Ability of medical students to calculate drug doses in children after their paediatric attachment
Directory of Open Access Journals (Sweden)
Oshikoya KA
2008-12-01
Full Text Available Dose calculation errors constitute a significant part of prescribing errors which might have resulted from informal teaching of the topic in medical schools. Objectives: To determine adequacy of knowledge and skills of drug dose calculations in children acquired by medical students during their clinical attachment in paediatrics.Methods: Fifty two 5th year medical students of the Lagos State University College of Medicine (LASUCOM, Ikeja were examined on drug dose calculations from a vial and ampoules of injections, syrup and suspension, and tablet formulation. The examination was with a structured questionnaire mostly in the form of multiple choice questions.Results: Thirty-six (69.2% and 30 (57.7% students were taught drug dose calculation in neonatal posting and during ward rounds/ bed-side teaching, respectively. Less than 50% of the students were able to calculate the correct doses of each of adrenaline, gentamicin, chloroquine and sodium bicarbonate injections required by the patient. Dose calculation was however relatively better with adrenalin when compared with the other injections. The proportion of female students that calculated the correct doses of quinine syrup and cefuroxime suspension were significantly higher than those of their male counterparts (p<0.05 and p<0.01, respectively; Chi-square test. When doses calculated in mg/dose and mL/dose was compared for adrenalin injection and each of quinine syrup and cefuroxime suspension, there were significant differences (adrenaline and quinine, p=0.005; adrenaline and cefuroxime, p=0.003: Fischer’s exact test. Dose calculation errors of similar magnitude to injections, syrup and suspension were also observed with tablet formulation.Conclusions: LASUCOM medical students lacked the basic knowledge of paediatric drug dose calculations but were willing to learn if the topic was formally taught. Drug dose calculations should be given a prominent consideration in the undergraduate medical
Radioactive cloud dose calculations
International Nuclear Information System (INIS)
Radiological dosage principles, as well as methods for calculating external and internal dose rates, following dispersion and deposition of radioactive materials in the atmosphere are described. Emphasis has been placed on analytical solutions that are appropriate for hand calculations. In addition, the methods for calculating dose rates from ingestion are discussed. A brief description of several computer programs are included for information on radionuclides. There has been no attempt to be comprehensive, and only a sampling of programs has been selected to illustrate the variety available
Population dose calculation technique
International Nuclear Information System (INIS)
An original method is suggested for calculating the population doses from gas and aerosol radioactive releases. The method is based on the assumption of uniform population and arable land distribution. The validity of this assumption has been proved for a rather large condition range. Though, some modified formulae are given to take into account the non-uniformity of population distribution, connected with large cities, on the one hand, and with woods, shores, regional borders, on the other hand. Employment of the suggested method results in an apriciable calculation accuracy rise for the long-living slowly precipitating radionuclides as compared with the existing methods
Weldon Spring dose calculations
International Nuclear Information System (INIS)
In response to a request by the Oak Ridge Operations (ORO) Office of the Department of Energy (DOE) for assistance to the Department of the Army (DA) on the decommissioning of the Weldon Spring Chemical Plant, the Health and Safety Research Division of the Oak Ridge National Laboratory (ORNL) performed limited dose assessment calculations for that site. Based upon radiological measurements from a number of soil samples analyzed by ORNL and from previously acquired radiological data for the Weldon Spring site, source terms were derived to calculate radiation doses for three specific site scenarios. These three hypothetical scenarios are: a wildlife refuge for hunting, fishing, and general outdoor recreation; a school with 40 hr per week occupancy by students and a custodian; and a truck farm producing fruits, vegetables, meat, and dairy products which may be consumed on site. Radiation doses are reported for each of these scenarios both for measured uranium daughter equilibrium ratios and for assumed secular equilibrium. Doses are lower for the nonequilibrium case
Evaluation of radiation doses from radioactive drugs
International Nuclear Information System (INIS)
Radioactive new drugs are regulated by the Food and Drug Administration (FDA) in the United States. Before a new drug can be marketed it must have an approved New Drug Application (NDA). Clinical investigations of a radioactive new drug are carried out under a Notice of Claimed Investigational Exemption for a New Drug (IND), submitted to the FDA. In the review of the IND, radiation doses are projected on the basis of experimental data from animal models and from calculations based upon radiation characteristics, predicted biodistribution of the drug in humans, and activity to be administered. FDA physicians review anticipated doses and prevent clinical investigations in humans when the potential risk of the use of a radioactive substance outweighs the prospect of achieving beneficial results from the administration of the drug. In the evaluation of an NDA, FDA staff attempt to assure that the intended diagnostic or therapeutic effect is achievable with the lowest practicable radiation dose. Radiation doses from radioactive new drugs are evaluated by physicians within the FDA. Important radioactive new drugs are also evaluated by the Radiopharmaceuticals Advisory Committee. FDA also supports the Center for Internal Radiation Dosimetry at Oak Ridge, to provide information regarding in vivo distribution and dosimetry to critical organs and the whole body from radioactive new drugs. The process for evaluation of radiation doses from radioactive new drugs for protection against use of unnecessary radiation exposure by patients in nuclear medicine procedures, a
Prenatal radiation exposure. Dose calculation
International Nuclear Information System (INIS)
The unborn child requires special protection. In this context, the indication for an X-ray examination is to be checked critically. If thereupon radiation of the lower abdomen including the uterus cannot be avoided, the examination should be postponed until the end of pregnancy or alternative examination techniques should be considered. Under certain circumstances, either accidental or in unavoidable cases after a thorough risk assessment, radiation exposure of the unborn may take place. In some of these cases an expert radiation hygiene consultation may be required. This consultation should comprise the expected risks for the unborn while not perturbing the mother or the involved medical staff. For the risk assessment in case of an in-utero X-ray exposition deterministic damages with a defined threshold dose are distinguished from stochastic damages without a definable threshold dose. The occurrence of deterministic damages depends on the dose and the developmental stage of the unborn at the time of radiation. To calculate the risks of an in-utero radiation exposure a three-stage concept is commonly applied. Depending on the amount of radiation, the radiation dose is either estimated, roughly calculated using standard tables or, in critical cases, accurately calculated based on the individual event. The complexity of the calculation thereby increases from stage to stage. An estimation based on stage one is easily feasible whereas calculations based on stages two and especially three are more complex and often necessitate execution by specialists. This article demonstrates in detail the risks for the unborn child pertaining to its developmental phase and explains the three-stage concept as an evaluation scheme. It should be noted, that all risk estimations are subject to considerable uncertainties.
Directory of Open Access Journals (Sweden)
Gracieli Prado Elias
2005-06-01
Full Text Available The present study was conducted to evaluate the utilization of Clark's, Salisbury and Penna's rules and the Body Surface Area (BSA formula for calculation of pediatric drug dosage, as well as their reliability and viability in the clinical use. These rules are frequently cited in the literature, but much controversy still exists with regards to their use. The pediatric drug dosage was calculated by utilization of the aforementioned rules and using the drugs Paracetamol, Dipyrone, Diclofenac Potassium, Nimesulide, Amoxicillin and Erythromycin, widely employed in Pediatric Dentistry. Weight and body surface areas were considered of children with ages between 1 and 12 years old as well as the dosage for the adult. The pediatric dosages achieved were compared to the predetermined dosages in mg kg-1 herein-named standard dosages. The results were submitted to the parametric test ANOVA and to the Tukey test (pO presente estudo foi realizado com a finalidade de avaliar as fórmulas de Clark, Salisbury, Área da Superfície Corpórea (ASC e Penna, quanto a sua confiabilidade e viabilidade de uso clínico para o cálculo de doses medicamentosas infantis, uma vez que tais fórmulas são freqüentemente citadas na literatura, mas muita controvérsia ainda existe com relação ao seu uso. As doses infantis foram calculadas utilizando as fórmulas descritas e os medicamentos Paracetamol, Dipirona, Diclofenaco de Potássio, Nimesulida, Amoxicilina e Eritromicina, largamente usados na clínica odontopediátrica. Foram considerados parâmetros como o peso e área da superfície corpórea de crianças com idades entre 1 e 12 anos e a dose para o adulto. As doses obtidas foram comparadas às doses em mg/kg consideradas como padrão de referência para os medicamentos. Os resultados foram submetidos ao teste paramétrico ANOVA e de Tukey (P<0,05. Os antibióticos e o Diclofenaco propiciam utilização aceitável das fórmulas na Odontopediatria, porém para a
Calculational Tool for Skin Contamination Dose Assessment
Hill, R L
2002-01-01
Spreadsheet calculational tool was developed to automate the calculations preformed for dose assessment of skin contamination. This document reports on the design and testing of the spreadsheet calculational tool.
Tank Z-361 dose rate calculations
International Nuclear Information System (INIS)
Neutron and gamma ray dose rates were calculated above and around the 6-inch riser of tank Z-361 located at the Plutonium Finishing Plant. Dose rates were also determined off of one side of the tank. The largest dose rate 0.029 mrem/h was a gamma ray dose and occurred 76.2 cm (30 in.) directly above the open riser. All other dose rates were negligible. The ANSI/ANS 1991 flux to dose conversion factor for neutrons and photons were used in this analysis. Dose rates are reported in units of mrem/h with the calculated uncertainty shown within the parentheses
Basak, Tulay; Yildiz, Dilek
2014-01-01
Objective: The aim of this study was to compare the effectiveness of cooperative learning and traditional learning methods on the development of drug-calculation skills. Design: Final-year nursing students ("n" = 85) undergoing internships during the 2010-2011 academic year at a nursing school constituted the study group of this…
Methods of bone marrow dose calculation
International Nuclear Information System (INIS)
Several methods of bone marrow dose calculation for photon irradiation were analised. After a critical analysis, the author proposes the adoption, by the Instituto de Radioprotecao e Dosimetria/CNEN, of Rosenstein's method for dose calculations in Radiodiagnostic examinations and Kramer's method in case of occupational irradiation. It was verified by Eckerman and Simpson that for monoenergetic gamma emitters uniformly distributed within the bone mineral of the skeleton the dose in the bone surface can be several times higher than dose in skeleton. In this way, is also proposed the Calculation of tissue-air ratios for bone surfaces in some irradiation geometries and photon energies to be included in the Rosenstein's method for organ dose calculation in Radiodiagnostic examinations. (Author)
Dose calculation system for remotely supporting radiotherapy
International Nuclear Information System (INIS)
The dose calculation system IMAGINE is being developed keeping in mind remotely supporting external radiation therapy using photon beams. The system is expected to provide an accurate picture of the dose distribution in a patient body, using a Monte Carlo calculation that employs precise models of the patient body and irradiation head. The dose calculation will be performed utilising super-parallel computing at the dose calculation centre, which is equipped with the ITBL computer, and the calculated results will be transferred through a network. The system is intended to support the quality assurance of current, widely carried out radiotherapy and, further, to promote the prevalence of advanced radiotherapy. Prototypes of the modules constituting the system have already been constructed and used to obtain basic data that are necessary in order to decide on the concrete design of the system. The final system will be completed in 2007. (authors)
Equivalent-spherical-shield neutron dose calculations
International Nuclear Information System (INIS)
Neutron doses through 162-cm-thick spherical shields were calculated to be 1090 and 448 mrem/h for regular and magnetite concrete, respectively. These results bracket the measured data, for reinforced regular concrete, of /approximately/600 mrem/h. The calculated fraction of the high-energy (>20 MeV) dose component also bracketed the experimental data. The measured and calculated doses were for a graphite beam stop bombarded with 100 nA of 800-MeV protons. 6 refs., 2 figs., 1 tab
Radiological Dose Calculations for Fusion Facilities
Energy Technology Data Exchange (ETDEWEB)
Michael L. Abbott; Lee C. Cadwallader; David A. Petti
2003-04-01
This report summarizes the results and rationale for radiological dose calculations for the maximally exposed individual during fusion accident conditions. Early doses per unit activity (Sieverts per TeraBecquerel) are given for 535 magnetic fusion isotopes of interest for several release scenarios. These data can be used for accident assessment calculations to determine if the accident consequences exceed Nuclear Regulatory Commission and Department of Energy evaluation guides. A generalized yearly dose estimate for routine releases, based on 1 Terabecquerel unit releases per radionuclide, has also been performed using averaged site parameters and assumed populations. These routine release data are useful for assessing designs against US Environmental Protection Agency yearly release limits.
Historical river flow rates for dose calculations
International Nuclear Information System (INIS)
Annual average river flow rates are required input to the LADTAP Computer Code for calculating offsite doses from liquid releases of radioactive materials to the Savannah River. The source of information on annual river flow rates used in dose calculations varies, depending on whether calculations are for retrospective releases or prospective releases. Examples of these types of releases are: Retrospective - releases from routine operations (annual environmental reports) and short term release incidents that have occurred. Prospective - releases that might be expected in the future from routine or abnormal operation of existing or new facilities (EIS's, EID'S, SAR'S, etc.). This memorandum provides historical flow rates at the downstream gauging station at Highway 301 for use in retrospective dose calculations and derives flow rate data for the Beaufort-Jasper and Port Wentworth water treatment plants
Validation of dose calculation programmes for recycling
International Nuclear Information System (INIS)
This report contains the results from an international project initiated by the SSI in 1999. The primary purpose of the project was to validate some of the computer codes that are used to estimate radiation doses due to the recycling of scrap metal. The secondary purpose of the validation project was to give a quantification of the level of conservatism in clearance levels based on these codes. Specifically, the computer codes RESRAD-RECYCLE and CERISE were used to calculate radiation doses to individuals during the processing of slightly contaminated material, mainly in Studsvik, Sweden. Calculated external doses were compared with measured data from different steps of the process. The comparison of calculations and measurements shows that the computer code calculations resulted in both overestimations and underestimations of the external doses for different recycling activities. The SSI draws the conclusion that the accuracy is within one order of magnitude when experienced modellers use their programmes to calculate external radiation doses for a recycling process involving material that is mainly contaminated with cobalt-60. No errors in the codes themselves were found. Instead, the inaccuracy seems to depend mainly on the choice of some modelling parameters related to the receptor (e.g., distance, time, etc.) and simplifications made to facilitate modelling with the codes (e.g., object geometry). Clearance levels are often based on studies on enveloping scenarios that are designed to cover all realistic exposure pathways. It is obvious that for most practical cases, this gives a margin to the individual dose constraint (in the order of 10 micro sievert per year within the EC). This may be accentuated by the use of conservative assumptions when modelling the enveloping scenarios. Since there can obviously be a fairly large inaccuracy in the calculations, it seems reasonable to consider some degree of conservatism when establishing clearance levels based on
Evolution of dose distribution calculations in brachytherapy
International Nuclear Information System (INIS)
In this report the evolution of dose distribution calculations is revised in detail, considering the simplest case (a point source in free space) and the more complex situation of a real encapsulated line source embedded in a scattering medium. The most recent formalism to perform the dosimetry of interstitial brachytherapy sources is presented, where measured or measurable dose rates from actual sources in a tissue equivalent phantom are required as input data
Multigroup neutron dose calculations for proton therapy
International Nuclear Information System (INIS)
We have developed tools for the preparation of coupled multigroup proton/neutron cross section libraries. Our method is to use NJOY to process evaluated nuclear data files for incident particles below 150 MeV and MCNPX to produce data for higher energies. We modified the XSEX3 program of the MCNPX code system to produce Legendre expansions of scattering matrices generated by sampling the physics models that are comparable to the output of the GROUPR routine of NJOY. Our code combines the low and high energy scattering data with user input stopping powers and energy deposition cross sections that we also calculated using MCNPX. Our code also calculates momentum transfer coefficients for the library and optionally applies an energy straggling model to the scattering cross sections and stopping powers. The motivation was initially for deterministic solution of space radiation shielding calculations using Attila, but noting that proton therapy treatment planning may neglect secondary neutron dose assessments because of difficulty and expense, we have also investigated the feasibility of multi group methods for this application. We have shown that multigroup MCNPX solutions for secondary neutron dose compare well with continuous energy solutions and are obtainable with less than half computational cost. This efficiency comparison neglects the cost of preparing the library data, but this becomes negligible when distributed over many multi group calculations. Our deterministic calculations illustrate recognized obstacles that may have to be overcome before discrete ordinates methods can be efficient alternatives for proton therapy neutron dose calculations
Multigroup neutron dose calculations for proton therapy
Energy Technology Data Exchange (ETDEWEB)
Kelsey Iv, Charles T [Los Alamos National Laboratory; Prinja, Anil K [Los Alamos National Laboratory
2009-01-01
We have developed tools for the preparation of coupled multigroup proton/neutron cross section libraries. Our method is to use NJOY to process evaluated nuclear data files for incident particles below 150 MeV and MCNPX to produce data for higher energies. We modified the XSEX3 program of the MCNPX code system to produce Legendre expansions of scattering matrices generated by sampling the physics models that are comparable to the output of the GROUPR routine of NJOY. Our code combines the low and high energy scattering data with user input stopping powers and energy deposition cross sections that we also calculated using MCNPX. Our code also calculates momentum transfer coefficients for the library and optionally applies an energy straggling model to the scattering cross sections and stopping powers. The motivation was initially for deterministic solution of space radiation shielding calculations using Attila, but noting that proton therapy treatment planning may neglect secondary neutron dose assessments because of difficulty and expense, we have also investigated the feasibility of multi group methods for this application. We have shown that multigroup MCNPX solutions for secondary neutron dose compare well with continuous energy solutions and are obtainable with less than half computational cost. This efficiency comparison neglects the cost of preparing the library data, but this becomes negligible when distributed over many multi group calculations. Our deterministic calculations illustrate recognized obstacles that may have to be overcome before discrete ordinates methods can be efficient alternatives for proton therapy neutron dose calculations.
Agriculture-related radiation dose calculations
International Nuclear Information System (INIS)
Estimates of radiation dose to the public must be made at each stage in the identification and qualification process leading to siting a high-level nuclear waste repository. Specifically considering the ingestion pathway, this paper examines questions of reliability and adequacy of dose calculations in relation to five stages of data availability (geologic province, region, area, location, and mass balance) and three methods of calculation (population, population/food production, and food production driven). Calculations were done using the model PABLM with data for the Permian and Palo Duro Basins and the Deaf Smith County area. Extra effort expended in gathering agricultural data at succeeding environmental characterization levels does not appear justified, since dose estimates do not differ greatly; that effort would be better spent determining usage of food types that contribute most to the total dose; and that consumption rate and the air dispersion factor are critical to assessment of radiation dose via the ingestion pathway. 17 refs., 9 figs., 32 tabs
Agriculture-related radiation dose calculations
Energy Technology Data Exchange (ETDEWEB)
Furr, J.M.; Mayberry, J.J.; Waite, D.A.
1987-10-01
Estimates of radiation dose to the public must be made at each stage in the identification and qualification process leading to siting a high-level nuclear waste repository. Specifically considering the ingestion pathway, this paper examines questions of reliability and adequacy of dose calculations in relation to five stages of data availability (geologic province, region, area, location, and mass balance) and three methods of calculation (population, population/food production, and food production driven). Calculations were done using the model PABLM with data for the Permian and Palo Duro Basins and the Deaf Smith County area. Extra effort expended in gathering agricultural data at succeeding environmental characterization levels does not appear justified, since dose estimates do not differ greatly; that effort would be better spent determining usage of food types that contribute most to the total dose; and that consumption rate and the air dispersion factor are critical to assessment of radiation dose via the ingestion pathway. 17 refs., 9 figs., 32 tabs.
Dose calculation in brachytherapy with microcomputers
International Nuclear Information System (INIS)
The computer algorithms, that allow the calculation of brachytherapy doses and its graphic representation for implants, using programs developed for Pc microcomputers are presented. These algorithms allow to localized the sources in space, from their projection in radiographics images and trace isodose counter. (C.G.C.)
Calculation of external dose from distributed source
International Nuclear Information System (INIS)
This paper discusses a relatively simple calculational method, called the point kernel method (Fo68), for estimating external dose from distributed sources that emit photon or electron radiations. The principles of the point kernel method are emphasized, rather than the presentation of extensive sets of calculations or tables of numerical results. A few calculations are presented for simple source geometries as illustrations of the method, and references and descriptions are provided for other caluclations in the literature. This paper also describes exposure situations for which the point kernel method is not appropriate and other, more complex, methods must be used, but these methods are not discussed in any detail
Dose calculations for intakes of ore dust
International Nuclear Information System (INIS)
This report describes a methodology for calculating the committed effective dose for mixtures of radionuclides, such as those which occur in natural radioactive ores and dusts. The formulae are derived from first principles, with the use of reasonable assumptions concerning the nature and behaviour of the radionuclide mixtures. The calculations are complicated because these 'ores' contain a range of particle sizes, have different degrees of solubility in blood and other body fluids, and also have different biokinetic clearance characteristics from the organs and tissues in the body. The naturally occurring radionuclides also tend to occur in series, i.e. one is produced by the radioactive decay of another 'parent' radionuclide. The formulae derived here can be used, in conjunction with a model such as LUDEP, for calculating total dose resulting from inhalation and/or ingestion of a mixture of radionuclides, and also for deriving annual limits on intake and derived air concentrations for these mixtures
Recommendations for Insulin Dose Calculator Risk Management
Rees, Christen
2014-01-01
Several studies have shown the usefulness of an automated insulin dose bolus advisor (BA) in achieving improved glycemic control for insulin-using diabetes patients. Although regulatory agencies have approved several BAs over the past decades, these devices are not standardized in their approach to dosage calculation and include many features that may introduce risk to patients. Moreover, there is no single standard of care for diabetes worldwide and no guidance documents for BAs, specificall...
Phantoms for calculations of absorbed organ dose
International Nuclear Information System (INIS)
We have developed a computer code IDES (Internal Dose Estimation System). In this code, MIRD Transformation Method is used and photon simulation by Monte Carlo method is also possible. We have studied Japanese phantoms in two procedures, mathematical phantom and 'symbol phantoms'. Our mathematical phantoms realize their height and body weights but does not hold some of organ weights, which were measured by TANAKA and KAWAMURA. The symbol phantom can solve this discrepancy and realize a realistic phantom, although it remains problems of authorization and normalization. Errors were estimated for internal dose calculations and it was pointed out that to use realistic organ weights and parameters of kinetics was important competitively to reduce uncertainty of the results. (author)
Annual dose rate calculations for thermoluminescence dating
International Nuclear Information System (INIS)
Tabulations of decay data and dose rate calculations that are necessary for TL dating are presented. An effort has been made to collect the latest evaluated data and to catalog them in a form that is easily accessible, so that they may be updated as new revised values are reported. It is suggested that the largest error in thermoluminescence dating will come from sources other than the tabulated particle energies and branching ratios. These include: (a) the alpha to beta thermoluminescence efficiency determination; (b) concentration measurements of K, Rb, Th, and U; (c) all departures from secular equilibrium in the uranium and thorium decay chains; and (d) the imprecise calibration of laboratory radiation sources
Paramedics’ Ability to Perform Drug Calculations
Directory of Open Access Journals (Sweden)
Eastwood, Kathyrn J
2009-11-01
Full Text Available Background: The ability to perform drug calculations accurately is imperative to patient safety. Research into paramedics’ drug calculation abilities was first published in 2000 and for nurses’ abilities the research dates back to the late 1930s. Yet, there have been no studies investigating an undergraduate paramedic student’s ability to perform drug or basic mathematical calculations. The objective of this study was to review the literature and determine the ability of undergraduate and qualified paramedics to perform drug calculations.Methods: A search of the prehospital-related electronic databases was undertaken using the Ovid and EMBASE systems available through the Monash University Library. Databases searched included the Cochrane Central Register of Controlled Trials (CENTRAL, MEDLINE, CINAHL, JSTOR, EMBASE and Google Scholar, from their beginning until the end of August 2009. We reviewed references from articles retrieved.Results: The electronic database search located 1,154 articles for review. Six additional articles were identified from reference lists of retrieved articles. Of these, 59 were considered relevant. After reviewing the 59 articles only three met the inclusion criteria. All articles noted some level of mathematical deficiencies amongst their subjects.Conclusions: This study identified only three articles. Results from these limited studies indicate a significant lack of mathematical proficiency amongst the paramedics sampled. A need exists to identify if undergraduate paramedic students are capable of performing the required drug calculations in a non-clinical setting.[WestJEM. 2009;10:240-243.
Recommendations for Insulin Dose Calculator Risk Management
2014-01-01
Several studies have shown the usefulness of an automated insulin dose bolus advisor (BA) in achieving improved glycemic control for insulin-using diabetes patients. Although regulatory agencies have approved several BAs over the past decades, these devices are not standardized in their approach to dosage calculation and include many features that may introduce risk to patients. Moreover, there is no single standard of care for diabetes worldwide and no guidance documents for BAs, specifically. Given the emerging and more stringent regulations on software used in medical devices, the approval process is becoming more difficult for manufacturers to navigate, with some manufacturers opting to remove BAs from their products altogether. A comprehensive literature search was performed, including publications discussing: diabetes BA use and benefit, infusion pump safety and regulation, regulatory submissions, novel BAs, and recommendations for regulation and risk management of BAs. Also included were country-specific and international guidance documents for medical device, infusion pump, medical software, and mobile medical application risk management and regulation. No definitive worldwide guidance exists regarding risk management requirements for BAs, specifically. However, local and international guidance documents for medical devices, infusion pumps, and medical device software offer guidance that can be applied to this technology. In addition, risk management exercises that are algorithm-specific can help prepare manufacturers for regulatory submissions. This article discusses key issues relevant to BA use and safety, and recommends risk management activities incorporating current research and guidance. PMID:24876550
DEFF Research Database (Denmark)
Faralli, Adele; Melander, Fredrik; Larsen, Esben Kjær Unmack;
2014-01-01
Polyethylene glycol (PEG)-based hydrogels are widely used for biomedical applications, including matrices for controlled drug release. We present a method for defining drug dosing in screening assays by light-activated cross-linking of PEG-diacrylate hydrogels with embedded drug-loaded liposome n...
PRDC - A software package for personnel radiation dose calculation
International Nuclear Information System (INIS)
To determine effective dose, we usually need to use a very complicated human body model and a sophisticated computer code to transport radiations in the body model and surrounding medium, which is not very easy to practicing health physicists in the field. This study develops and tests a software package, called PRDC (Personnel Radiation Dose Calculation), which calculates effective dose and radiation doses to various organs/tissues and personal dosemeters based on a series of interpolations. (authors)
Monte Carlo dose calculations for dynamic IMRT treatments
International Nuclear Information System (INIS)
Dose calculations for intensity modulated radiation therapy (IMRT) face new challenges due to the complex leaf geometry and time dependent nature of the delivery. A fast method of particle transport through a dynamic multileaf collimator (MLC) geometry that accounts for photon attenuation and first-scattered Compton photon production has been incorporated into an existing Monte Carlo code used for patient dose calculations. Dosimetric agreement between calculation and measurement for two photon energies and MLC types is within experimental error for the sliding window tests. For a patient IMRT field, the Monte Carlo calculations are closer to measured dose than similar superposition or pencil beam calculations. (author)
Is it worth to calculate the dose of radioiodine?
International Nuclear Information System (INIS)
Full text: Administration of empirical doses of radioiodine (RAI) has been preferred to calculated doses in many hospitals, because the need to measure the size and the iodine uptake in the thyroid involves considerable inconvenience to the patient and additional costs. The preparation of RAI of varying activities also means extra work. Today there is no general consensus on whether radioiodine should be given as a fixed dose or should be calculated. There is also no consensus regarding the question of which radiation burden should be administered to a given volume of thyroid if the activity is calculated. However, while it is possible to deliver a relatively precise dose of radiation to the thyroid gland, maybe it is worth doing this?The aim of this study was to investigate the results of different uptake and volume dependent target doses on clinical outcome of patients with hyperthyroidism in Graves' disease, multi-nodular toxic goiter or toxic adenoma after radioiodine therapy. We reviewed the records of 428 patients (389 women and 39 men, mean age 56.8±12.9 years) who had received radioiodine treatment for Graves' disease and multinodular toxic goiter (n=312) or toxic adenoma (n=116) during the period of 2000-2004 in Kaunas Medical University Hospital. Most patients were given antithyroid drug therapy in order to achieve euthyroidism before treatment with RAI. Radioiodine uptake test with repeated measurements at 2, 6, 24, 48 and/or 72 and/or 96 hr to define the effective half-life was performed. In addition, all the patients underwent thyroid ultrasonography and scintigraphy to define the volume of the thyroid. The 131I activities were calculated according to the formula of Marinelli. In addition to the normal calculation individual target doses were adjusted to the thyroid volumes of each patient before therapy. For statistical evaluation, the patients were divided into four groups: group I included those with a thyroid volume 51 ml. Statistical analysis was
DICOM organ dose does not accurately represent calculated dose in mammography
Suleiman, Moayyad E.; Brennan, Patrick C.; McEntee, Mark F.
2016-03-01
This study aims to analyze the agreement between the mean glandular dose estimated by the mammography unit (organ dose) and mean glandular dose calculated using Dance et al published method (calculated dose). Anonymised digital mammograms from 50 BreastScreen NSW centers were downloaded and exposure information required for the calculation of dose was extracted from the DICOM header along with the organ dose estimated by the system. Data from quality assurance annual tests for the included centers were collected and used to calculate the mean glandular dose for each mammogram. Bland-Altman analysis and a two-tailed paired t-test were used to study the agreement between calculated and organ dose and the significance of any differences. A total of 27,869 dose points from 40 centers were included in the study, mean calculated dose and mean organ dose (+/- standard deviation) were 1.47 (+/-0.66) and 1.38 (+/-0.56) mGy respectively. A statistically significant 0.09 mGy bias (t = 69.25; p<0.0001) with 95% limits of agreement between calculated and organ doses ranging from -0.34 and 0.52 were shown by Bland-Altman analysis, which indicates a small yet highly significant difference between the two means. The use of organ dose for dose audits is done at the risk of over or underestimating the calculated dose, hence, further work is needed to identify the causal agents for differences between organ and calculated doses and to generate a correction factor for organ dose.
Study of dose calculation on breast brachytherapy using prism TPS
International Nuclear Information System (INIS)
PRISM is one of non-commercial Treatment Planning System (TPS) and is developed at the University of Washington. In Indonesia, many cancer hospitals use expensive commercial TPS. This study aims to investigate Prism TPS which been applied to the dose distribution of brachytherapy by taking into account the effect of source position and inhomogeneities. The results will be applicable for clinical Treatment Planning System. Dose calculation has been implemented for water phantom and CT scan images of breast cancer using point source and line source. This study used point source and line source and divided into two cases. On the first case, Ir-192 seed source is located at the center of treatment volume. On the second case, the source position is gradually changed. The dose calculation of every case performed on a homogeneous and inhomogeneous phantom with dimension 20 × 20 × 20 cm3. The inhomogeneous phantom has inhomogeneities volume 2 × 2 × 2 cm3. The results of dose calculations using PRISM TPS were compared to literature data. From the calculation of PRISM TPS, dose rates show good agreement with Plato TPS and other study as published by Ramdhani. No deviations greater than ±4% for all case. Dose calculation in inhomogeneous and homogenous cases show similar result. This results indicate that Prism TPS is good in dose calculation of brachytherapy but not sensitive for inhomogeneities. Thus, the dose calculation parameters developed in this study were found to be applicable for clinical treatment planning of brachytherapy
Study of dose calculation on breast brachytherapy using prism TPS
Fendriani, Yoza; Haryanto, Freddy
2015-09-01
PRISM is one of non-commercial Treatment Planning System (TPS) and is developed at the University of Washington. In Indonesia, many cancer hospitals use expensive commercial TPS. This study aims to investigate Prism TPS which been applied to the dose distribution of brachytherapy by taking into account the effect of source position and inhomogeneities. The results will be applicable for clinical Treatment Planning System. Dose calculation has been implemented for water phantom and CT scan images of breast cancer using point source and line source. This study used point source and line source and divided into two cases. On the first case, Ir-192 seed source is located at the center of treatment volume. On the second case, the source position is gradually changed. The dose calculation of every case performed on a homogeneous and inhomogeneous phantom with dimension 20 × 20 × 20 cm3. The inhomogeneous phantom has inhomogeneities volume 2 × 2 × 2 cm3. The results of dose calculations using PRISM TPS were compared to literature data. From the calculation of PRISM TPS, dose rates show good agreement with Plato TPS and other study as published by Ramdhani. No deviations greater than ±4% for all case. Dose calculation in inhomogeneous and homogenous cases show similar result. This results indicate that Prism TPS is good in dose calculation of brachytherapy but not sensitive for inhomogeneities. Thus, the dose calculation parameters developed in this study were found to be applicable for clinical treatment planning of brachytherapy.
Fast dose calculation in magnetic fields with GPUMCD
Energy Technology Data Exchange (ETDEWEB)
Hissoiny, S; Ozell, B [Ecole Polytechnique de Montreal, Departement de genie informatique et genie logiciel, 2500 Chemin de Polytechnique, Montreal, Quebec H3T 1J4 (Canada); Raaijmakers, A J E; Raaymakers, B W [Department of Radiotherapy, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht (Netherlands); Despres, P, E-mail: sami.hissoiny@polymtl.ca [Departement de physique, Universite Laval, Quebec (Canada)
2011-08-21
A new hybrid imaging-treatment modality, the MRI-Linac, involves the irradiation of the patient in the presence of a strong magnetic field. This field acts on the charged particles, responsible for depositing dose, through the Lorentz force. These conditions require a dose calculation engine capable of taking into consideration the effect of the magnetic field on the dose distribution during the planning stage. Also in the case of a change in anatomy at the time of treatment, a fast online replanning tool is desirable. It is improbable that analytical solutions such as pencil beam calculations can be efficiently adapted for dose calculations within a magnetic field. Monte Carlo simulations have therefore been used for the computations but the calculation speed is generally too slow to allow online replanning. In this work, GPUMCD, a fast graphics processing unit (GPU)-based Monte Carlo dose calculation platform, was benchmarked with a new feature that allows dose calculations within a magnetic field. As a proof of concept, this new feature is validated against experimental measurements. GPUMCD was found to accurately reproduce experimental dose distributions according to a 2%-2 mm gamma analysis in two cases with large magnetic field-induced dose effects: a depth-dose phantom with an air cavity and a lateral-dose phantom surrounded by air. Furthermore, execution times of less than 15 s were achieved for one beam in a prostate case phantom for a 2% statistical uncertainty while less than 20 s were required for a seven-beam plan. These results indicate that GPUMCD is an interesting candidate, being fast and accurate, for dose calculations for the hybrid MRI-Linac modality.
Aviation route dose calculation and its numerical basis
International Nuclear Information System (INIS)
The European Directive 96/12 requires that aircrew be considered as occupationally exposed persons and that measures are taken to determine the individual doses of air crew and cabin personnel. Consequently, several European research institutes have undertaken an extensive programme of air borne and mountain based experiments to measure the radiation field in the earth's atmosphere. Furthermore, Monte Carlo radiation transport calculations were done to follow the radiation cascades from the top of the atmosphere down to the earth's surface. Though the basic physical processes and radiation components have been studied previously, the determination of dose quantities require more physical information: Both operational (ambient dose equivalent) and risk related quantities (effective dose) contain non-physical information which is described by quality and radiation weighting factors, respectively. The radiation transport calculations show that at normal flight altitudes the spectral shapes of the particle fluences are essentially invariable. This permits to use calculated conversion coefficients to determine the dose quantities from calculated and experimental spectral data. This appears necessary especially for those radiation components whose dose contribution can not experimentally separated, but may considerably contribute to the effective dose considering the radiation factors presently recommended by the ICRP, e.g. for protons. The European Computer Package EPCARD for the Calculation of Aviation Route Doses was designed to combine the experimental and theoretical data in the best available way. The concept is to treat each major component of the cosmic rays separately, i.e. muons, electrons and photons, neutrons, protons and charged particles. The influence of geomagnetic shielding is considered based on calculations and experimental data, and the magnitude of solar modulation is inferred from neutron monitor data. Route doses are calculated along any specified
A program for synchrotron radiation dose calculations
International Nuclear Information System (INIS)
The computer program PHOTON was obtained from Brookhaven National Laboratory (courtesy D. Chapman, NSLS), and has now been installed at APS VAX. In the following a brief description of the program and how to access to it is described with an example. A detailed manual for the program is also available. The program is developed to calculate the transmitted and scattered spectra of the synchrotron radiation, as it passes through series of filters. The source can be a bending magnet or a wiggler. This can be generated for any bending magnet or a wiggler source by varying ring energy, the critical energy and opening angles of the radiation beam. Monochromatic beams to white radiation can be treated. Filter materials can be pure elements or composites. The absorption cross-sections of all elements for covering 10-2 to 106 keV are now included in a table, which can be accessed by giving the atomic symbol
Weighting of secondary radiations in organ dose calculations
International Nuclear Information System (INIS)
The current system of dose quantities in radiological protection is based, in addition to the absorbed dose, on the concepts of equivalent dose and effective dose. This system has been developed mainly with uniform whole-body exposures in mind. Conceptual and practical problems arise when the system is applied to more general exposure situations where the radiation quality is altered within the human body. In this article these problems are discussed, using proton beam radiotherapy as a specific example, and a proposition is made that dose equivalent quantities should be used instead of equivalent doses when organ doses are of interest. The calculations of out-of-field organ doses in proton therapy show that the International Commission on Radiological Protection-prescribed use of the proton weighting factor generally leads to an underestimation of the stochastic risks, while the use of neutron weighting factors in the way as practised in the literature leads to a significant overestimation of these risks. (authors)
International Nuclear Information System (INIS)
The Hanford Dose Overview Program is a Hanford site-wide service established to provide a method of assuring the consistency of Hanford-related environmental dose assessments. This document serves as a guide to the Hanford contractors for obtaining or performing Hanford-related environmental dose calculations. The program serves as a focal point for Hanford environmental dose calculation activities and provides a number of services for Hanford contractors involved in calculation of environmental doses. Site specific input data and assumptions have been compiled and are maintained for use by the contractors in calculating Hanford environmental doses. The data and assumptions, to the extent they apply, should be used in Hanford calculations. These data are not all inclusive and will be modified should additional or more appropriate information become available
Biases affecting injected doses of an experimental drug during clinical trials
Perrottet, Nancy; Brunner-Ferber, Françoise; Grouzmann, Eric; Spertini, François; Biollaz, Jérôme; Buclin, Thierry; Widmer, Nicolas
2016-01-01
Background During clinical trials, researchers rarely question nominal doses specified on labels of investigational products, overlooking the potential for inaccuracies that may result when calculating pharmacokinetic and pharmacodynamic parameters. This study evaluated the disparity between nominal doses and the doses actually administered in two Phase I trials of a biosimilar drug. Methods In Trial A, 12 healthy volunteers received various doses of an interferon β-1a biosimilar via either s...
Application of a sitting MIRD phantom for effective dose calculations
International Nuclear Information System (INIS)
In typical realistic scenarios, dose factors due to 60Co contaminated steel, used in consumer products, cannot be approximated by standard exposure geometries. It is then necessary to calculate the effective dose using an appropriate anthropomorphic phantom. MCNP calculations were performed using a MIRD human model in two settings. In the first, a male office worker is sitting in a chair containing contaminated steel, surrounded by contaminated furniture. In the second, a male driver is seated inside an automobile, the steel of which is uniformly contaminated. To accurately calculate the dose to lower body organs, especially the gonads, it was essential to modify the MIRD model to simulate two sitting postures: chair and driving position. The phantom modifications are described, and the results of the calculations are presented. In the case of the automobile scenarios, results are compared to those obtained using an isotropic fluence-to-dose conversion function. (authors)
Verification of Calculated Skin Doses in Postmastectomy Helical Tomotherapy
International Nuclear Information System (INIS)
Purpose: To verify the accuracy of calculated skin doses in helical tomotherapy for postmastectomy radiation therapy (PMRT). Methods and Materials: In vivo thermoluminescent dosimeters (TLDs) were used to measure the skin dose at multiple points in each of 14 patients throughout the course of treatment on a TomoTherapy Hi.Art II system, for a total of 420 TLD measurements. Five patients were evaluated near the location of the mastectomy scar, whereas 9 patients were evaluated throughout the treatment volume. The measured dose at each location was compared with calculations from the treatment planning system. Results: The mean difference and standard error of the mean difference between measurement and calculation for the scar measurements was -1.8% ± 0.2% (standard deviation [SD], 4.3%; range, -11.1% to 10.6%). The mean difference and standard error of the mean difference between measurement and calculation for measurements throughout the treatment volume was -3.0% ± 0.4% (SD, 4.7%; range, -18.4% to 12.6%). The mean difference and standard error of the mean difference between measurement and calculation for all measurements was -2.1% ± 0.2% (standard deviation, 4.5%: range, -18.4% to 12.6%). The mean difference between measured and calculated TLD doses was statistically significant at two standard deviations of the mean, but was not clinically significant (i.e., was <5%). However, 23% of the measured TLD doses differed from the calculated TLD doses by more than 5%. Conclusions: The mean of the measured TLD doses agreed with TomoTherapy calculated TLD doses within our clinical criterion of 5%.
Outline of the dose calculation system imagine for radiotherapy
International Nuclear Information System (INIS)
The dose calculation system IMAGINE is under development for supporting X-ray radiotherapy by rapidly providing the accurate dose distribution in a patient body utilizing precise models of the patient body and accelerator assembly incorporated with Monte Carlo calculations. The system will be used for the quality assurance of the current radiotherapy widely carried out at present, and further for promoting the prevalence of advanced therapy. The system is scheduled to be completed in 2007 after the five-year project. (author)
Study of dose calculation on breast brachytherapy using prism TPS
Energy Technology Data Exchange (ETDEWEB)
Fendriani, Yoza; Haryanto, Freddy [Nuclear Physics and Biophysics Research Division, FMIPA Institut Teknologi Bandung, Physics Buildings, Jl. Ganesha 10, Bandung 40132 (Indonesia)
2015-09-30
PRISM is one of non-commercial Treatment Planning System (TPS) and is developed at the University of Washington. In Indonesia, many cancer hospitals use expensive commercial TPS. This study aims to investigate Prism TPS which been applied to the dose distribution of brachytherapy by taking into account the effect of source position and inhomogeneities. The results will be applicable for clinical Treatment Planning System. Dose calculation has been implemented for water phantom and CT scan images of breast cancer using point source and line source. This study used point source and line source and divided into two cases. On the first case, Ir-192 seed source is located at the center of treatment volume. On the second case, the source position is gradually changed. The dose calculation of every case performed on a homogeneous and inhomogeneous phantom with dimension 20 × 20 × 20 cm{sup 3}. The inhomogeneous phantom has inhomogeneities volume 2 × 2 × 2 cm{sup 3}. The results of dose calculations using PRISM TPS were compared to literature data. From the calculation of PRISM TPS, dose rates show good agreement with Plato TPS and other study as published by Ramdhani. No deviations greater than ±4% for all case. Dose calculation in inhomogeneous and homogenous cases show similar result. This results indicate that Prism TPS is good in dose calculation of brachytherapy but not sensitive for inhomogeneities. Thus, the dose calculation parameters developed in this study were found to be applicable for clinical treatment planning of brachytherapy.
International Nuclear Information System (INIS)
This document serves as a guide to Hanford contractors for obtaining or performing Hanford-related environmental dose calculations. Because environmental dose estimation techniques are state-of-the-art and are continually evolving, the data and standard methods presented herein will require periodic revision. This document is scheduled to be updated annually, but actual changes to the program will be made more frequently if required. For this reason, PNL's Occupational and Environmental Protection Department should be contacted before any Hanford-related environmental dose calculation is performed. This revision of the Hanford Dose Overview Program Report primarily reflects changes made to the data and models used in calculating atmospheric dispersion of airborne effluents at Hanford. The modified data and models are described in detail. In addition, discussions of dose calculation methods and the review of calculation results have been expanded to provide more explicit guidance to the Hanford contractors. 19 references, 30 tables
Calculation of the dose caused by internal radiation
Energy Technology Data Exchange (ETDEWEB)
NONE
2000-07-01
For the purposes of monitoring radiation exposure it is necessary to determine or to estimate the dose caused by both external and internal radiation. When comparing the value of exposure to the dose limits, account must be taken of the total dose incurred from different sources. This guide explains how to calculate the committed effective dose caused by internal radiation and gives the conversion factors required for the calculation. Application of the maximum values for radiation exposure is dealt with in ST guide 7.2, which also sets out the definitions of the quantities and concepts most commonly used in the monitoring of radiation exposure. The monitoring of exposure and recording of doses are dealt with in ST Guides 7.1 and 7.4.
PLUTONIUM/HIGH-LEVEL VITRIFIED WASTE BDBE DOSE CALCULATION
International Nuclear Information System (INIS)
The purpose of this calculation is to provide a dose consequence analysis of high-level waste (HLW) consisting of plutonium immobilized in vitrified HLW to be handled at the proposed Monitored Geologic Repository at Yucca Mountain for a beyond design basis event (BDBE) under expected conditions using best estimate values for each calculation parameter. In addition to the dose calculation, a plutonium respirable particle size for dose calculation use is derived. The current concept for this waste form is plutonium disks enclosed in cans immobilized in canisters of vitrified HLW (i.e., glass). The plutonium inventory at risk used for this calculation is selected from Plutonium Immobilization Project Input for Yucca Mountain Total Systems Performance Assessment (Shaw 1999). The BDBE examined in this calculation is a nonmechanistic initiating event and the sequence of events that follow to cause a radiological release. This analysis will provide the radiological releases and dose consequences for a postulated BDBE. Results may be considered in other analyses to determine or modify the safety classification and quality assurance level of repository structures, systems, and components. This calculation uses best available technical information because the BDBE frequency is very low (i.e., less than 1.0E-6 events/year) and is not required for License Application for the Monitored Geologic Repository. The results of this calculation will not be used as part of a licensing or design basis
Calculation method for gamma dose rates from Gaussian puffs
International Nuclear Information System (INIS)
The Lagrangian puff models are widely used for calculation of the dispersion of releases to the atmosphere. Basic output from such models is concentration of material in the air and on the ground. The most simple method for calculation of the gamma dose from the concentration of airborne activity is based on the semi-infinite cloud model. This method is however only applicable for puffs with large dispersion parameters, i.e. for receptors far away from the release point. The exact calculation of the cloud dose using volume integral requires large computer time usually exceeding what is available for real time calculations. The volume integral for gamma doses could be approximated by using the semi-infinite cloud model combined with correction factors. This type of calculation procedure is very fast, but usually the accuracy is poor because only a few of the relevant parameters are considered. A multi-parameter method for calculation of gamma doses is described here. This method uses precalculated values of the gamma dose rates as a function of Eγ, σy, the asymmetry factor - σy/σz, the height of puff center - H and the distance from puff center Rxy. To accelerate the calculations the release energy, for each significant radionuclide in each energy group, has been calculated and tabulated. Based on the precalculated values and suitable interpolation procedure the calculation of gamma doses needs only short computing time and it is almost independent of the number of radionuclides considered. (au) 2 tabs., 15 ills., 12 refs
Quantification of Proton Dose Calculation Accuracy in the Lung
Energy Technology Data Exchange (ETDEWEB)
Grassberger, Clemens, E-mail: Grassberger.Clemens@mgh.harvard.edu [Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts (United States); Center for Proton Radiotherapy, Paul Scherrer Institute, Villigen (Switzerland); Daartz, Juliane; Dowdell, Stephen; Ruggieri, Thomas; Sharp, Greg; Paganetti, Harald [Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts (United States)
2014-06-01
Purpose: To quantify the accuracy of a clinical proton treatment planning system (TPS) as well as Monte Carlo (MC)–based dose calculation through measurements and to assess the clinical impact in a cohort of patients with tumors located in the lung. Methods and Materials: A lung phantom and ion chamber array were used to measure the dose to a plane through a tumor embedded in the lung, and to determine the distal fall-off of the proton beam. Results were compared with TPS and MC calculations. Dose distributions in 19 patients (54 fields total) were simulated using MC and compared to the TPS algorithm. Results: MC increased dose calculation accuracy in lung tissue compared with the TPS and reproduced dose measurements in the target to within ±2%. The average difference between measured and predicted dose in a plane through the center of the target was 5.6% for the TPS and 1.6% for MC. MC recalculations in patients showed a mean dose to the clinical target volume on average 3.4% lower than the TPS, exceeding 5% for small fields. For large tumors, MC also predicted consistently higher V5 and V10 to the normal lung, because of a wider lateral penumbra, which was also observed experimentally. Critical structures located distal to the target could show large deviations, although this effect was highly patient specific. Range measurements showed that MC can reduce range uncertainty by a factor of ∼2: the average (maximum) difference to the measured range was 3.9 mm (7.5 mm) for MC and 7 mm (17 mm) for the TPS in lung tissue. Conclusion: Integration of Monte Carlo dose calculation techniques into the clinic would improve treatment quality in proton therapy for lung cancer by avoiding systematic overestimation of target dose and underestimation of dose to normal lung. In addition, the ability to confidently reduce range margins would benefit all patients by potentially lowering toxicity.
The effect of dose calculation accuracy on inverse treatment planning
Jeraj, Robert; Keall, Paul J.; Siebers, Jeffrey V.
2002-02-01
The effect of dose calculation accuracy during inverse treatment planning for intensity modulated radiotherapy (IMRT) was studied in this work. Three dose calculation methods were compared: Monte Carlo, superposition and pencil beam. These algorithms were used to calculate beamlets, which were subsequently used by a simulated annealing algorithm to determine beamlet weights which comprised the optimal solution to the objective function. Three different cases (lung, prostate and head and neck) were investigated and several different objective functions were tested for their effect on inverse treatment planning. It is shown that the use of inaccurate dose calculation introduces two errors in a treatment plan, a systematic error and a convergence error. The systematic error is present because of the inaccuracy of the dose calculation algorithm. The convergence error appears because the optimal intensity distribution for inaccurate beamlets differs from the optimal solution for the accurate beamlets. While the systematic error for superposition was found to be ~1% of Dmax in the tumour and slightly larger outside, the error for the pencil beam method is typically ~5% of Dmax and is rather insensitive to the given objectives. On the other hand, the convergence error was found to be very sensitive to the objective function, is only slightly correlated to the systematic error and should be determined for each case individually. Our results suggest that because of the large systematic and convergence errors, inverse treatment planning systems based on pencil beam algorithms alone should be upgraded either to superposition or Monte Carlo based dose calculations.
Automatic computed tomography patient dose calculation using header metadata
International Nuclear Information System (INIS)
The present work describes a method that calculates the patient dose values in computed tomography (CT) based on metadata contained in DICOM images in support of patient dose studies. The DICOM metadata is pre-processed to extract necessary calculation parameters. Vendor-specific DICOM header information is harmonized using vendor translation tables and unavailable DICOM tags can be completed with a graphical user interface. CT-Expo, an MS Excel application for calculating the radiation dose, is used to calculate the patient doses. All relevant data and calculation results are stored for further analysis in a relational database. Final results are compiled by utilizing data mining tools. This solution was successfully used for the 2009 CT dose study in Luxembourg. National diagnostic reference levels for standard examinations were calculated based on each of the countries' hospitals. The benefits using this new automatic system saved time as well as resources during the data acquisition and the evaluation when compared with earlier questionnaire-based surveys. (authors)
Calculation method for gamma-dose rates from spherical puffs
International Nuclear Information System (INIS)
The Lagrangian puff-models are widely used for calculation of the dispersion of atmospheric releases. Basic output from such models are concentrations of material in the air and on the ground. The most simple method for calculation of the gamma dose from the concentration of airborne activity is based on semi-infinite cloud model. This method is however only applicable for points far away from the release point. The exact calculation of the cloud dose using the volume integral requires significant computer time. The volume integral for the gamma dose could be approximated by using the semi-infinite cloud model combined with correction factors. This type of calculation procedure is very fast, but usually the accuracy is poor due to the fact that the same correction factors are used for all isotopes. The authors describe a more elaborate correction method. This method uses precalculated values of the gamma-dose rate as a function of the puff dispersion parameter (δp) and the distance from the puff centre for four energy groups. The release of energy for each radionuclide in each energy group has been calculated and tabulated. Based on these tables and a suitable interpolation procedure the calculation of gamma doses takes very short time and is almost independent of the number of radionuclides. (au) (7 tabs., 7 ills., 12 refs.)
DS86 and DS02 organ dose calculations.
Kerr, George D
2012-03-01
A brief review of the techniques used to calculate organ doses for the atomic-bomb survivors at Hiroshima and Nagasaki is provided using the original dosimetry system 1986 (DS86) and revised dosimetry system 2002 (DS02). The DS02 study was undertaken to address a serious discrepancy between calculated and measured values for neutron activation at Hiroshima that had caused a lack of confidence in the previous dosimetry, designated as DS86. Some potential improvements to the organ dose calculations that were not considered during the DS02 study due to time and funding limitations are recommended in this paper. PMID:21725078
International Nuclear Information System (INIS)
Transporting and processing of radioisotopes and irradiated targets inside hot cells generate a significant contamination. The majority of contamination comes from dispersion of radioactive materials during processing the samples after irradiation. Processing includes opening, extracting the irradiated samples, and preparing the samples in a shield prior to transportation. A model of dispersion of radioactive products inside the cell is postulated. Before decontaminating the cell, the expected dose received by the worker must be evaluated. A RESRAD-BUILD code is used in this study to calculate the dose and the corresponding risk. The calculated dose received during the decontamination process is more than the permissible dose and many proposals are presented in the study to decrease the level of received doses
Calculation of surface dose in rotational total skin electron irradiation
International Nuclear Information System (INIS)
A single-field rotational total skin electron irradiation technique has recently been developed at the McGill University for treatment of skin malignancies. The dose received by a given surface point during rotation in a uniform large electron field depends on the radius of rotation of the surface point, on the local radius of curvature of the contour in the vicinity of the point of interest, and on the shadows cast by limbs (arms upon trunk or head and neck, and legs upon each other). A method for calculating the surface dose distribution on a patient is presented accounting for the various parameters affecting the dose. A series of measurements were performed with polystyrene and a humanoid phantom, and an excellent agreement between measured and calculated dose distributions was obtained
Comparison of dose calculation methods for brachytherapy of intraocular tumors
Energy Technology Data Exchange (ETDEWEB)
Rivard, Mark J.; Chiu-Tsao, Sou-Tung; Finger, Paul T.; Meigooni, Ali S.; Melhus, Christopher S.; Mourtada, Firas; Napolitano, Mary E.; Rogers, D. W. O.; Thomson, Rowan M.; Nath, Ravinder [Department of Radiation Oncology, Tufts University School of Medicine, Boston, Massachusetts 02111 (United States); Quality MediPhys LLC, Denville, New Jersey 07834 (United States); New York Eye Cancer Center, New York, New York 10065 (United States); Department of Radiation Oncology, Comprehensive Cancer Center of Nevada, Las Vegas, Nevada 89169 (United States); Department of Radiation Oncology, Tufts University School of Medicine, Boston, Massachusetts 02111 (United States); Department of Radiation Physics, University of Texas, M.D. Anderson Cancer Center, Houston, Texas 77030 (United States) and Department of Experimental Diagnostic Imaging, University of Texas, M.D. Anderson Cancer Center, Houston, Texas 77030 (United States); Physics, Elekta Inc., Norcross, Georgia 30092 (United States); Department of Physics, Carleton University, Ottawa, Ontario K1S 5B6 (Canada); Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, Connecticut 06520 (United States)
2011-01-15
Purpose: To investigate dosimetric differences among several clinical treatment planning systems (TPS) and Monte Carlo (MC) codes for brachytherapy of intraocular tumors using {sup 125}I or {sup 103}Pd plaques, and to evaluate the impact on the prescription dose of the adoption of MC codes and certain versions of a TPS (Plaque Simulator with optional modules). Methods: Three clinical brachytherapy TPS capable of intraocular brachytherapy treatment planning and two MC codes were compared. The TPS investigated were Pinnacle v8.0dp1, BrachyVision v8.1, and Plaque Simulator v5.3.9, all of which use the AAPM TG-43 formalism in water. The Plaque Simulator software can also handle some correction factors from MC simulations. The MC codes used are MCNP5 v1.40 and BrachyDose/EGSnrc. Using these TPS and MC codes, three types of calculations were performed: homogeneous medium with point sources (for the TPS only, using the 1D TG-43 dose calculation formalism); homogeneous medium with line sources (TPS with 2D TG-43 dose calculation formalism and MC codes); and plaque heterogeneity-corrected line sources (Plaque Simulator with modified 2D TG-43 dose calculation formalism and MC codes). Comparisons were made of doses calculated at points-of-interest on the plaque central-axis and at off-axis points of clinical interest within a standardized model of the right eye. Results: For the homogeneous water medium case, agreement was within {approx}2% for the point- and line-source models when comparing between TPS and between TPS and MC codes, respectively. For the heterogeneous medium case, dose differences (as calculated using the MC codes and Plaque Simulator) differ by up to 37% on the central-axis in comparison to the homogeneous water calculations. A prescription dose of 85 Gy at 5 mm depth based on calculations in a homogeneous medium delivers 76 Gy and 67 Gy for specific {sup 125}I and {sup 103}Pd sources, respectively, when accounting for COMS-plaque heterogeneities. For off
Optimizing an analytical dose calculation algorithm for fast 2D calculations
Energy Technology Data Exchange (ETDEWEB)
Lorenz, Friedlieb [Dept. of Radiation Oncology, Mannheim Medical Centre, Univ. of Heidelberg, Mannheim (Germany); Richter, Henning [Technical Univ. of Kaiserslautern (Germany); Zygmanski, Piotr [Dept. of Radiation Oncology, Dana Farber/Brigham and Women' s Cancer Centre, Harvard Medical School, Boston (United States)
2010-07-01
Previously, an analytical dose calculation algorithm for MLC-based radiotherapy was developed and commissioned, which includes a detailed model of various MLC effects as a unique feature [1]. The algorithm was originally developed as an independent verification of the treatment planning system's dose calculation and it explicitly modeled spatial and depth dependent MLC effects such as interleaf transmission, the tongue-and-groove effect, rounded leaf ends, MLC scatter, beam hardening, and gradual MLC transmission fall-off with increasing off-axis distance. Originally the algorithm was implemented in Mathematica trademark (Wolfram). To speed up the calculation time and to be able to calculate high resolution 2D dose distributions within a reasonable time frame (<2 s) the algorithm needs to be optimized and to be embedded in a user friendly environment. To achieve this goal, the dose calculation model is implemented in Visual Basic 6.0, which decreases the calculation time moderately. More importantly, the numerical algorithm for dose calculation is changed at two levels: the dose contributions are split into their x- and y-contributions and the calculation is aperture- rather than as originally point-based. Implementing these three major changes, the calculation time is reduced considerably without loosing accuracy. The time for a typical IMRT field with about 2500 calculation points decreased from 2387 seconds to 0.624 seconds (a factor of about 3800). The mean agreement of the optimized and the not optimized calculation algorithm at the isocenter for a fairly complex IMRT plan with 23 fields is better than 1% relative to the local dose at the measuring point. (orig.)
Development of a computational methodology for internal dose calculations
Yoriyaz, H
2000-01-01
A new approach for calculating internal dose estimates was developed through the use of a more realistic computational model of the human body and a more precise tool for the radiation transport simulation. The present technique shows the capability to build a patient-specific phantom with tomography data (a voxel-based phantom) for the simulation of radiation transport and energy deposition using Monte Carlo methods such as in the MCNP-4B code. In order to utilize the segmented human anatomy as a computational model for the simulation of radiation transport, an interface program, SCMS, was developed to build the geometric configurations for the phantom through the use of tomographic images. This procedure allows to calculate not only average dose values but also spatial distribution of dose in regions of interest. With the present methodology absorbed fractions for photons and electrons in various organs of the Zubal segmented phantom were calculated and compared to those reported for the mathematical phanto...
Impact of dose calculation algorithm on radiation therapy
Institute of Scientific and Technical Information of China (English)
Wen-Zhou; Chen; Ying; Xiao; Jun; Li
2014-01-01
The quality of radiation therapy depends on the ability to maximize the tumor control probability while minimizing the normal tissue complication probability.Both of these two quantities are directly related to the accuracy of dose distributions calculated by treatment planning systems.The commonly used dose calculation algorithms in the treatment planning systems are reviewed in this work.The accuracy comparisons among these algorithms are illustrated by summarizing the highly cited research papers on this topic.Further,the correlation between the algorithms and tumor control probability/normal tissue complication probability values are manifested by several recent studies from different groups.All the cases demonstrate that dose calculation algorithms play a vital role in radiation therapy.
Dose calculation of 6 MV Truebeam using Monte Carlo method
International Nuclear Information System (INIS)
The purpose of this work is to simulate 6 MV Varian Truebeam linac dosimeter characteristics using Monte Carlo method and to investigate the availability of phase space file and the accuracy of the simulation. With the phase space file at linac window supplied by Varian to be a source, the patient-dependent part was simulated. Dose distributions in a water phantom with a 10 cm × 10 cm field were calculated and compared with measured data for validation. Evident time reduction was obtained from 4-5 h which a whole simulation cost on the same computer to around 48 minutes. Good agreement between simulations and measurements in water was observed. Dose differences are less than 3% for depth doses in build-up region and also for dose profiles inside the 80% field size, and the effect in penumbra is good. It demonstrate that the simulation using existing phase space file as the EGSnrc source is efficient. Dose differences between calculated data and measured data could meet the requirements for dose calculation. (authors)
Predictive Models for Maximum Recommended Therapeutic Dose of Antiretroviral Drugs
Directory of Open Access Journals (Sweden)
Michael Lee Branham
2012-01-01
Full Text Available A novel method for predicting maximum recommended therapeutic dose (MRTD is presented using quantitative structure property relationships (QSPRs and artificial neural networks (ANNs. MRTD data of 31 structurally diverse Antiretroviral drugs (ARVs were collected from FDA MRTD Database or package inserts. Molecular property descriptors of each compound, that is, molecular mass, aqueous solubility, lipophilicity, biotransformation half life, oxidation half life, and biodegradation probability were calculated from their SMILES codes. A training set (=23 was used to construct multiple linear regression and back propagation neural network models. The models were validated using an external test set (=8 which demonstrated that MRTD values may be predicted with reasonable accuracy. Model predictability was described by root mean squared errors (RMSEs, Kendall's correlation coefficients (tau, P-values, and Bland Altman plots for method comparisons. MRTD was predicted by a 6-3-1 neural network model (RMSE=13.67, tau=0.643, =0.035 more accurately than by the multiple linear regression (RMSE=27.27, tau=0.714, =0.019 model. Both models illustrated a moderate correlation between aqueous solubility of antiretroviral drugs and maximum therapeutic dose. MRTD prediction may assist in the design of safer, more effective treatments for HIV infection.
Satory, P R
2012-03-01
This work is the development of a MOSFET based surface in vivo dosimetry system for total body irradiation patients treated with bilateral extended SSD beams using PMMA missing tissue compensators adjacent to the patient. An empirical formula to calculate midplane dose from MOSFET measured entrance and exit doses has been derived. The dependency of surface dose on the air-gap between the spoiler and the surface was investigated by suspending a spoiler above a water phantom, and taking percentage depth dose measurements (PDD). Exit and entrances doses were measured with MOSFETs in conjunction with midplane doses measured with an ion chamber. The entrance and exit doses were combined using an exponential attenuation formula to give an estimate of midplane dose and were compared to the midplane ion chamber measurement for a range of phantom thicknesses. Having a maximum PDD at the surface simplifies the prediction of midplane dose, which is achieved by ensuring that the air gap between the compensator and the surface is less than 10 cm. The comparison of estimated midplane dose and measured midplane dose showed no dependence on phantom thickness and an average correction factor of 0.88 was found. If the missing tissue compensators are kept within 10 cm of the patient then MOSFET measurements of entrance and exit dose can predict the midplane dose for the patient. PMID:22298238
Monte Carlo dose calculation in dental amalgam phantom.
Aziz, Mohd Zahri Abdul; Yusoff, A L; Osman, N D; Abdullah, R; Rabaie, N A; Salikin, M S
2015-01-01
It has become a great challenge in the modern radiation treatment to ensure the accuracy of treatment delivery in electron beam therapy. Tissue inhomogeneity has become one of the factors for accurate dose calculation, and this requires complex algorithm calculation like Monte Carlo (MC). On the other hand, computed tomography (CT) images used in treatment planning system need to be trustful as they are the input in radiotherapy treatment. However, with the presence of metal amalgam in treatment volume, the CT images input showed prominent streak artefact, thus, contributed sources of error. Hence, metal amalgam phantom often creates streak artifacts, which cause an error in the dose calculation. Thus, a streak artifact reduction technique was applied to correct the images, and as a result, better images were observed in terms of structure delineation and density assigning. Furthermore, the amalgam density data were corrected to provide amalgam voxel with accurate density value. As for the errors of dose uncertainties due to metal amalgam, they were reduced from 46% to as low as 2% at d80 (depth of the 80% dose beyond Zmax) using the presented strategies. Considering the number of vital and radiosensitive organs in the head and the neck regions, this correction strategy is suggested in reducing calculation uncertainties through MC calculation. PMID:26500401
Monte carlo dose calculation in dental amalgam phantom
Directory of Open Access Journals (Sweden)
Mohd Zahri Abdul Aziz
2015-01-01
Full Text Available It has become a great challenge in the modern radiation treatment to ensure the accuracy of treatment delivery in electron beam therapy. Tissue inhomogeneity has become one of the factors for accurate dose calculation, and this requires complex algorithm calculation like Monte Carlo (MC. On the other hand, computed tomography (CT images used in treatment planning system need to be trustful as they are the input in radiotherapy treatment. However, with the presence of metal amalgam in treatment volume, the CT images input showed prominent streak artefact, thus, contributed sources of error. Hence, metal amalgam phantom often creates streak artifacts, which cause an error in the dose calculation. Thus, a streak artifact reduction technique was applied to correct the images, and as a result, better images were observed in terms of structure delineation and density assigning. Furthermore, the amalgam density data were corrected to provide amalgam voxel with accurate density value. As for the errors of dose uncertainties due to metal amalgam, they were reduced from 46% to as low as 2% at d80 (depth of the 80% dose beyond Zmax using the presented strategies. Considering the number of vital and radiosensitive organs in the head and the neck regions, this correction strategy is suggested in reducing calculation uncertainties through MC calculation.
Monte Carlo dose calculation in dental amalgam phantom
Mohd Zahri Abdul Aziz; Yusoff, A. L.; N D Osman; R. Abdullah; Rabaie, N. A.; M S Salikin
2015-01-01
It has become a great challenge in the modern radiation treatment to ensure the accuracy of treatment delivery in electron beam therapy. Tissue inhomogeneity has become one of the factors for accurate dose calculation, and this requires complex algorithm calculation like Monte Carlo (MC). On the other hand, computed tomography (CT) images used in treatment planning system need to be trustful as they are the input in radiotherapy treatment. However, with the presence of metal amalgam in treatm...
A Monte Carlo dose calculation tool for radiotherapy treatment planning
Ma, C.-M.; Li, J. S.; Pawlicki, T.; Jiang, S. B.; Deng, J.; Lee, M. C.; Koumrian, T.; Luxton, M.; Brain, S.
2002-05-01
A Monte Carlo user code, MCDOSE, has been developed for radiotherapy treatment planning (RTP) dose calculations. MCDOSE is designed as a dose calculation module suitable for adaptation to host RTP systems. MCDOSE can be used for both conventional photon/electron beam calculation and intensity modulated radiotherapy (IMRT) treatment planning. MCDOSE uses a multiple-source model to reconstruct the treatment beam phase space. Based on Monte Carlo simulated or measured beam data acquired during commissioning, source-model parameters are adjusted through an automated procedure. Beam modifiers such as jaws, physical and dynamic wedges, compensators, blocks, electron cut-outs and bolus are simulated by MCDOSE together with a 3D rectilinear patient geometry model built from CT data. Dose distributions calculated using MCDOSE agreed well with those calculated by the EGS4/DOSXYZ code using different beam set-ups and beam modifiers. Heterogeneity correction factors for layered-lung or layered-bone phantoms as calculated by both codes were consistent with measured data to within 1%. The effect of energy cut-offs for particle transport was investigated. Variance reduction techniques were implemented in MCDOSE to achieve a speedup factor of 10-30 compared to DOSXYZ.
Calculation and measurement of depth dose distributions in bricks
International Nuclear Information System (INIS)
The dose accumulated in bricks exposed to gamma radiation can be measured as a function of depth using luminescence methods. The dependence of dose on depth has the potential of providing information on the energy as well as on the angular distribution of the incident radiation, which could give indications on the configuration of the radiation sources. A prerequisite for such an analysis is a comprehensive knowledge on the dependence of dose on depth for different source energies and for specific source configurations. Depth dose distribution in brick walls have been calculated by Monte Carlo simulations for a source distribution on a wall, for a source distribution on the ground and for a parallel photon beam, for source energies ranging from 140 keV to 1600 keV. It is shown that depth dose distributions depend substantially on source configuration and energy. Depth dose distributions measured in ceramic materials irradiated in the laboratory and in a brick from a contaminated area are compared with results of Monte Carlo calculations. (Author)
Tissue heterogeneity in IMRT dose calculation for lung cancer.
Pasciuti, Katia; Iaccarino, Giuseppe; Strigari, Lidia; Malatesta, Tiziana; Benassi, Marcello; Di Nallo, Anna Maria; Mirri, Alessandra; Pinzi, Valentina; Landoni, Valeria
2011-01-01
The aim of this study was to evaluate the differences in accuracy of dose calculation between 3 commonly used algorithms, the Pencil Beam algorithm (PB), the Anisotropic Analytical Algorithm (AAA), and the Collapsed Cone Convolution Superposition (CCCS) for intensity-modulated radiation therapy (IMRT). The 2D dose distributions obtained with the 3 algorithms were compared on each CT slice pixel by pixel, using the MATLAB code (The MathWorks, Natick, MA) and the agreement was assessed with the γ function. The effect of the differences on dose-volume histograms (DVHs), tumor control, and normal tissue complication probability (TCP and NTCP) were also evaluated, and its significance was quantified by using a nonparametric test. In general PB generates regions of over-dosage both in the lung and in the tumor area. These differences are not always in DVH of the lung, although the Wilcoxon test indicated significant differences in 2 of 4 patients. Disagreement in the lung region was also found when the Γ analysis was performed. The effect on TCP is less important than for NTCP because of the slope of the curve at the level of the dose of interest. The effect of dose calculation inaccuracy is patient-dependent and strongly related to beam geometry and to the localization of the tumor. When multiple intensity-modulated beams are used, the effect of the presence of the heterogeneity on dose distribution may not always be easily predictable. PMID:20970989
Analytical probabilistic proton dose calculation and range uncertainties
International Nuclear Information System (INIS)
We introduce the concept of analytical probabilistic modeling (APM) to calculate the mean and the standard deviation of intensity-modulated proton dose distributions under the influence of range uncertainties in closed form. For APM, range uncertainties are modeled with a multivariate Normal distribution p(z) over the radiological depths z. A pencil beam algorithm that parameterizes the proton depth dose d(z) with a weighted superposition of ten Gaussians is used. Hence, the integrals ∫ dz p(z) d(z) and ∫ dz p(z) d(z)2 required for the calculation of the expected value and standard deviation of the dose remain analytically tractable and can be efficiently evaluated. The means μk, widths δk, and weights ωk of the Gaussian components parameterizing the depth dose curves are found with least squares fits for all available proton ranges. We observe less than 0.3% average deviation of the Gaussian parameterizations from the original proton depth dose curves. Consequently, APM yields high accuracy estimates for the expected value and standard deviation of intensity-modulated proton dose distributions for two dimensional test cases. APM can accommodate arbitrary correlation models and account for the different nature of random and systematic errors in fractionated radiation therapy. Beneficial applications of APM in robust planning are feasible.
Touch screen man machine interfere for emergency dose calculations
International Nuclear Information System (INIS)
Emergency dose calculation systems generally use a keyboard to provide the interface between the user and the computer. This interface is preferred by users who work daily with computers; however, for many plant personnel who are not continuously involved with computer operations, the use of a keyboard can be cumbersome and time consuming. This is particularly true when the user is under pressure during a drill or an actual emergency. Experience in many applications of Pickard, Lowe and Garrick's PLG's Meteorological Information and Dose Assessment System (MIDAS) has shown that user friendliness is a key ingredient toward achieving acceptance of computerized systems. Hardware to support to touch screen interface is now available and has been implemented in MIDAS. Recent experience has demonstrated that selection times for dose calculations are reduced, data entry errors have been minimized, and confusion over appropriate entries has been avoided due to the built-in logic. A 10-yr search for an acceptable keyboard replacement has ended
Development of new methodology for dose calculation in photographic dosimetry
International Nuclear Information System (INIS)
The personal dosemeter system of IPEN is based on film dosimetry. Personal doses at IPEN are mainly due to X or gamma radiation. The use of personal photographic dosemeters involves two steps: firstly, data acquisition including their evaluation with respect to the calibration quantity and secondly, the interpretation of the data in terms of effective dose. The effective dose was calculated using artificial intelligence techniques by means of neural network. The learning of the neural network was performed by taking the readings of optical density as a function of incident energy and exposure from the calibration curve. The obtained output in the daily grind is the mean effective energy and the effective dose. (author)
Dose Calculation Evolution for Internal Organ Irradiation in Humans
Jimenez V., Reina A.
2007-10-01
The International Commission of Radiation Units (ICRU) has established through the years, a discrimination system regarding the security levels on the prescription and administration of doses in radiation treatments (Radiotherapy, Brach therapy, Nuclear Medicine). The first level is concerned with the prescription and posterior assurance of dose administration to a point of interest (POI), commonly located at the geometrical center of the region to be treated. In this, the effects of radiation around that POI, is not a priority. The second level refers to the dose specifications in a particular plane inside the patient, mostly the middle plane of the lesion. The dose is calculated to all the structures in that plane regardless if they are tumor or healthy tissue. In this case, the dose is not represented by a point value, but by level curves called "isodoses" as in a topographic map, so you can assure the level of doses to this particular plane, but it also leave with no information about how this values go thru adjacent planes. This is why the third level is referred to the volumetrical description of doses so these isodoses construct now a volume (named "cloud") that give us better assurance about tissue irradiation around the volume of the lesion and its margin (sub clinical spread or microscopic illness). This work shows how this evolution has resulted, not only in healthy tissue protection improvement but in a rise of tumor control, quality of life, better treatment tolerance and minimum permanent secuelae.
Dose Calculation Evolution for Internal Organ Irradiation in Humans
International Nuclear Information System (INIS)
The International Commission of Radiation Units (ICRU) has established through the years, a discrimination system regarding the security levels on the prescription and administration of doses in radiation treatments (Radiotherapy, Brach therapy, Nuclear Medicine). The first level is concerned with the prescription and posterior assurance of dose administration to a point of interest (POI), commonly located at the geometrical center of the region to be treated. In this, the effects of radiation around that POI, is not a priority. The second level refers to the dose specifications in a particular plane inside the patient, mostly the middle plane of the lesion. The dose is calculated to all the structures in that plane regardless if they are tumor or healthy tissue. In this case, the dose is not represented by a point value, but by level curves called 'isodoses' as in a topographic map, so you can assure the level of doses to this particular plane, but it also leave with no information about how this values go thru adjacent planes. This is why the third level is referred to the volumetrical description of doses so these isodoses construct now a volume (named 'cloud') that give us better assurance about tissue irradiation around the volume of the lesion and its margin (sub clinical spread or microscopic illness). This work shows how this evolution has resulted, not only in healthy tissue protection improvement but in a rise of tumor control, quality of life, better treatment tolerance and minimum permanent secuelae
Automated objective thyroid ablation dose calculations using interactive computer program
International Nuclear Information System (INIS)
Aim: Development of an interactive computer program allowing automatic calculation of an optimized dose of I-131 required for the effective ablation of remnants of thyroid tissue. Materials and methods: The Standard Thyroid Uptake Neck Phantom (Nucl.Assoc.) was used for measurements of efficiency of high energy (for I-131) and low energy (for I-123) collimator mounted on the Picker Prism 2000 gamma camera. The efficiency was calculated for a wide range of distances between the patient's neck and the camera head and for different sizes of remnant thyroid tissue and activities. These data were built into the computer memory (Picker Odyssey FX 729) and then were used for calculation of percentage uptake in the neck (regular quality control and maintenance of gamma camera secures the stability of its performance). On the basis of the uptake on an early and late image after the administration of radioisotope, its biological and effective half lives in the patient are calculated and the dose required for delivery of 50mGy per gram of I-131 radiation to the remaining thyroid tissue is evaluated. Results: The technologist selects the appropriate isotope, enters the patient's dose and the neck to collimator distance then draws the regions of interests around the thyroid remnants on each of anterior images. No other operator interventions are required. When regions are assigned the percentage uptake, biological half life, effective half life and required I-131 activity in MBq per gram are calculated automatically. It was found that efficiency is independent of activity over the range seen clinically. The need for a standard is eliminated and automated calculations ensure accuracy. Estimation of remnant mass and desired radiation dose is required to complete the dose calculations. The program works for both I-131 (using 1 to 3 day and 5 to 10 day images) and I-123 (using 6 and 24 hrs images). The program automatically corrects for the exact imaging time. Results are displayed
Interpretation of animal data in the calculation of doses from new radiolabelled compounds
International Nuclear Information System (INIS)
The Radionuclide Biokinetics Group of the Biomedical Effects Department at NRPB provides a dose calculation service for pharmaceutical companies and associated laboratories which plan to administer radiolabelled drugs to human volunteers as part of their research and development programmes for new compounds. Animal data provided by these companies are used to estimate the likely doses to humans from administration of the compound. The dose estimate then accompanies the pharmaceutical company's application for approval from the UK Administration of Radioactive Substances Advisory Committee (ARSAC). The method of calculation, the interpretation of the animal data and the range of results obtained are discussed. In addition, the effect of the use of the new ICRP tissue weighting factors in the calculations is considered. (Author)
Internal dose conversion factors for calculation of dose to the public
International Nuclear Information System (INIS)
This publication contains 50-year committed dose equivalent factors, in tabular form. The document is intended to be used as the primary reference by the US Department of Energy (DOE) and its contractors for calculating radiation dose equivalents for members of the public, resulting from ingestion or inhalation of radioactive materials. Its application is intended specifically for such materials released to the environment during routine DOE operations, except in those instances where compliance with 40 CFR 61 (National Emission Standards for Hazardous Air Pollutants) requires otherwise. However, the calculated values may be equally applicable to unusual releases or to occupational exposures. The use of these committed dose equivalent tables should ensure that doses to members of the public from internal exposures are calculated in a consistent manner at all DOE facilities
Fast optimization and dose calculation in scanned ion beam therapy
Energy Technology Data Exchange (ETDEWEB)
Hild, S. [Department of Biophysics, GSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt (Germany); Department of Radiation Oncology, University Clinic Erlangen and Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen (Germany); Institute for Medical Physics and Radiation Protection, University of Applied Sciences, 35390 Giessen (Germany); Graeff, C.; Trautmann, J.; Kraemer, M. [Department of Biophysics, GSI Helmholtzzentrum für Schwerionenforschung GmbH, 64289 Darmstadt (Germany); Zink, K. [Institute for Medical Physics and Radiation Protection, University of Applied Sciences, 35390 Giessen, Germany and Department of Radiotherapy and Radiooncology, University Hospital Giessen-Marburg, 35043 Marburg (Germany); Durante, M. [Department of Biophysics, GSI Helmholtzzentrum für Schwerionenforschung GmbH, 64289 Darmstadt, Germany and Faculty of Physics, Technische Universität Darmstadt, 64289 Darmstadt (Germany); Bert, C., E-mail: christoph.bert@uk-erlangen.de [Department of Biophysics, GSI Helmholtzzentrum für Schwerionenforschung GmbH, 64289 Darmstadt, Germany and Department of Radiation Oncology, University Clinic Erlangen and Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen (Germany)
2014-07-15
Purpose: Particle therapy (PT) has advantages over photon irradiation on static tumors. An increased biological effectiveness and active target conformal dose shaping are strong arguments for PT. However, the sensitivity to changes of internal geometry complicates the use of PT for moving organs. In case of interfractionally moving objects adaptive radiotherapy (ART) concepts known from intensity modulated radiotherapy (IMRT) can be adopted for PT treatments. One ART strategy is to optimize a new treatment plan based on daily image data directly before a radiation fraction is delivered [treatment replanning (TRP)]. Optimizing treatment plans for PT using a scanned beam is a time consuming problem especially for particles other than protons where the biological effective dose has to be calculated. For the purpose of TRP, fast optimization and fast dose calculation have been implemented into the GSI in-house treatment planning system (TPS) TRiP98. Methods: This work reports about the outcome of a code analysis that resulted in optimization of the calculation processes as well as implementation of routines supporting parallel execution of the code. To benchmark the new features, the calculation time for therapy treatment planning has been studied. Results: Compared to the original version of the TPS, calculation times for treatment planning (optimization and dose calculation) have been improved by a factor of 10 with code optimization. The parallelization of the TPS resulted in a speedup factor of 12 and 5.5 for the original version and the code optimized version, respectively. Hence the total speedup of the new implementation of the authors' TPS yielded speedup factors up to 55. Conclusions: The improved TPS is capable of completing treatment planning for ion beam therapy of a prostate irradiation considering organs at risk in this has been overseen in the review process. Also see below 6 min.
Fast optimization and dose calculation in scanned ion beam therapy
International Nuclear Information System (INIS)
Purpose: Particle therapy (PT) has advantages over photon irradiation on static tumors. An increased biological effectiveness and active target conformal dose shaping are strong arguments for PT. However, the sensitivity to changes of internal geometry complicates the use of PT for moving organs. In case of interfractionally moving objects adaptive radiotherapy (ART) concepts known from intensity modulated radiotherapy (IMRT) can be adopted for PT treatments. One ART strategy is to optimize a new treatment plan based on daily image data directly before a radiation fraction is delivered [treatment replanning (TRP)]. Optimizing treatment plans for PT using a scanned beam is a time consuming problem especially for particles other than protons where the biological effective dose has to be calculated. For the purpose of TRP, fast optimization and fast dose calculation have been implemented into the GSI in-house treatment planning system (TPS) TRiP98. Methods: This work reports about the outcome of a code analysis that resulted in optimization of the calculation processes as well as implementation of routines supporting parallel execution of the code. To benchmark the new features, the calculation time for therapy treatment planning has been studied. Results: Compared to the original version of the TPS, calculation times for treatment planning (optimization and dose calculation) have been improved by a factor of 10 with code optimization. The parallelization of the TPS resulted in a speedup factor of 12 and 5.5 for the original version and the code optimized version, respectively. Hence the total speedup of the new implementation of the authors' TPS yielded speedup factors up to 55. Conclusions: The improved TPS is capable of completing treatment planning for ion beam therapy of a prostate irradiation considering organs at risk in this has been overseen in the review process. Also see below 6 min
External dose-rate conversion factors for calculation of dose to the public
Energy Technology Data Exchange (ETDEWEB)
1988-07-01
This report presents a tabulation of dose-rate conversion factors for external exposure to photons and electrons emitted by radionuclides in the environment. This report was prepared in conjunction with criteria for limiting dose equivalents to members of the public from operations of the US Department of Energy (DOE). The dose-rate conversion factors are provided for use by the DOE and its contractors in performing calculations of external dose equivalents to members of the public. The dose-rate conversion factors for external exposure to photons and electrons presented in this report are based on a methodology developed at Oak Ridge National Laboratory. However, some adjustments of the previously documented methodology have been made in obtaining the dose-rate conversion factors in this report. 42 refs., 1 fig., 4 tabs.
A convolution-superposition dose calculation engine for GPUs
International Nuclear Information System (INIS)
Purpose: Graphic processing units (GPUs) are increasingly used for scientific applications, where their parallel architecture and unprecedented computing power density can be exploited to accelerate calculations. In this paper, a new GPU implementation of a convolution/superposition (CS) algorithm is presented. Methods: This new GPU implementation has been designed from the ground-up to use the graphics card's strengths and to avoid its weaknesses. The CS GPU algorithm takes into account beam hardening, off-axis softening, kernel tilting, and relies heavily on raytracing through patient imaging data. Implementation details are reported as well as a multi-GPU solution. Results: An overall single-GPU acceleration factor of 908x was achieved when compared to a nonoptimized version of the CS algorithm implemented in PlanUNC in single threaded central processing unit (CPU) mode, resulting in approximatively 2.8 s per beam for a 3D dose computation on a 0.4 cm grid. A comparison to an established commercial system leads to an acceleration factor of approximately 29x or 0.58 versus 16.6 s per beam in single threaded mode. An acceleration factor of 46x has been obtained for the total energy released per mass (TERMA) calculation and a 943x acceleration factor for the CS calculation compared to PlanUNC. Dose distributions also have been obtained for a simple water-lung phantom to verify that the implementation gives accurate results. Conclusions: These results suggest that GPUs are an attractive solution for radiation therapy applications and that careful design, taking the GPU architecture into account, is critical in obtaining significant acceleration factors. These results potentially can have a significant impact on complex dose delivery techniques requiring intensive dose calculations such as intensity-modulated radiation therapy (IMRT) and arc therapy. They also are relevant for adaptive radiation therapy where dose results must be obtained rapidly.
A convolution-superposition dose calculation engine for GPUs
Energy Technology Data Exchange (ETDEWEB)
Hissoiny, Sami; Ozell, Benoit; Despres, Philippe [Departement de genie informatique et genie logiciel, Ecole polytechnique de Montreal, 2500 Chemin de Polytechnique, Montreal, Quebec H3T 1J4 (Canada); Departement de radio-oncologie, CRCHUM-Centre hospitalier de l' Universite de Montreal, 1560 rue Sherbrooke Est, Montreal, Quebec H2L 4M1 (Canada)
2010-03-15
Purpose: Graphic processing units (GPUs) are increasingly used for scientific applications, where their parallel architecture and unprecedented computing power density can be exploited to accelerate calculations. In this paper, a new GPU implementation of a convolution/superposition (CS) algorithm is presented. Methods: This new GPU implementation has been designed from the ground-up to use the graphics card's strengths and to avoid its weaknesses. The CS GPU algorithm takes into account beam hardening, off-axis softening, kernel tilting, and relies heavily on raytracing through patient imaging data. Implementation details are reported as well as a multi-GPU solution. Results: An overall single-GPU acceleration factor of 908x was achieved when compared to a nonoptimized version of the CS algorithm implemented in PlanUNC in single threaded central processing unit (CPU) mode, resulting in approximatively 2.8 s per beam for a 3D dose computation on a 0.4 cm grid. A comparison to an established commercial system leads to an acceleration factor of approximately 29x or 0.58 versus 16.6 s per beam in single threaded mode. An acceleration factor of 46x has been obtained for the total energy released per mass (TERMA) calculation and a 943x acceleration factor for the CS calculation compared to PlanUNC. Dose distributions also have been obtained for a simple water-lung phantom to verify that the implementation gives accurate results. Conclusions: These results suggest that GPUs are an attractive solution for radiation therapy applications and that careful design, taking the GPU architecture into account, is critical in obtaining significant acceleration factors. These results potentially can have a significant impact on complex dose delivery techniques requiring intensive dose calculations such as intensity-modulated radiation therapy (IMRT) and arc therapy. They also are relevant for adaptive radiation therapy where dose results must be obtained rapidly.
Adjoint Monte Carlo techniques and codes for organ dose calculations
International Nuclear Information System (INIS)
Adjoint Monte Carlo simulations can be effectively used for the estimation of doses in small targets when the sources are extended in large volumes or surfaces. The main features of two computer codes for calculating doses at free points or in organs of an anthropomorphic phantom are described. In the first program (REBEL-3) natural gamma-emitting sources are contained in the walls of a dwelling room; in the second one (POKER-CAMP) the user can specify arbitrary gamma sources with different spatial distributions in the environment: in (or on the surface of) the ground and in the air. 3 figures
An efficient dose calculation strategy for intensity modulated proton therapy
International Nuclear Information System (INIS)
While intensity-modulated proton therapy (IMPT) has great potential to improve the therapeutic efficacy of radiotherapy, IMPT optimization can be computationally demanding, particularly for large and complex tumors. Here we propose a dose calculation strategy to accelerate IMPT optimization while reducing memory requirements. By using two adjustable threshold parameters, our method separates dose contributions from proton beamlets into major and minor components for each dose voxel. The optimization proceeds with two levels of iterations: in inner iterations, doses are updated in correspondence with changes in beamlet intensities from only the major contributions while keeping the portions from the minor contributions constant; in outer iterations, doses are recalculated exactly by considering both major and minor contributions. Since the number of elements in the influence matrix for major contributions is relatively small, each inner iteration proceeds quickly. Each outer iteration requires a longer computation time, but only a few such iterations are needed. Our study shows that the proposed strategy leads to nearly identical dose distributions as those optimized with the full influence matrix, but reducing computing time by at least a factor of 3 and internal memory requirements by a factor of 10 or more. In addition, we show that the proposed approach could enhance other optimization-related applications such as optimizing beam angles. By using an advanced lung cancer case that would demand large computing resources by conventional optimization approach, we show how our method may potentially help improve IMPT treatment planning in real clinical situations. (note)
Prenatal radiation exposure. Dose calculation; Praenatale Strahlenexposition. Dosisermittlung
Energy Technology Data Exchange (ETDEWEB)
Scharwaechter, C.; Schwartz, C.A.; Haage, P. [University Hospital Witten/Herdecke, Wuppertal (Germany). Dept. of Diagnostic and Interventional Radiology; Roeser, A. [University Hospital Witten/Herdecke, Wuppertal (Germany). Dept. of Radiotherapy and Radio-Oncology
2015-05-15
The unborn child requires special protection. In this context, the indication for an X-ray examination is to be checked critically. If thereupon radiation of the lower abdomen including the uterus cannot be avoided, the examination should be postponed until the end of pregnancy or alternative examination techniques should be considered. Under certain circumstances, either accidental or in unavoidable cases after a thorough risk assessment, radiation exposure of the unborn may take place. In some of these cases an expert radiation hygiene consultation may be required. This consultation should comprise the expected risks for the unborn while not perturbing the mother or the involved medical staff. For the risk assessment in case of an in-utero X-ray exposition deterministic damages with a defined threshold dose are distinguished from stochastic damages without a definable threshold dose. The occurrence of deterministic damages depends on the dose and the developmental stage of the unborn at the time of radiation. To calculate the risks of an in-utero radiation exposure a three-stage concept is commonly applied. Depending on the amount of radiation, the radiation dose is either estimated, roughly calculated using standard tables or, in critical cases, accurately calculated based on the individual event. The complexity of the calculation thereby increases from stage to stage. An estimation based on stage one is easily feasible whereas calculations based on stages two and especially three are more complex and often necessitate execution by specialists. This article demonstrates in detail the risks for the unborn child pertaining to its developmental phase and explains the three-stage concept as an evaluation scheme. It should be noted, that all risk estimations are subject to considerable uncertainties.
A calculation of the dose distributions in a dog phantom
International Nuclear Information System (INIS)
In the research of radiobiology, animals sometimes receive non-uniform irradiation and the severity of radiation injury greatly depends on the uniformity of the dose in objects. It is necessary to obtain depth dose distributions to express the severity of injury. The dose distributions were calculated in a dog-sized cylindrical phantom using Monte Carlo methods in the paper. It was assumed that the phantom was composed of tissue equivalent material (10.2%H, 12.3%C, 3.5%N, 72.9%O, etc.) and that parallel beams of non-energetic neutrons from 0.3 eV to 14 MeV injected into the phantom with a direction perpendicular to the cylindrical axis
A unique manual method for emergency offsite dose calculations
International Nuclear Information System (INIS)
This paper describes a manual method developed for performance of emergency offsite dose calculations for PP and L's Susquehanna Steam Electric Station. The method is based on a three-part carbonless form. The front page guides the user through selection of the appropriate accident case and inclusion of meteorological and effluent data data. By circling the applicable accident descriptors, the user circles the dose factors on pages 2 and 3 which are then simply multiplied to yield the whole body and thyroid dose rates at the plant boundary, two, five, and ten miles. The process used to generate the worksheet is discussed, including the method used to incorporate the observed terrain effects on airflow patterns caused by the Susquehanna River Valley topography
A Monte Carlo dose calculation algorithm for proton therapy
International Nuclear Information System (INIS)
A Monte Carlo (MC) code (VMCpro) for treatment planning in proton beam therapy of cancer is introduced. It is based on ideas of the Voxel Monte Carlo algorithm for photons and electrons and is applicable to human tissue for clinical proton energies. In the present paper the implementation of electromagnetic and nuclear interactions is described. They are modeled by a Class II condensed history algorithm with continuous energy loss, ionization, multiple scattering, range straggling, δ-electron transport, nuclear elastic proton nucleus scattering and inelastic proton nucleus reactions. VMCpro is faster than the general purpose MC codes FLUKA by a factor of 13 and GEANT4 by a factor of 35 for simulations in a phantom with inhomogeneities. For dose calculations in patients the speed improvement is larger, because VMCpro has only a weak dependency on the heterogeneity of the calculation grid. Dose distributions produced with VMCpro are in agreement with GEANT4 results. Integrated or broad beam depth dose curves show maximum deviations not larger than 1% or 0.5 mm in regions with large dose gradients for the examples presented here
NAC-1 cask dose rate calculations for LWR spent fuel
Energy Technology Data Exchange (ETDEWEB)
CARLSON, A.B.
1999-02-24
A Nuclear Assurance Corporation nuclear fuel transport cask, NAC-1, is being considered as a transport and storage option for spent nuclear fuel located in the B-Cell of the 324 Building. The loaded casks will be shipped to the 200 East Area Interim Storage Area for dry interim storage. Several calculations were performed to assess the photon and neutron dose rates. This report describes the analytical methods, models, and results of this investigation.
NAC-1 cask dose rate calculations for LWR spent fuel
International Nuclear Information System (INIS)
A Nuclear Assurance Corporation nuclear fuel transport cask, NAC-1, is being considered as a transport and storage option for spent nuclear fuel located in the B-Cell of the 324 Building. The loaded casks will be shipped to the 200 East Area Interim Storage Area for dry interim storage. Several calculations were performed to assess the photon and neutron dose rates. This report describes the analytical methods, models, and results of this investigation
Data base for terrestrial food pathways dose commitment calculations
International Nuclear Information System (INIS)
A computer program is under development to allow calculation of the dose-to-man in Georgia and South Carolina from ingestion of radionuclides in terrestrial foods resulting from deposition of airborne radionuclides. This program is based on models described in Regulatory Guide 1.109 (USNRC, 1977). The data base describes the movement of radionuclides through the terrestrial food chain, growth and consumption factors for a variety of radionuclides
Off-center ratios for three-dimensional dose calculations
International Nuclear Information System (INIS)
A new method is proposed for computing the off-center ratios (OCR's) in three-dimensional dose calculations. For an open field, the OCR at a point is computed as the product of the primary OCR (POCR) and the boundary factors (BF's). The POCR describes the beam profile for an infinite field, that is, without the effect of the collimators. It is defined as the ratio of the dose at a point off the central ray to the dose at the point on the central ray at the same depth for an infinite field. The POCR is a function of radial distance from the beam central ray and depth. The BF describes the shape of the beam in the neighborhood of the field boundary defined by the collimators. It is defined as the ratio of the OCR at a point for a finite field to the OCR at the same point for an infinite field. The BF is a function of distance from the field boundary, depth, and field size. For a wedged field, we assume that the boundary factors remain the same as for open fields but the POCR's are altered. The changes in beam profiles are described by a factor called the wedge profile factor (WPF), defined as the ratio of the dose at a point for the largest wedged field to the dose at the same point for an open field of the same field size. The WPF is a function of lateral distance from the beam central plane and depth. Calculated OCR's using this new method are in agreement with the measured data along both the transverse and the diagonal directions of the field
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Purpose: Treatment plans for the TomoTherapy unit are produced with a planning system that is integral to the unit. The authors have produced an independent dose calculation system, to enable plans to be recalculated in three dimensions, using the patient's CT data. Methods: Software has been written using MATLAB. The DICOM-RT plan object is used to determine the treatment parameters used, including the treatment sinogram. Each projection of the sinogram is segmented and used to calculate dose at multiple calculation points in a three-dimensional grid using tables of measured beam data. A fast ray-trace algorithm is used to determine effective depth for each projection angle at each calculation point. Calculations were performed on a standard desktop personal computer, with a 2.6 GHz Pentium, running Windows XP. Results: The time to perform a calculation, for 3375 points averaged 1 min 23 s for prostate plans and 3 min 40 s for head and neck plans. The mean dose within the 50% isodose was calculated and compared with the predictions of the TomoTherapy planning system. When the modified CT (which includes the TomoTherapy couch) was used, the mean difference for ten prostate patients, was -0.4% (range -0.9% to +0.3%). With the original CT (which included the CT couch), the mean difference was -1.0% (range -1.7% to 0.0%). The number of points agreeing with a gamma 3%/3 mm averaged 99.2% with the modified CT, 96.3% with the original CT. For ten head and neck patients, for the modified and original CT, respectively, the mean difference was +1.1% (range -0.4% to +3.1%) and 1.1% (range -0.4% to +3.0%) with 94.4% and 95.4% passing a gamma 4%/4 mm. The ability of the program to detect a variety of simulated errors has been tested. Conclusions: By using the patient's CT data, the independent dose calculation performs checks that are not performed by a measurement in a cylindrical phantom. This enables it to be used either as an additional check or to replace phantom
Implementation of spot scanning dose optimization and dose calculation for helium ions in Hyperion
DEFF Research Database (Denmark)
Fuchs, Hermann; Alber, Markus; Schreiner, Thomas;
2015-01-01
PURPOSE: Helium ions ((4)He) may supplement current particle beam therapy strategies as they possess advantages in physical dose distribution over protons. To assess potential clinical advantages, a dose calculation module accounting for relative biological effectiveness (RBE) was developed and...... Bragg-peak region, which was then kept constant over the fragmentation tail. To account for a variable proton RBE, the same model concept was also applied to protons with a maximum RBE of 1.6. Both RBE models were added to a previously developed pencil beam algorithm for physical dose calculation and...... included into the treatment planning system Hyperion. The implementation was validated against Monte Carlo simulations within a water phantom using γ-index evaluation. The potential benefits of (4)He based treatment plans were explored in a preliminary treatment planning comparison (against protons) for...
Kanematsu, Nobuyuki
2007-01-01
A simple and efficient variant of the pencil-beam algorithm for dose distribution calculation is proposed. Compared to the conventional pencil-beam algorithms, the new algorithm is intrinsically faster due to minimized computation within the convolution integral. Namely, computation for physical interaction is decoupled from the convolution integral and the convolution kernel is approximated by simple grid-to-grid correlation. Implementation to a treatment planning system for carbon-ion radiotherapy has enabled realistic beam blurring with marginal speed decrease from the broad-beam calculation. Evaluation of a modeled proton pencil beam exhibits inaccuracy within its spread at the Bragg peak when the beam incidence is angled to all the dose grid axes, which will be minimized in broad-beam formation and may be acceptable depending on its relative significance to the other sources of errors. The new algorithm will provide balanced accuracy and speed without technical difficulty for high-resolution dose distrib...
Source term calculations for assessing radiation dose to equipment
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This study examines results of analyses performed with the Source Term Code Package to develop updated source terms using NUREG-0956 methods. The updated source terms are to be used to assess the adequacy of current regulatory source terms used as the basis for equipment qualification. Time-dependent locational distributions of radionuclides within a containment following a severe accident have been developed. The Surry reactor has been selected in this study as representative of PWR containment designs. Similarly, the Peach Bottom reactor has been used to examine radionuclide distributions in boiling water reactors. The time-dependent inventory of each key radionuclide is provided in terms of its activity in curies. The data are to be used by Sandia National Laboratories to perform shielding analyses to estimate radiation dose to equipment in each containment design. See NUREG/CR-5175, ''Beta and Gamma Dose Calculations for PWR and BWR Containments.'' 6 refs., 11 tabs
Development of software for internal dose calculation from bioassay measurements
International Nuclear Information System (INIS)
Recently developed biokinetic models of ICRP permit increasingly realistic descriptions of the behaviour of radionuclides in the human body. This, however, has made the interpretation of bioassay data extremely difficult. Thus computer programs for implementing these models are in need, but very few are available. The present work describes personal-computer-based software, MONDAL2 (monitoring to dose calculation ver. 2), that enables users to estimate intake activity and the resulting effective doses from bioassay measurements for both workers and members of the public. This software runs on Microsoft Windows 95, 98, Millennium edition, 2000 or XP. If the system is to be fully copied to a hard disk, hard disk space of 23 MB is required. This software is distributed by the National Inst. of Radiological Sciences free of charge. (authors)
Bicalho, Millena Drumond; Soares, Danielly Botelho; Botoni, Fernando Antonio; Reis, Adriano Max Moreira; Martins, Maria Auxiliadora Parreiras
2015-09-01
: Hospitalized patients require the use of a variety of drugs, many of which individually or in combination have the potential to cause kidney damage. The use of potentially nephrotoxic drugs is often unavoidable, and the need for dose adjustment should be evaluated. This study is aimed at assessing concordance in information on drug-induced nephrotoxicity and dose adjustment recommendations by comparing four drug information sources (DRUGDEX(®), UpToDate(®), Medscape(®) and the Brazilian Therapeutic Formulary) using the formulary of a Brazilian public hospital. A total of 218 drugs were investigated. The global Fleiss' kappa coefficient was 0.265 for nephrotoxicity (p < 0.001; CI 95%, 0.211-0.319) and 0.346 for recommendations (p < 0.001; CI 95%, 0.292-0.401), indicating fair concordance among the sources. Anti-infectives and anti-hypertensives were the main drugs cited as nephrotoxic by the different sources. There were no clear definitions for qualitative data or quantitative values for dose adjustments among the four information sources. There was no advice for dosing for a large number of the drugs in the international databases. The National Therapeutic Formulary offered imprecise dose adjustment recommendations for many nephrotoxic drugs. Discrepancies among information sources may have a clinical impact on patient care and contribute to drug-related morbidity and mortality. PMID:26371029
Measurements and calculations of doses from radioactive particles
International Nuclear Information System (INIS)
Three Mile Island (TMI) and Tchernobyl reactor accidents have revealed the importance of the skin exposure to beta radiation produced by small high activity sources, named 'hot particles'. In nuclear power reactors, they may arise as small fragments of irradiated fuel or material which have been neutron activated by passing through the reactor co. In recent years, skin exposure to hot particles has been subject to different limitation criteria, formulated by AIEA, ICRP, NCRP working groups. The present work is the contribution of CEA Grenoble to a contract of the Commission of the European communities in cooperation with several laboratories: University of Birmingham, University of Toulouse and University of Montpellier with the main goal to check experiments and calculations of tissue dose from 60Co radioactive particles. This report is split up into two parts: hot particle dosimetry close to a 60Co spherical sample with an approximately 200 μm diameter, using a PTW extrapolation chamber model 233991; dose calculations from two codes: the Varskin Mod 2 computer code and the Hot 25 S2 Monte Carlo algorithm. The two codes lead to similar results; nevertheless there is a large discrepancy (of about 2) between calculations and PTW measurements which are higher by a factor of 1.9. At a 70 μm skin depth and for 1 cm2 irradiated area, the total (β + γ) tissue dose rate delivered by a spherical ( φ = 200 μm) 60Co source, in contact with skin, is of the order of 6.1 10-2 nGy s-1 Bq-1. (author)
Deterministic calculations of radiation doses from brachytherapy seeds
International Nuclear Information System (INIS)
Brachytherapy is used for treating certain types of cancer by inserting radioactive sources into tumours. CDTN/CNEN is developing brachytherapy seeds to be used mainly in prostate cancer treatment. Dose calculations play a very significant role in the characterization of the developed seeds. The current state-of-the-art of computation dosimetry relies on Monte Carlo methods using, for instance, MCNP codes. However, deterministic calculations have some advantages, as, for example, short computer time to find solutions. This paper presents a software developed to calculate doses in a two-dimensional space surrounding the seed, using a deterministic algorithm. The analysed seeds consist of capsules similar to IMC6711 (OncoSeed), that are commercially available. The exposure rates and absorbed doses are computed using the Sievert integral and the Meisberger third order polynomial, respectively. The software also allows the isodose visualization at the surface plan. The user can choose between four different radionuclides (192Ir, 198Au, 137Cs and 60Co). He also have to enter as input data: the exposure rate constant; the source activity; the active length of the source; the number of segments in which the source will be divided; the total source length; the source diameter; and the actual and effective source thickness. The computed results were benchmarked against results from literature and developed software will be used to support the characterization process of the source that is being developed at CDTN. The software was implemented using Borland Delphi in Windows environment and is an alternative to Monte Carlo based codes. (author)
Comparison between calculation methods of dose rates in gynecologic brachytherapy
International Nuclear Information System (INIS)
In treatments with radiations for gynecologic tumors is necessary to evaluate the quality of the results obtained by different calculation methods for the dose rates on the points of clinical interest (A, rectal, vesicle). The present work compares the results obtained by two methods. The Manual Calibration Method (MCM) tri dimensional (Vianello E., et.al. 1998), using orthogonal radiographs for each patient in treatment, and the Theraplan/T P-11 planning system (Thratonics International Limited 1990) this last one verified experimentally (Vianello et.al. 1996). The results show that MCM can be used in the physical-clinical practice with a percentile difference comparable at the computerized programs. (Author)
Mathematical models for calculating radiation dose to the fetus
International Nuclear Information System (INIS)
Estimates of radiation dose from radionuclides inside the body are calculated on the basis of energy deposition in mathematical models representing the organs and tissues of the human body. Complex models may be used with radiation transport codes to calculate the fraction of emitted energy that is absorbed in a target tissue even at a distance from the source. Other models may be simple geometric shapes for which absorbed fractions of energy have already been calculated. Models of Reference Man, the 15-year-old (Reference Woman), the 10-year-old, the five-year-old, the one-year-old, and the newborn have been developed and used for calculating specific absorbed fractions (absorbed fractions of energy per unit mass) for several different photon energies and many different source-target combinations. The Reference woman model is adequate for calculating energy deposition in the uterus during the first few weeks of pregnancy. During the course of pregnancy, the embryo/fetus increases rapidly in size and thus requires several models for calculating absorbed fractions. In addition, the increases in size and changes in shape of the uterus and fetus result in the repositioning of the maternal organs and in different geometric relationships among the organs and the fetus. This is especially true of the excretory organs such as the urinary bladder and the various sections of the gastrointestinal tract. Several models have been developed for calculating absorbed fractions of energy in the fetus, including models of the uterus and fetus for each month of pregnancy and complete models of the pregnant woman at the end of each trimester. In this paper, the available models and the appropriate use of each will be discussed. (Author) 19 refs., 7 figs
Midplane dose determination and verification of calculated doses in total body irradiation
Directory of Open Access Journals (Sweden)
Özlem ÖZDEMİR
2014-06-01
Full Text Available OBJECTIVES To compare calculated and measured doses for different regions of anthropomorphic phantom and patients using ion chamber and thermoluminescence dosimetry (TLD for total body irradiation. METHODS Measurements were done for lateral fields with 6 MV, gantry 82º, 40x40 cm2 field and 400 cm source-axis distance (SAD. Entrance-exit and midline doses were measured on anthropomorphic phantom by TLD and entrance-exit doses were measured by TLD and ion chamber on patients. RESULTS For anthropomorphic phantom measurements differences between calculated and measured entrance-exit doses of head, neck, shoulder, lung and thick pelvis were 0.8%, 2.7%, 26.4%, 4.4% and 4.9% and for midline doses were 1.6%, 1.6%, 6.3%, -1.4% and 7.4% respectively. For patients; TLD differences were within -4.13% ile 6.7%, -3.3% ile 3.9%, 5.1% ile 16.6%, -7.8% ile 2.4%, and 3.6% ile 7.1% respectively. For thick pelvis measurements with ion chamber differences were within %0.1-1.9. CONCLUSION Total body irradiation is being applied in limit values in our clinic.
Effects of sterilising doses of gamma radiation on drugs
International Nuclear Information System (INIS)
Effects of gamma radiation on drugs in solid state and aqueous solution were studied after application of doses of 2.5 and 5.0 Mrad (dose rate 0.1 Mrad/hour). Whereas solid substances only showed colour changes dissolved substances were decomposed to a somewhat higher degree than by heating in an autoclave at a temperature of 120 0C. (author)
Japanese internet system for calculation of route doses (JISCARD)
International Nuclear Information System (INIS)
JISCARD was developed in 2005 by the National Institute of Radiological Sciences (NIRS), Japan. The present report explains how to use the system to calculate exposure doses to be received by aircraft crew or passengers making a flight by international regular routes connecting Japan and the principle 35 cities of the world. Entering home page of NIRS, the user is requested to select the starting and arriving airports on graphical interface, the traveling date (year, month) which should be within 2001 - 2011, and the internet tool. The calculation is based on the code CARI-6, developed by FAA (the Federal Aviation Administration), and takes into consideration altitude effect as well as an 11-year cycle of the solar activity. (S. Ohno)
International Nuclear Information System (INIS)
Full text: With the growing need of energy all over the world there is no doubt that nuclear energy will be an important alternative. Nuclear energy is not only a good alternative energy source but also is getting more safe. In contrary to fossil fuels nuclear energy does not produce green house gases. With all adventages of nuclear energy, the safety of nuclear power plants must be taken into care. From the radiological point of view the atmospheric dispersion of radionuclides and radiation dose calculations in case of a reactor accident is important. This study investigates the deposition and air concentration of 137Cs and 131I radionuclides and the radiation doses exposed to people living in different cities in Turkey after Chernobyl nuclear reactor accident. WRF results and HYSPLIT results were compared with observation data and the 'Atlas on the cesium deposition across Europe' that published by European Commission respectively. Both WRF and HYSPLIT results were consistent with reference data. (author)
PFP vertical calciner shield wall dose rate calculations using MCNP
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This report yields a neutron shield wall design for a full time occupancy dose rate of 0.25 mrem/h. ORIGEN2 generated gamma ray spectrum and neutron intensity for plutonium. MCNP modeled the calciner glovebox and room for reflection of neutrons off concrete walls and ceiling. Neutron calculations used MCNP in mode n, p to include neutron capture gammas. Photon calculations used MCNP in mode p for gamma rays. Neutron shield with lower 137.16 cm (4.5 feet) of 12.7 cm (5 inch) thick Lucite reg-sign and 0.3175 cm (0.125 inch) stainless steel on both sides, and upper 76.2 cm (2.5 feet) of 10.16 cm (4 inch) thick Lucite reg-sign and 1.905 cm (0.75 inch) thick glass on each side gave a total weighted dose rate of 0.23 mrem/h, fulfilling the design goal. Lucite reg-sign is considered to be equivalent to Plexiglas reg-sign since both are methylmethacrylate polymers
International Nuclear Information System (INIS)
The computer code HADOC (Hanford Acute Dose Calculations) is described and instructions for its use are presented. The code calculates external dose from air submersion and inhalation doses following acute radionuclide releases. Atmospheric dispersion is calculated using the Hanford model with options to determine maximum conditions. Building wake effects and terrain variation may also be considered. Doses are calculated using dose conversion factor supplied in a data library. Doses are reported for one and fifty year dose commitment periods for the maximum individual and the regional population (within 50 miles). The fractional contribution to dose by radionuclide and exposure mode are also printed if requested
Assessment of X-ray output dose in the dose calculation of linear accelerators
International Nuclear Information System (INIS)
Many structural types of MLC (multiple-leaf collimator) are now introduced for linear accelerators and are important factors influencing the exposure dose to patients. In other words, the formula for dose calculation would differ depending on the type which, however, does not always require the different method of dose assessment for different MLC type. Rather, the assessment can be generalized and be applicable in any case of irradiation conditions when the concept of output factors is used. This article described the concept now recognized globally: The output factors consists from field factors and scatter factors, which are further divided in some factors attributable to the apparatus with MLC and irradiation object. The review also demonstrated the effectiveness of the concept by experiments using phantoms under various irradiation conditions. (K.H.)
Effects of TPS calculation grid on dose calculation accuracy for 125I seed implantation
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Objective: To study the influence of TPS calculation grid on the dose calculation accuracy for 125I seed implantation. Methods: Ten verification plans were selected randomly. Calculating grids were modulated into four groups: 128 × 128, 96 × 96, 64 × 64 and 32 × 32. Under the conditions of same seeds number, location, activity and target volume, the doses resulting from every plan were calculated using TPS to obtain D90, V90, V100 and V150. Data were grouped into A, B, C and D by means of the calculating grid of 128 × 128, 96 × 96, 64 × 64 and 32 × 32. The percentage errors of four groups were calculated. Results: The arithmetic mean D90 of group A, B, C and D were (7 178.8 ± 2 237.7), (7 072.7 ±2 240.8), (6 889.1 ±2 305.5) and (6 351.0 ±2 515.7) cGy, respectively. The arithmetic mean of percentage errors of the four groups were (0.74 ± 0.6)%, (-0.89 ± 2.2)%, (-3.85 ± 4.7)% and (-10.46 ±4.8)% (F=8.95, P <0.05). The V90 of group A, B, C and D were (93.12 ± 0.32)%, (92.75 ±0.29)%, (91.87±1.28)% and (88.06 ±5.06)% (F=7.85, P<0.05). The V100 of group A, B, C and D were (90.21 ±0.14)%, (89.67 ±0.64)%, (88.68 ± 1.80)% and (84.10±6.56)% (F=6.64, P<0.05). The V150 of group A, B, C and D were (73.48 ±3.49)%,(72.66±3.96)%,(71.33±4.83)% and (65.41 ±9.49)% (F=3.90, P<0.05). Conclusions: The dose calculating accuracy of 125I seeds implantation is influenced significantly by TPS calculating grid. The calculating grid of 128 × 128 should be used as long as the calculating speed is not reduced. (authors)
Effect of tissue inhomogeneity on beta dose calculation
International Nuclear Information System (INIS)
Appropriate monoclonal antibodies labeled with beta-emitting nuclides of high specific activity have been suggested for treatment of specific tumors. In a homogeneous medium the radiation dose rate distribution R due to a distributed activity distribution C can be calculated by convolution of the beta dose point kernel of the radionuclide in soft tissue with C. Prototype computer programs using Fast Fourier Transform techniques have been developed to evaluate the three dimensional spatial convolution efficiently. To study the effect of tissue inhomogeneity on R, the authors simulated a soft tissue-bone interface by a polystyrene (PST)-aluminum (A1) interface and considered the backscattering of beta rays from a point source and a plane source of 32P. LiF thermoluminescent dosimeters were used. With the point source at the PST-A1 interface, R at 0-31, 125-156, and 283-314 mg/cm2 separations from the interface were increased by (12 +/- 3)%, (8 +/-2)%, and (3 +/- 2)%, respectively, compared with a PST-PST interface. With the plane source, the increases were (8 +/- 3)%, (6 +/- 3)%, and (5 +/- 5)% for separations of 23-58, 150-184, and 277-311 mg/cm2, respectively. With the point source at a PST-air interface to simulate soft tissue-air interface, R at 0-31, 139-170, and 283-314 mg/cm2 from the interface were decreased by (25 +/- 4)%, (11 +/- 7)%, and (5 +/-2)%, respectively. The changes in R have also been measured with degraded spectra of 32P. Comparison of the experimental data with Monte Carlo calculation and the Two-Group method of calculation will be discussed. 20 references, 6 figures, 2 tables
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Full text: For nuclear medicine patients who are breast feeding an infant, special radiation safety precautions may need to be taken. An estimate of the potential radiation dose to the child from ingested milk must be made, and breast-feeding may need to be suspended until levels of radioactivity in the breast-milk have fallen to acceptable levels. The risk of radiation to the child must be weighed against the benefits of breast-feeding and the possible trauma to both mother and child arising from interruption or cessation of the milk supply. In the United States, the Nuclear Regulatory Commission (NRC) has already published regulations which will necessitate an estimate of the infant's dose from breast milk to be made, in principle, for every breast-feeding patient. There is obviously, therefore, a need to provide a rapid and reliable means of estimating such doses. A spreadsheet template which automatically calculates the cumulative dose to breast feeding infants based on any multi-exponential clearance of activity from the breast milk, and any pattern of feeding, has been developed by the authors. The time (post administration) for which breast-feeding should be interrupted in order to constrain the radiation dose to a selected limit is also calculated along with the concentration of activity in breast milk at which feeding can resume. The effect of changing dose limits, feeding patterns and using individually derived breast milk clearance rates may be readily modelled using this spreadsheet template. Data has been included for many of the most commonly used radiopharmaceuticals and new data can readily be incorporated as it becomes available. Copyright (2000) The Australian and New Zealand Society of Nuclear Medicine Inc
Biokinetics in repeated-dosing in vitro drug toxicity studies
Kramer, Nynke I; Di Consiglio, Emma; Blaauboer, Bas J; Testai, Emanuela
2015-01-01
The aim of the EU FP7 Predict-IV project was to improve the predictivity of in vitro assays for unwanted effects of drugs after repeated dosing. The project assessed the added benefit of integrating long-lived in vitro organotypic cell systems with 'omics' technologies and in silico modelling, inclu
The models of internal dose calculation in ICRP
International Nuclear Information System (INIS)
There are a lot discussions about internal dose calculation in ICRP. Many efforts are devoted to improvement in models and parameters. In this report, we discuss what kind of models and parameters are used in ICRP. Models are divided into two parts, the dosimetric model and biokinetic model. The former is a mathematical phantom model, and it is mainly developed in ORNL. The results are used in many researchers. The latter is a compartment model and it has a difficulty to decide the parameter values. They are not easy to estimate because of their age dependency. ICRP officially sets values at ages of 3 month, 1 year, 5 year, 10 year, 15 year and adult, and recommends to get values among ages by linear age interpolate. But it is very difficult to solve the basic equation with these values, so we calculate by use of computers. However, it has complex shame and needs long CPU time. We should make approximated equations. The parameter values include much uncertainty because of less experimental data, especially for a child. And these models and parameter values are for Caucasian. We should inquire whether they could correctly describe other than Caucasian. The body size affects the values of calculated SAF, and the differences of metabolism change the biokinetic pattern. (author)
International Nuclear Information System (INIS)
The objective of this study was to evaluate the patient effective dose and scattered dose from recently developed dental mobile equipment in Korea. The MCNPX 2.6 (Los Alamos National Laboratory, USA) was used in a Monte Carlo simulation to calculate both the effective and scattered doses. The MCNPX code was constructed identically as in the general use of equipment and the effective dose and scattered dose were calculated using the KTMAN-2 digital phantom. The effective dose was calculated as 906 μSv. The equivalent doses per organ were calculated via the MCNPX code, and were 32 174 and 19 μSv in the salivary gland and oesophagus, respectively. The scattered dose of 22.5-32.6 μSv of the tube side at 25 cm from the centre in anterior and posterior planes was measured as 1.4-3 times higher than the detector side of 10.5-16.0 μSv. (authors)
Emergency Doses (ED) - Revision 3: A calculator code for environmental dose computations
International Nuclear Information System (INIS)
The calculator program ED (Emergency Doses) was developed from several HP-41CV calculator programs documented in the report Seven Health Physics Calculator Programs for the HP-41CV, RHO-HS-ST-5P (Rittman 1984). The program was developed to enable estimates of offsite impacts more rapidly and reliably than was possible with the software available for emergency response at that time. The ED - Revision 3, documented in this report, revises the inhalation dose model to match that of ICRP 30, and adds the simple estimates for air concentration downwind from a chemical release. In addition, the method for calculating the Pasquill dispersion parameters was revised to match the GENII code within the limitations of a hand-held calculator (e.g., plume rise and building wake effects are not included). The summary report generator for printed output, which had been present in the code from the original version, was eliminated in Revision 3 to make room for the dispersion model, the chemical release portion, and the methods of looping back to an input menu until there is no further no change. This program runs on the Hewlett-Packard programmable calculators known as the HP-41CV and the HP-41CX. The documentation for ED - Revision 3 includes a guide for users, sample problems, detailed verification tests and results, model descriptions, code description (with program listing), and independent peer review. This software is intended to be used by individuals with some training in the use of air transport models. There are some user inputs that require intelligent application of the model to the actual conditions of the accident. The results calculated using ED - Revision 3 are only correct to the extent allowed by the mathematical models. 9 refs., 36 tabs
A brachytherapy model-based dose calculation algorithm -AMIGOBrachy
International Nuclear Information System (INIS)
Brachytherapy treatments have been performed based on TG-43U1 water dose formalism which neglects human tissues density and composition, body interfaces and applicator effects. As these effects could be relevant for brachytherapy energy range, modern treatment planning systems (TPS) are now available that are based on model-based dose calculation algorithms (MBDCA) enabling heterogeneity corrections, which are needed to replace the TG-43U1 water dose formalism for a more accurate approach. The recently published AAPM TG-186 report is the first step towards to a TPS taking into account heterogeneities, applicators and human body complexities. This report presents the current status, recommendations for clinical implementation and specifies research areas where considerable efforts are necessary to move forward with MBDCA. Monte Carlo (MC) codes are an important part of the current algorithms due their flexibility and accuracy, although, almost all MC codes present no interface to process the large amount of data necessary to perform clinical cases simulations, which may include hundreds of dwell positions, inter-seed attenuation, image processing and others time consuming issues that can make MC simulation unfeasible without a pre-processing interface. This work presents the AMIGOBrachy interface tool (Algorithm for Medical Image-based Generating Object - Brachytherapy module) which provides all the pre-processing task needed for the simulation. This software can import and edit treatments plans from BrachyVision™ (Varian Medical Systems, Inc., Palo Alto, CA) and ONCENTRA™ (Elekta AB, Stockholm, Sweden), and also create a new plan through contouring resources, needle recognition, HU segmentation, combining voxels phantoms with analytical geometries to define applicators and other resources used to create MCNP5 input and analyze the results. This work presents some results used to validate the software and to evaluate the heterogeneities impact in a clinical case
Considerations of beta and electron transport in internal dose calculations
Energy Technology Data Exchange (ETDEWEB)
Bolch, W.E.; Poston, J.W. Sr.
1990-12-01
Ionizing radiation has broad uses in modern science and medicine. These uses often require the calculation of energy deposition in the irradiated media and, usually, the medium of interest is the human body. Energy deposition from radioactive sources within the human body and the effects of such deposition are considered in the field of internal dosimetry. In July of 1988, a three-year research project was initiated by the Nuclear Engineering Department at Texas A M University under the sponsorship of the US Department of Energy. The main thrust of the research was to consider, for the first time, the detailed spatial transport of electron and beta particles in the estimation of average organ doses under the Medical Internal Radiation Dose (MIRD) schema. At the present time (December of 1990), research activities are continuing within five areas. Several are new initiatives begun within the second or third year of the current contract period. They include: (1) development of small-scale dosimetry; (2) development of a differential volume phantom; (3) development of a dosimetric bone model; (4) assessment of the new ICRP lung model; and (5) studies into the mechanisms of DNA damage. A progress report is given for each of these tasks within the Comprehensive Report. In each case, preliminary results are very encouraging and plans for further research are detailed within this document.
Considerations of beta and electron transport in internal dose calculations
International Nuclear Information System (INIS)
Ionizing radiation has broad uses in modern science and medicine. These uses often require the calculation of energy deposition in the irradiated media and, usually, the medium of interest is the human body. Energy deposition from radioactive sources within the human body and the effects of such deposition are considered in the field of internal dosimetry. In July of 1988, a three-year research project was initiated by the Nuclear Engineering Department at Texas A ampersand M University under the sponsorship of the US Department of Energy. The main thrust of the research was to consider, for the first time, the detailed spatial transport of electron and beta particles in the estimation of average organ doses under the Medical Internal Radiation Dose (MIRD) schema. At the present time (December of 1990), research activities are continuing within five areas. Several are new initiatives begun within the second or third year of the current contract period. They include: (1) development of small-scale dosimetry; (2) development of a differential volume phantom; (3) development of a dosimetric bone model; (4) assessment of the new ICRP lung model; and (5) studies into the mechanisms of DNA damage. A progress report is given for each of these tasks within the Comprehensive Report. In each case, preliminary results are very encouraging and plans for further research are detailed within this document
Considerations of beta and electron transport in internal dose calculations
International Nuclear Information System (INIS)
Ionizing radiation has broad uses in modern science and medicine. These uses often require the calculation of energy deposition in the irradiated media and, usually, the medium of interest is the human body. Energy deposition from radioactive sources within the human body and the effects of such deposition are considered in the field of internal dosimetry. In July of 1988, a three-year research project was initiated by the Nuclear Engineering Department at Texas A ampersand M University under the sponsorship of the US Department of Energy. The main thrust of the research was to consider, for the first time, the detailed spatial transport of electron and beta particles in the estimation of average organ doses under the Medical Internal Radiation Dose (MIRD) schema. At the present time (December of 1990), research activities are continuing within five areas. Several are new initiatives begun within the second or third year of the current contract period. They include: (1) development of small-scale dosimetry; (2) development of a differential volume phantom; (3) development of a dosimetric bone model; (4) assessment of the new ICRP lung model; and (5) studies into the mechanisms of DNA damage. A progress report is given for each of these tasks within the Comprehensive Report. In each use, preliminary results are very encouraging and plans for further research are detailed within this document. 22 refs., 13 figs., 1 tab
Pion dose distribution calculations and measurements for dynamic radiotherapy
International Nuclear Information System (INIS)
Routine three dimensional conformation therapy with negative pions is done with the PIOTRON at SIN since two years. More than 60 patients have been treated by spot scan with the 60 converging beams for deep seated tumors in the pelvic region. Extensive measurements have been performed on various phantoms, homogeneous and anthropomorphic, to investigate the influence of tissue inhomogeneities and verify treatment planning calculations. Total dose has been measured by T.E. ionization chambers and TLD, two dimensional stop distributions exposed in planes between phantom slices. In vivo measurements with ionization chambers, as well as catheters filled with /sup 7/LiF TLD's and rolled Al foils, introduced in bladder or rectum, have been used to confirm dose distributions in patients. To check predictions of differences of RBE due to variations in treatment volumes or beam configuration, treatment plans, reflecting typical situation in therapy, have been created for radiobiological investigations. Various user groups have measured biological effects by cell survival experiments with mammalian cells or with mouse intestinal crypt cell assay
Considerations of beta and electron transport in internal dose calculations
Energy Technology Data Exchange (ETDEWEB)
Bolch, W.E.; Poston, J.W. Sr. (Texas A and M Univ., College Station, TX (USA). Dept. of Nuclear Engineering)
1990-12-01
Ionizing radiation has broad uses in modern science and medicine. These uses often require the calculation of energy deposition in the irradiated media and, usually, the medium of interest is the human body. Energy deposition from radioactive sources within the human body and the effects of such deposition are considered in the field of internal dosimetry. In July of 1988, a three-year research project was initiated by the Nuclear Engineering Department at Texas A M University under the sponsorship of the US Department of Energy. The main thrust of the research was to consider, for the first time, the detailed spatial transport of electron and beta particles in the estimation of average organ doses under the Medical Internal Radiation Dose (MIRD) schema. At the present time (December of 1990), research activities are continuing within five areas. Several are new initiatives begun within the second or third year of the current contract period. They include: (1) development of small-scale dosimetry; (2) development of a differential volume phantom; (3) development of a dosimetric bone model; (4) assessment of the new ICRP lung model; and (5) studies into the mechanisms of DNA damage. A progress report is given for each of these tasks within the Comprehensive Report. In each use, preliminary results are very encouraging and plans for further research are detailed within this document. 22 refs., 13 figs., 1 tab.
Directory of Open Access Journals (Sweden)
Peiman Haddad
2014-02-01
Conclusion: In this study, the mean testis dose of radiation was 3.77 Gy, similar to the dose calculated by the planning software (4.11 Gy. This dose could be significantly harmful for spermatogenesis, though low doses of scattered radiation to the testis in fractionated radiotherapy might be followed with better recovery. Based on above findings, careful attention to testicular dose in radiotherapy of rectal cancer for the males desiring continued fertility seems to be required.
Review of dose-response curves for acute antimigraine drugs
DEFF Research Database (Denmark)
Hougaard, Anders; Tfelt-Hansen, Peer
2015-01-01
calcitonin-gene related peptide receptor antagonists (telcagepant, MK-3207, BI 44370 TA and BMS-927711) in placebo-controlled trials were reviewed. In addition, dose-response curves for adverse events (AEs) were reviewed. Expert opinion: For most triptans, the dose-response curve for efficacy is flat......, there are many unmet needs. Although upcoming drugs may not be superior to triptans, migraine patients will potentially benefit greatly from these, especially patients who are triptan non-responders and patients with cardiovascular disease....
Radiopharmaceuticals introduction to drug evaluation and dose estimation
Williams, Lawerence E
2010-01-01
Nanoengineering, energized by the desire to find specific targeting agents, is leading to dramatic acceleration in novel drug design. However, in this flurry of activity, some issues may be overlooked. This is especially true in the area of determining dosage and evaluating the effects of multiple agents designed to target more than one site of metastasis. Offering the unique perspective of a medical physicist who has worked directly with cancer patients for over three decades, Radiopharmaceuticals: Introduction to Drug Evaluation and Dose Estimation starts by exploring the recent history and
Off-site dose calculation computer code based on ICRP-60(II) - liquid radioactive effluents -
International Nuclear Information System (INIS)
The development of computer code for calculating off-site doses(K-DOSE60) was based on ICRP-60 and the dose calculationi equations of Reg. Guide 1.109. In this paper, the methodology to compute dose for liquid effluents was described. To examine reliability of the K-DOSE60 code the results obtained from K-DOSE60 were compared with analytic solutions. For liquid effluents. The results by K-DOSE60 are in agreement with analytic solution
Determination of Appropriate Dosing of Influenza Drugs in Pediatric Patients
Acosta, EP; Kimberlin, DW
2010-01-01
Dose-finding studies of influenza antiviral drugs are challenging because it is difficult to enroll subjects in pediatric interventional studies and also because of the lack of concentration (or toxicity)–response relationships, the short duration of antiviral therapy, and the continually developing metabolic profiles of infants and young children. The evaluation of influenza antiviral agents in premature infants adds even more complexity. Recent advances in exposure-targeted study designs an...
International Nuclear Information System (INIS)
We assessed the reliability of the program with 80 patients in the usual points of prescription of each pathology. The average error of the calculation points is less than 0.3% in 95% of cases, finding the major differences in the axes of the applicators (maximum error -0.798%). The program has proved effective previously testing him with erroneous dosimetry. Thanks to the implementation of this program is achieved by the calculation of the dose and part of the process of quality assurance program in a few minutes, highlighting the case of HDR prostate due to having a limited time. Having separate data sheet allows each institution to its protocols modify parameters. (Author)
BENCHMARKING UPGRADED HOTSPOT DOSE CALCULATIONS AGAINST MACCS2 RESULTS
Energy Technology Data Exchange (ETDEWEB)
Brotherton, Kevin
2009-04-30
The radiological consequence of interest for a documented safety analysis (DSA) is the centerline Total Effective Dose Equivalent (TEDE) incurred by the Maximally Exposed Offsite Individual (MOI) evaluated at the 95th percentile consequence level. An upgraded version of HotSpot (Version 2.07) has been developed with the capabilities to read site meteorological data and perform the necessary statistical calculations to determine the 95th percentile consequence result. These capabilities should allow HotSpot to join MACCS2 (Version 1.13.1) and GENII (Version 1.485) as radiological consequence toolbox codes in the Department of Energy (DOE) Safety Software Central Registry. Using the same meteorological data file, scenarios involving a one curie release of {sup 239}Pu were modeled in both HotSpot and MACCS2. Several sets of release conditions were modeled, and the results compared. In each case, input parameter specifications for each code were chosen to match one another as much as the codes would allow. The results from the two codes are in excellent agreement. Slight differences observed in results are explained by algorithm differences.
Considerations of beta and electron transport in internal dose calculations
International Nuclear Information System (INIS)
A computer program has been developed at Texas A ampersand M University to model the transport and energy deposition of electrons and photons for use in internal dose estimation. The code incorporates photon and electron transport subroutines with the geometry subroutine from ALGAM. A user code, called INDOSE, was used to provide estimates of the absorbed fraction of energy for selected target organs of a mathematically described human phantom. The INDOSE code is comprised of three primary sections: the MAIN program, AUSGAB, the scoring routine, and POSITIN, the geometry tracking routine. The geometry routine contains a mathematical representation of Reference Man. The total-body phantom consists of three principal sections and of three types of tissue: lung, skeletal tissue, and soft tissue. The skeletal system represents the total content of the intact skeleton and includes both bone and marrow. This material is considered to be distributed homogeneously throughout the phantom. In 1988, a research proposal was submitted to the Department of Energy (DOE) to continue the code development for use in internal dosimetry calculations, particularly those related to diagnostic nuclear medicine procedures. This document presents a progress report for the completion of tasks accomplished over the period of July 1989 through January 1990. 39 refs., 45 figs., 24 tabs
International Nuclear Information System (INIS)
A computer program, PABLM, was written to facilitate the calculation of internal radiation doses to man from radionuclides in food products and external radiation doses from radionuclides in the environment. This report contains details of mathematical models used and calculational procedures required to run the computer program. Radiation doses from radionuclides in the environment may be calculated from deposition on the soil or plants during an atmospheric or liquid release, or from exposure to residual radionuclides in the environment after the releases have ended. Radioactive decay is considered during the release of radionuclides, after they are deposited on the plants or ground, and during holdup of food after harvest. The radiation dose models consider several exposure pathways. Doses may be calculated for either a maximum-exposed individual or for a population group. The doses calculated are accumulated doses from continuous chronic exposure. A first-year committed dose is calculated as well as an integrated dose for a selected number of years. The equations for calculating internal radiation doses are derived from those given by the International Commission on Radiological Protection (ICRP) for body burdens and MPC's of each radionuclide. The radiation doses from external exposure to contaminated water and soil are calculated using the basic assumption that the contaminated medium is large enough to be considered an infinite volume or plane relative to the range of the emitted radiations. The equations for calculations of the radiation dose from external exposure to shoreline sediments include a correction for the finite width of the contaminated beach
Monte Carlo calculation of ''skyshine'' neutron dose from ALS [Advanced Light Source
International Nuclear Information System (INIS)
This report discusses the following topics on ''skyshine'' neutron dose from ALS: Sources of radiation; ALS modeling for skyshine calculations; MORSE Monte-Carlo; Implementation of MORSE; Results of skyshine calculations from storage ring; and Comparison of MORSE shielding calculations
Performance of independent dose calculation in helical tomotherapy: implementation of the MCSIM code
International Nuclear Information System (INIS)
Currently, a software-based second check dose calculation for helical tomotherapy (HT) is not available. The goal of this study is to evaluate the dose calculation accuracy of the in-house software using EGS4 /MCSIM Monte Carlo environment against the treatment planning system calculations. In-house software was used to convert HT treatment plan information into a non-helical format. The MCSIM dose calculation code was evaluated by comparing point dose calculations and dose profiles against those from the HT treatment plan. Fifteen patients, representing five treatment sites, were used in this comparison. Point dose calculations between the HT treatment planning system and the EGS4 /MCSIM Monte Carlo environment had percent difference values below 5 % for the majority of this study. Vertical and horizontal planar profiles also had percent difference values below 5 % for the majority of this study. Down sampling was seen to improve speed without much loss of accuracy. EGS4 /MCSIM Monte Carlo environment showed good agreement with point dose measurements, compared to the HT treatment plans. Vertical and horizontal profiles also showed good agreement. Significant time saving may be obtained by down-sampling beam projections. The dose calculation accuracy of the in-house software using the MCSIM code against the treatment planning system calculations was evaluated. By comparing point doses and dose profiles, the EGS4 /MCSIM Monte Carlo environment was seen to provide an accurate independent dose calculation.
International Nuclear Information System (INIS)
It is important to ensure that as low as reasonably achievable (ALARA) concept during the radiopharmaceutical (RPH) dose administration in pediatric patients. Several methods have been suggested over the years for the calculation of individualized RPH dose, sometimes requiring complex calculations and large variability exists for administered dose in children. The aim of the present study was to develop a software application that can calculate and store RPH dose along with patient record. We reviewed the literature to select the dose formula and used Microsoft Access (a software package) to develop this application. We used the Microsoft Excel to verify the accurate execution of the dose formula. The manual and computer time using this program required for calculating the RPH dose were compared. The developed application calculates RPH dose for pediatric patients based on European Association of Nuclear Medicine dose card, weight based, body surface area based, Clark, Solomon Fried, Young and Webster's formula. It is password protected to prevent the accidental damage and stores the complete record of patients that can be exported to Excel sheet for further analysis. It reduces the burden of calculation and saves considerable time i.e., 2 min computer time as compared with 102 min (manual calculation with the calculator for all seven formulas for 25 patients). The software detailed above appears to be an easy and useful method for calculation of pediatric RPH dose in routine clinical practice. This software application will help in helping the user to routinely applied ALARA principle while pediatric dose administration. (author)
Hanford Site Annual Report Radiological Dose Calculation Upgrade Evaluation
Energy Technology Data Exchange (ETDEWEB)
Snyder, Sandra F.
2010-02-28
Operations at the Hanford Site, Richland, Washington, result in the release of radioactive materials to offsite residents. Site authorities are required to estimate the dose to the maximally exposed offsite resident. Due to the very low levels of exposure at the residence, computer models, rather than environmental samples, are used to estimate exposure, intake, and dose. A DOS-based model has been used in the past (GENII version 1.485). GENII v1.485 has been updated to a Windows®-based software (GENII version 2.08). Use of the updated software will facilitate future dose evaluations, but must be demonstrated to provide results comparable to those of GENII v1.485. This report describes the GENII v1.485 and GENII v2.08 dose exposure, intake, and dose estimates for the maximally exposed offsite resident reported for calendar year 2008. The GENII v2.08 results reflect updates to implemented algorithms. No two environmental models produce the same results, as was again demonstrated in this report. The aggregated dose results from 2008 Hanford Site airborne and surface water exposure scenarios provide comparable dose results. Therefore, the GENII v2.08 software is recommended for future offsite resident dose evaluations.
Directory of Open Access Journals (Sweden)
Atsushi Komemushi
2012-01-01
Full Text Available Purpose. To assess differences in dose distribution of a vertebral body injected with bone cement as calculated by radiation treatment planning system (RTPS and actual dose distribution. Methods. We prepared two water-equivalent phantoms with cement, and the other two phantoms without cement. The bulk density of the bone cement was imported into RTPS to reduce error from high CT values. A dose distribution map for the phantoms with and without cement was calculated using RTPS with clinical setting and with the bulk density importing. Actual dose distribution was measured by the film density. Dose distribution as calculated by RTPS was compared to the dose distribution measured by the film dosimetry. Results. For the phantom with cement, dose distribution was distorted for the areas corresponding to inside the cement and on the ventral side of the cement. However, dose distribution based on film dosimetry was undistorted behind the cement and dose increases were seen inside cement and around the cement. With the equivalent phantom with bone cement, differences were seen between dose distribution calculated by RTPS and that measured by the film dosimetry. Conclusion. The dose distribution of an area containing bone cement calculated using RTPS differs from actual dose distribution.
International Nuclear Information System (INIS)
Purpose. To assess differences in dose distribution of a vertebral body injected with bone cement as calculated by radiation treatment planning system (RTPS) and actual dose distribution. Methods. We prepared two water-equivalent phantoms with cement, and the other two phantoms without cement. The bulk density of the bone cement was imported into RTPS to reduce error from high CT values. A dose distribution map for the phantoms with and without cement was calculated using RTPS with clinical setting and with the bulk density importing. Actual dose distribution was measured by the film density. Dose distribution as calculated by RTPS was compared to the dose distribution measured by the film dosimetry. Results. For the phantom with cement, dose distribution was distorted for the areas corresponding to inside the cement and on the ventral side of the cement. However, dose distribution based on film dosimetry was undistorted behind the cement and dose increases were seen inside cement and around the cement. With the equivalent phantom with bone cement, differences were seen between dose distribution calculated by RTPS and that measured by the film dosimetry. Conclusion. The dose distribution of an area containing bone cement calculated using RTPS differs from actual dose distribution
International Nuclear Information System (INIS)
Purpose: We describe computer software that performs, quickly and accurately, secondary dose calculations for high-dose-rate (HDR) treatment plans, including those employed for prostate treatments. Methods: The program takes as primary input the data file used by the HDR remote afterloader console for treatment. Dosimetric calculations are performed using the Meisberger polynomial and the anisotropy table for the HDR Iridium-192 source. For standard applicators, treatment geometry is automatically reconstructed and the dose is calculated at relevant reference point(s). Template-based treatment plans (e.g., prostate) require additional user input; the dose calculation is then performed at user-selected reference points. A total dwell time calculation for volume and planar implants using the Manchester tables was also implemented. Results: For fixed-geometry HDR procedures, secondary dose calculations are within 2% of the treatment plan, and results are available for review instantly. For more general applications, the calculated and planned doses are typically within 3% at the prescription isodose line. The Manchester-based dwell time calculation is within 10% of the planned time
The interpretation of animal data in the calculation of doses from new radiolabeled compounds
International Nuclear Information System (INIS)
At NRPB, dose calculations are performed for pharmaceutical companies wishing to obtain approval for human volunteer experiments. Animal data from one or more species are used to estimate the radiation doses to humans that would result from the administration of novel radiolabeled compounds. The calculations themselves are straightforward, but the animal data can be interpreted in different ways, leading to variations in the calculated dose. Doses to the gut compartments usually dominate the committed effective dose equivalent, but retention in other tissues may be important for some compounds. Long-term retention components in tissues can affect doses considerably, and the binding of many radiopharmaceuticals to melanin means that doses to the eye are particularly important. The effect of these considerations on calculating doses are considered, as well as the effect of changes in risk estimates and tissue weighting factors
International Nuclear Information System (INIS)
The analysis described in this report develops the Unit Liter Doses for use in the TWRS FSAR. The Unit Liter Doses provide a practical way to calculate conservative radiological consequences for a variety of potential accidents for the tank farms
Analysis of offsite dose calculation methodology for a nuclear power reactor
International Nuclear Information System (INIS)
This technical study reviews the methodology for calculating offsite dose estimates as described in the offsite dose calculation manual (ODCM) for Pennsylvania Power and Light - Susquehanna Steam Electric Station (SSES). An evaluation of the SSES ODCM dose assessment methodology indicates that it conforms with methodology accepted by the US Nuclear Regulatory Commission (NRC). Using 1993 SSES effluent data, dose estimates are calculated according to SSES ODCM methodology and compared to the dose estimates calculated according to SSES ODCM and the computer model used to produce the reported 1993 dose estimates. The 1993 SSES dose estimates are based on the axioms of Publication 2 of the International Commission of Radiological Protection (ICRP). SSES Dose estimates based on the axioms of ICRP Publication 26 and 30 reveal the total body estimates to be the most affected
Digital Breast Tomosynthesis: Comparison of Different Methods to Calculate Patient Doses
International Nuclear Information System (INIS)
Different methods have been proposed in the literature to calculate the dose to the patient's breast in 3-D mammography. The methods described by Dance et al. and Sechopoulos et al. have been compared in this study using the two tomosynthesis systems available in the authors' hospitals (Siemens and Hologic). There is a small but significant difference of 23% for the first X ray system and 13% for the second system between dose calculations performed with Dance's method and Sechopoulos' method. These differences are mainly due to the fact that the two sets of authors used different breast models for their Monte Carlo calculations. For each system, the calculated breast doses were compared with the dose values indicated on the system console. Good agreement was found when the method of Dance et al. was used for a breast glandularity based on the patient age. For the Siemens system, the calculated doses were 5% lower than the indicated dose and for the Hologic system, the calculated doses were 12% higher. Finally, the 3-D dose values were compared with the doses found in a large 2-D dosimetry study. The dose values for tomosynthesis on the Siemens system were almost double the doses in one view 2-D digital mammography. For a typical breast of thickness 45 mm, the dose of one 2-D view was 0.83 mGy and for one 3-D view 1.79 mGy. (author)
Calculation of mean kidney dose for a Co-57 external radiation source
International Nuclear Information System (INIS)
A description is given of the numerical integration method for the calculation of the mean kidney dose for a Co-57 external radiation source. Based on this theory, a computer program was written. Initial calculation of the kidney volume shows that the method has a good accuracy. For the mean kidney dose, this method gives satisfactory result, since the calculated value lies within the acceptable range of the central axis depth dose
International Nuclear Information System (INIS)
The gantry for proton radiotherapy at the Paul Scherrer Institute (PSI) is designed specifically for the spot-scanning technique. Use of this technique to its full potential requires dose calculation algorithms which are capable of precisely simulating each scanned beam individually. Different specialized analytical dose calculations have been developed, which attempt to model the effects of density heterogeneities in the patient's body on the dose. Their accuracy has been evaluated by a comparison with Monte Carlo calculated dose distributions in the case of a simple geometrical density interface parallel to the beam and typical anatomical situations. A specialized ray casting model which takes range dilution effects (broadening of the spectrum of proton ranges) into account has been found to produce results of good accuracy. This algorithm can easily be implemented in the iterative optimization procedure used for the calculation of the optimal contribution of each individual scanned pencil beam. In most cases an elemental pencil beam dose calculation has been found to be most accurate. Due to the long computing time, this model is currently used only after the optimization procedure as an alternative method of calculating the dose. (author)
International Nuclear Information System (INIS)
In this research, total effective dose equivalent (TEDE) and collective dose (CD) are calculated for the most adverse potential accident in Bushehr Nuclear Power Plant from the viewpoint of radionuclides release to the environment. Calculations are performed using a Gaussian diffusion model and a slightly modified version of AIREM computer code to adopt for conditions in Bushehr. The results are comparable with the final safety analysis report which used DOZAM code. Results of our calculations show no excessive dose in populated regions. Maximum TEDE is determined to be in the WSW direction. CD in the area around the nuclear power plant by a distance of 30 km (138 man Sv) is far below the accepted limits. Thyroid equivalent dose is also calculated for the WSW direction (maximum 25.6 mSv) and is below the limits at various distances from the reactor stack. (authors)
Monte-Carlo Method Python Library for dose distribution Calculation in Brachytherapy
International Nuclear Information System (INIS)
The Cs-137 Brachytherapy treatment is performed in Madagascar since 2005. Time treatment calculation for prescribed dose is made manually. Monte-Carlo Method Python library written at Madagascar INSTN is experimentally used to calculate the dose distribution on the tumour and around it. The first validation of the code was done by comparing the library curves with the Nucletron company curves. To reduce the duration of the calculation, a Grid of PC's is set up with listner patch run on each PC. The library will be used to modelize the dose distribution in the CT scan patient picture for individual and better accuracy time calculation for a prescribed dose.
Vibrational spectra and quantum mechanical calculations of antiretroviral drugs: Nevirapine
Ayala, A. P.; Siesler, H. W.; Wardell, S. M. S. V.; Boechat, N.; Dabbene, V.; Cuffini, S. L.
2007-02-01
Nevirapine (11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'e][1,4]diazepin-6-one) is an antiretroviral drug belonging to the class of the non-nucleoside inhibitors of the HIV-1 virus reverse transcriptase. As most of this kind of antiretroviral drugs, nevirapine displays a butterfly-like conformation which is preserved in complexes with the HIV-1 reverse transcriptase. In this work, we present a detailed vibrational spectroscopy investigation of nevirapine by using mid-infrared, near-infrared, and Raman spectroscopies. These data are supported by quantum mechanical calculations, which allow us to characterize completely the vibrational spectra of this compound. Based on these results, we discuss the correlation between the vibrational modes and the crystalline structure of the most stable form of nevirapine.
Radial Dose Profiles: Calculation Refinements and Sensitivities to Single Event Effects Analysis
Patterson, Jeffrey; Swimm, Randall
2005-01-01
Comparisons of radial dose calculation are performed, as well as the introduction of important physics to improve the calculation techniques. Also, the consequences to device performance are explored via numerical simulations.
Paradigm shift in LUNG SBRT dose calculation associated with Heterogeneity correction
International Nuclear Information System (INIS)
Treatment of lung injury SBRT requires great dosimetric accuracy, the increasing clinical importance of dose calculation heterogeneities introducing algorithms that adequately model the transport of particles narrow beams in media of low density, as with Monte Carlo calculation. (Author)
Experimental validation of Monte Carlo calculations for organ dose
International Nuclear Information System (INIS)
The problem of validating estimates of absorbed dose due to photon energy deposition is examined. The computational approaches used for the estimation of the photon energy deposition is examined. The limited data for validation of these approaches is discussed and suggestions made as to how better validation information might be obtained
Improving dosing of gentamicin in the obese patient: a 3-cycle drug chart and case note audit
Manjaly, Joseph G.; Alexander M. Reece-Smith; Sivaloganathan, Sivan S; Thuraisamy, Christina; Smallwood, Katie LM; Jonas, Elizabeth; Longman, Robert J.
2012-01-01
Objectives To assess the use of an electronic dose calculator to improve accuracy in the use of a complex Gentamicin prescription policy and assess turnaround time of blood sampling to dose delivery in an NHS hospital. Design Retrospective review of drug chart, case notes and hospital antibiotic database. Setting University Hospitals Bristol, UK Participants Patients receiving once daily intravenous gentamicin using the trust protocol, during the same time window for 3 consecutive years. Main...
Probabilistic calculation of dose commitment from uranium mill tailings
International Nuclear Information System (INIS)
The report discusses in a general way considerations of uncertainty in relation to probabilistic modelling. An example of a probabilistic calculation applied to the behaviour of uranium mill tailings is given
Energy Technology Data Exchange (ETDEWEB)
Napier, B.A.; Kennedy, W.E. Jr.; Soldat, J.K.
1980-03-01
A computer program, PABLM, was written to facilitate the calculation of internal radiation doses to man from radionuclides in food products and external radiation doses from radionuclides in the environment. This report contains details of mathematical models used and calculational procedures required to run the computer program. Radiation doses from radionuclides in the environment may be calculated from deposition on the soil or plants during an atmospheric or liquid release, or from exposure to residual radionuclides in the environment after the releases have ended. Radioactive decay is considered during the release of radionuclides, after they are deposited on the plants or ground, and during holdup of food after harvest. The radiation dose models consider several exposure pathways. Doses may be calculated for either a maximum-exposed individual or for a population group. The doses calculated are accumulated doses from continuous chronic exposure. A first-year committed dose is calculated as well as an integrated dose for a selected number of years. The equations for calculating internal radiation doses are derived from those given by the International Commission on Radiological Protection (ICRP) for body burdens and MPC's of each radionuclide. The radiation doses from external exposure to contaminated water and soil are calculated using the basic assumption that the contaminated medium is large enough to be considered an infinite volume or plane relative to the range of the emitted radiations. The equations for calculations of the radiation dose from external exposure to shoreline sediments include a correction for the finite width of the contaminated beach.
International Nuclear Information System (INIS)
Model-based dose calculation algorithms (MBDCAs), recently introduced in treatment planning systems (TPS) for brachytherapy, calculate tissue absorbed doses. In the TPS framework, doses have hereto been reported as dose to water and water may still be preferred as a dose specification medium. Dose to tissue medium Dmed then needs to be converted into dose to water in tissue Dw,med. Methods to calculate absorbed dose to differently sized water compartments/cavities inside tissue, infinitesimal (used for definition of absorbed dose), small, large or intermediate, are reviewed. Burlin theory is applied to estimate photon energies at which cavity sizes in the range 1 nm–10 mm can be considered small or large. Photon and electron energy spectra are calculated at 1 cm distance from the central axis in cylindrical phantoms of bone, muscle and adipose tissue for 20, 50, 300 keV photons and photons from 125I, 169Yb and 192Ir sources; ratios of mass-collision-stopping powers and mass energy absorption coefficients are calculated as applicable to convert Dmed into Dw,med for small and large cavities. Results show that 1–10 nm sized cavities are small at all investigated photon energies; 100 µm cavities are large only at photon energies w,med/Dmed is discussed in terms of the cavity size in relation to the size of important cellular targets. Free radicals from DNA bound water of nanometre dimensions contribute to DNA damage and cell killing and may be the most important water compartment in cells implying use of ratios of mass-collision-stopping powers for converting Dmed into Dw,med. (paper)
International Nuclear Information System (INIS)
The presence of heterogeneous media can produce significant perturbations of dose distribution in brachytherapy. In a companion paper, we proposed a dose decomposition approach for dose calculation in a heterogeneous medium, which separately treats dose contributions from primary, once-scattered and multiple-scattered photons. The companion paper also describes and verifies a micro-beam ray-tracing method for evaluating the once-scatter dose. This paper deals with the calculation of the multiple-scatter dose. We present two empirical formulations for evaluating the heterogeneity correction factor for a 27 keV point source in a water sphere containing a disc-shaped heterogeneity. The empirical formulations are based on nonlinear curve fitting of the Monte Carlo multiple-scatter dose estimates calculated for the heterogeneous system. Extensive benchmark comparisons show that these formulations provide results for the multiple-scatter dose that agree within 10% (and mostly within 5%) with corresponding Monte Carlo dose estimates. Combining them with the algorithms for primary and once-scatter dose calculation described in the companion paper yields results for the total dose of equivalent accuracy. The empirical formulations are expressed in simple mathematical forms which involve a separation of the geometry and position variables of the heterogeneous system. Such representation provides a good tool to investigate the heterogeneity-induced perturbation of a multiple-scatter dose at low photon energy
Recommended environmental dose calculation methods and Hanford-specific parameters
International Nuclear Information System (INIS)
This document was developed to support the Hanford Environmental Dose overview Panel (HEDOP). The Panel is responsible for reviewing all assessments of potential doses received by humans and other biota resulting from the actual or possible environmental releases of radioactive and other hazardous materials from facilities and/or operations belonging to the US Department of Energy on the Hanford Site in south-central Washington. This document serves as a guide to be used for developing estimates of potential radiation doses, or other measures of risk or health impacts, to people and other biota in the environs on and around the Hanford Site. It provides information to develop technically sound estimates of exposure (i.e., potential or actual) to humans or other biotic receptors that could result from the environmental transport of potentially harmful materials that have been, or could be, released from Hanford operations or facilities. Parameter values and information that are specific to the Hanford environs as well as other supporting material are included in this document
Recommended environmental dose calculation methods and Hanford-specific parameters
Energy Technology Data Exchange (ETDEWEB)
Schreckhise, R.G.; Rhoads, K.; Napier, B.A.; Ramsdell, J.V. (Pacific Northwest Lab., Richland, WA (United States)); Davis, J.S. (Westinghouse Hanford Co., Richland, WA (United States))
1993-03-01
This document was developed to support the Hanford Environmental Dose overview Panel (HEDOP). The Panel is responsible for reviewing all assessments of potential doses received by humans and other biota resulting from the actual or possible environmental releases of radioactive and other hazardous materials from facilities and/or operations belonging to the US Department of Energy on the Hanford Site in south-central Washington. This document serves as a guide to be used for developing estimates of potential radiation doses, or other measures of risk or health impacts, to people and other biota in the environs on and around the Hanford Site. It provides information to develop technically sound estimates of exposure (i.e., potential or actual) to humans or other biotic receptors that could result from the environmental transport of potentially harmful materials that have been, or could be, released from Hanford operations or facilities. Parameter values and information that are specific to the Hanford environs as well as other supporting material are included in this document.
International Nuclear Information System (INIS)
A method is described for determining an effective, depth dose consistent bremsstrahlung spectra for high-energy photon beams using depth dose curves measured in water. A simple, analytical model with three parameters, together with the nominal accelerating potential is used to characterise the bremsstrahlung spectra. The model is used to compute weights for depth dose curves from monoenergetic photons. These monoenergetic depth doses, calculated with the convolution method from Monte Carlo generated point spread functions (PSF), are added to yield the pure photon depth dose distribution. The parameters of the analytical spectrum model are determined using an iterative technique to minimise the difference between calculated and measured depth dose curves. The influence from contaminant electrons is determined from the difference between the calculated and the measured depth dose. (author)
Evaluation of a new commercial Monte Carlo dose calculation algorithm for electron beams
International Nuclear Information System (INIS)
Purpose: In this report the authors present the validation of a Monte Carlo dose calculation algorithm (XiO EMC from Elekta Software) for electron beams. Methods: Calculated and measured dose distributions were compared for homogeneous water phantoms and for a 3D heterogeneous phantom meant to approximate the geometry of a trachea and spine. Comparisons of measurements and calculated data were performed using 2D and 3D gamma index dose comparison metrics. Results: Measured outputs agree with calculated values within estimated uncertainties for standard and extended SSDs for open applicators, and for cutouts, with the exception of the 17 MeV electron beam at extended SSD for cutout sizes smaller than 5 × 5 cm2. Good agreement was obtained between calculated and experimental depth dose curves and dose profiles (minimum number of measurements that pass a 2%/2 mm agreement 2D gamma index criteria for any applicator or energy was 97%). Dose calculations in a heterogeneous phantom agree with radiochromic film measurements (>98% of pixels pass a 3 dimensional 3%/2 mm γ-criteria) provided that the steep dose gradient in the depth direction is considered. Conclusions: Clinically acceptable agreement (at the 2%/2 mm level) between the measurements and calculated data for measurements in water are obtained for this dose calculation algorithm. Radiochromic film is a useful tool to evaluate the accuracy of electron MC treatment planning systems in heterogeneous media
Calculation of age-dependent effective doses for external exposure using the MCNP code
Energy Technology Data Exchange (ETDEWEB)
Hung, Tran Van [Research and Development Center for Radiation Technology, ThuDuc, HoChiMinh City (VT)
2013-07-15
Age-dependent effective dose for external exposure to photons uniformly distributed in air were calculated. Firstly, organ doses were calculated with a series of age-specific MIRD-5 type phantoms using the Monte Carlo code MCNP. The calculations were performed for mono-energetic photon sources with source energies from 10 keV to 5 MeV and for phantoms of newborn, 1, 5, 10, and 15 years-old and adult. Then, the effective doses to the different age-phantoms from the mono-energetic photon sources were estimated based on the obtained organ doses. From the calculated results, it is shown that the effective doses depend on the body size; the effective doses in younger phantoms are higher than those in the older phantoms, especially below 100 keV. (orig.)
Drug interaction with radiopharmaceuticals and the importance for the radiation dose to the patient
International Nuclear Information System (INIS)
A central aspect of the profession of health physics is to establish practical scientifically based radiation protection standards with the worthy aim of minimizing the detriment while at the same time enhancing the benefits derived from sources of ionizing radiation. The biodistribution or pharmacokinetics of radiopharmaceuticals may be altered by drugs and it can lead to misdiagnosis or the necessity to repeat the examination, increasing the dose to the patient. Vincristine (0.03mg/ml) was administered into female mice. One hour after the last dose, 99mTc-GHA (7.4 MBq) was administered and the animals (n=15) were sacrificed. The organs were isolated and the percentages of radioactivity (%ATI/g) in the organs were calculated. We calculated the Drug Interaction Factor (DIF) and the Effect Mass Factor (EMF). The results were statistically significant (Wilcoxon test, p99mTc-GHA was to thymus 1.70, to pancreas 1.68, to uterus 0.42, to spleen 0.78, to lymph node inguinal 0.55, to kidney 0.45, to heart 0.59. The EMF was to ovary 0.28, to uterus 0.64, to thymus 0.17, to spleen 0.45, to lymph node inguinal 0.24, to kidney 0.80, to liver 0.77, to pancreas 0.61. The effects could be explained by the metabolization and/or therapeutic action of these drug. (author)
Fixed-dose combinations of drugs versus single-drug formulations for treating pulmonary tuberculosis
Gallardo, Carmen R; Rigau Comas, David; Valderrama Rodríguez, Angélica; Roqué i Figuls, Marta; Parker, Lucy Anne; Caylà, Joan; Bonfill Cosp, Xavier
2016-01-01
Background People who are newly diagnosed with pulmonary tuberculosis (TB) typically receive a standard first-line treatment regimen that consists of two months of isoniazid, rifampicin, pyrazinamide, and ethambutol followed by four months of isoniazid and rifampicin. Fixed-dose combinations (FDCs) of these drugs are widely recommended. Objectives To compare the efficacy, safety, and acceptability of anti-tuberculosis regimens given as fixed-dose combinations compared to single-drug formulations for treating people with newly diagnosed pulmonary tuberculosis. Search methods We searched the Cochrane Infectious Disease Group Specialized Register; the Cochrane Central Register of Controlled Trials (CENTRAL, published in the Cochrane Library, Issue 11 2015); MEDLINE (1966 to 20 November 2015); EMBASE (1980 to 20 November 2015); LILACS (1982 to 20 November 2015); the metaRegister of Controlled Trials; and the World Health Organization International Clinical Trials Registry Platform (WHO ICTRP), without language restrictions, up to 20 November 2015. Selection criteria Randomized controlled trials that compared the use of FDCs with single-drug formulations in adults (aged 15 years or more) newly diagnosed with pulmonary TB. Data collection and analysis Two review authors independently assessed studies for inclusion, and assessed the risk of bias and extracted data from the included trials. We used risk ratios (RRs) for dichotomous data and mean differences (MDs) for continuous data with 95% confidence intervals (CIs). We attempted to assess the effect of treatment for time-to-event measures with hazard ratios and their 95% CIs. We used the Cochrane 'Risk of bias' assessment tool to determine the risk of bias in included trials. We used the fixed-effect model when there was little heterogeneity and the random-effects model with moderate heterogeneity. We used an I² statistic value of 75% or greater to denote significant heterogeneity, in which case we did not perform a
佐藤, 薫; 遠藤 章; 斎藤 公明
2008-01-01
At the Japan Atomic Energy Agency, high-resolution five Japanese adult voxel phantoms have been constructed up to now to clarify the variation of organ doses due to the anatomical characteristics of Japanese. This report presents a complete set of conversion coefficients of organ doses and effective doses calculated for external photon exposure using five Japanese voxel phantoms. The calculated conversion coefficients are compared with those of Caucasian voxel phantoms and the recommended val...
Calculating integral dose using data exported from a commercial record and verify system.
Fox, C; Hardcastle, N; Lim, A; Khor, R
2015-06-01
Integral dose has been useful in investigations into the incidence of second primary malignancies in radiotherapy patients. This note outlines an approach to calculation of integral dose for a group of prostate patients using only data exported from a commercial record and verify system. Even though it was necessary to make some assumptions about patient anatomy, comparison with integral dose calculated from data exported from the planning system showed good agreement. PMID:25869674
Sakamoto, Y
2002-01-01
In the prevention of nuclear disaster, there needs the information on the dose equivalent rate distribution inside and outside the site, and energy spectra. The three dimensional radiation transport calculation code is a useful tool for the site specific detailed analysis with the consideration of facility structures. It is important in the prediction of individual doses in the future countermeasure that the reliability of the evaluation methods of dose equivalent rate distribution and energy spectra by using of Monte Carlo radiation transport calculation code, and the factors which influence the dose equivalent rate distribution outside the site are confirmed. The reliability of radiation transport calculation code and the influence factors of dose equivalent rate distribution were examined through the analyses of critical accident at JCO's uranium processing plant occurred on September 30, 1999. The radiation transport calculations including the burn-up calculations were done by using of the structural info...
International Nuclear Information System (INIS)
Due to secondary cosmic radiation (SCR), pilots and flight attendants receive elevated effective doses at flight altitudes. For this reason, since 2003 aircrew members are considered as occupationally exposed, in Germany. This work deals with the calculation of dose conversion coefficients (DCC) for protons, neutrons, electrons, positrons, photons and myons, which are crucial for estimation of effective dose from SCR. For the first time, calculations were performed combining Geant4 - a Monte Carlo code developed at CERN - with the voxel phantoms for the reference female and male published in 2008 by ICRP and ICRU. Furthermore, measurements of neutron fluence spectra - which contribute the major part to the effective dose of SCR - were carried out at the Environmental Research Station Schneefernerhaus (UFS) located at 2650 m above sea level nearby the Zugspitze mountain, Germany. These measured neutron spectra, and additionally available calculated spectra, were then folded with the DCC calculated in this work, and effective dose rates for different heights were calculated.
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To report the result of independent absorbed-dose calculations based on a Monte Carlo (MC) algorithm in volumetric modulated arc therapy (VMAT) for various treatment sites. All treatment plans were created by the superposition/convolution (SC) algorithm of SmartArc (Pinnacle V9.2, Philips). The beam information was converted into the format of the Monaco V3.3 (Elekta), which uses the X-ray voxel-based MC (XVMC) algorithm. The dose distribution was independently recalculated in the Monaco. The dose for the planning target volume (PTV) and the organ at risk (OAR) were analyzed via comparisons with those of the treatment plan. Before performing an independent absorbed-dose calculation, the validation was conducted via irradiation from 3 different gantry angles with a 10- × 10-cm2 field. For the independent absorbed-dose calculation, 15 patients with cancer (prostate, 5; lung, 5; head and neck, 3; rectal, 1; and esophageal, 1) who were treated with single-arc VMAT were selected. To classify the cause of the dose difference between the Pinnacle and Monaco TPSs, their calculations were also compared with the measurement data. In validation, the dose in Pinnacle agreed with that in Monaco within 1.5%. The agreement in VMAT calculations between Pinnacle and Monaco using phantoms was exceptional; at the isocenter, the difference was less than 1.5% for all the patients. For independent absorbed-dose calculations, the agreement was also extremely good. For the mean dose for the PTV in particular, the agreement was within 2.0% in all the patients; specifically, no large difference was observed for high-dose regions. Conversely, a significant difference was observed in the mean dose for the OAR. For patients with prostate cancer, the mean rectal dose calculated in Monaco was significantly smaller than that calculated in Pinnacle. There was no remarkable difference between the SC and XVMC calculations in the high-dose regions. The difference observed in the low-dose regions may
RADIATION DOSE CALCULATION FOR FUEL HANDLING FACILITY CLOSURE CELL EQUIPMENT
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This calculation evaluates the energy deposition rates in silicon, gamma and neutron flux spectra at various locations of interest throughout FHF closure cell. The physical configuration features a complex geometry, with particle flux attenuation of many orders of magnitude that cannot be modeled by computer codes that use deterministic methods. Therefore, in this calculation the Monte Carlo method was used to solve the photon and neutron transport. In contrast with the deterministic methods, Monte Carlo does not solve an explicit transport equation, but rather obtain answers by simulating individual particles, recording the aspects of interest of their average behavior, and estimates the statistical precision of the results
A new finite cloud method for calculating external exposure dose in a nuclear emergency
International Nuclear Information System (INIS)
A new finite cloud method (5/μ method) for calculating external exposure dose in a nuclear emergency is presented in this paper. The method calculates external exposure dose over a specially constructed three-dimensional columned space, whose underside center is the location of the receptor and underside radius and height are both five times mean free path of a gamma-photon. Then, the space is divided into many grid cells for integral to calculate external exposure dose (or dose rate). The calculation values of air external exposure dose rate conversion factors and air-absorbed dose rate conversion factors by the 5/μ method are accordant with the values presented in related references. Comparing with the discrete point approximation method (DPA) [USNRC, The MESORAD Dose Assessment Model. NUREG/CR-4000 Vol. 1, 1986] and the Nomogram method [USNRC, Nomogram for Evaluation of Doses from Finite Noble Gas Clouds, NUREG-0851, 1983], which are two traditional finite cloud methods for calculating external exposure dose, the 5/μ method has a distinct advantage of more fast calculation speed, which is very important in a nuclear emergency. What is more, the 5/μ method can be applied together with three-dimensional atmospheric dispersion models
A new finite cloud method for calculating external exposure dose in a nuclear emergency
Energy Technology Data Exchange (ETDEWEB)
Wang, X.Y.; Ling, Y.S. E-mail: lingyongsheng00@mails.tsinghua.edu.cn; Shi, Z.Q
2004-06-01
A new finite cloud method (5/{mu} method) for calculating external exposure dose in a nuclear emergency is presented in this paper. The method calculates external exposure dose over a specially constructed three-dimensional columned space, whose underside center is the location of the receptor and underside radius and height are both five times mean free path of a gamma-photon. Then, the space is divided into many grid cells for integral to calculate external exposure dose (or dose rate). The calculation values of air external exposure dose rate conversion factors and air-absorbed dose rate conversion factors by the 5/{mu} method are accordant with the values presented in related references. Comparing with the discrete point approximation method (DPA) [USNRC, The MESORAD Dose Assessment Model. NUREG/CR-4000 Vol. 1, 1986] and the Nomogram method [USNRC, Nomogram for Evaluation of Doses from Finite Noble Gas Clouds, NUREG-0851, 1983], which are two traditional finite cloud methods for calculating external exposure dose, the 5/{mu} method has a distinct advantage of more fast calculation speed, which is very important in a nuclear emergency. What is more, the 5/{mu} method can be applied together with three-dimensional atmospheric dispersion models.
Wuelfing, W Peter; Daublain, Pierre; Kesisoglou, Filippos; Templeton, Allen; McGregor, Caroline
2015-04-01
In the drug discovery setting, the ability to rapidly identify drug absorption risk in preclinical species at high doses from easily measured physical properties is desired. This is due to the large number of molecules being evaluated and their high attrition rate, which make resource-intensive in vitro and in silico evaluation unattractive. High-dose in vivo data from rat, dog, and monkey are analyzed here, using a preclinical dose number (PDo) concept based on the dose number described by Amidon and other authors (Pharm. Res., 1993, 10, 264-270). PDo, as described in this article, is simply calculated as dose (mg/kg) divided by compound solubility in FaSSIF (mg/mL) and approximates the volume of biorelevant media per kilogram of animal that would be needed to fully dissolve the dose. High PDo values were found to be predictive of difficulty in achieving drug exposure (AUC)-dose proportionality in in vivo studies, as could be expected; however, this work analyzes a large data set (>900 data points) and provides quantitative guidance to identify drug absorption risk in preclinical species based on a single solubility measurement commonly carried out in drug discovery. Above the PDo values defined, >50% of all in vivo studies exhibited poor AUC-dose proportionality in rat, dog, and monkey, and these values can be utilized as general guidelines in discovery and early development to rapidly assess risk of solubility-limited absorption for a given compound. A preclinical dose number generated by biorelevant dilutions of formulated compounds (formulated PDo) was also evaluated and defines solubility targets predictive of suitable AUC-dose proportionality in formulation development efforts. Application of these guidelines can serve to efficiently identify compounds in discovery that are likely to present extreme challenges with respect to solubility-limited absorption in preclinical species as well as reduce the testing of poor formulations in vivo, which is a key
The calculation, presentation and use of collective doses for routine discharges
International Nuclear Information System (INIS)
Over recent decades concerns have been expressed about the way collective doses have been used. In particular, there is general agreement that using the fully aggregated collective dose masks a lot of useful information on levels of individual dose and their distribution over space and time, which decision makers may consider important. The International Commission on Radiological Protection has suggested a 'collective dose matrix' approach as a solution to this. A study has been carried out to explore some of the issues involved in the development and use of such matrices. In particular, practical issues regarding the disaggregation of collective dose in relation to individual dose rates and the temporal and spatial distribution of exposures have been addressed. Calculations have been undertaken to illustrate ways in which the estimated collective dose from routine discharges can be broken down. The nuclear site chosen was the Sellafield reprocessing plant but additional calculations were also undertaken for the Cap de La Hague reprocessing plant for comparative purposes. It was found that useful information on the temporal and spatial elements of collective doses can be obtained and that per-caput doses can be used to give an indication of the likely individual doses that make up the collective dose. At long times following discharges of radionuclides to the environment doses due to global circulation will dominate the collective dose and there is likely to be little requirement for obtaining information on individual dose distributions. (author)
The economics of polypharmacology: fixed dose combinations and drug cocktails.
Wertheimer, A I
2013-01-01
The history of Fixed Dose Combination (FDC) oral drug products has been tumultuous over its history. Some FDCs were prepared for marketing purposes and others for clinical improvements. Often, the products prepared for marketing advantage ended up causing negative outcomes. However, in recent years, there has been a resurgence of FDCs as clinicians have found them adventitious for treatment of AIDS/HIV and for oral contraceptives, just to name two examples. International regulatory Agencies and most major drug regulatory agencies have established guidelines along with regulations concerning preparation, labeling and marketing for FDCs. The advantages of FDCs are said to be in the clinical realm where simplified therapy regimens are thought to enhance patient's medication taking compliance. On the financial side, health insurers and other payers normally save money from a decreased number of dispensing fees, the use of fewer bottles, labels, etc., and from the possible situation where the price of the FDC is less than the medication price of the two separate ingredients dispensed individually. Overall, there is a great deal of evidence in favor of appropriate FDCs. PMID:23410163
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Purpose: To investigate the correlation of size-specific dose estimate (SSDE) with absorbed organ dose, and to develop a simple methodology for estimating patient organ dose in a pediatric population (5–55 kg). Methods: Four physical anthropomorphic phantoms representing a range of pediatric body habitus were scanned with metal oxide semiconductor field effect transistor (MOSFET) dosimeters placed at 23 organ locations to determine absolute organ dose. Phantom absolute organ dose was divided by phantom SSDE to determine correlation between organ dose and SSDE. Organ dose correlation factors (CFSSDEorgan) were then multiplied by patient-specific SSDE to estimate patient organ dose. The CFSSDEorgan were used to retrospectively estimate individual organ doses from 352 chest and 241 abdominopelvic pediatric CT examinations, where mean patient weight was 22 kg ± 15 (range 5–55 kg), and mean patient age was 6 yrs ± 5 (range 4 months to 23 yrs). Patient organ dose estimates were compared to published pediatric Monte Carlo study results. Results: Phantom effective diameters were matched with patient population effective diameters to within 4 cm; thus, showing appropriate scalability of the phantoms across the entire pediatric population in this study. IndividualCFSSDEorgan were determined for a total of 23 organs in the chest and abdominopelvic region across nine weight subcategories. For organs fully covered by the scan volume, correlation in the chest (average 1.1; range 0.7–1.4) and abdominopelvic region (average 0.9; range 0.7–1.3) was near unity. For organ/tissue that extended beyond the scan volume (i.e., skin, bone marrow, and bone surface), correlation was determined to be poor (average 0.3; range: 0.1–0.4) for both the chest and abdominopelvic regions, respectively. A means to estimate patient organ dose was demonstrated. Calculated patient organ dose, using patient SSDE and CFSSDEorgan, was compared to previously published pediatric patient doses that
Aliasgharzadeh, Akbar; Mihandoost, Ehsan; Masoumbeigi, Mahboubeh; Salimian, Morteza; Mohseni, Mehran
2015-01-01
The knowledge of the radiation dose received by the patient during the radiological examination is essential to prevent risks of exposures. The aim of this work is to study patient doses for common diagnostic radiographic examinations in hospitals affiliated to Kashan University of Medical sciences, Iran. The results of this survey are compared with those published by some national and international values. Entrance surface dose (ESD) was measured based on the exposure parameters used for the actual examination and effective dose (ED) was calculated by use of conversion coefficients calculated by Monte Carlo methods. The mean entrance surface dose and effective dose for examinations of the chest (PA, Lat), abdomen (AP), pelvis (AP), lumbar spine (AP, Lat) and skull (AP, Lat) are 0.37, 0.99, 2.01, 1.76, 2.18, 5.36, 1.39 and 1.01 mGy, and 0.04, 0.1, 0.28, 0,28, 0.23, 0.13, 0.01 and 0.01 mSv, respectively. The ESDs and EDs reported in this study, except for examinations of the chest, are generally lower than comparable reference dose values published in the literature. On the basis of the results obtained in this study can conclude that use of newer equipment and use of the proper radiological parameter can significantly reduce the absorbed dose. It is recommended that radiological parameter in chest examinations be revised. PMID:26156930
International Nuclear Information System (INIS)
This report presents a complete set of conversion coefficients of organ doses and effective doses calculated for external photon exposure using five Japanese adult voxel phantoms developed at the Japan Atomic Energy Agency (JAEA). At the JAEA, high-resolution Japanese voxel phantoms have been developed to clarify the variation of organ doses due to the anatomical characteristics of Japanese, and three male phantoms (JM, JM2 and Otoko) and two female phantoms (JF and Onago) have been constructed up to now. The conversion coefficients of organ doses and effective doses for the five voxel phantoms have been calculated for six kinds of idealized irradiation geometries from monoenergetic photons ranging from 0.01 to 10 MeV using EGS4, a Monte Carlo code for the simulation of coupled electron-photon transport. The dose conversion coefficients are given as absorbed dose and effective dose per unit air-kerma free-in-air, and are presented in tables and figures. The calculated dose conversion coefficients are compared with those of voxel phantoms based on the Caucasian and the recommended values in ICRP74 in order to discuss (1) variation of organ dose due to the body size and individual anatomy, such as position and shape of organs, and (2) effect of posture on organ doses. The present report provides valuable data to study the influence of the body characteristics of Japanese upon the organ doses and to discuss developing reference Japanese and Asian phantoms. (author)
International Nuclear Information System (INIS)
The comparatively high dose and increasing frequency of computed tomography (CT) examinations have spurred the development of techniques for reducing radiation dose to imaging patients. Among these is the application of tube current modulation (TCM), which can be applied either longitudinally along the body or rotationally along the body, or both. Existing computational models for calculating dose from CT examinations do not include TCM techniques. Dose calculations using Monte Carlo methods have been previously prepared for constant-current rotational exposures at various positions along the body and for the principle exposure projections for several sets of computational phantoms, including adult male and female and pregnant patients. Dose calculations from CT scans with TCM are prepared by appropriately weighting the existing dose data. Longitudinal TCM doses can be obtained by weighting the dose at the z-axis scan position by the relative tube current at that position. Rotational TCM doses are weighted using the relative organ doses from the principle projections as a function of the current at the rotational angle. Significant dose reductions of 15% to 25% to fetal tissues are found from simulations of longitudinal TCM schemes to pregnant patients of different gestational ages. Weighting factors for each organ in rotational TCM schemes applied to adult male and female patients have also been found. As the application of TCM techniques becomes more prevalent, the need for including TCM in CT dose estimates will necessarily increase. (author)
2010-07-01
... Human Services that applicant did not act with due diligence; (iii) One-half the number of days... extension for a human drug, antibiotic drug or human biological product. 1.775 Section 1.775 Patents... Review § 1.775 Calculation of patent term extension for a human drug, antibiotic drug or human...
Institute of Scientific and Technical Information of China (English)
GAO Ci-xiu; XU Shi-xiong; JIANG Yu-ping; TU Jiang-long
2009-01-01
This work aims to investigate the effects of dosing regiments on drug delivery in solid tumors and to validate them with experiments on rats.The lumped parameter models of pharmacokinetics and of drug delivery in tumor were developed to simulate time courses of average drug concentration(Ct)of tumor interstitium in two types of dosing regiments(i.e.,single-shot and triple-shot ones).The two regiments were performed via antitumor drug,hydroxycamptothecin(HCPT),on rats,to measure the drug concentration in the tumor.The simulations of the drug concentration in the tumor of the two dosing regiments were conducted and compared with the experimental data on rats.The coefficients in the models were investigated.It is concluded that the triple-shot method is more effective than that of single-shot injection.The present lumped-parameter model is quantitatively competent for drug delivery in solid tumor.
Vitale, Gail A.
2011-01-01
The purpose of this study was to examine how nursing efficacy for drug-dosage calculation instruction is determined. Medication administration is a critical function of nurses in healthcare settings. An essential component of safe medication administration is accurate drug-dosage calculation, but instruction in drug-dosage calculation methods…
Application of the peregrine Monte Carlo dose calculation system to stereotactic radiosurgery
International Nuclear Information System (INIS)
Purpose/Objective: This work describes the capability to perform Monte Carlo dose calculations for stereotactic radiosurgery within the framework of the PEREGRINE dose calculation system. A future study will use this capability to assess the clinical benefits to this technique of higher accuracy in dose calculation. Materials and Methods: PEREGRINE is a first-principles 3D Monte Carlo dose calculation system for clinical radiation therapy treatment planning (RTP) systems. By taking advantage of recent advances in low-cost computer commodity hardware, modern symmetric multiprocessor architectures and state-of-the-art Monte Carlo transport algorithms, PEREGRINE performs high-resolution (1 mm), high accuracy, Monte Carlo RTP calculations in times that are reasonable for clinical use (< 30 minutes.) The PEREGRINE source model provides a compact, accurate representation of the radiation source and the effects of beam modifiers. Our experience in implementing blocks, wedges, and static MLC ports in PEREGRINE as beam modifiers provides physics models that accurately reproduce the transmitted and scattered fluence at the patient surface. Adapting PEREGRINE to calculate stereotactic radiosurgery dose distributions requires extending the PEREGRINE source model to include stereotactic apertures and treatment arcs. The physics models used for other modifiers will accurately determine stereotactic aperture effects. We only need to provide a new geometry module to describe the physical properties of the apertures. Treatment arcs are easily implemented as a probability distribution in beam direction as a function of delivered dose. Results: A comparison of results from PEREGRINE calculations and experimental measurements made at the University of Wisconsin/Madison is presented. The distribution of direct, transmitted and scattered radiation and the resulting contributions to dose from stereotactic apertures are shown. The accuracy and calculational efficiency of the physics
A computer code for calculating a γ-external dose from a randomly distributed radioactive cloud
International Nuclear Information System (INIS)
A computer code ( CIDE ) has been developed to calculate a γ-external dose from a randomly distributed radioactive cloud. Atmospheric dispersion of radioactive materials accidentally released from a nuclear reactor needs to be estimated considering time-dependent meteorological data and terrain heights. Particle-in-Cell model is useful for that purpose, but it is not easy to calculate the dose from the randomly distributed concentration by numerical integration. In this study the mean concentration in a cell evaluated by PIC model was assumed to be uniformly distributed over that cell, which was integrated as a constant concentration by a point kernel method. The dose was obtained by summing the attributable cell doses. When the concentration of plume had a Gaussian distribution, the results of CIDE code well agreed with those of GAMPLE, which was the code for calculating the dose from the Gaussian distribution. The choice of cell sizes affecting the accuracy of the calculated results was discussed. (author)
International Nuclear Information System (INIS)
Purpose: Implantable devices routinely used for increasing spatial accuracy in modern image-guided radiation treatments (IGRT), such as fiducials or brachytherapy spacers, encompass the potential for in situ release of biologically active drugs, providing an opportunity to enhance the therapeutic ratio. We model this new approach for two types of treatment. Methods and Materials: Radiopaque fiducials used in IGRT, or prostate brachytherapy spacers ('eluters'), were assumed to be loaded with radiosensitizer for in situ drug slow release. An analytic function describing the concentration of radiosensitizer versus distance from eluters, depending on diffusion-elimination properties of the drug in tissue, was developed. Tumor coverage by the drug was modeled for tumors typical of lung stereotactic body radiation therapy treatments for various eluter dimensions and drug properties. Six prostate 125I brachytherapy cases were analyzed by assuming implantation of drug-loaded spacers. Radiosensitizer-induced subvolume boost was simulated from which biologically effective doses for typical radiosensitizers were calculated in one example. Results: Drug distributions from three-dimensional arrangements of drug eluters versus eluter size and drug properties were tabulated. Four radiosensitizer-loaded fiducials provide adequate radiosensitization for ∼4-cm-diameter lung tumors, thus potentially boosting biologically equivalent doses in centrally located stereotactic body treated lesions. Similarly, multiple drug-loaded spacers provide prostate brachytherapy with flexible shaping of 'biologically equivalent doses' to fit requirements difficult to meet by using radiation alone, e.g., boosting a high-risk region juxtaposed to the urethra while respecting normal tissue tolerance of both the urethra and the rectum. Conclusions: Drug loading of implantable devices routinely used in IGRT provides new opportunities for therapy modulation via biological in situ dose painting.
International Nuclear Information System (INIS)
Age-dependent dose conversion coefficients for external exposure to photons emitted by radionuclides uniformly distributed in air were calculated. The size of the source region in the calculation was assumed to be effectively semi-infinite in extent. Firstly, organ doses were calculated with a series of age-specific MIRD-5 type phantoms using MCNP code, a Monte Carlo transport code. The calculations were performed for mono-energetic photon sources of twelve energies from 10 keV to 5 MeV and for phantoms of newborn, 1, 5, 10 and 15 years, and adult. Then, the effective doses to the different age-phantoms from the mono-energetic photon sources were estimated based on the obtained organ doses. The calculated effective doses were used to interpolate the conversion coefficients of the effective doses for 160 radionuclides, which are important for dose assessment of nuclear facilities. In the calculation, energies and intensities of emitted photons from radionuclides were taken from DECDC, a recent compilation of decay data for radiation dosimetry developed at JAERI. The results are tabulated in the form of effective dose per unit concentration and time (Sv per Bq s m-3). (author)
Energy Technology Data Exchange (ETDEWEB)
NONE
2000-07-01
The guide sets out the mathematical definitions and principles involved in the calculation of the equivalent dose and the effective dose, and the instructions concerning the application of the maximum values of these quantities. further, for monitoring the dose caused by internal radiation, the guide defines the limits derived from annual dose limits (the Annual Limit on Intake and the Derived Air Concentration). Finally, the guide defines the operational quantities to be used in estimating the equivalent dose and the effective dose, and also sets out the definitions of some other quantities and concepts to be used in monitoring radiation exposure. The guide does not include the calculation of patient doses carried out for the purposes of quality assurance.
International Nuclear Information System (INIS)
The guide sets out the mathematical definitions and principles involved in the calculation of the equivalent dose and the effective dose, and the instructions concerning the application of the maximum values of these quantities. further, for monitoring the dose caused by internal radiation, the guide defines the limits derived from annual dose limits (the Annual Limit on Intake and the Derived Air Concentration). Finally, the guide defines the operational quantities to be used in estimating the equivalent dose and the effective dose, and also sets out the definitions of some other quantities and concepts to be used in monitoring radiation exposure. The guide does not include the calculation of patient doses carried out for the purposes of quality assurance
A note on vector flux models for radiation dose calculations
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This paper reviews and extends modelling of anisotropic fluxes for radiation belt protons to provide closed-form equations for vector proton fluxes and proton flux anisotropy in terms of standard omnidirectional flux models. These equations provide a flexible alternative to the date-based vector flux models currently available. At higher energies, anisotropy of trapped proton flux in the upper atmosphere depends strongly on the variation of atmospheric density with altitude. Calculations of proton flux anisotropies using present models require specification of the average atmospheric density along trapped particle trajectories and its variation with mirror point altitude. For an isothermal atmosphere, calculations show that in a dipole magnetic field, the scale height of this trajectory-averaged density closely approximates the scale height of the atmosphere at the mirror point of the trapped particle. However, for the earth's magnetic field, the altitudes of mirror points vary for protons drifting in longitude. This results in a small increase in longitude-averaged scale heights compared to the atmospheric scale heights at minimum mirror point altitudes. The trajectory-averaged scale heights are increased by about 10-20% over scale heights from standard atmosphere models for protons mirroring at altitudes less than 500 km in the South Atlantic Anomaly Atmospheric losses of protons in the geomagnetic field minimum in the South Atlantic Anomaly control proton flux anisotropies of interest for radiation studies in low earth orbit. Standard atmosphere models provide corrections for diurnal, seasonal and solar activity-driven variations. Thus, determination of an ''equilibrium'' model of trapped proton fluxes of a given energy requires using a scale height that is time-averaged over the lifetime of the protons. The trajectory-averaged atmospheric densities calculated here lead to estimates for trapped proton lifetimes. These lifetimes provide appropriate time
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The purpose of this study was to compare dose distributions from three different algorithms with the x-ray Voxel Monte Carlo (XVMC) calculations, in actual computed tomography (CT) scans for use in stereotactic radiotherapy (SRT) of small lung cancers. Slow CT scan of 20 patients was performed and the internal target volume (ITV) was delineated on Pinnacle3. All plans were first calculated with a scatter homogeneous mode (SHM) which is compatible with Clarkson algorithm using Pinnacle3 treatment planning system (TPS). The planned dose was 48 Gy in 4 fractions. In a second step, the CT images, structures and beam data were exported to other treatment planning systems (TPSs). Collapsed cone convolution (CCC) from Pinnacle3, superposition (SP) from XiO, and XVMC from Monaco were used for recalculating. The dose distributions and the Dose Volume Histograms (DVHs) were compared with each other. The phantom test revealed that all algorithms could reproduce the measured data within 1% except for the SHM with inhomogeneous phantom. For the patient study, the SHM greatly overestimated the isocenter (IC) doses and the minimal dose received by 95% of the PTV (PTV95) compared to XVMC. The differences in mean doses were 2.96 Gy (6.17%) for IC and 5.02 Gy (11.18%) for PTV95. The DVH's and dose distributions with CCC and SP were in agreement with those obtained by XVMC. The average differences in IC doses between CCC and XVMC, and SP and XVMC were -1.14% (p = 0.17), and -2.67% (p = 0.0036), respectively. Our work clearly confirms that the actual practice of relying solely on a Clarkson algorithm may be inappropriate for SRT planning. Meanwhile, CCC and SP were close to XVMC simulations and actual dose distributions obtained in lung SRT
Babcock, Kerry Kent Ronald
2009-04-01
The goal of this thesis was to explore the effects of dose resolution, respiratory variation and dose calculation method on dose accuracy. To achieve this, two models of lung were created. The first model, called TISSUE, approximated the connective alveolar tissues of the lung. The second model, called BRANCH, approximated the lungs bronchial, arterial and venous branching networks. Both models were varied to represent the full inhalation, full exhalation and midbreath phases of the respiration cycle. To explore the effects of dose resolution and respiratory variation on dose accuracy, each model was converted into a CT dataset and imported into a Monte Carlo simulation. The resulting dose distributions were compared and contrasted against dose distributions from Monte Carlo simulations which included the explicit model geometries. It was concluded that, regardless of respiratory phase, the exclusion of the connective tissue structures in the CT representation did not significantly effect the accuracy of dose calculations. However, the exclusion of the BRANCH structures resulted in dose underestimations as high as 14% local to the branching structures. As lung density decreased, the overall dose accuracy marginally decreased. To explore the effects of dose calculation method on dose accuracy, CT representations of the lung models were imported into the Pinnacle 3 treatment planning system. Dose distributions were calculated using the collapsed cone convolution method and compared to those derived using the Monte Carlo method. For both lung models, it was concluded that the accuracy of the collapsed cone algorithm decreased with decreasing density. At full inhalation lung density, the collapsed cone algorithm underestimated dose by as much as 15%. Also, the accuracy of the CCC method decreased with decreasing field size. Further work is needed to determine the source of the discrepancy.
Directory of Open Access Journals (Sweden)
Eduardo de Paiva
2015-01-01
Full Text Available Concave beta sources of 106Ru/106Rh are used in radiotherapy to treat ophthalmic tumors. However, a problem that arises is the difficult determination of absorbed dose distributions around such sources mainly because of the small range of the electrons and the steep dose gradients. In this sense, numerical methods have been developed to calculate the dose distributions around the beta applicators. In this work a simple code in Fortran language is developed to estimate the dose rates along the central axis of 106Ru/106Rh curved plaques by numerical integration of the beta point source function and results are compared with other calculated data.
de Paiva, Eduardo
Concave beta sources of 106Ru/106Rh are used in radiotherapy to treat ophthalmic tumors. However, a problem that arises is the difficult determination of absorbed dose distributions around such sources mainly because of the small range of the electrons and the steep dose gradients. In this sense, numerical methods have been developed to calculate the dose distributions around the beta applicators. In this work a simple code in Fortran language is developed to estimate the dose rates along the central axis of 106Ru/106Rh curved plaques by numerical integration of the beta point source function and results are compared with other calculated data.
Calculation of radiation dose rate arisen from radionuclide contained in building materials
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This paper presents some results that we used MCNP5 program to calculate radiation dose rate arisen from radionuclide in building materials. Since then, the limits of radionuclide content in building materials are discussed. The calculation results by MCNP are compared with those calculated by analytical method. (author)
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Calculations with the quadratic lineal model for medium rate using the equation dose-effect. Several calculations for system of low dose rate brachytherapy plus teletherapy, calculations for brachytherapy with medium dose rate together with teletherapy, dose for fraction and the one numbers of fractions in medium rate
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A series of scoping calculations have been undertaken to evaluate The absolute and relative contribution of different exposure pathways to doses that may have been received by individuals living in the vicinity of the Hanford site. This scoping calculation (Calculation 001) examined the contributions of the various exposure pathways associated with environmental transport and accumulation of iodine-131 in the pasture-cow-milk pathway. Addressed in this calculation were the contributions to thyroid dose of infants and adult from (1) the ingestion by dairy cattle of various feedstuffs (pasturage, silage, alfalfa hay, and grass hay) in four different feeding regimes; (2) ingestion of soil by dairy cattle; (3) ingestion of stared feed on which airborne iodine-131 had been deposited; and (4) inhalation of airborne iodine-131 by dairy cows
Independent dose calculation in IMRT for the Tps Iplan using the Clarkson modified integral
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Intensity-Modulated Radiation Therapy (IMRT) treatments require a quality assurance (Q A) specific patient before delivery. These controls include the experimental verification in dose phantom of the total plan as well as dose distributions. The use of independent dose calculation (IDC) is used in 3D-Crt treatments; however its application in IMRT requires the implementation of an algorithm that allows considering a non-uniform intensity beam. The purpose of this work was to develop IDC software in IMRT with MLC using the algorithm proposed by Kung (Kung et al. 2000). The software was done using Matlab programming. The Clarkson modified integral was implemented on each flowing, applying concentric rings for the dose determination. From the integral of each field was calculated the dose anywhere. One time finished a planning; all data are exported to a phantom where a Q A plan is generated. On this is calculated the half dose in a representative volume of the ionization chamber and the dose at the center of it. Until now 230 IMRT planning were analyzed carried out ??in the treatment planning system (Tps) Iplan. For each one of them Q A plan was generated, were calculated and compared calculated dose with the Tps, IDC system and measurement with ionization chamber. The average difference between measured and calculated dose with the IDC system was 0.4% ± 2.2% [-6.8%, 6.4%]. The difference between the measured and the calculated doses by the pencil-beam algorithm (Pb) of Tps was 2.6% ± 1.41% [-2.0%, 5.6%] and with the Monte Carlo algorithm was 0.4% ± 1.5% [-4.9%, 3.7%]. The differences of the carried out software are comparable to the obtained with the ionization chamber and Tps in Monte Carlo mode. (author)
CT-based dose calculations and in vivo dosimetry for lung cancer treatment
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Reliable CT-based dose calculations and dosimetric quality control are essential for the introduction of new conformal techniques for the treatment of lung cancer. The first aim of this study was therefore to check the accuracy of dose calculations based on CT-densities, using a simple inhomogeneity correction model, for lung cancer patients irradiated with an AP-PA treatment technique. Second, the use of diodes for absolute exit dose measurements and an Electronic Portal Imaging Device (EPID) for relative transmission dose verification was investigated for 22 and 12 patients, respectively. The measured dose values were compared with calculations performed using our 3-dimensional treatment planning system, using CT-densities or assuming the patient to be water-equivalent. Using water-equivalent calculations, the actual exit dose value under lung was, on average, underestimated by 30%, with an overall spread of 10% (1 SD). Using inhomogeneity corrections, the exit dose was, on average, overestimated by 4%, with an overall spread of 6% (1 SD). Only 2% of the average deviation was due to the inhomogeneity correction model. An uncertainty in exit dose calculation of 2.5% (1 SD) could be explained by organ motion, resulting from the ventilatory or cardiac cycle. The most important reason for the large overall spread was, however, the uncertainty involved in performing point measurements: about 4% (1 SD). This difference resulted from the systematic and random deviation in patient set-up and therefore in diode position with respect to patient anatomy. Transmission and exit dose values agreed with an average difference of 1.1%. Transmission dose profiles also showed good agreement with calculated exit dose profiles. Our study shows that, for this treatment technique, the dose in the thorax region is quite accurately predicted using CT-based dose calculations, even if a simple inhomogeneity correction model is used. Point detectors such as diodes are not suitable for exit
Jeraj, Robert; Keall, Paul
2000-12-01
The effect of the statistical uncertainty, or noise, in inverse treatment planning for intensity modulated radiotherapy (IMRT) based on Monte Carlo dose calculation was studied. Sets of Monte Carlo beamlets were calculated to give uncertainties at Dmax ranging from 0.2% to 4% for a lung tumour plan. The weights of these beamlets were optimized using a previously described procedure based on a simulated annealing optimization algorithm. Several different objective functions were used. It was determined that the use of Monte Carlo dose calculation in inverse treatment planning introduces two errors in the calculated plan. In addition to the statistical error due to the statistical uncertainty of the Monte Carlo calculation, a noise convergence error also appears. For the statistical error it was determined that apparently successfully optimized plans with a noisy dose calculation (3% 1σ at Dmax ), which satisfied the required uniformity of the dose within the tumour, showed as much as 7% underdose when recalculated with a noise-free dose calculation. The statistical error is larger towards the tumour and is only weakly dependent on the choice of objective function. The noise convergence error appears because the optimum weights are determined using a noisy calculation, which is different from the optimum weights determined for a noise-free calculation. Unlike the statistical error, the noise convergence error is generally larger outside the tumour, is case dependent and strongly depends on the required objectives.
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AQUAMAN is an interactive computer code for calculating values of dose (50-year dose commitment) to man from aqueous releases of radionuclides from nuclear facilities. The data base contains values of internal and external dose conversion factors, and bioaccumulation (freshwater and marine) factors for 56 radionuclides. A maximum of 20 radionuclides may be selected for any one calculation. Dose and cumulative exposure index (CUEX) values are calculated for total body, GI tract, bone, thyroid, lungs, liver, kidneys, testes, and ovaries for each of three exposure pathways: water ingestion, fish ingestion, and submersion. The user is provided the option at the time of execution to change the default values of most of the variables, with the exception of the dose conversion factor values. AQUAMAN is written in FORTRAN for the PDP-10 computer
Comparison of measured and calculated peripheral doses in patients undergoing radiation therapy
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Background and purpose: Many papers have been published on the measurement for specific treatment machines and/or techniques of the dose to points outside the primary beam, often called the peripheral dose (PD). Most papers concern measurements in phantoms. We report on the results of a comparison of estimates of the PD, based on these phantom measurements, with PDs measured on patients. Material and methods: A special holder with thermoluminescent dosimeters was placed against the perineum of patients referred to our institute for radiation therapy. The measured dose was then compared with the dose calculated on the basis of published PD data. Results: For all measurements together, the calculated values exceeded the measured PDs by about 9%, with a standard deviation of 35%. The correlation varied between specific subgroups but the difference between measurement and calculation did not exceed 50%. Conclusions: We conclude that published PD data can be used to accurately predict the peripheral dose in the clinical situation
Effects of microdistribution of tritium on dose calculations
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Literature and data pertaining to the microdosimetry, relative biological effectiveness, subcellular distribution, organ uptake and retention for organically-bound tritium are reviewed. The quality factor for the electron degradation spectrum associated with the radiation field of tritium β-rays in water was calculated. The value was found to be 1.9 ± .2. A related experimental measure of quality with value 1.6 ± .2 and an estimate of 1.3 based on simulation studies are cited. The average value for relative biological effectiveness for a data base of 55 values was found to be 1.8 ± .1. The influence of reference radiation, in vivo versus in vitro methodologies, and the use of tritiated thymidine or tritiated water are discussed. A methodology designed to estimate the effects of subcellular distribution is described and a suitable parameter, the localization factor defined. Estimates of this factor are made for both nuclear-bound and organically-bound tritium. Values of 4 and 1.5 respectively are suggested. Organ uptake studies in rodents following long-term feeding of organically-bound tritium are compared. The tritium is found to be unequally distributed among the tissues studied. The highest specific activity occurs in liver, with the lowest in femur. The specific activity of tritium in tissue-free water slightly exceeds that of organically-bound tritium in liver. Retention studies reveal a three-component exponential decrease of organically-bound tritium. No discernible trends of the periods of the three components with specific organs could be established. Average values of the periods are 1.2 ± .2, 10 ± 2, and 65 ± 8 days. It is concluded that specific enhancement of radiobiological effectiveness due to incorporation of tritium in DNA does probably not occur. The radiotoxicological impact of organically-bound tritium could warrant the use of a radiation weighing factor between 2 and 3
Dose calculation from a D-D-reaction-based BSA for boron neutron capture synovectomy
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Monte Carlo simulations were carried out to calculate dose in a knee phantom from a D-D-reaction-based Beam Shaping Assembly (BSA) for Boron Neutron Capture Synovectomy (BNCS). The BSA consists of a D(d,n)-reaction-based neutron source enclosed inside a polyethylene moderator and graphite reflector. The polyethylene moderator and graphite reflector sizes were optimized to deliver the highest ratio of thermal to fast neutron yield at the knee phantom. Then neutron dose was calculated at various depths in a knee phantom loaded with boron and therapeutic ratios of synovium dose/skin dose and synovium dose/bone dose were determined. Normalized to same boron loading in synovium, the values of the therapeutic ratios obtained in the present study are 12-30 times higher than the published values.
Dose calculation from a D-D-reaction-based BSA for boron neutron capture synovectomy
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Abdalla, Khalid [Department of Physics, Hail University, Hail (Saudi Arabia)], E-mail: khalidafnan@uoh.edu.sa; Naqvi, A.A. [Department of Physics, King Fahd University of Petroleum and Minerals and Center for Applied Physical Sciences, Box No. 1815, Dhahran 31261 (Saudi Arabia)], E-mail: aanaqvi@kfupm.edu.sa; Maalej, N.; Elshahat, B. [Department of Physics, King Fahd University of Petroleum and Minerals and Center for Applied Physical Sciences, Box No. 1815, Dhahran 31261 (Saudi Arabia)
2010-04-15
Monte Carlo simulations were carried out to calculate dose in a knee phantom from a D-D-reaction-based Beam Shaping Assembly (BSA) for Boron Neutron Capture Synovectomy (BNCS). The BSA consists of a D(d,n)-reaction-based neutron source enclosed inside a polyethylene moderator and graphite reflector. The polyethylene moderator and graphite reflector sizes were optimized to deliver the highest ratio of thermal to fast neutron yield at the knee phantom. Then neutron dose was calculated at various depths in a knee phantom loaded with boron and therapeutic ratios of synovium dose/skin dose and synovium dose/bone dose were determined. Normalized to same boron loading in synovium, the values of the therapeutic ratios obtained in the present study are 12-30 times higher than the published values.
Determination of uncertainties in the calculation of dose rates at transport and storage casks
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The compliance with the dose rate limits for transport and storage casks (TLB) for spent nuclear fuel from pressurised water reactors can be proved by calculation. This includes the determination of the radioactive sources and the shielding-capability of the cask. In this thesis the entire computational chain, which extends from the determination of the source terms to the final Monte-Carlo-transport-calculation is analysed and the arising uncertainties are quantified not only by benchmarks but also by variational calculi. The background of these analyses is that the comparison with measured dose rates at different TLBs shows an overestimation by the values calculated. Regarding the studies performed, the overestimation can be mainly explained by the detector characteristics for the measurement of the neutron dose rate and additionally in case of the gamma dose rates by the energy group structure, which the calculation is based on. It turns out that the consideration of the uncertainties occurring along the computational chain can lead to even greater overestimation. Concerning the dose rate calculation at cask loadings with spent uranium fuel assemblies an uncertainty of ((+21-28) ±2) % (rel.) for the total gamma dose rate and of (+28±23-55±4) % (rel.) for the total neutron dose rate are estimated. For mixed-loadings with spent uranium and MOX fuel assemblies an uncertainty of (+24±3-27±2) % (rel.) for the total gamma dose rate and of (+28±23-55±4) % (rel.) for the total neutron dose rate are quantified. The results show that the computational chain has not to be modified, because the calculations performed lead to conservative dose rate predictions, even if high uncertainties at neutron dose rate measurements arise. Thus at first the uncertainties of the neutron dose rate measurement have to be decreased to enable a reduction of the overestimation of the calculated dose rate afterwards. In the present thesis the deviation of the measured and calculated
Influence of polarization and a source model for dose calculation in MRT
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Bartzsch, Stefan, E-mail: s.bartzsch@dkfz.de; Oelfke, Uwe [The Institute of Cancer Research, 15 Cotswold Road, Belmont, Sutton, Surrey SM2 5NG, United Kingdom and Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 280, D-69120 Heidelberg (Germany); Lerch, Michael; Petasecca, Marco [Centre for Medical Radiation Physics, University of Wollongong, Northfields Avenue, Wollongong 2522 (Australia); Bräuer-Krisch, Elke [European Synchrotron Radiation Facility, 6 Rue Jules Horowitz, 38000 Grenoble (France)
2014-04-15
Purpose: Microbeam Radiation Therapy (MRT), an alternative preclinical treatment strategy using spatially modulated synchrotron radiation on a micrometer scale, has the great potential to cure malignant tumors (e.g., brain tumors) while having low side effects on normal tissue. Dose measurement and calculation in MRT is challenging because of the spatial accuracy required and the arising high dose differences. Dose calculation with Monte Carlo simulations is time consuming and their accuracy is still a matter of debate. In particular, the influence of photon polarization has been discussed in the literature. Moreover, it is controversial whether a complete knowledge of phase space trajectories, i.e., the simulation of the machine from the wiggler to the collimator, is necessary in order to accurately calculate the dose. Methods: With Monte Carlo simulations in the Geant4 toolkit, the authors investigate the influence of polarization on the dose distribution and the therapeutically important peak to valley dose ratios (PVDRs). Furthermore, the authors analyze in detail phase space information provided byMartínez-Rovira et al. [“Development and commissioning of a Monte Carlo photon model for the forthcoming clinical trials in microbeam radiation therapy,” Med. Phys. 39(1), 119–131 (2012)] and examine its influence on peak and valley doses. A simple source model is developed using parallel beams and its applicability is shown in a semiadjoint Monte Carlo simulation. Results are compared to measurements and previously published data. Results: Polarization has a significant influence on the scattered dose outside the microbeam field. In the radiation field, however, dose and PVDRs deduced from calculations without polarization and with polarization differ by less than 3%. The authors show that the key consequences from the phase space information for dose calculations are inhomogeneous primary photon flux, partial absorption due to inclined beam incidence outside
A CT-based analytical dose calculation method for HDR 192Ir brachytherapy
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Purpose: This article presents an analytical dose calculation method for high-dose-rate 192Ir brachytherapy, taking into account the effects of inhomogeneities and reduced photon backscatter near the skin. The adequacy of the Task Group 43 (TG-43) two-dimensional formalism for treatment planning is also assessed. Methods: The proposed method uses material composition and density data derived from computed tomography images. The primary and scatter dose distributions for each dwell position are calculated first as if the patient is an infinite water phantom. This is done using either TG-43 or a database of Monte Carlo (MC) dose distributions. The latter can be used to account for the effects of shielding in water. Subsequently, corrections for photon attenuation, scatter, and spectral variations along medium- or low-Z inhomogeneities are made according to the radiological paths determined by ray tracing. The scatter dose is then scaled by a correction factor that depends on the distances between the point of interest, the body contour, and the source position. Dose calculations are done for phantoms with tissue and lead inserts, as well as patient plans for head-and-neck, esophagus, and MammoSite balloon breast brachytherapy treatments. Gamma indices are evaluated using a dose-difference criterion of 3% and a distance-to-agreement criterion of 2 mm. PTRANCT MC calculations are used as the reference dose distributions. Results: For the phantom with tissue and lead inserts, the percentages of the voxels of interest passing the gamma criteria (Pγ≥1) are 100% for the analytical calculation and 91% for TG-43. For the breast patient plan, TG-43 overestimates the target volume receiving the prescribed dose by 4% and the dose to the hottest 0.1 cm3 of the skin by 9%, whereas the analytical and MC results agree within 0.4%. Pγ≥1 are 100% and 48% for the analytical and TG-43 calculations, respectively. For the head-and-neck and esophagus patient plans, Pγ≥1 are ≥99
Monte Carlo calculation of 60Co γ-ray's albedo-dose rate from the air
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The Monte Carlo calculation of 60Co γ-ray's albedo-dose rate from the air is reported. A formula is presented with which the relations of the albedo-doserate with some parameters are simulated and fitted
Liang, X.; Penagaricano, J.; Zheng, D.; Morrill, S.; Zhang, X; Corry, P.; Griffin, R. J.; Han, E. Y.; Hardee, M.; Ratanatharathom, V.
2016-01-01
Background The aim of this study is to evaluate the radiobiological impact of Acuros XB (AXB) vs. Anisotropic Analytic Algorithm (AAA) dose calculation algorithms in combined dose-volume and biological optimized IMRT plans of SBRT treatments for non-small-cell lung cancer (NSCLC) patients. Methods Twenty eight patients with NSCLC previously treated SBRT were re-planned using Varian Eclipse (V11) with combined dose-volume and biological optimization IMRT sliding window technique. The total dos...
An energy transfer method for 4D Monte Carlo dose calculation
Siebers, Jeffrey V; Zhong, Hualiang
2008-01-01
This article presents a new method for four-dimensional Monte Carlo dose calculations which properly addresses dose mapping for deforming anatomy. The method, called the energy transfer method (ETM), separates the particle transport and particle scoring geometries: Particle transport takes place in the typical rectilinear coordinate system of the source image, while energy deposition scoring takes place in a desired reference image via use of deformable image registration. Dose is the energy ...
Calculating patient specific doses in X-ray diagnostics and from radiopharmaceuticals
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The risk associated with exposure to ionising radiation is dependent on the characteristics of the exposed individual. The size and structure of the individual influences the absorbed dose distribution in the organs. Traditional methods used to calculate the patient organ doses are based on standardised calculation phantoms, which neglect the variance of the patient size or even sex. When estimating the radiation dose of an individual patient, patient specific calculation methods must be used. Methods for patient specific dosimetry in the fields of X-ray diagnostics and diagnostic and therapeutic use of radiopharmaceuticals were proposed in this thesis. A computer program, ODS-60, for calculating organ doses from diagnostic X-ray exposures was presented. The calculation is done in a patient specific phantom with depth dose and profile algorithms fitted to Monte Carlo simulation data from a previous study. Improvements to the version reported earlier were introduced, e.g. bone attenuation was implemented. The applicability of the program to determine patient doses from complex X-ray examinations (barium enema examination) was studied. The conversion equations derived for female and male patients as a function of patient weight gave the smallest deviation from the actual patient doses when compared to previous studies. Another computer program, Intdose, was presented for calculation of the dose distribution from radiopharmaceuticals. The calculation is based on convolution of an isotope specific point dose kernel with activity distribution, obtained from single photon emission computed tomography (SPECT) images. Anatomical information is taken from magnetic resonance (MR) or computed tomography (CT) images. According to a phantom study, Intdose agreed within 3 % with measurements. For volunteers administered diagnostic radiopharmaceuticals, the results given by Intdose were found to agree with traditional methods in cases of medium sized patients. For patients
Calculations of received dose for different points in the enrichment uranium oxide warehouse at 4%
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In order to verifying that the received dose so much inside as outside of the warehouse of enriched uranium dioxide to 4% it doesn't represent risk to the personnel, the modelling of this and the corresponding calculations for the extreme case of dose at contact are made. (Author)
Monte Carlo calculation of received dose from ingestion and inhalation of natural uranium
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For the purpose of this study eighty samples are taken from the area Bela Crkva and Vrsac. The activity of radionuclide in the soil is determined by gamma- ray spectrometry. Monte Carlo method is used to calculate effective dose received by population resulting from the inhalation and ingestion of natural uranium. The estimated doses were compared with the legally prescribed levels. (author)
Calculation of the dose to lymphocytes in external beam radiation therapy
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Lymphopenia is known to occur in patients undergoing external beam radiation therapy when the radiation fields encompass major blood vessels and lymphatic tissue. The dose received by the lymphocytes has up to now not been determined. We present here a general formalism for the calculation of the lymphocyte dose for a patient undergoing fractionated radiation therapy at any irradiation site. The calculation procedure is demonstrated for a typical case of pelvic irradiation
Calculation of the dose to lymphocytes in external beam radiation therapy
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Ekstrand, K.E.; Dixon, R.L.; Plunkett, S.; Raben, M.
1981-02-01
Lymphopenia is known to occur in patients undergoing external beam radiation therapy when the radiation fields encompass major blood vessels and lymphatic tissue. The dose received by the lymphocytes has up to now not been determined. We present here a general formalism for the calculation of the lymphocyte dose for a patient undergoing fractionated radiation therapy at any irradiation site. The calculation procedure is demonstrated for a typical case of pelvic irradiation.
A clinical study of lung cancer dose calculation accuracy with Monte Carlo simulation
Zhao, Yanqun; Qi, Guohai; Yin, Gang; Wang, Xianliang; Wang, Pei; Li, Jian; Xiao, Mingyong; Li, Jie; Kang, Shengwei; Liao, Xiongfei
2014-01-01
Background The accuracy of dose calculation is crucial to the quality of treatment planning and, consequently, to the dose delivered to patients undergoing radiation therapy. Current general calculation algorithms such as Pencil Beam Convolution (PBC) and Collapsed Cone Convolution (CCC) have shortcomings in regard to severe inhomogeneities, particularly in those regions where charged particle equilibrium does not hold. The aim of this study was to evaluate the accuracy of the PBC and CCC alg...
Calculation of 131I-ortho-iodohippurate absorbed kidney dose: A literature review
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Extensive information has been made available relative to the physical aspects necessary for calculation of radiation absorbed dose from radiopharmaceuticals. A similar data base for the biological factors involved in these calculations has not been documented as thoroughly. The authors present an extensive literature review for the radiation absorbed dose of 131I-ortho-iodohippurate and discuss the rationale for adjusting previously accepted values with new biodistribution information
International Nuclear Information System (INIS)
A method is presented for estimating the total treatment time for a brachytherapy radiation fraction with a planar flexible intraoperative template (FIT), using an 192Ir high dose rate afterloading device. The FIT can be rectangular or irregularly shaped. The manual calculation serves as an independent check of the treatment time calculated by the treatment planning system for applications with varying sizes, shapes and dose prescription depths. The parameters required for the calculation are the number of active dwell positions, the catheter spacing and dwell position spacing, the source strength, the applied dose and the depth of dose prescription. For a fixed depth of dose prescription (1.25 cm) and fixed dwell position and catheter spacing (0.5 and 1 cm respectively) the manual calculation accurately predicts (usually within 2%) the total treatment time as calculated by the treatment planning system. For varying catheter and dwell position spacings and dose prescription depths the accuracy is still within 7%. An action threshold of 5% allows detection of errors made in the number of active dwell positions (±9), catheter spacing (±1 mm) and dose prescription depth (±1 mm). Errors in dwell position spacing (0.25 cm or more) could also be accurately detected. (author)
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Dose quantity in the shielding design calculation was changed from the 1 cm depth dose equivalent to effective dose on the occasion of the introduction of the International Commission on Radiological Protection (ICRP) 1990 Recommendations (ICRP Publication 60) into domestic laws. As dose conversion coefficients in the shielding design calculation for accelerator facilities, the values for front irradiation (AP irradiation geometry) of neutrons below 20 MeV based on the ICRP Publication 74 are listed in the accompanying table of the domestic laws, but the values for neutrons above 20 MeV are not shown in the accompanying table. The status of dose conversion coefficients for neutrons above 20 MeV was surveyed and the effective dose rates behind the concrete shield of proton accelerator facilities were obtained by using typical neutron spectra and various dose conversion coefficients. As a result of consideration, the effective dose conversion coefficients for front irradiation of neutrons above 20 MeV evaluated by using HERMES code system was recommended for high energy neutrons in the shielding design calculation of proton accelerator facilities and 77 energy group averaged dose conversion coefficients was produced from thermal energy to 2 GeV. (author)
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The γ-index test has been commonly adopted to quantify the degree of agreement between a reference dose distribution and an evaluation dose distribution. Monte Carlo (MC) simulation has been widely used for the radiotherapy dose calculation for both clinical and research purposes. The goal of this work is to investigate both theoretically and experimentally the impact of the MC statistical fluctuation on the γ-index test when the fluctuation exists in the reference, the evaluation, or both dose distributions. To the first order approximation, we theoretically demonstrated in a simplified model that the statistical fluctuation tends to overestimate γ-index values when existing in the reference dose distribution and underestimate γ-index values when existing in the evaluation dose distribution given the original γ-index is relatively large for the statistical fluctuation. Our numerical experiments using realistic clinical photon radiation therapy cases have shown that (1) when performing a γ-index test between an MC reference dose and a non-MC evaluation dose, the average γ-index is overestimated and the gamma passing rate decreases with the increase of the statistical noise level in the reference dose; (2) when performing a γ-index test between a non-MC reference dose and an MC evaluation dose, the average γ-index is underestimated when they are within the clinically relevant range and the gamma passing rate increases with the increase of the statistical noise level in the evaluation dose; (3) when performing a γ-index test between an MC reference dose and an MC evaluation dose, the gamma passing rate is overestimated due to the statistical noise in the evaluation dose and underestimated due to the statistical noise in the reference dose. We conclude that the γ-index test should be used with caution when comparing dose distributions computed with MC simulation. (paper)
Energy Technology Data Exchange (ETDEWEB)
Chibani, Omar, E-mail: omar.chibani@fccc.edu; C-M Ma, Charlie [Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111 (United States)
2014-05-15
Purpose: To present a new accelerated Monte Carlo code for CT-based dose calculations in high dose rate (HDR) brachytherapy. The new code (HDRMC) accounts for both tissue and nontissue heterogeneities (applicator and contrast medium). Methods: HDRMC uses a fast ray-tracing technique and detailed physics algorithms to transport photons through a 3D mesh of voxels representing the patient anatomy with applicator and contrast medium included. A precalculated phase space file for the{sup 192}Ir source is used as source term. HDRM is calibrated to calculated absolute dose for real plans. A postprocessing technique is used to include the exact density and composition of nontissue heterogeneities in the 3D phantom. Dwell positions and angular orientations of the source are reconstructed using data from the treatment planning system (TPS). Structure contours are also imported from the TPS to recalculate dose-volume histograms. Results: HDRMC was first benchmarked against the MCNP5 code for a single source in homogenous water and for a loaded gynecologic applicator in water. The accuracy of the voxel-based applicator model used in HDRMC was also verified by comparing 3D dose distributions and dose-volume parameters obtained using 1-mm{sup 3} versus 2-mm{sup 3} phantom resolutions. HDRMC can calculate the 3D dose distribution for a typical HDR cervix case with 2-mm resolution in 5 min on a single CPU. Examples of heterogeneity effects for two clinical cases (cervix and esophagus) were demonstrated using HDRMC. The neglect of tissue heterogeneity for the esophageal case leads to the overestimate of CTV D90, CTV D100, and spinal cord maximum dose by 3.2%, 3.9%, and 3.6%, respectively. Conclusions: A fast Monte Carlo code for CT-based dose calculations which does not require a prebuilt applicator model is developed for those HDR brachytherapy treatments that use CT-compatible applicators. Tissue and nontissue heterogeneities should be taken into account in modern HDR
Development of the Calculation Module for Uncertainty of Internal Dose Coefficients
International Nuclear Information System (INIS)
The ICRP (International Commission on Radiological Protection) provides the coefficients as point values without uncertainties, it is important to understand sources of uncertainty in the derivation of the coefficients. When internal dose coefficients are calculated, numerous factors are involved such as transfer rate in biokinetic models, absorption rates and deposition in respiratory tract model, fractional absorption in alimentary tract model, absorbed fractions (AF), nuclide information and organ mass. These factors have uncertainty respectively, which increases the uncertainty of internal dose coefficients by uncertainty propagation. Since the procedure of internal dose coefficients calculation is somewhat complicated, it is difficult to propagate the each uncertainty analytically. The development of module and calculation were performed by MATLAB. In this study, we developed the calculation module for uncertainty of the internal dose coefficient. In this module, uncertainty of various factor used to calculate the internal dose coefficient can be considered using the Monte Carlo sampling method. After developing the module, we calculated the internal dose coefficient for inhalation of 90Sr with the uncertainty and obtained the distribution and percentile values. It is expected that this study will contribute greatly to the uncertainty research on internal dosimetry. In the future, we will update the module to consider more uncertainties
Dose calculation for neutrons of thermal to 10 MeV
International Nuclear Information System (INIS)
In the ICRP publication 60 adopted in 1990, the drastic change was proposed regarding the definition of the dose used for radiation protection. The main changes were the introduction of radiation weighting factor, the definition of tissue equivalent dose, the change of tissue weighting factor and the change of the equation for defining radiation quality factor (the equation for Q-L relation). In the exposure to neutrons, all these changes exert influence. In the case of neutrons, the conservativeness of operational quantity in relation to the limit of exposure may break down. Effective dose is defined as the sum of weighted risks of the equivalent doses of 12 organs and tissues and the rest of tissues. Also it has been recommended to take the mass-weighted average value for 10 specified organs and tissues as the equivalent dose. As to the effective dose for neutrons, the calculating method, the effective dose for adults, the comparison of effective dose and effective dose equivalent, and the age dependence of effective dose are explained. It is difficult to directly measure effective dose which is the limiting quantity of exposure. Therefore, ICRU defined operational quantity for area monitoring and individual monitoring. The relation of effective dose with operational quantity is shown. (K.I.)
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Pilots, flight attendants, and passengers aboard jet aircrafts are subjected to higher cosmic radiation levels at high altitude than on the ground. Additional dose, received during flight is called 'aviation route dose'. Addressing the needs for precise and easy determination of aviation route doses (Sv), the authors have developed a new application 'JISCARD GUI' with a graphical user interface which provides dose rate (Sv/h) distribution along a flight route and aviation route dose. The graphical interface made with Adobe Flash provide functions to select airports on dynamic map or to search by airport/city names, and to report resulting aviation route doses and graphs of dose rate change through a flight. Dose rate data at several cut off rigidity, Rc and force field potential, FFP were calculated in advance using a PHITS-based analytical model and stored in the server as matrix data. Upon user's request of departure/arrival airports and flight date, interpolation using matrix data substantiates derivation of dose rate distribution in a simple and quick manner with sufficient accuracy. Precision of the dose calculation was verified by comparison with JISCARD EX (MS-Excel version) released in September 2008. This advanced application will be open to public through the website of the National Institute of Radiological Sciences in the near future. (author)
Analysis of the dose calculation accuracy for IMRT in lung: A 2D approach
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Dvorak, Pavel; Stock, Markus; Kroupa, Bernhard; Bogner, Joachim; Georg, Diet mar [Div. of Medical Radiation Physics, Dept. of Radiotherapy and Radiobiology, AKH Vienna, Medical Univ. Vienna, Vienna (Austria)
2007-10-15
The purpose of this study was to compare the dosimetric accuracy of IMRT plans for targets in lung with the accuracy of standard uniform-intensity conformal radiotherapy for different dose calculation algorithms. Tests were performed utilizing a special phantom manufactured from cork and polystyrene in order to quantify the uncertainty of two commercial TPS for IMRT in the lung. Ionization and film measurements were performed at various measuring points/planes. Additionally, single-beam and uniform-intensity multiple-beam tests were performed, in order to investigate deviations due to other characteristics of IMRT. Helax-TMS V6.1(A) was tested for 6, 10 and 25 MV and BrainSCAN 5.2 for 6 MV photon beams, respectively. Pencil beam (PB) with simple inhomogeneity correction and 'collapsed cone' (CC) algorithms were applied for dose calculations. However, the latter was not incorporated during optimization hence only post-optimization recalculation was tested. Two-dimensional dose distributions were evaluated applying the b.gamma index concept. Conformal plans showed the same accuracy as IMRT plans. Ionization chamber measurements detected deviations of up to 5% when a PB algorithm was used for IMRT dose calculations. Significant improvement was observed when IMRT plans were recalculated with the CC algorithm, especially for the highest nominal energy. All b.gamma evaluations confirmed substantial improvement with the CC algorithm in 2D. While PB dose distributions showed most discrepancies in lower (<50%) and high (>90%) dose regions, the CC dose distributions deviated mainly in the high dose gradient (20-80%) region. The advantages of IMRT (conformity, intra-target dose control) should be counterbalanced with possible calculation inaccuracies for targets in the lung. Until no superior dose calculation algorithms are involved in the iterative optimization process it should be used with great care. When only PB algorithm with simple inhomogeneity correction is
Analysis of the dose calculation accuracy for IMRT in lung: a 2D approach.
Dvorak, Pavel; Stock, Markus; Kroupa, Bernhard; Bogner, Joachim; Georg, Dietmar
2007-01-01
The purpose of this study was to compare the dosimetric accuracy of IMRT plans for targets in lung with the accuracy of standard uniform-intensity conformal radiotherapy for different dose calculation algorithms. Tests were performed utilizing a special phantom manufactured from cork and polystyrene in order to quantify the uncertainty of two commercial TPS for IMRT in the lung. Ionization and film measurements were performed at various measuring points/planes. Additionally, single-beam and uniform-intensity multiple-beam tests were performed, in order to investigate deviations due to other characteristics of IMRT. Helax-TMS V6.1(A) was tested for 6, 10 and 25 MV and BrainSCAN 5.2 for 6 MV photon beams, respectively. Pencil beam (PB) with simple inhomogeneity correction and 'collapsed cone' (CC) algorithms were applied for dose calculations. However, the latter was not incorporated during optimization hence only post-optimization recalculation was tested. Two-dimensional dose distributions were evaluated applying the gamma index concept. Conformal plans showed the same accuracy as IMRT plans. Ionization chamber measurements detected deviations of up to 5% when a PB algorithm was used for IMRT dose calculations. Significant improvement (deviations approximately 2%) was observed when IMRT plans were recalculated with the CC algorithm, especially for the highest nominal energy. All gamma evaluations confirmed substantial improvement with the CC algorithm in 2D. While PB dose distributions showed most discrepancies in lower (90%) dose regions, the CC dose distributions deviated mainly in the high dose gradient (20-80%) region. The advantages of IMRT (conformity, intra-target dose control) should be counterbalanced with possible calculation inaccuracies for targets in the lung. Until no superior dose calculation algorithms are involved in the iterative optimization process it should be used with great care. When only PB algorithm with simple inhomogeneity correction is
Analysis of the dose calculation accuracy for IMRT in lung: A 2D approach
International Nuclear Information System (INIS)
The purpose of this study was to compare the dosimetric accuracy of IMRT plans for targets in lung with the accuracy of standard uniform-intensity conformal radiotherapy for different dose calculation algorithms. Tests were performed utilizing a special phantom manufactured from cork and polystyrene in order to quantify the uncertainty of two commercial TPS for IMRT in the lung. Ionization and film measurements were performed at various measuring points/planes. Additionally, single-beam and uniform-intensity multiple-beam tests were performed, in order to investigate deviations due to other characteristics of IMRT. Helax-TMS V6.1(A) was tested for 6, 10 and 25 MV and BrainSCAN 5.2 for 6 MV photon beams, respectively. Pencil beam (PB) with simple inhomogeneity correction and 'collapsed cone' (CC) algorithms were applied for dose calculations. However, the latter was not incorporated during optimization hence only post-optimization recalculation was tested. Two-dimensional dose distributions were evaluated applying the b.gamma index concept. Conformal plans showed the same accuracy as IMRT plans. Ionization chamber measurements detected deviations of up to 5% when a PB algorithm was used for IMRT dose calculations. Significant improvement was observed when IMRT plans were recalculated with the CC algorithm, especially for the highest nominal energy. All b.gamma evaluations confirmed substantial improvement with the CC algorithm in 2D. While PB dose distributions showed most discrepancies in lower (90%) dose regions, the CC dose distributions deviated mainly in the high dose gradient (20-80%) region. The advantages of IMRT (conformity, intra-target dose control) should be counterbalanced with possible calculation inaccuracies for targets in the lung. Until no superior dose calculation algorithms are involved in the iterative optimization process it should be used with great care. When only PB algorithm with simple inhomogeneity correction is used, lower energy photon
Comparison of methods for calculating rectal dose after 125I prostate brachytherapy implants
International Nuclear Information System (INIS)
Purpose: To compare several different methods of calculating the rectal dose and examine how accurately they represent rectal dose surface area measurements and, also, their practicality for routine use. Methods and Materials: This study comprised 55 patients, randomly selected from 295 prostate brachytherapy patients implanted at the Vancouver Cancer Center between 1998 and 2000. All implants used a nonuniform loading of 0.33 mCi (NIST-99) 125I seeds and a prescribed dose of 144 Gy. Pelvic CT scans were obtained for each patient ∼30 days after implantation. For the purposes of calculating the rectal dose, several structures were contoured on the CT images: (1) a 1-mm-thick anterior rectal wall, (2) the anterior half rectum, and (3) the whole rectum. Point doses were also obtained along the anterior rectal surface. The thin wall contour provided a surrogate for a dose-surface histogram (DSH) and was our reference standard rectal dose measurement. Alternate rectal dose measurements (volume, surface area, and length of rectum receiving a dose of interest [DOI] of ≥144 Gy and 216 Gy, as well as point dose measures) were calculated using several methods (VariSeed software) and compared with the surrogate DSH measure (SADOI). Results: The best correlation with SA144Gy was the dose volumes (whole or anterior half rectum) (R = 0.949). The length of rectum receiving ≥144 Gy also correlated well with SA144Gy (R ≥0.898). Point dose measures, such as the average and maximal anterior dose, correlated poorly with SA144Gy (R ≤0.649). The 216-Gy measurements supported these results. In addition, dose-volume measurements were the most practical (∼6 min/patient), with our surrogate DSH the least practical (∼20 min/patient). Conclusion: Dose-volume measurements for the whole or anterior half rectum, because they were the most practical measures and best represented the DSH measurements, should be considered a standard method of reporting the rectal dose when
Assessing the Clinical Impact of Approximations in Analytical Dose Calculations for Proton Therapy
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Schuemann, Jan, E-mail: jschuemann@mgh.harvard.edu; Giantsoudi, Drosoula; Grassberger, Clemens; Moteabbed, Maryam; Min, Chul Hee; Paganetti, Harald
2015-08-01
Purpose: To assess the impact of approximations in current analytical dose calculation methods (ADCs) on tumor control probability (TCP) in proton therapy. Methods: Dose distributions planned with ADC were compared with delivered dose distributions as determined by Monte Carlo simulations. A total of 50 patients were investigated in this analysis with 10 patients per site for 5 treatment sites (head and neck, lung, breast, prostate, liver). Differences were evaluated using dosimetric indices based on a dose-volume histogram analysis, a γ-index analysis, and estimations of TCP. Results: We found that ADC overestimated the target doses on average by 1% to 2% for all patients considered. The mean dose, D95, D50, and D02 (the dose value covering 95%, 50% and 2% of the target volume, respectively) were predicted within 5% of the delivered dose. The γ-index passing rate for target volumes was above 96% for a 3%/3 mm criterion. Differences in TCP were up to 2%, 2.5%, 6%, 6.5%, and 11% for liver and breast, prostate, head and neck, and lung patients, respectively. Differences in normal tissue complication probabilities for bladder and anterior rectum of prostate patients were less than 3%. Conclusion: Our results indicate that current dose calculation algorithms lead to underdosage of the target by as much as 5%, resulting in differences in TCP of up to 11%. To ensure full target coverage, advanced dose calculation methods like Monte Carlo simulations may be necessary in proton therapy. Monte Carlo simulations may also be required to avoid biases resulting from systematic discrepancies in calculated dose distributions for clinical trials comparing proton therapy with conventional radiation therapy.
Dose rates from a C-14 source using extrapolation chamber and MC calculations
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The extrapolation chamber technique and the Monte Carlo (MC) calculation technique based on the EGS4 system have been studied for application for determination of dose rates in a low-energy β radiation field e.g., that from a 14C source. The extrapolation chamber measurement method is the basic method for determination of dose rates in β radiation fields. Applying a number of correction factors and the stopping power ratio, tissue to air, the measured dose rate in an air volume surrounded by tissue equivalent material is converted into dose to tissue. Various details of the extrapolation chamber measurement method and evaluation procedure have been studied and further developed, and a complete procedure for the experimental determination of dose rates from a14C source is presented. A number of correction factors and other parameters used in the evaluation procedure for the measured data have been obtained by MC calculations. The whole extrapolation chamber measurement procedure was simulated using the MC method. The measured dose rates showed an increasing deviation from the MC calculated dose rates as the absorber thickness increased. This indicates that the EGS4 code may have some limitations for transport of very low-energy electrons. i.e., electrons with estimated energies less than 10 - 20 keV. MC calculations of dose to tissue were performed using two models: a cylindrical tissue phantom and a computer model of the extrapolation chamber. The dose to tissue in the extrapolation chamber model showed an additional buildup dose compared to the dose in the tissue model. (au) 10 tabs., 11 ills., 18 refs
The impact of dose calculation algorithms on partial and whole breast radiation treatment plans
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Berrang Tanya
2010-12-01
Full Text Available Abstract Background This paper compares the calculated dose to target and normal tissues when using pencil beam (PBC, superposition/convolution (AAA and Monte Carlo (MC algorithms for whole breast (WBI and accelerated partial breast irradiation (APBI treatment plans. Methods Plans for 10 patients who met all dosimetry constraints on a prospective APBI protocol when using PBC calculations were recomputed with AAA and MC, keeping the monitor units and beam angles fixed. Similar calculations were performed for WBI plans on the same patients. Doses to target and normal tissue volumes were tested for significance using the paired Student's t-test. Results For WBI plans the average dose to target volumes when using PBC calculations was not significantly different than AAA calculations, the average PBC dose to the ipsilateral breast was 10.5% higher than the AAA calculations and the average MC dose to the ipsilateral breast was 11.8% lower than the PBC calculations. For ABPI plans there were no differences in dose to the planning target volume, ipsilateral breast, heart, ipsilateral lung, or contra-lateral lung. Although not significant, the maximum PBC dose to the contra-lateral breast was 1.9% higher than AAA and the PBC dose to the clinical target volume was 2.1% higher than AAA. When WBI technique is switched to APBI, there was significant reduction in dose to the ipsilateral breast when using PBC, a significant reduction in dose to the ipsilateral lung when using AAA, and a significant reduction in dose to the ipsilateral breast and lung and contra-lateral lung when using MC. Conclusions There is very good agreement between PBC, AAA and MC for all target and most normal tissues when treating with APBI and WBI and most of the differences in doses to target and normal tissues are not clinically significant. However, a commonly used dosimetry constraint, as recommended by the ASTRO consensus document for APBI, that no point in the contra
A clinical study of lung cancer dose calculation accuracy with Monte Carlo simulation
International Nuclear Information System (INIS)
The accuracy of dose calculation is crucial to the quality of treatment planning and, consequently, to the dose delivered to patients undergoing radiation therapy. Current general calculation algorithms such as Pencil Beam Convolution (PBC) and Collapsed Cone Convolution (CCC) have shortcomings in regard to severe inhomogeneities, particularly in those regions where charged particle equilibrium does not hold. The aim of this study was to evaluate the accuracy of the PBC and CCC algorithms in lung cancer radiotherapy using Monte Carlo (MC) technology. Four treatment plans were designed using Oncentra Masterplan TPS for each patient. Two intensity-modulated radiation therapy (IMRT) plans were developed using the PBC and CCC algorithms, and two three-dimensional conformal therapy (3DCRT) plans were developed using the PBC and CCC algorithms. The DICOM-RT files of the treatment plans were exported to the Monte Carlo system to recalculate. The dose distributions of GTV, PTV and ipsilateral lung calculated by the TPS and MC were compared. For 3DCRT and IMRT plans, the mean dose differences for GTV between the CCC and MC increased with decreasing of the GTV volume. For IMRT, the mean dose differences were found to be higher than that of 3DCRT. The CCC algorithm overestimated the GTV mean dose by approximately 3% for IMRT. For 3DCRT plans, when the volume of the GTV was greater than 100 cm3, the mean doses calculated by CCC and MC almost have no difference. PBC shows large deviations from the MC algorithm. For the dose to the ipsilateral lung, the CCC algorithm overestimated the dose to the entire lung, and the PBC algorithm overestimated V20 but underestimated V5; the difference in V10 was not statistically significant. PBC substantially overestimates the dose to the tumour, but the CCC is similar to the MC simulation. It is recommended that the treatment plans for lung cancer be developed using an advanced dose calculation algorithm other than PBC. MC can accurately
Dose calculation for 40K ingestion in samples of beans using spectrometry and MCNP
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A method based on gamma spectroscopy and on the use of voxel phantoms to calculate dose due to ingestion of 40K contained in bean samples are presented in this work. To quantify the activity of radionuclide, HPGe detector was used and the data entered in the input file of MCNP code. The highest value of equivalent dose was 7.83 μSv.y-1 in the stomach for white beans, whose activity 452.4 Bq.Kg-1 was the highest of the five analyzed. The tool proved to be appropriate when you want to calculate the dose in organs due to ingestion of food. (author)
An Automated Approach to Calculating the Daily Dose of Tacrolimus in Electronic Health Records
Xu, Hua; Doan, Son; Birdwell, Kelly A.; Cowan, James D; Vincz, Andrew J.; Haas, David W.; Basford, Melissa A; Denny, Joshua C.
2010-01-01
Clinical research often requires extracting detailed drug information, such as medication names and dosages, from Electronic Health Records (EHR). Since medication information is often recorded as both structured and unstructured formats in the EHR, extracting all the relevant drug mentions and determining the daily dose of a medication for a selected patient at a given date can be a challenging and time-consuming task. In this paper, we present an automated approach using natural language pr...
GTV-based prescription in SBRT for lung lesions using advanced dose calculation algorithms
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The aim of current study was to investigate the way dose is prescribed to lung lesions during SBRT using advanced dose calculation algorithms that take into account electron transport (type B algorithms). As type A algorithms do not take into account secondary electron transport, they overestimate the dose to lung lesions. Type B algorithms are more accurate but still no consensus is reached regarding dose prescription. The positive clinical results obtained using type A algorithms should be used as a starting point. In current work a dose-calculation experiment is performed, presenting different prescription methods. Three cases with three different sizes of peripheral lung lesions were planned using three different treatment platforms. For each individual case 60 Gy to the PTV was prescribed using a type A algorithm and the dose distribution was recalculated using a type B algorithm in order to evaluate the impact of the secondary electron transport. Secondly, for each case a type B algorithm was used to prescribe 48 Gy to the PTV, and the resulting doses to the GTV were analyzed. Finally, prescriptions based on specific GTV dose volumes were evaluated. When using a type A algorithm to prescribe the same dose to the PTV, the differences regarding median GTV doses among platforms and cases were always less than 10% of the prescription dose. The prescription to the PTV based on type B algorithms, leads to a more important variability of the median GTV dose among cases and among platforms, (respectively 24%, and 28%). However, when 54 Gy was prescribed as median GTV dose, using a type B algorithm, the variability observed was minimal. Normalizing the prescription dose to the median GTV dose for lung lesions avoids variability among different cases and treatment platforms of SBRT when type B algorithms are used to calculate the dose. The combination of using a type A algorithm to optimize a homogeneous dose in the PTV and using a type B algorithm to prescribe the
Effects of the difference in tube voltage of the CT scanner on dose calculation
Rhee, Dong Joo; Kim, Sung-woo; Jeong, Dong Hyeok; Moon, Young Min; Kim, Jung Ki
2015-07-01
Computed tomography (CT) measures the attenuation coefficient of an object and converts the value assigned to each voxel into a CT number. In radiation therapy, the CT number, which is directly proportional to the linear attenuation coefficient, must be converted to an electron density for radiation dose calculations for cancer treatment. However, if various tube voltages are applied to take the patient's CT image without applying the specific CT number to the electron density conversion curve, the accuracy of the dose calculation is not assured. In this study, changes in CT numbers for different materials due to changes in the tube voltage were demonstrated, and the dose calculation errors in the percentage depth dose (PDD), along with a clinical case were analyzed. The maximum dose difference in the PDD from the treatment planning system (TPS) dose calculation and from the Monte Carlo simulation were 1.3% and 1.1%, respectively, when applying the same CT number to the electron density conversion curve for the 80-kVp and 140-kVp images. In the clinical case, different CT number to electron density conversion curves at tube voltage of 80 kVp and 140 kVp were applied to the same image and the maximum differences in the mean, maximum, and minimum doses were 1.1%, 1.2%, and 1.0%, respectively, at the central region of the phantom and 0.6%, 0.9%, and 0.8%, respectively, at the peripheral region of the phantom.
Fast Monte Carlo Simulation for Patient-specific CT/CBCT Imaging Dose Calculation
Jia, Xun; Gu, Xuejun; Jiang, Steve B
2011-01-01
Recently, X-ray imaging dose from computed tomography (CT) or cone beam CT (CBCT) scans has become a serious concern. Patient-specific imaging dose calculation has been proposed for the purpose of dose management. While Monte Carlo (MC) dose calculation can be quite accurate for this purpose, it suffers from low computational efficiency. In response to this problem, we have successfully developed a MC dose calculation package, gCTD, on GPU architecture under the NVIDIA CUDA platform for fast and accurate estimation of the x-ray imaging dose received by a patient during a CT or CBCT scan. Techniques have been developed particularly for the GPU architecture to achieve high computational efficiency. Dose calculations using CBCT scanning geometry in a homogeneous water phantom and a heterogeneous Zubal head phantom have shown good agreement between gCTD and EGSnrc, indicating the accuracy of our code. In terms of improved efficiency, it is found that gCTD attains a speed-up of ~400 times in the homogeneous water ...
International Nuclear Information System (INIS)
Background and purpose: A series of phase I/II clinical trials are being initiated in several UK centres to explore the use of dose-escalated schedules for the treatment of non-small cell lung cancer (NSCLC). Among them the IDEAL-CRT trial (ISRCTN12155469) will investigate the introduction of individualised 'isotoxic' treatment schedules based on the relative mean lung normalised total dose (rNTDmean), an estimator related to lung toxicity. Since treatment planning will be performed using different treatment planning systems (TPSs), for the quality assurance of the trial we have carried out work to quantify the influence of dose calculation algorithms based on the determination of rNTDmean and on the choice of individualised prescription doses. Material and methods: Twenty-five patient plans with stage I, II and III NSCLC were calculated, with the same prescription dose, using the Adaptive Convolve (AC) and Collapsed Cone (CC) algorithms of the Pinnacle TPS, the pencil beam convolution (PBC) and AAA algorithms of Eclipse, and the CC and pencil beam (PB) algorithms of Oncentra Masterplan (OMP). For the paired-lungs-GTV structure, dose-volume histograms were obtained and used to calculate the corresponding rNTDmean values and results obtained with the different algorithms were compared. Results: For most (19 out of 25) of the patients studied, no algorithm-to-algorithm differences were seen in dose prescription based on rNTDmean. For the other 6 patients differences were within 2.3 Gy, except in one case where the difference was 4 Gy. Conclusions: For the IDEAL-CRT trial no corrections need to be applied to the value of rNTDmean calculated using any of the more advanced convolution/superposition algorithms studied in this work. For the two pencil beam algorithms analysed, no correction is necessary for the data obtained with the Eclipse-PBC, while for OMP-PB data a small correction needs to be applied, by using a scaling factor, to make prescription doses consistent
Wilson, J. W.; Khandelwal, G. S.
1976-01-01
Calculational methods for estimation of dose from external proton exposure of arbitrary convex bodies are briefly reviewed. All the necessary information for the estimation of dose in soft tissue is presented. Special emphasis is placed on retaining the effects of nuclear reaction, especially in relation to the dose equivalent. Computer subroutines to evaluate all of the relevant functions are discussed. Nuclear reaction contributions for standard space radiations are in most cases found to be significant. Many of the existing computer programs for estimating dose in which nuclear reaction effects are neglected can be readily converted to include nuclear reaction effects by use of the subroutines described herein.
Dose calculations with SERA for the application of the BNCT at the TRIGA Mainz
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The BNCT shall be applied for an explantated organ with metastases at the TRIGA reactor Mainz, Germany. After the treatment of the patient with 10B pharmaceutical the liver will be explanted, irradiated in the thermal column and then implantated again (autotransplantation). This was first successfully done in 12/2001 for a 48 years old male patient at the TRIGA reactor in Pavia. For a treatment with BNCT it is necessary to determine the total dose and partial radiation doses like the boron and gamma dose. Since several parts of the dose can not be measured, calculations are necessary. For this procedure the program Simulation Environment for Radiotherapy Applications (SERA) developed by INEEL, Idaho, U.S., can be applied, which allows an individual dosimetry for the patient. The SERA program consists of a manual and semi-automated geometric modeling of the treatment objects like the liver derived from MRI, CT or other medical imaging modalities. The dose for these geometric models is calculated with the INEEL radiation transport computer code and the dose contouring is also derived. The SERA program was adapted at MHH to calculate the radiation dose in the case of liver autotransplantation. Also, the technical characteristics and the physical environment of the thermal column were programmed for SERA. For the first reactor model the core of the MHH TRIGA reactor and the thermal column of the Mainz TRIGA reactor were used. The thermal column was modulated with layers of bismuth and lead to minimize the gamma dose. (author)
Calculation of dose in quartz for comparison with thermoluminescence dosimetry measurements
International Nuclear Information System (INIS)
Gamma radiation from the atomic bombs detonated over Hiroshima and Nagasaki left a record in the quartz grains constituent to the tile and brick in city structures. That record has been read to determine the gamma-ray dose deposited in these grains, using thermoluminescence (TL) dosimetry techniques. Because the quartz grains are imbedded in dense tile and brick material located on structures of complex geometry, the dose in quarts is not an exact measure of the free-field kerma. Therefore, calculations of dose deposition in the quartz grains were performed, using the same free-field fluence data and shielding computation methods as those incorporated in the dosimetry system delivered to the Radiation Effects Research Foundation (RERF) in 1986. This report presents a summary description of the experimental results, including total dose and background dose, as well as the salient features of the tiles and brick, including their locations on the various structures. The report provides a description of the approach used to calculate the dose to the quartz in the tile and brick samples, as well as a detailed tabulation of the calculated dose, including the contribution from each component of A-bomb radiation. Finally, the report provides a comparison of DS86 and T65D dose values with measured results and a discussion of issues raised in the process of that comparison
International Nuclear Information System (INIS)
In order to compare the internal effective dose evaluation in past and present, an automatic calculation sheet was developed using the parameters such as the dose conversion factors and intake of foods etc. in ICRP Pub.60, Pub72, the new 'Environmental Radiation Monitoring Guide' revised on March 29, 2001. It makes possible to sum up monitoring data in each year, to evaluate dose and to compare them to the past data. The equation, parameters of ingestion and inhalation, nuclides detected, subject nuclides, dose conversion factor of committed dose equivalent by ingestion and inhalation, fundamental principles, limits, model, monitoring results, calculation for estimation and valuation and discussion are described. This article must be handled with the utmost care on parameters, model, ND of monitoring results. (S.Y.)
International Nuclear Information System (INIS)
Uncertainty analysis of the dose calculation module of the COSYMA accident consequence assessment code has been undertaken, involving the following steps: (1) Expert judgement techniques were applied to assess uncertainties in measurable parameters determining external and internal doses. (2) The data obtained were used to calculate distributions on the dose quantities required as code input parameters. (3) The effect of uncertainties in dose quantities was analysed for a range of COSYMA end points, including the extent of countermeasures and incidences of early and late health effects, and the most important uncertainties were identified for inclusion in an overall uncertainty analysis of COSYMA. Parameters identified as making the largest contributions to uncertainty included external doses and location factors, residence times of materials on skin, breathing rates, and respiratory tract deposition and retention parameters, for the extent of countermeasures and early health effects, and caesium and iodine retention parameters for late effects. (author)
FOOD: an interactive code to calculate internal radiation doses from contaminated food products
International Nuclear Information System (INIS)
An interactive code, FOOD, has been written in BASIC for the UNIVAC 1108 to facilitate calculation of internal radiation doses to man from radionuclides in food products. In the dose model, vegetation may be contaminated by either air or irrigation water containing radionuclides. The model considers two mechanisms for radionuclide contamination of vegetation: direct deposition on leaves and uptake from soil through the root system. The user may select up to 14 food categories with corresponding consumption rates, growing periods and either irrigation rates or atmospheric deposition rates. These foods include various kinds of produce, grains and animal products. At present, doses may be calculated for the skin, total body and five internal organs from 190 radionuclides. Dose summaries can be displayed at the local terminal. Further details on percent contribution to dose by nuclide and by food type are available from an auxiliary high-speed printer. This output also includes estimated radionuclide concentrations in soil, plants and animal products
International Nuclear Information System (INIS)
Verification of calculated lung dose in an anthropomorphic phantom is performed using two dosimetry media. Dosimetry is complicated by factors such as variations in density at slice interfaces and appropriate position on CT scanning slice to accommodate these factors. Dose in lung for a 6 MV and 10 MV anterior-posterior field was calculated with a collapsed cone convolution method using an ADAC Pinnacle, 3D planning system. Up to 5% variations between doses calculated at the centre and near the edge of the 2 cm phantom slice positioned at the beam central axis were seen, due to the composition of each phantom slice. Validation of dose was performed with LiF thermoluminescent dosimeters (TLDs) and X-Omat V radiographic film. Both dosimetry media produced dose results which agreed closely with calculated results nearest their physical positioning in the phantom. The collapsed cone convolution method accurately calculates dose within inhomogeneous lung regions at 6 MV and 10 MV x-ray energy. (author)
Incorporating partial shining effects in proton pencil-beam dose calculation
International Nuclear Information System (INIS)
A range modulator wheel (RMW) is an essential component in passively scattered proton therapy. We have observed that a proton beam spot may shine on multiple steps of the RMW. Proton dose calculation algorithms normally do not consider the partial shining effect, and thus overestimate the dose at the proximal shoulder of spread-out Bragg peak (SOBP) compared with the measurement. If the SOBP is adjusted to better fit the plateau region, the entrance dose is likely to be underestimated. In this work, we developed an algorithm that can be used to model this effect and to allow for dose calculations that better fit the measured SOBP. First, a set of apparent modulator weights was calculated without considering partial shining. Next, protons spilled from the accelerator reaching the modulator wheel were simplified as a circular spot of uniform intensity. A weight-splitting process was then performed to generate a set of effective modulator weights with the partial shining effect incorporated. The SOBPs of eight options, which are used to label different combinations of proton-beam energy and scattering devices, were calculated with the generated effective weights. Our algorithm fitted the measured SOBP at the proximal and entrance regions much better than the ones without considering partial shining effect for all SOBPs of the eight options. In a prostate patient, we found that dose calculation without considering partial shining effect underestimated the femoral head and skin dose
Incorporating partial shining effects in proton pencil-beam dose calculation
Energy Technology Data Exchange (ETDEWEB)
Li Yupeng; Zhang Xiaodong; Lii Mingfwu; Sahoo, Narayan; Zhu, Ron X; Gillin, Michael; Mohan, Radhe [Department of Radiation Physics, University of Texas, MD Anderson Cancer Center, Houston, TX 77030 (United States)
2008-02-07
A range modulator wheel (RMW) is an essential component in passively scattered proton therapy. We have observed that a proton beam spot may shine on multiple steps of the RMW. Proton dose calculation algorithms normally do not consider the partial shining effect, and thus overestimate the dose at the proximal shoulder of spread-out Bragg peak (SOBP) compared with the measurement. If the SOBP is adjusted to better fit the plateau region, the entrance dose is likely to be underestimated. In this work, we developed an algorithm that can be used to model this effect and to allow for dose calculations that better fit the measured SOBP. First, a set of apparent modulator weights was calculated without considering partial shining. Next, protons spilled from the accelerator reaching the modulator wheel were simplified as a circular spot of uniform intensity. A weight-splitting process was then performed to generate a set of effective modulator weights with the partial shining effect incorporated. The SOBPs of eight options, which are used to label different combinations of proton-beam energy and scattering devices, were calculated with the generated effective weights. Our algorithm fitted the measured SOBP at the proximal and entrance regions much better than the ones without considering partial shining effect for all SOBPs of the eight options. In a prostate patient, we found that dose calculation without considering partial shining effect underestimated the femoral head and skin dose.
Inverse treatment planning for radiation therapy based on fast Monte Carlo dose calculation
International Nuclear Information System (INIS)
An inverse treatment planning system based on fast Monte Carlo (MC) dose calculation is presented. It allows optimisation of intensity modulated dose distributions in 15 to 60 minutes on present day personal computers. If a multi-processor machine is available, parallel simulation of particle histories is also possible, leading to further calculation time reductions. The optimisation process is divided into two stages. The first stage results influence profiles based on pencil beam (PB) dose calculation. The second stage starts with MC verification and post-optimisation of the PB dose and fluence distributions. Because of the potential to accurately model beam modifiers, MC based inverse planning systems are able to optimise compensator thicknesses and leaf trajectories instead of intensity profiles only. The corresponding techniques, whose implementation is the subject for future work, are also presented here. (orig.)
Dose calculation accuracy of lung planning with a commercial IMRT treatment planning system.
McDermott, Patrick N; He, Tongming; DeYoung, A
2003-01-01
The dose calculation accuracy of a commercial pencil beam IMRT planning system is evaluated by comparison with Monte Carlo calculations and measurements in an anthropomorphic phantom. The target volume is in the right lung and mediastinum and thus significant tissue inhomogeneities are present. The Monte Carlo code is an adaptation of the MCNP code and the measurements were made with TLD and film. Both the Monte Carlo code and the measurements show very good agreement with the treatment planning system except in regions where the dose is high and the electron density is low. In these regions the commercial system shows doses up to 10% higher than Monte Carlo and film. The average calculated dose for the CTV is 5% higher with the commercial system as compared to Monte Carlo. PMID:14604424
International Nuclear Information System (INIS)
Purpose: The dosimetric verification of treatment plans in helical tomotherapy usually is carried out via verification measurements. In this study, a method for independent dose calculation of tomotherapy treatment plans is presented, that uses a conventional treatment planning system with a pencil kernel dose calculation algorithm for generation of verification dose distributions based on patient CT data. Methods: A pencil beam algorithm that directly uses measured beam data was configured for dose calculation for a tomotherapy machine. Tomotherapy treatment plans were converted into a format readable by an in-house treatment planning system by assigning each projection to one static treatment field and shifting the calculation isocenter for each field in order to account for the couch movement. The modulation of the fluence for each projection is read out of the delivery sinogram, and with the kernel-based dose calculation, this information can directly be used for dose calculation without the need for decomposition of the sinogram. The sinogram values are only corrected for leaf output and leaf latency. Using the converted treatment plans, dose was recalculated with the independent treatment planning system. Multiple treatment plans ranging from simple static fields to real patient treatment plans were calculated using the new approach and either compared to actual measurements or the 3D dose distribution calculated by the tomotherapy treatment planning system. In addition, dose–volume histograms were calculated for the patient plans. Results: Except for minor deviations at the maximum field size, the pencil beam dose calculation for static beams agreed with measurements in a water tank within 2%/2 mm. A mean deviation to point dose measurements in the cheese phantom of 0.89% ± 0.81% was found for unmodulated helical plans. A mean voxel-based deviation of −0.67% ± 1.11% for all voxels in the respective high dose region (dose values >80%), and a mean local
Directory of Open Access Journals (Sweden)
Tuncay Bayram
2012-04-01
Full Text Available Objective: In this study, we aimed to make a computer program that calculates approximate radiation dose received by embryo/fetus in nuclear medicine applications. Material and Methods: Radiation dose values per MBq-1 received by embryo/fetus in nuclear medicine applications were gathered from literature for various stages of pregnancy. These values were embedded in the computer code, which was written in Fortran 90 program language. Results: The computer program called nmfdose covers almost all radiopharmaceuticals used in nuclear medicine applications. Approximate radiation dose received by embryo/fetus can be calculated easily at a few steps using this computer program. Conclusion: Although there are some constraints on using the program for some special cases, nmfdose is useful and it provides practical solution for calculation of approximate dose to embryo/fetus in nuclear medicine applications. (MIRT 2012;21:19-22
Study on the GEANT4 code applications to the dose calculation using imaging data
Lee, JeongOk; Kim, JhinKee; Kwon, HyeongCheol; Kim, JungSoo; Kim, BuGil; Jeong, DongHyeok
2015-01-01
The use of GEANT4 code has increased in the medical field. There are various studies to calculate the patient dose distributions with the GEANT4 code using the imaging data. In present study, the Monte Carlo simulations based on the DICOM data were performed to calculate absorbed dose in the patient's body. Various visualization tools were equipped in the GEANT4 code to display the detector construction, however there are limitations to display the DICOM images. In addition, it is difficult to display the dose distributions on the imaging data of the patient. Recently, gMocren code, volume visualization tool for GEANT4 simulation, has been developed and used in volume visualization of image files. In this study, the imaging data based absorbed dose distributions in patient were performed by using the gMocren code. The dosimetric evaluations with TLD and film dosimetry methods were carried out to verify the calculation results.
Study on GEANT4 code applications to dose calculation using imaging data
Lee, Jeong Ok; Kang, Jeong Ku; Kim, Jhin Kee; Kwon, Hyeong Cheol; Kim, Jung Soo; Kim, Bu Gil; Jeong, Dong Hyeok
2015-07-01
The use of the GEANT4 code has increased in the medical field. Various studies have calculated the patient dose distributions by users the GEANT4 code with imaging data. In present study, Monte Carlo simulations based on DICOM data were performed to calculate the dose absorb in the patient's body. Various visualization tools are installed in the GEANT4 code to display the detector construction; however, the display of DICOM images is limited. In addition, to displaying the dose distributions on the imaging data of the patient is difficult. Recently, the gMocren code, a volume visualization tool for GEANT4 simulation, was developed and has been used in volume visualization of image files. In this study, the imaging based on the dose distributions absorbed in the patients was performed by using the gMocren code. Dosimetric evaluations with were carried out by using thermo luminescent dosimeter and film dosimetry to verify the calculated results.
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Klüter, Sebastian, E-mail: sebastian.klueter@med.uni-heidelberg.de; Schubert, Kai; Lissner, Steffen; Sterzing, Florian; Oetzel, Dieter; Debus, Jürgen [Department of Radiation Oncology, Heidelberg University Hospital, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany, and Heidelberg Institute for Radiation Oncology (HIRO), Im Neuenheimer Feld 400, 69120 Heidelberg, Germany, and German Consortium for Translational Cancer Research (DKTK), Im Neuenheimer Feld 400, 69120 Heidelberg (Germany); Schlegel, Wolfgang [German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg (Germany); Oelfke, Uwe [German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany and Joint Department of Physics at The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London SM2 5NG (United Kingdom); Nill, Simeon [Joint Department of Physics at The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London SM2 5NG (United Kingdom)
2014-08-15
Purpose: The dosimetric verification of treatment plans in helical tomotherapy usually is carried out via verification measurements. In this study, a method for independent dose calculation of tomotherapy treatment plans is presented, that uses a conventional treatment planning system with a pencil kernel dose calculation algorithm for generation of verification dose distributions based on patient CT data. Methods: A pencil beam algorithm that directly uses measured beam data was configured for dose calculation for a tomotherapy machine. Tomotherapy treatment plans were converted into a format readable by an in-house treatment planning system by assigning each projection to one static treatment field and shifting the calculation isocenter for each field in order to account for the couch movement. The modulation of the fluence for each projection is read out of the delivery sinogram, and with the kernel-based dose calculation, this information can directly be used for dose calculation without the need for decomposition of the sinogram. The sinogram values are only corrected for leaf output and leaf latency. Using the converted treatment plans, dose was recalculated with the independent treatment planning system. Multiple treatment plans ranging from simple static fields to real patient treatment plans were calculated using the new approach and either compared to actual measurements or the 3D dose distribution calculated by the tomotherapy treatment planning system. In addition, dose–volume histograms were calculated for the patient plans. Results: Except for minor deviations at the maximum field size, the pencil beam dose calculation for static beams agreed with measurements in a water tank within 2%/2 mm. A mean deviation to point dose measurements in the cheese phantom of 0.89% ± 0.81% was found for unmodulated helical plans. A mean voxel-based deviation of −0.67% ± 1.11% for all voxels in the respective high dose region (dose values >80%), and a mean local
Calculation of the dose rate for the spent fuel assembly from VVER-1000 type reactors
International Nuclear Information System (INIS)
The dose rate from the spent fuel assembly presented in this paper was obtained by using of the SAS2H control module in Version 4.3 of the SCALE code system. The calculations were performed for a VVER-1000 type fuel assembly with 4.4wt% initial 235U enrichment and different storage time. The calculations may be divided into two steps: calculation of the characteristics - concentrations of fission products, actinides, neutron and gamma source emissions, and determination of the equivalent dose rate on the surface and at some distance from a single assembly. SAS2H computes neutron and gamma source spectrum and evaluates equivalent dose rates from spent nuclear fuel assembly using a 1-D transport shielding analysis. Obtained results presented in this paper are necessary step in shielding analysis of spent fuel casks and interim storage facilities. (author) Keywords: equivalent dose rate, spent fuel assembly, VVER-1000
Calculation of Ambient (H*(10)) and Personal (Hp(10)) Dose Equivalent from a 252Cf Neutron Source
Energy Technology Data Exchange (ETDEWEB)
Traub, Richard J.
2010-03-26
The purpose of this calculation is to calculate the neutron dose factors for the Sr-Cf-3000 neutron source that is located in the 318 low scatter room (LSR). The dose factors were based on the dose conversion factors published in ICRP-21 Appendix 6, and the Ambient dose equivalent (H*(10)) and Personal dose equivalent (Hp(10)) dose factors published in ICRP Publication 74.
Patient-specific dose calculations for pediatric CT of the chest, abdomen and pelvis
International Nuclear Information System (INIS)
Organ dose is essential for accurate estimates of patient dose from CT. To determine organ doses from a broad range of pediatric patients undergoing diagnostic chest-abdomen-pelvis CT and investigate how these relate to patient size. We used a previously validated Monte Carlo simulation model of a Philips Brilliance 64 multi-detector CT scanner (Philips Healthcare, Best, The Netherlands) to calculate organ doses for 40 pediatric patients (M:F = 21:19; range 0.6-17 years). Organ volumes and positions were determined from the images using standard segmentation techniques. Non-linear regression was performed to determine the relationship between volume CT dose index (CTDIvol)-normalized organ doses and abdominopelvic diameter. We then compared results with values obtained from independent studies. We found that CTDIvol-normalized organ dose correlated strongly with exponentially decreasing abdominopelvic diameter (R2 > 0.8 for most organs). A similar relationship was determined for effective dose when normalized by dose-length product (R2 = 0.95). Our results agreed with previous studies within 12% using similar scan parameters (e.g., bowtie filter size, beam collimation); however results varied up to 25% when compared to studies using different bowtie filters. Our study determined that organ doses can be estimated from measurements of patient size, namely body diameter, and CTDIvol prior to CT examination. This information provides an improved method for patient dose estimation. (orig.)
Comparison of organ dosimetry methods and effective dose calculation methods for paediatric CT
International Nuclear Information System (INIS)
Computed tomography (CT) is the single biggest ionising radiation risk from anthropogenic exposure. Reducing unnecessary carcinogenic risks from this source requires the determination of organ and tissue absorbed doses to estimate detrimental stochastic effects. In addition, effective dose can be used to assess comparative risk between exposure situations and facilitate dose reduction through optimisation. Children are at the highest risk from radiation induced carcinogenesis and therefore dosimetry for paediatric CT recipients is essential in addressing the ionising radiation health risks of CT scanning. However, there is no well-defined method in the clinical environment for routinely and reliably performing paediatric CT organ dosimetry and there are numerous methods utilised for estimating paediatric CT effective dose. Therefore, in this study, eleven computational methods for organ dosimetry and/or effective dose calculation were investigated and compared with absorbed doses measured using thermoluminescent dosemeters placed in a physical anthropomorphic phantom representing a 10 year old child. Three common clinical paediatric CT protocols including brain, chest and abdomen/pelvis examinations were evaluated. Overall, computed absorbed doses to organs and tissues fully and directly irradiated demonstrated better agreement (within approximately 50 %) with the measured absorbed doses than absorbed doses to distributed organs or to those located on the periphery of the scan volume, which showed up to a 15-fold dose variation. The disparities predominantly arose from differences in the phantoms used. While the ability to estimate CT dose is essential for risk assessment and radiation protection, identifying a simple, practical dosimetry method remains challenging.
Patient-specific dose calculations for pediatric CT of the chest, abdomen and pelvis
Energy Technology Data Exchange (ETDEWEB)
Kost, Susan D.; Carver, Diana E.; Stabin, Michael G. [Vanderbilt University, Physics and Astronomy Department, Nashville, TN (United States); Vanderbilt University Medical Center, Department of Radiology and Radiological Sciences, Nashville, TN (United States); Fraser, Nicholas D.; Pickens, David R.; Price, Ronald R.; Hernanz-Schulman, Marta [Vanderbilt University Medical Center, Department of Radiology and Radiological Sciences, Nashville, TN (United States)
2015-11-15
Organ dose is essential for accurate estimates of patient dose from CT. To determine organ doses from a broad range of pediatric patients undergoing diagnostic chest-abdomen-pelvis CT and investigate how these relate to patient size. We used a previously validated Monte Carlo simulation model of a Philips Brilliance 64 multi-detector CT scanner (Philips Healthcare, Best, The Netherlands) to calculate organ doses for 40 pediatric patients (M:F = 21:19; range 0.6-17 years). Organ volumes and positions were determined from the images using standard segmentation techniques. Non-linear regression was performed to determine the relationship between volume CT dose index (CTDI{sub vol})-normalized organ doses and abdominopelvic diameter. We then compared results with values obtained from independent studies. We found that CTDI{sub vol}-normalized organ dose correlated strongly with exponentially decreasing abdominopelvic diameter (R{sup 2} > 0.8 for most organs). A similar relationship was determined for effective dose when normalized by dose-length product (R{sup 2} = 0.95). Our results agreed with previous studies within 12% using similar scan parameters (e.g., bowtie filter size, beam collimation); however results varied up to 25% when compared to studies using different bowtie filters. Our study determined that organ doses can be estimated from measurements of patient size, namely body diameter, and CTDI{sub vol} prior to CT examination. This information provides an improved method for patient dose estimation. (orig.)
Tolerances for the accuracy of photon beam dose calculations of treatment planning systems
International Nuclear Information System (INIS)
Background and purpose: To design a consistent set of criteria for acceptability of photon beam dose calculations of treatment planning systems. The set should be applicable in combination with a test package used for evaluation of a treatment planning system, such as the ones proposed by the AAPM Task Group 23 or by the Netherlands Commission on Radiation Dosimetry. Results: Tolerances have been defined for the accuracy with which a treatment planning system should be able to calculate the dose in different parts of a photon beam: the central beam axis and regions with large and small dose gradients. For increasing complexity of the geometry, wider tolerances are allowed, varying between 2 and 5%. For the evaluation of a large number of data points an additional quantity, the confidence limit, has been introduced, which combines the influence of systematic and random deviations. The proposed tolerances have been compared with other recommendations for a number of clinically relevant examples, showing considerable differences, which are partly due to the way the complexity of the geometry is taken into account. Furthermore differences occur if criteria for acceptability of dose calculations are related either to the local dose value or to a normalized dose value. Conclusions: Although it is acknowledged that the general aim must be to have good agreement between dose calculation and the actual dose value, e.g. within 2% or 2 mm, current day algorithms and their implementation into commercial treatment planning systems result often in larger deviations. A high accuracy can at present only be achieved in relatively simple cases. The new set of tolerances and the quantity confidence limit have proven to be useful tools for the acceptance of photon beam dose calculation algorithms of treatment planning systems
A design of a DICOM-RT-based tool box for nonrigid 4D dose calculation.
Wong, Victy Y W; Baker, Colin R; Leung, T W; Tung, Stewart Y
2016-01-01
The study was aimed to introduce a design of a DICOM-RT-based tool box to facilitate 4D dose calculation based on deformable voxel-dose registration. The computational structure and the calculation algorithm of the tool box were explicitly discussed in the study. The tool box was written in MATLAB in conjunction with CERR. It consists of five main functions which allow a) importation of DICOM-RT-based 3D dose plan, b) deformable image registration, c) tracking voxel doses along breathing cycle, d) presentation of temporal dose distribution at different time phase, and e) derivation of 4D dose. The efficacy of using the tool box for clinical application had been verified with nine clinical cases on retrospective-study basis. The logistic and the robustness of the tool box were tested with 27 applications and the results were shown successful with no computational errors encountered. In the study, the accumulated dose coverage as a function of planning CT taken at end-inhale, end-exhale, and mean tumor position were assessed. The results indicated that the majority of the cases (67%) achieved maximum target coverage, while the planning CT was taken at the temporal mean tumor position and 56% at the end-exhale position. The comparable results to the literature imply that the studied tool box can be reliable for 4D dose calculation. The authors suggest that, with proper application, 4D dose calculation using deformable registration can provide better dose evaluation for treatment with moving target. PMID:27074476
Calculation of dose decrease in a finite phantom of a 192Ir point source
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The purpose of this study was to calculate the dose decrease in a finite phantom of a 192Ir-point source by using a new algorithm based on field theory. The methods used included the phenomenological application of the principle ''mirror image of an electric point source in front of a dielectric semi-plateau'' to a radioactive source in a finite phantom results in a function to calculate the dose decrease near the surface. Measurements were done in a water phantom in three different experimental setups. To verify the calculated results Monte Carlo (MC) simulations of dose distribution of a 192Ir point source in 34x40x40 cm3 water were carried out. The strength of mirror source was found -0.103 of the real source. A lack scatter function was necessary to handle the dose decrease very close to surface. The measured and calculated dose values differed less than 0.9%. Both MC simulations and the new algorithm show the dose decrease near phantom surface with differences less than 2% between each other. The new algorithm based on field theory calculated the dose decrease of a 192Ir point source in a finite phantom with a very good agreement to measured and simulated data. A clinical example, which affects only a single planar boundary, is given by using molds in the treatment of skin tumors. This was calculated with the new algorithm presented in this article. The comparison with the common algorithm demonstrates the differences that might cause an overestimation of the dose, which probably leads an underdosing of the tumor. The general use of the new algorithm in brachytherapy where a variety of boundary shapes are encountered has to be verified seriously
Fast pencil beam dose calculation for proton therapy using a double-Gaussian beam model
Directory of Open Access Journals (Sweden)
Joakim eda Silva
2015-12-01
Full Text Available The highly conformal dose distributions produced by scanned proton pencil beams are more sensitive to motion and anatomical changes than those produced by conventional radiotherapy. The ability to calculate the dose in real time as it is being delivered would enable, for example, online dose monitoring, and is therefore highly desirable. We have previously described an implementation of a pencil beam algorithm running on graphics processing units (GPUs intended specifically for online dose calculation. Here we present an extension to the dose calculation engine employing a double-Gaussian beam model to better account for the low-dose halo. To the best of our knowledge, it is the first such pencil beam algorithm for proton therapy running on a GPU. We employ two different parametrizations for the halo dose, one describing the distribution of secondary particles from nuclear interactions found in the literature and one relying on directly fitting the model to Monte Carlo simulations of pencil beams in water. Despite the large width of the halo contribution, we show how in either case the second Gaussian can be included whilst prolonging the calculation of the investigated plans by no more than 16%, or the calculation of the most time-consuming energy layers by about 25%. Further, the calculation time is relatively unaffected by the parametrization used, which suggests that these results should hold also for different systems. Finally, since the implementation is based on an algorithm employed by a commercial treatment planning system, it is expected that with adequate tuning, it should be able to reproduce the halo dose from a general beam line with sufficient accuracy.
SU-E-I-28: Evaluating the Organ Dose From Computed Tomography Using Monte Carlo Calculations
International Nuclear Information System (INIS)
Purpose: To evaluate organ doses from computed tomography (CT) using Monte Carlo (MC) calculations. Methods: A Philips Brilliance CT scanner (64 slice) was simulated using the GMctdospp (IMPS, Germany) based on the EGSnrc user code. The X-ray spectra and a bowtie filter for MC simulations were determined to coincide with measurements of half-value layer (HVL) and off-center ratio (OCR) profile in air. The MC dose was calibrated from absorbed dose measurements using a Farmer chamber and a cylindrical water phantom. The dose distribution from CT was calculated using patient CT images and organ doses were evaluated from dose volume histograms. Results: The HVLs of Al at 80, 100, and 120 kV were 6.3, 7.7, and 8.7 mm, respectively. The calculated HVLs agreed with measurements within 0.3%. The calculated and measured OCR profiles agreed within 3%. For adult head scans (CTDIvol) =51.4 mGy), mean doses for brain stem, eye, and eye lens were 23.2, 34.2, and 37.6 mGy, respectively. For pediatric head scans (CTDIvol =35.6 mGy), mean doses for brain stem, eye, and eye lens were 19.3, 24.5, and 26.8 mGy, respectively. For adult chest scans (CTDIvol=19.0 mGy), mean doses for lung, heart, and spinal cord were 21.1, 22.0, and 15.5 mGy, respectively. For adult abdominal scans (CTDIvol=14.4 mGy), the mean doses for kidney, liver, pancreas, spleen, and spinal cord were 17.4, 16.5, 16.8, 16.8, and 13.1 mGy, respectively. For pediatric abdominal scans (CTDIvol=6.76 mGy), mean doses for kidney, liver, pancreas, spleen, and spinal cord were 8.24, 8.90, 8.17, 8.31, and 6.73 mGy, respectively. In head scan, organ doses were considerably different from CTDIvol values. Conclusion: MC dose distributions calculated by using patient CT images are useful to evaluate organ doses absorbed to individual patients
SU-E-I-28: Evaluating the Organ Dose From Computed Tomography Using Monte Carlo Calculations
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Ono, T; Araki, F [Faculty of Life Sciences, Kumamoto University, Kumamoto (Japan)
2014-06-01
Purpose: To evaluate organ doses from computed tomography (CT) using Monte Carlo (MC) calculations. Methods: A Philips Brilliance CT scanner (64 slice) was simulated using the GMctdospp (IMPS, Germany) based on the EGSnrc user code. The X-ray spectra and a bowtie filter for MC simulations were determined to coincide with measurements of half-value layer (HVL) and off-center ratio (OCR) profile in air. The MC dose was calibrated from absorbed dose measurements using a Farmer chamber and a cylindrical water phantom. The dose distribution from CT was calculated using patient CT images and organ doses were evaluated from dose volume histograms. Results: The HVLs of Al at 80, 100, and 120 kV were 6.3, 7.7, and 8.7 mm, respectively. The calculated HVLs agreed with measurements within 0.3%. The calculated and measured OCR profiles agreed within 3%. For adult head scans (CTDIvol) =51.4 mGy), mean doses for brain stem, eye, and eye lens were 23.2, 34.2, and 37.6 mGy, respectively. For pediatric head scans (CTDIvol =35.6 mGy), mean doses for brain stem, eye, and eye lens were 19.3, 24.5, and 26.8 mGy, respectively. For adult chest scans (CTDIvol=19.0 mGy), mean doses for lung, heart, and spinal cord were 21.1, 22.0, and 15.5 mGy, respectively. For adult abdominal scans (CTDIvol=14.4 mGy), the mean doses for kidney, liver, pancreas, spleen, and spinal cord were 17.4, 16.5, 16.8, 16.8, and 13.1 mGy, respectively. For pediatric abdominal scans (CTDIvol=6.76 mGy), mean doses for kidney, liver, pancreas, spleen, and spinal cord were 8.24, 8.90, 8.17, 8.31, and 6.73 mGy, respectively. In head scan, organ doses were considerably different from CTDIvol values. Conclusion: MC dose distributions calculated by using patient CT images are useful to evaluate organ doses absorbed to individual patients.
International Nuclear Information System (INIS)
The purpose of this study is to perform a clinical evaluation of the first commercial (MDS Nordion, now Nucletron) treatment planning system for electron beams incorporating Monte Carlo dose calculation module. This software implements Kawrakow's VMC++ voxel-based Monte Carlo calculation algorithm. The accuracy of the dose distribution calculations is evaluated by direct comparisons with extensive sets of measured data in homogeneous and heterogeneous phantoms at different source-to-surface distances (SSDs) and gantry angles. We also verify the accuracy of the Monte Carlo module for monitor unit calculations in comparison with independent hand calculations for homogeneous water phantom at two different SSDs. All electron beams in the range 6-20 MeV are from a Siemens KD-2 linear accelerator. We used 10 000 or 50 000 histories/cm2 in our Monte Carlo calculations, which led to about 2.5% and 1% relative standard error of the mean of the calculated dose. The dose calculation time depends on the number of histories, the number of voxels used to map the patient anatomy, the field size, and the beam energy. The typical run time of the Monte Carlo calculations (10 000 histories/cm2) is 1.02 min on a 2.2 GHz Pentium 4 Xeon computer for a 9 MeV beam, 10x10 cm2 field size, incident on the phantom 15x15x10 cm3 consisting of 31 CT slices and voxels size of 3x3x3 mm3 (total of 486 720 voxels). We find good agreement (discrepancies smaller than 5%) for most of the tested dose distributions. We also find excellent agreement (discrepancies of 2.5% or less) for the monitor unit calculations relative to the independent manual calculations. The accuracy of monitor unit calculations does not depend on the SSD used, which allows the use of one virtual machine for each beam energy for all arbitrary SSDs. In some cases the test results are found to be sensitive to the voxel size applied such that bigger systematic errors (>5%) occur when large voxel sizes interfere with the extensions of
Estimates of Columbia River radionuclide concentrations: Data for Phase 1 dose calculations
International Nuclear Information System (INIS)
Pacific Northwest Laboratory is conducting the Hanford Environmental Dose Reconstruction Project to estimate the radiation doses people may have received from historical Hanford Site operations. Under the direction of an independent Technical Steering Panel, the project is being conducted in phases. The objective of the first phase is to assess the feasibility of the project-wide technical approach for acquiring data and developing models needed to calculate potential radiation doses. This report summarizes data that were generated for the Phase 1 dose calculations. These included monthly average concentrations of specific radionuclides in Columbia River water and sediments between Priest Rapids Dam and McNary Dam for the years 1964 to 1966. Nine key radionuclides were selected for analysis based on estimation of their contribution to dose. Concentrations of these radionuclides in the river were estimated using existing measurements and hydraulic calculations based on the simplifying assumption that dilution and decay were the primary processes controlling the fate of radionuclides released to the river. Five sub-reaches between Priest Rapids Dam and McNary Dam, corresponding to population centers and tributary confluences, were identified and monthly average radionuclide concentrations were calculated for each sub-reach. The hydraulic calculations were performed to provide radionuclide concentration estimates for time periods and geographic locations where measured data were not available. The validity of the calculation method will be evaluated in Phase 2. 12 refs., 13 figs., 49 tabs
Monte Carlo calculation of dose to water of a 106Ru COB-type ophthalmic plaque
International Nuclear Information System (INIS)
The concave eye applicators with 106Ru/106Rh or 90Sr/90Y beta-ray sources are worldwide used in brachytherapy for treating intraocular tumors. It raises the need to know the exact dose delivered by beta radiation to tumors but measurement of the dose to water (or tissue) is very difficult due to short range of electrons. The Monte Carlo technique provides a powerful tool for calculation of the dose and dose distributions which helps to predict and determine the doses from different shapes of various types of eye applicators more accurately. The Monte Carlo code MCNPX has been used to calculate dose distributions from a COB-type 106Ru/106Rh ophthalmic applicator manufactured by Eckert and Ziegler BEBIG GmbH. This type of a concave eye applicator has a cut-out whose purpose is to protect the eye nerve which makes the dose distribution more complicated. Several calculations have been performed including depth dose along the applicator central axis and various dose distributions. The depth dose along the applicator central axis and the dose distribution on a spherical surface 1 mm above the plaque inner surface have been compared with measurement data provided by the manufacturer. For distances from 0.5 to 4 mm above the surface, the agreement was within 2.5% and from 5 mm the difference increased from 6% up to 25% at 10 mm whereas the uncertainty on manufacturer data is 20% (2s). It is assumed that the difference is caused by nonuniformly distributed radioactivity over the applicator radioactive layer
Implementation of Monte Carlo Dose calculation for CyberKnife treatment planning
Ma, C.-M.; Li, J. S.; Deng, J.; Fan, J.
2008-02-01
Accurate dose calculation is essential to advanced stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT) especially for treatment planning involving heterogeneous patient anatomy. This paper describes the implementation of a fast Monte Carlo dose calculation algorithm in SRS/SRT treatment planning for the CyberKnife® SRS/SRT system. A superposition Monte Carlo algorithm is developed for this application. Photon mean free paths and interaction types for different materials and energies as well as the tracks of secondary electrons are pre-simulated using the MCSIM system. Photon interaction forcing and splitting are applied to the source photons in the patient calculation and the pre-simulated electron tracks are repeated with proper corrections based on the tissue density and electron stopping powers. Electron energy is deposited along the tracks and accumulated in the simulation geometry. Scattered and bremsstrahlung photons are transported, after applying the Russian roulette technique, in the same way as the primary photons. Dose calculations are compared with full Monte Carlo simulations performed using EGS4/MCSIM and the CyberKnife treatment planning system (TPS) for lung, head & neck and liver treatments. Comparisons with full Monte Carlo simulations show excellent agreement (within 0.5%). More than 10% differences in the target dose are found between Monte Carlo simulations and the CyberKnife TPS for SRS/SRT lung treatment while negligible differences are shown in head and neck and liver for the cases investigated. The calculation time using our superposition Monte Carlo algorithm is reduced up to 62 times (46 times on average for 10 typical clinical cases) compared to full Monte Carlo simulations. SRS/SRT dose distributions calculated by simple dose algorithms may be significantly overestimated for small lung target volumes, which can be improved by accurate Monte Carlo dose calculations.
Implementation of Monte Carlo Dose calculation for CyberKnife treatment planning
International Nuclear Information System (INIS)
Accurate dose calculation is essential to advanced stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT) especially for treatment planning involving heterogeneous patient anatomy. This paper describes the implementation of a fast Monte Carlo dose calculation algorithm in SRS/SRT treatment planning for the CyberKnife (registered) SRS/SRT system. A superposition Monte Carlo algorithm is developed for this application. Photon mean free paths and interaction types for different materials and energies as well as the tracks of secondary electrons are pre-simulated using the MCSIM system. Photon interaction forcing and splitting are applied to the source photons in the patient calculation and the pre-simulated electron tracks are repeated with proper corrections based on the tissue density and electron stopping powers. Electron energy is deposited along the tracks and accumulated in the simulation geometry. Scattered and bremsstrahlung photons are transported, after applying the Russian roulette technique, in the same way as the primary photons. Dose calculations are compared with full Monte Carlo simulations performed using EGS4/MCSIM and the CyberKnife treatment planning system (TPS) for lung, head and neck and liver treatments. Comparisons with full Monte Carlo simulations show excellent agreement (within 0.5%). More than 10% differences in the target dose are found between Monte Carlo simulations and the CyberKnife TPS for SRS/SRT lung treatment while negligible differences are shown in head and neck and liver for the cases investigated. The calculation time using our superposition Monte Carlo algorithm is reduced up to 62 times (46 times on average for 10 typical clinical cases) compared to full Monte Carlo simulations. SRS/SRT dose distributions calculated by simple dose algorithms may be significantly overestimated for small lung target volumes, which can be improved by accurate Monte Carlo dose calculations
Implementation of Monte Carlo Dose calculation for CyberKnife treatment planning
Energy Technology Data Exchange (ETDEWEB)
Ma, C-M; Li, J S; Deng, J; Fan, J [Radiation Oncology Department, Fox Chase Cancer Center, Philadelphia, PA (United States)], E-mail: Charlie.ma@fccc.edu
2008-02-01
Accurate dose calculation is essential to advanced stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT) especially for treatment planning involving heterogeneous patient anatomy. This paper describes the implementation of a fast Monte Carlo dose calculation algorithm in SRS/SRT treatment planning for the CyberKnife (registered) SRS/SRT system. A superposition Monte Carlo algorithm is developed for this application. Photon mean free paths and interaction types for different materials and energies as well as the tracks of secondary electrons are pre-simulated using the MCSIM system. Photon interaction forcing and splitting are applied to the source photons in the patient calculation and the pre-simulated electron tracks are repeated with proper corrections based on the tissue density and electron stopping powers. Electron energy is deposited along the tracks and accumulated in the simulation geometry. Scattered and bremsstrahlung photons are transported, after applying the Russian roulette technique, in the same way as the primary photons. Dose calculations are compared with full Monte Carlo simulations performed using EGS4/MCSIM and the CyberKnife treatment planning system (TPS) for lung, head and neck and liver treatments. Comparisons with full Monte Carlo simulations show excellent agreement (within 0.5%). More than 10% differences in the target dose are found between Monte Carlo simulations and the CyberKnife TPS for SRS/SRT lung treatment while negligible differences are shown in head and neck and liver for the cases investigated. The calculation time using our superposition Monte Carlo algorithm is reduced up to 62 times (46 times on average for 10 typical clinical cases) compared to full Monte Carlo simulations. SRS/SRT dose distributions calculated by simple dose algorithms may be significantly overestimated for small lung target volumes, which can be improved by accurate Monte Carlo dose calculations.
Development of dose calculation system of brachytherapy with a personal computer. 138
International Nuclear Information System (INIS)
A dose calculation system for the brachytherapy was developed with a personal computer. The system was made up of a 16 bits personal computer and a digitizer with a light panel. As the operating system, MS-DOS version 2.1 was used and the programs were written in the BASIC (compiler version) and the assembler. The followings are characteristics of the systeM1; (1) low cost, (2) high performances in the speed of calculation and the data-transfer, (3) high accuracy of the calculated dose-distribution, (4) consideration of the absorption of gamma rays within sources themselves and their containers. In this paper, functions of the system and the performances are described minutely. Moreover, we show the results of estimation of the accuracy of the calculated dose. 10 refs.; 5 figs.; 1 table
Evaluation of an electron Monte Carlo dose calculation algorithm for treatment planning.
Chamberland, Eve; Beaulieu, Luc; Lachance, Bernard
2015-01-01
The purpose of this study is to evaluate the accuracy of the electron Monte Carlo (eMC) dose calculation algorithm included in a commercial treatment planning system and compare its performance against an electron pencil beam algorithm. Several tests were performed to explore the system's behavior in simple geometries and in configurations encountered in clinical practice. The first series of tests were executed in a homogeneous water phantom, where experimental measurements and eMC-calculated dose distributions were compared for various combinations of energy and applicator. More specifically, we compared beam profiles and depth-dose curves at different source-to-surface distances (SSDs) and gantry angles, by using dose difference and distance to agreement. Also, we compared output factors, we studied the effects of algorithm input parameters, which are the random number generator seed, as well as the calculation grid size, and we performed a calculation time evaluation. Three different inhomogeneous solid phantoms were built, using high- and low-density materials inserts, to clinically simulate relevant heterogeneity conditions: a small air cylinder within a homogeneous phantom, a lung phantom, and a chest wall phantom. We also used an anthropomorphic phantom to perform comparison of eMC calculations to measurements. Finally, we proceeded with an evaluation of the eMC algorithm on a clinical case of nose cancer. In all mentioned cases, measurements, carried out by means of XV-2 films, radiographic films or EBT2 Gafchromic films. were used to compare eMC calculations with dose distributions obtained from an electron pencil beam algorithm. eMC calculations in the water phantom were accurate. Discrepancies for depth-dose curves and beam profiles were under 2.5% and 2 mm. Dose calculations with eMC for the small air cylinder and the lung phantom agreed within 2% and 4%, respectively. eMC calculations for the chest wall phantom and the anthropomorphic phantom also
International Nuclear Information System (INIS)
A planning study was carried out on a cohort of CT datasets from breast patients scanned during different respiratory phases. The aim of the study was to investigate the influence of different air filling in lungs on the calculation accuracy of photon dose algorithms and to identify potential patterns of failure with clinical implications. Selected respiratory phases were free breathing (FB), representative of typical end expiration, and deep inspiration breath hold (DIBH), a typical condition for clinical treatment with respiratory gating. Algorithms investigated were the pencil beam (PBC), the anisotropic analytical algorithm (AAA) and the collapsed cone (CC) from the Varian Eclipse or Philips Pinnacle planning system. Reference benchmark calculations were performed with the Voxel Monte Carlo (VMC++). An analysis was performed in terms of physical quantities inspecting either dose-volume or dose-mass histograms and in terms of an extension to three dimensions of the γ index of Low. Results were stratified according to a breathing phase and algorithm. Collectives acquired in FB or DIBH showed well-separated average lung density distributions with mean densities of 0.27 ± 0.04 and 0.16 ± 0.02 g cm-3, respectively, and average peak densities of 0.17 ± 0.03 and 0.09 ± 0.02 g cm-3. Analysis of volume-dose or mass-dose histograms proved the expected deviations on PBC results due to the missing lateral transport of electrons with underestimations in the low dose region and overestimations in the high dose region. From the γ analysis, it resulted that PBC is systematically defective compared to VMC++ over the entire range of lung densities and dose levels with severe violations in both respiratory phases. The fraction of lung voxels with γ > 1 for PBC reached 25% in DIBH and about 15% in FB. CC and AAA performed, in contrast, similarly and with fractions of lung voxels with γ > 1 in average inferior to 2% in FB and 4-5% (AAA) or 6-8% (CC) in DIBH. In summary, PBC
Energy Technology Data Exchange (ETDEWEB)
Fogliata, Antonella; Nicolini, Giorgia; Vanetti, Eugenio; Clivio, Alessandro; Cozzi, Luca [Oncology Institute of Southern Switzerland, Medical Physics Unit, 6504 Bellinzona (Switzerland); Winkler, Peter [Department of Therapeutic Radiology and Oncology, University Hospital Graz (Austria)], E-mail: lucozzi@iosi.ch
2008-05-07
A planning study was carried out on a cohort of CT datasets from breast patients scanned during different respiratory phases. The aim of the study was to investigate the influence of different air filling in lungs on the calculation accuracy of photon dose algorithms and to identify potential patterns of failure with clinical implications. Selected respiratory phases were free breathing (FB), representative of typical end expiration, and deep inspiration breath hold (DIBH), a typical condition for clinical treatment with respiratory gating. Algorithms investigated were the pencil beam (PBC), the anisotropic analytical algorithm (AAA) and the collapsed cone (CC) from the Varian Eclipse or Philips Pinnacle planning system. Reference benchmark calculations were performed with the Voxel Monte Carlo (VMC++). An analysis was performed in terms of physical quantities inspecting either dose-volume or dose-mass histograms and in terms of an extension to three dimensions of the {gamma} index of Low. Results were stratified according to a breathing phase and algorithm. Collectives acquired in FB or DIBH showed well-separated average lung density distributions with mean densities of 0.27 {+-} 0.04 and 0.16 {+-} 0.02 g cm{sup -3}, respectively, and average peak densities of 0.17 {+-} 0.03 and 0.09 {+-} 0.02 g cm{sup -3}. Analysis of volume-dose or mass-dose histograms proved the expected deviations on PBC results due to the missing lateral transport of electrons with underestimations in the low dose region and overestimations in the high dose region. From the {gamma} analysis, it resulted that PBC is systematically defective compared to VMC++ over the entire range of lung densities and dose levels with severe violations in both respiratory phases. The fraction of lung voxels with {gamma} > 1 for PBC reached 25% in DIBH and about 15% in FB. CC and AAA performed, in contrast, similarly and with fractions of lung voxels with {gamma} > 1 in average inferior to 2% in FB and 4
Fogliata, Antonella; Nicolini, Giorgia; Vanetti, Eugenio; Clivio, Alessandro; Winkler, Peter; Cozzi, Luca
2008-05-01
A planning study was carried out on a cohort of CT datasets from breast patients scanned during different respiratory phases. The aim of the study was to investigate the influence of different air filling in lungs on the calculation accuracy of photon dose algorithms and to identify potential patterns of failure with clinical implications. Selected respiratory phases were free breathing (FB), representative of typical end expiration, and deep inspiration breath hold (DIBH), a typical condition for clinical treatment with respiratory gating. Algorithms investigated were the pencil beam (PBC), the anisotropic analytical algorithm (AAA) and the collapsed cone (CC) from the Varian Eclipse or Philips Pinnacle planning system. Reference benchmark calculations were performed with the Voxel Monte Carlo (VMC++). An analysis was performed in terms of physical quantities inspecting either dose-volume or dose-mass histograms and in terms of an extension to three dimensions of the γ index of Low. Results were stratified according to a breathing phase and algorithm. Collectives acquired in FB or DIBH showed well-separated average lung density distributions with mean densities of 0.27 ± 0.04 and 0.16 ± 0.02 g cm-3, respectively, and average peak densities of 0.17 ± 0.03 and 0.09 ± 0.02 g cm-3. Analysis of volume-dose or mass-dose histograms proved the expected deviations on PBC results due to the missing lateral transport of electrons with underestimations in the low dose region and overestimations in the high dose region. From the γ analysis, it resulted that PBC is systematically defective compared to VMC++ over the entire range of lung densities and dose levels with severe violations in both respiratory phases. The fraction of lung voxels with γ > 1 for PBC reached 25% in DIBH and about 15% in FB. CC and AAA performed, in contrast, similarly and with fractions of lung voxels with γ > 1 in average inferior to 2% in FB and 4-5% (AAA) or 6-8% (CC) in DIBH. In summary, PBC
Monte Carlo Calculations of Dose to Medium and Dose to Water for Carbon Ion Beams in Various Media
DEFF Research Database (Denmark)
Herrmann, Rochus; Petersen, Jørgen B.B.; Jäkel, Oliver;
materials exposed to carbon ion beams. The scored track-length fluence spectrum Φi for a given particle i at the energy E, is multiplied with the mass stopping power for target material for calculating Dm . Similarly, Dw is calculated by multiplying the same fluence spectrum with the mass stopping power...... the PSTAR, ASTAR stopping power routines available at NIST1 and MSTAR2 provided by H. Paul et al. 3 Results For a pristine carbon ion beam we encountered a maximum deviation between Dw and Dm up to 8% for bone. In addition we investigate spread out Bragg peak configurations which dilutes the effect......1 Background In clinical practice the quantity dose to water (Dw ) is used as a reference standard for dosimeters and treatment planning systems. Treatment planning systems usually rely on analytical representation of the particle beam, which are normally expressed as dose with respect to water...
Impact of dose calculation accuracy during optimization on lung IMRT plan quality.
Li, Ying; Rodrigues, Anna; Li, Taoran; Yuan, Lulin; Yin, Fang-Fang; Wu, Q Jackie
2015-01-01
The purpose of this study was to evaluate the effect of dose calculation accuracy and the use of an intermediate dose calculation step during the optimization of intensity-modulated radiation therapy (IMRT) planning on the final plan quality for lung cancer patients. This study included replanning for 11 randomly selected free-breathing lung IMRT plans. The original plans were optimized using a fast pencil beam convolution algorithm. After optimization, the final dose calculation was performed using the analytical anisotropic algorithm (AAA). The Varian Treatment Planning System (TPS) Eclipse v11, includes an option to perform intermediate dose calculation during optimization using the AAA. The new plans were created using this intermediate dose calculation during optimization with the same planning objectives and dose constraints as in the original plan. Differences in dosimetric parameters for the planning target volume (PTV) dose coverage, organs-at-risk (OARs) dose sparing, and the number of monitor units (MU) between the original and new plans were analyzed. Statistical significance was determined with a p-value of less than 0.05. All plans were normalized to cover 95% of the PTV with the prescription dose. Compared with the original plans, the PTV in the new plans had on average a lower maximum dose (69.45 vs. 71.96Gy, p = 0.005), a better homogeneity index (HI) (0.08 vs. 0.12, p = 0.002), and a better conformity index (CI) (0.69 vs. 0.59, p = 0.003). In the new plans, lung sparing was increased as the volumes receiving 5, 10, and 30 Gy were reduced when compared to the original plans (40.39% vs. 42.73%, p = 0.005; 28.93% vs. 30.40%, p = 0.001; 14.11%vs. 14.84%, p = 0.031). The volume receiving 20 Gy was not significantly lower (19.60% vs. 20.38%, p = 0.052). Further, the mean dose to the lung was reduced in the new plans (11.55 vs. 12.12 Gy, p = 0.024). For the esophagus, the mean dose, the maximum dose, and the volumes receiving 20 and 60 Gy were lower in
Calculation of dose-rate conversion factors for external exposure to photons and electrons
International Nuclear Information System (INIS)
Methods are presented for the calculation of dose-rate conversion factors for external exposure to photon and electron radiation from radioactive decay. A dose-rate conversion factor is defined as the dose-equivalent rate per unit radionuclide concentration. Exposure modes considered are immersion in contaminated air, immersion in contaminated water, and irradiation from a contaminated ground surface. For each radiation type and exposure mode, dose-rate conversion factors are derived for tissue-equivalent material at the body surface of an exposed individual. In addition, photon dose-rate conversion factors are estimated for 22 body organs. The calculations are based on the assumption that the exposure medium is infinite in extent and that the radionuclide concentration is uniform. The dose-rate conversion factors for immersion in contaminated air and water then follow from the requirement that all of the energy emitted in the radioactive decay is absorbed in the infinite medium. Dose-rate conversion factors for ground-surface exposure are calculated at a reference location above a smooth, infinite plane using the point-kernel integration method and known specific absorbed fractions for photons and electrons in air
Improvement of neutron dose calculation algorithm using panasonic UD-809P type albedo TLD
International Nuclear Information System (INIS)
Panasonic UD-809P type albedo TLD mounted on a water phantom were used to measure neutron personal dose equivalent in a Korean nuclear power plant. From the measured TL readings, personal dose equivalents from thermal, epithermal and fast neutrons were evaluated by using a method adopted in a neutron dose calculation algorithm for Panasonic UD-809P type albedo TLD, which was recommended in a Panasonic TLD System User's Manual. The results showed that personal dose equivalent for fast neutrons could not be adequately evaluated in a field with high thermal neutron fraction. This seems to be related to the incomplete incidence of albedo thermal neutrons to the TLD. In order to calculate the personal dose equivalent from fast neutrons in the field condition to be encountered in a nuclear power plant, new method for the neutron dose calculation algorithm were suggested. For a known energy spectrum, it is very easy and simple to use this method for the evaluation of neutron personal dose equivalent
Influence of respiration on calculation and delivery of the prescribed dose in external radiotherapy
International Nuclear Information System (INIS)
During the delivery of the prescribed dose in external beam radiotherapy, respiration alters the patient's body outline and consequently the basis for dose calculations. The influence of this effect was studied on both healthy volunteers and patients. In a sub-group of volunteers, we measured that respiratory movements modify a person's thickness, in particular in the antero-posterior direction at the lower abdominal level, by more than 4% implying a variation in absorbed dose of more than 2%. In view of the I.C.R.U. requirements for absorbed dose accuracy, these variations must be taken into account. Extension of the study to a group of 160 patients confirmed that for a subgroup of about 25%, respiration induces an important deviation from the prescribed dose as dose calculations are based on a body outline taken at an unknown stage during the respiratory cycle. Our results indicate that dose calculations should be based on an average body outline which takes the respiratory movements into account
Effects of the difference in tube voltage of the CT scanner on dose calculation
Rhee, Dong Joo; Moon, Young Min; Kim, Jung Ki; Jeong, Dong Hyeok
2015-01-01
Computed Tomography (CT) measures the attenuation coefficient of an object and converts the value assigned to each voxel into a CT number. In radiation therapy, CT number, which is directly proportional to the linear attenuation coefficient, is required to be converted to electron density for radiation dose calculation for cancer treatment. However, if various tube voltages were applied to take the patient CT image without applying the specific CT number to electron density conversion curve, the accuracy of dose calculation would be unassured. In this study, changes in CT numbers for different materials due to change in tube voltage were demonstrated and the dose calculation errors in percentage depth dose (PDD) and a clinical case were analyzed. The maximum dose difference in PDD from TPS dose calculation and Monte Carlo simulation were 1.3 % and 1.1 % respectively when applying the same CT number to electron density conversion curve to the 80 kVp and 140 kVp images. In the clinical case, the different CT nu...
Postimplant Dosimetry Using a Monte Carlo Dose Calculation Engine: A New Clinical Standard
International Nuclear Information System (INIS)
Purpose: To use the Monte Carlo (MC) method as a dose calculation engine for postimplant dosimetry. To compare the results with clinically approved data for a sample of 28 patients. Two effects not taken into account by the clinical calculation, interseed attenuation and tissue composition, are being specifically investigated. Methods and Materials: An automated MC program was developed. The dose distributions were calculated for the target volume and organs at risk (OAR) for 28 patients. Additional MC techniques were developed to focus specifically on the interseed attenuation and tissue effects. Results: For the clinical target volume (CTV) D90 parameter, the mean difference between the clinical technique and the complete MC method is 10.7 Gy, with cases reaching up to 17 Gy. For all cases, the clinical technique overestimates the deposited dose in the CTV. This overestimation is mainly from a combination of two effects: the interseed attenuation (average, 6.8 Gy) and tissue composition (average, 4.1 Gy). The deposited dose in the OARs is also overestimated in the clinical calculation. Conclusions: The clinical technique systematically overestimates the deposited dose in the prostate and in the OARs. To reduce this systematic inaccuracy, the MC method should be considered in establishing a new standard for clinical postimplant dosimetry and dose-outcome studies in a near future
International Nuclear Information System (INIS)
The conversion coefficients, H'(d,α)/φ, for monoenergetic positrons and positron-emitting radionuclides were calculated by using the user code UCICRPM of the Monte Carlo code EGS5 to estimate the radiation dose for medical staff involved in positron emission tomography examinations. From these coefficients, the dose equivalent rates per unit activity at 0.07 and 10 mm depths in a soft tissue for a straight-line source of 2-deoxy-2-[18F]fluoro-d-glucose (18F-FDG) were calculated by using the developed user code UCF18DOSE. The dose equivalent rates per unit activity at 0.07 and 10 mm depths were measured by using a personal dosemeter (DOSE 3) under the same conditions as those considered in the calculation. The calculated dose equivalent rates per unit activity at 0.07 and 10 mm depths were 0.116 and 0.0352 pSv min-1 Bq-1, respectively, at 20 cm from the 18F-FDG injection tube. (authors)
Estimation of the uncertainty in internal dose calculation for two contamination cases
International Nuclear Information System (INIS)
Full text: The result of dosimetric expertise after internal contamination is usually presented as a 'best estimate' calculated from the available monitoring data and information about the conditions of exposure. Reference assumptions are applied to make up for unknown parameter values. However, previous intercomparisons demonstrated that the evaluation of internal dose is subject to a large uncertainty coming from both the technical limits of measuring apparatus and the assumptions made by the expert. In this work we propose an alternative approach to the assessment of internal dose that enables to report the confidence interval associated with the evaluated dose value. So far, four sources of uncertainties on input data have been considered: the physicochemical characteristics of the radioactive material (absorption type and diameter of aerosols), the time pattern of intake, the counting error and the stochastic variability of excretion or bioassay sampling. Three successive steps of approximation are suggested, depending on the expected level of dose, for which increasingly realistic parameter values should be sought and applied. The propagation of errors from input data to dose result is performed through Monte Carlo calculation. Finally, the results of dose calculation are presented in the form of mean possible dose value, medium possible dose value and upper 95th percentile. This approach has been implemented in internal dose calculation softwares and applied to two example cases of routine monitoring of uranium and special monitoring of caesium. It provides a useful tool for both reporting the results of expertise and designing realistic monitoring programs, and it will be improved in the future by further investigation of the sources of uncertainty in internal dosimetry. (author)
SU-E-T-27: A Tool for Routine Quality Assurance of Radiotherapy Dose Calculation Software
International Nuclear Information System (INIS)
Purpose: Dose calculation software is thoroughly evaluated when it is commissioned; however, evaluation of periodic software updates is typically limited in scope due to staffing constraints and the need to quickly return the treatment planning system to clinical service. We developed a tool for quickly and comprehensively testing and documenting dose calculation software against measured data. Methods: A tool was developed using MatLab (The MathWorks, Natick, MA) for evaluation of dose calculation algorithms against measured data. Inputs to the tool are measured data, reference DICOM RT PLAN files describing the measurements, and dose calculations in DICOM format. The tool consists of a collection of extensible modules that can perform analysis of point dose, depth dose curves, and profiles using dose difference, distance-to-agreement, and the gamma-index. Each module generates a report subsection that is incorporated into a master template, which is converted to final form in portable document format (PDF). Results: After each change to the treatment planning system, a report can be generated in approximately 90 minutes. The tool has been in use for more than 5 years, spanning 5 versions of the eMC and 4 versions of the AAA. We have detected changes to the algorithms that affected clinical practice once during this period. Conclusion: Our tool provides an efficient method for quality assurance of dose calculation software, providing a complete set of tests for an update. Future work includes the addition of plan level tests, allowing incorporation of, for example, the TG-119 test suite for IMRT, and integration with the treatment planning system via an application programming interface. Integration with the planning system will permit fully-automated testing and reporting at scheduled intervals
SU-E-T-27: A Tool for Routine Quality Assurance of Radiotherapy Dose Calculation Software
Energy Technology Data Exchange (ETDEWEB)
Popple, R; Cardan, R; Duan, J; Wu, X; Shen, S; Brezovich, I [The University of Alabama at Birmingham, Birmingham, AL (United States)
2014-06-01
Purpose: Dose calculation software is thoroughly evaluated when it is commissioned; however, evaluation of periodic software updates is typically limited in scope due to staffing constraints and the need to quickly return the treatment planning system to clinical service. We developed a tool for quickly and comprehensively testing and documenting dose calculation software against measured data. Methods: A tool was developed using MatLab (The MathWorks, Natick, MA) for evaluation of dose calculation algorithms against measured data. Inputs to the tool are measured data, reference DICOM RT PLAN files describing the measurements, and dose calculations in DICOM format. The tool consists of a collection of extensible modules that can perform analysis of point dose, depth dose curves, and profiles using dose difference, distance-to-agreement, and the gamma-index. Each module generates a report subsection that is incorporated into a master template, which is converted to final form in portable document format (PDF). Results: After each change to the treatment planning system, a report can be generated in approximately 90 minutes. The tool has been in use for more than 5 years, spanning 5 versions of the eMC and 4 versions of the AAA. We have detected changes to the algorithms that affected clinical practice once during this period. Conclusion: Our tool provides an efficient method for quality assurance of dose calculation software, providing a complete set of tests for an update. Future work includes the addition of plan level tests, allowing incorporation of, for example, the TG-119 test suite for IMRT, and integration with the treatment planning system via an application programming interface. Integration with the planning system will permit fully-automated testing and reporting at scheduled intervals.
Energy Technology Data Exchange (ETDEWEB)
García-Garduño, O. A., E-mail: oagarciag@innn.edu.mx, E-mail: amanda.garcia.g@gmail.com [Laboratorio de Física Médica, Instituto Nacional de Neurología y Neurocirugía, Mexico City 14269, México and Centro de Investigación en Ciencia Aplicada y Tecnología Avanzada, Unidad Legaria, Instituto Politécnico Nacional, Legaria 694, México City 11500, México (Mexico); Rodríguez-Ponce, M. [Departamento de Biofísica, Instituto Nacional de Cancerología, Mexico City 14080, México (Mexico); Gamboa-deBuen, I. [Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico City 04510 (Mexico); Rodríguez-Villafuerte, M. [Instituto de Física, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico City 04510 (Mexico); Galván de la Cruz, O. O. [Laboratorio de Física Médica, Instituto Nacional de Neurología y Neurocirugía, Mexico City 14269, México (Mexico); and others
2014-09-15
Purpose: To assess the impact of the detector used to commission small photon beams on the calculated dose distribution in stereotactic radiosurgery (SRS). Methods: In this study, six types of detectors were used to characterize small photon beams: three diodes [a silicon stereotactic field diode SFD, a silicon diode SRS, and a silicon diode E], an ionization chamber CC01, and two types of radiochromic film models EBT and EBT2. These detectors were used to characterize circular collimated beams that were generated by a Novalis linear accelerator. This study was conducted in two parts. First, the following dosimetric data, which are of particular interest in SRS, were compared for the different detectors: the total scatter factor (TSF), the tissue phantom ratios (TPRs), and the off-axis ratios (OARs). Second, the commissioned data sets were incorporated into the treatment planning system (TPS) to compare the calculated dose distributions and the dose volume histograms (DVHs) that were obtained using the different detectors. Results: The TSFs data measured by all of the detectors were in good agreement with each other within the respective statistical uncertainties: two exceptions, where the data were systematically below those obtained for the other detectors, were the CC01 results for all of the circular collimators and the EBT2 film results for circular collimators with diameters below 10.0 mm. The OAR results obtained for all of the detectors were in excellent agreement for all of the circular collimators. This observation was supported by the gamma-index test. The largest difference in the TPR data was found for the 4.0 mm circular collimator, followed by the 10.0 and 20.0 mm circular collimators. The results for the calculated dose distributions showed that all of the detectors passed the gamma-index test at 100% for the 3 mm/3% criteria. The aforementioned observation was true regardless of the size of the calculation grid for all of the circular collimators
Recent developments in biokinetic models and the calculation of internal dose coefficients
International Nuclear Information System (INIS)
In most cases the measurement of radioactivity in an environmental or biological sample will be followed by some estimation of dose and possibly risk, either to a population or an individual. This will normally involve the use of a dose coefficient (dose per unit intake value) taken from a compendium. In recent years the calculation of dose coefficients has seen many developments in both biokinetic modelling and computational capabilities. ICRP has recommended new models for the respiratory tract and for the systemic behavior of many of the more important elements. As well as this, a general age-dependent calculation method has been developed which involves an effectively continuous variation of both biokinetic and dosimetric parameters, facilitating more realistic estimation of doses to young people. These new developments were used in work for recent ICRP, IAEA and CEC compendia of dose coefficients for both members of the public (including children) and workers. This paper presents a general overview of the method of calculation of internal doses with particular reference to the actinides. Some of the implications for dose coefficients of the new models are discussed. For example it is shown that compared with data in ICRP Publications 30 and 54: the new respiratory tract model generally predicts lower deposition in systemic tissues per unit intake; the new biokinetic models for actinides allow for burial of material deposited on bone surfaces; age-dependent models generally feature faster turnover of material in young people. All of these factors can lead to substantially different estimates of dose and examples of the new dose coefficients are given to illustrate these differences. During the development of the new models for actinides, human bioassay data were used to validate the model. Thus, one would expect the new models to give reasonable predictions of bioassay quantities. Some examples of the bioassay applications, e.g., excretion data for the
An energy transfer method for 4D Monte Carlo dose calculation.
Siebers, Jeffrey V; Zhong, Hualiang
2008-09-01
This article presents a new method for four-dimensional Monte Carlo dose calculations which properly addresses dose mapping for deforming anatomy. The method, called the energy transfer method (ETM), separates the particle transport and particle scoring geometries: Particle transport takes place in the typical rectilinear coordinate system of the source image, while energy deposition scoring takes place in a desired reference image via use of deformable image registration. Dose is the energy deposited per unit mass in the reference image. ETM has been implemented into DOSXYZnrc and compared with a conventional dose interpolation method (DIM) on deformable phantoms. For voxels whose contents merge in the deforming phantom, the doses calculated by ETM are exactly the same as an analytical solution, contrasting to the DIM which has an average 1.1% dose discrepancy in the beam direction with a maximum error of 24.9% found in the penumbra of a 6 MV beam. The DIM error observed persists even if voxel subdivision is used. The ETM is computationally efficient and will be useful for 4D dose addition and benchmarking alternative 4D dose addition algorithms. PMID:18841862
Neutrons and Gamma-Ray Dose Calculations in Subcritical Reactor Facility Using MCNP
Directory of Open Access Journals (Sweden)
Ned Xoubi
2016-06-01
Full Text Available In nuclear experimental, training and teaching laboratories such as a subcritical reactor facility, huge measures of external radiation doses could be caused by neutron and gamma radiation. It becomes imperative to place the health and safety of staff and students in the reactor facility under proper scrutiny. The protection of these individuals against ionization radiation is facilitated by expected dose mapping and shielding calculations. A three-dimensional (3D Monte Carlo model was developed to calculate the dose rate from neutrons and gamma, using the ANSI/ANS-6.1.1 and the ICRP-74 flux-to-dose conversion factors. Estimation for the dose was conducted across 39 areas located throughout the reactor hall of the facility and its training platform. It was found that the range of the dose rate magnitude is between 7.50 E−01 μSv/h and 1.96 E−04 μSv/h in normal operation mode. During reactor start-up/shut-down mode, it was observed that a large area of the facility can experience exposure to a significant radiation field. This field ranges from 2.99 E+03 μSv/h to 3.12 E+01 μSv/h. There exists no noticeable disparity between results using the ICRP-74 or ANSI/ANS-6.1.1 flux-to-dose rate conversion factors. It was found that the dose rate due to gamma rays is higher than that of neutrons.
Directory of Open Access Journals (Sweden)
Takashi Kadowaki
Full Text Available BACKGROUND: Pragmatic methods for dose optimization are required for the successful basal management in daily clinical practice. To derive a useful formula for calculating recommended glargine doses, we analyzed data from the Add-on Lantus® to Oral Hypoglycemic Agents (ALOHA study, a 24-week observation of Japanese type 2 diabetes patients. METHODOLOGY/PRINCIPAL FINDINGS: The patients who initiated insulin glargine in basal-supported oral therapy (BOT regimen (n = 3506 were analyzed. The correlations between average changes in glargine dose and HbA1c were calculated, and its regression formula was estimated from grouped data categorized by baseline HbA1c levels. Starting doses of the background-subgroup achieving the HbA1c target with a last-observed dose above the average were compared to an assumed optimal starting dose of 0.15 U/kg/day. The difference in regression lines between background-subgroups was examined. A formula for determining the optimal starting and titration doses was thereby derived. The correlation coefficient between changes in dose and HbA1c was -0.9043. The estimated regression line formula was -0.964 × change in HbA1c+2.000. A starting dose of 0.15 U/kg/day was applicable to all background-subgroups except for patients with retinopathy (0.120 U/kg/day and/or with eGFR<60 mL/min/1.73 m(2 (0.114 U/kg/day. Additionally, women (0.135 U/kg/day and patients with sulfonylureas (0.132 U/kg/day received a slightly decreased starting dose. CONCLUSIONS/SIGNIFICANCE: We suggest a simplified and pragmatic dose calculation formula for type 2 diabetes patients starting glargine BOT optimal daily dose at 24 weeks = starting dose (0.15×weight + incremental dose (baseline HbA1c - target HbA1c+2. This formula should be further validated using other samples in a prospective follow-up, especially since several patient groups required lower starting doses.
Dose Distribution Calculation Using MCNPX Code in the Gamma-ray Irradiation Cell
International Nuclear Information System (INIS)
60Co-gamma irradiators have long been used for foods sterilization, plant mutation and development of radio-protective agents, radio-sensitizers and other purposes. The Applied Radiological Science Research Institute of Cheju National University has a multipurpose gamma irradiation facility loaded with a MDS Nordin standard 60Co source (C188), of which the initial activity was 400 TBq (10,800 Ci) on February 19, 2004. This panoramic gamma irradiator is designed to irradiate in all directions various samples such as plants, cultured cells and mice to administer given radiation doses. In order to give accurate doses to irradiation samples, appropriate methods of evaluating, both by calculation and measurement, the radiation doses delivered to the samples should be set up. Computational models have been developed to evaluate the radiation dose distributions inside the irradiation chamber and the radiation doses delivered to typical biolological samples which are frequently irradiated in the facility. The computational models are based on using the MCNPX code. The horizontal and vertical dose distributions has been calculated inside the irradiation chamber and compared the calculated results with measured data obtained with radiation dosimeters to verify the computational models. The radiation dosimeters employed are a Famer's type ion chamber and MOSFET dosimeters. Radiation doses were calculated by computational models, which were delivered to cultured cell samples contained in test tubes and to a mouse fixed in a irradiation cage, and compared the calculated results with the measured data. The computation models are also tested to see if they can accurately simulate the case where a thick lead shield is placed between the source and detector. Three tally options of the MCNPX code, F4, F5 and F6, are alternately used to see which option produces optimum results. The computation models are also used to calculate gamma ray energy spectra of a BGO scintillator at
Influence of metallic dental implants and metal artefacts on dose calculation accuracy
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Metallic dental implants cause severe streaking artefacts in computed tomography (CT) data, which inhibit the correct representation of shape and density of the metal and the surrounding tissue. The aim of this study was to investigate the impact of dental implants on the accuracy of dose calculations in radiation therapy planning and the benefit of metal artefact reduction (MAR). A second aim was to determine the treatment technique which is less sensitive to the presence of metallic implants in terms of dose calculation accuracy. Phantoms consisting of homogeneous water equivalent material surrounding dental implants were designed. Artefact-containing CT data were corrected using the correct density information. Intensity-modulated radiation therapy (IMRT) and volumetric modulated arc therapy (VMAT) plans were calculated on corrected and uncorrected CT data and compared to 2-dimensional dose measurements using GafChromic trademark EBT2 films. For all plans the accuracy of dose calculations is significantly higher if performed on corrected CT data (p = 0.015). The agreement of calculated and measured dose distributions is significantly higher for VMAT than for IMRT plans for calculations on uncorrected CT data (p = 0.011) as well as on corrected CT data (p = 0.029). For IMRT and VMAT the application of metal artefact reduction significantly increases the agreement of dose calculations with film measurements. VMAT was found to provide the highest accuracy on corrected as well as on uncorrected CT data. VMAT is therefore preferable over IMRT for patients with metallic implants, if plan quality is comparable for the two techniques. (orig.)
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Purpose: The approach to equilibrium function has been used previously to calculate the radiation dose to a shift-invariant medium undergoing CT scans with constant tube current [Li, Zhang, and Liu, Med. Phys. 39, 5347–5352 (2012)]. The authors have adapted this method to CT scans with tube current modulation (TCM). Methods: For a scan with variable tube current, the scan range was divided into multiple subscan ranges, each with a nearly constant tube current. Then the dose calculation algorithm presented previously was applied. For a clinical CT scan series that presented tube current per slice, the authors adopted an efficient approach that computed the longitudinal dose distribution for one scan length equal to the slice thickness, which center was at z = 0. The cumulative dose at a specific point was a summation of the contributions from all slices and the overscan. Results: The dose calculations performed for a total of four constant and variable tube current distributions agreed with the published results of Dixon and Boone [Med. Phys. 40, 111920 (14pp.) (2013)]. For an abdomen/pelvis scan of an anthropomorphic phantom (model ATOM 701-B, CIRS, Inc., VA) on a GE Lightspeed Pro 16 scanner with 120 kV, N × T = 20 mm, pitch = 1.375, z axis current modulation (auto mA), and angular current modulation (smart mA), dose measurements were performed using two lines of optically stimulated luminescence dosimeters, one of which was placed near the phantom center and the other on the surface. Dose calculations were performed on the central and peripheral axes of a cylinder containing water, whose cross-sectional mass was about equal to that of the ATOM phantom in its abdominal region, and the results agreed with the measurements within 28.4%. Conclusions: The described method provides an effective approach that takes into account subject size, scan length, and constant or variable tube current to evaluate CT dose to a shift-invariant medium. For a clinical CT scan
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Lesperance, Marielle; Inglis-Whalen, M.; Thomson, R. M., E-mail: rthomson@physics.carleton.ca [Carleton Laboratory for Radiotherapy Physics, Department of Physics, Carleton University, Ottawa K1S 5B6 (Canada)
2014-02-15
Purpose : To investigate the effects of the composition and geometry of ocular media and tissues surrounding the eye on dose distributions for COMS eye plaque brachytherapy with{sup 125}I, {sup 103}Pd, or {sup 131}Cs seeds, and to investigate doses to ocular structures. Methods : An anatomically and compositionally realistic voxelized eye model with a medial tumor is developed based on a literature review. Mass energy absorption and attenuation coefficients for ocular media are calculated. Radiation transport and dose deposition are simulated using the EGSnrc Monte Carlo user-code BrachyDose for a fully loaded COMS eye plaque within a water phantom and our full eye model for the three radionuclides. A TG-43 simulation with the same seed configuration in a water phantom neglecting the plaque and interseed effects is also performed. The impact on dose distributions of varying tumor position, as well as tumor and surrounding tissue media is investigated. Each simulation and radionuclide is compared using isodose contours, dose volume histograms for the lens and tumor, maximum, minimum, and average doses to structures of interest, and doses to voxels of interest within the eye. Results : Mass energy absorption and attenuation coefficients of the ocular media differ from those of water by as much as 12% within the 20–30 keV photon energy range. For all radionuclides studied, average doses to the tumor and lens regions in the full eye model differ from those for the plaque in water by 8%–10% and 13%–14%, respectively; the average doses to the tumor and lens regions differ between the full eye model and the TG-43 simulation by 2%–17% and 29%–34%, respectively. Replacing the surrounding tissues in the eye model with water increases the maximum and average doses to the lens by 2% and 3%, respectively. Substituting the tumor medium in the eye model for water, soft tissue, or an alternate melanoma composition affects tumor dose compared to the default eye model
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Purpose : To investigate the effects of the composition and geometry of ocular media and tissues surrounding the eye on dose distributions for COMS eye plaque brachytherapy with125I, 103Pd, or 131Cs seeds, and to investigate doses to ocular structures. Methods : An anatomically and compositionally realistic voxelized eye model with a medial tumor is developed based on a literature review. Mass energy absorption and attenuation coefficients for ocular media are calculated. Radiation transport and dose deposition are simulated using the EGSnrc Monte Carlo user-code BrachyDose for a fully loaded COMS eye plaque within a water phantom and our full eye model for the three radionuclides. A TG-43 simulation with the same seed configuration in a water phantom neglecting the plaque and interseed effects is also performed. The impact on dose distributions of varying tumor position, as well as tumor and surrounding tissue media is investigated. Each simulation and radionuclide is compared using isodose contours, dose volume histograms for the lens and tumor, maximum, minimum, and average doses to structures of interest, and doses to voxels of interest within the eye. Results : Mass energy absorption and attenuation coefficients of the ocular media differ from those of water by as much as 12% within the 20–30 keV photon energy range. For all radionuclides studied, average doses to the tumor and lens regions in the full eye model differ from those for the plaque in water by 8%–10% and 13%–14%, respectively; the average doses to the tumor and lens regions differ between the full eye model and the TG-43 simulation by 2%–17% and 29%–34%, respectively. Replacing the surrounding tissues in the eye model with water increases the maximum and average doses to the lens by 2% and 3%, respectively. Substituting the tumor medium in the eye model for water, soft tissue, or an alternate melanoma composition affects tumor dose compared to the default eye model simulation by up to 16
Independent dose calculation of the Tps Iplan in radiotherapy conformed with MLC
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The systems utilization of independent dose calculation in three dimensional-Conformal Radiation Therapy (3D-Crt) treatments allows a direct verification of the treatments times. The utilization of these systems allows diminishing the probability of errors occurrence generated by the treatment planning system (Tps), allowing a detailed analysis of the dose to delivering and review of the normalization point (Np) or prescription. The independent dose calculation is realized across the knowledge of dosimetric parameters of the treatment machine and particular characteristics of every individual field. The aim of this work is develops a calculation system of punctual doses for isocentric fields conformed with multi-leaf collimation systems (MLC), where the dose calculation is in conformity with the suggested ones by ICRU Report No. 42, 1987. Calculation software was realized in C ++ under a free platform of programming (Code::Blocks). The system uses files in format Rtp, exported from the Tps to systems of record and verification (Lantis). This file contains detailed information of the dose, Um, position of the MLC sheets and collimators for every field of treatment. The size of equivalent field is obtained from the positions of every sheet; the effective depth of calculation can be introduced from the dosimetric report of the Tps or automatically from the DFS of the field. The 3D coordinates of the isocenter and the Np for the treatment plan must be introduced manually. From this information the system looks the dosimetric parameters and calculates the Um. The calculations were realized in two accelerators a NOVALIS Tx (Varian) with 120 sheets of high definition (hd-MLC) and a PRIMUS Optifocus (Siemens) with 82 sheets. 705 patients were analyzed for a total of 1082, in plans made for both equipment s, the average uncertainty with regard to the calculation of the Tps is-0.43% ± 2.42% in a range between [-7.90 %, 7.50 %]. The major uncertainty was in Np near of the
Development of Japanese voxel models and their application to organ dose calculation
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Three Japanese voxel (volume pixel) phantoms in supine and upright postures, which are consisted of about 1 mm3 size voxels, have been developed on the basis of computed tomography (CT) images of healthy Japanese adult male and female volunteers. Their body structures are reproduced more realistically in comparison with most existing voxel phantoms. Organ doses due to internal or external exposures were calculated using the developed phantoms. In estimation of radiation dose from radionuclides incorporated into body, specific absorbed fractions (SAFs) for low energy photon were significantly influenced by the changes in postures. In estimation of organ doses due to external exposures, the doses of some organs of the developed phantom were calculated and were compared with those of a previous Japanese voxel phantom (voxel size: 0.98x0.98x10 mm3) and the reference values of ICRP Publication 74. (author)
Effects of human model configuration in Monte Carlo calculations on organ doses from CT examinations
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A new dosimetry system, WAZA-ARI, is being developed to estimate radiation dose from Computed Tomography (CT) examination in Japan. The dose estimation in WAZA-ARI utilizes organ dose data, which have been derived by Monte Carlo calculations using Particle and Heavy Ion Transport code System, PHITS. A Japanese adult male phantom, JM phantom, is adapted as a reference human model in the calculations, because the physique and inner organ masses agree well with the average values for Japanese adult males. On the other hand, each patient has arbitrary physical characteristics. Thus, the effects of human body configuration on organ doses are studied by applying another Japanese male model and the reference phantom by the International Commission on Radiological Protection (ICRP) to PHITS. In addition, this paper describes computation conditions for the three human models, which are constructed in the format of voxel phantom with different resolutions. (author)
Calculational methods for estimating skin dose from electrons in Co-60 gamma-ray beams
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Several methods have been employed to calculate the relative contribution to skin dose due to scattered electrons in Co-60 γ-ray beams. Either the Klein--Nishina differential scattering probability is employed to determine the number and initial energy of electrons scattered into the direction of a detector, or a Gaussian approximation is used to specify the surface distribution of initial pencil electron beams created by parallel or diverging photon fields. Results of these calculations are compared with experimental data. In addition, that fraction of relative surface dose resulting from photon interactions in air alone is estimated and compared with data extrapolated from measurements at large source--surface distance (SSD). The contribution to surface dose from electrons generated in air is 50% or more of the total skin dose for SSDs greater than 80 cm
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Before conducting human study on radiolabeled drug, internal radiation dose is evaluated based on the animal data. Generally, however, species difference in the elimination process of radioactivity, mostly in the hepatic metabolism, is ignored. The methodology of correction was described for drugs that are eliminated mostly by hepatic metabolism. We showed the validity of using the method where the hepatic clearance in animal and human are constructed by the hepatic blood flow, protein unbound fraction and metabolic rate in vitro, and the internal radiation exposure calculated is corrected by the animal/human ratio of the hepatic clearance. (author)
Calculation of depth-dose distribution of intermediate energy heavy-ion beams
Institute of Scientific and Technical Information of China (English)
无
2002-01-01
Based on the characteristics of the interactions between intermediate energy heavy-ion beam and target matter, a method to calculate the depth-dose distribution of heavy-ion beams with intermediate energy (10 -100 MeV/u) is presented. By comparing high energy beams where projectile fragmentation is overwhelm ing with lowenergies where energy straggling is the sole factor instead, a crescent energy spread with increasing depth and a simple fragmentation assumption were included for the depth-dose calculation of the intermediate energy beam. Rel ative depth-dose curves of carbon and oxygen ion beams with intermediate energie s were computed according to the method here. Comparisons between the calculated relative doses and measurements are shown. The calculated Bragg curves, especially the upstream and downstream Bragg peaks, agree with the measured data. Differences between the two results appear only around the peak regions because of th e limitations of the calculation and experimental conditions, but the calculated curves generally reproduce the measured data within the experimental errors. Th e reasons for the divergences were analyzed carefully and the magnitudes of the deviations are given.
Park, Yoon-Dong; Sun, Wei; Salas, Antonio; Antia, Avan; Carvajal, Cindy; Wang, Amy; Xu, Xin; Meng, Zhaojin; Zhou, Ming; Tawa, Gregory J.; Dehdashti, Jean; Zheng, Wei; Henderson, Christina M.; Zelazny, Adrian M.
2016-01-01
ABSTRACT Cryptococcus neoformans is a pathogenic fungus that is responsible for up to half a million cases of meningitis globally, especially in immunocompromised individuals. Common fungistatic drugs, such as fluconazole, are less toxic for patients but have low efficacy for initial therapy of the disease. Effective therapy against the disease is provided by the fungicidal drug amphotericin B; however, due to its high toxicity and the difficulty in administering its intravenous formulation, it is imperative to find new therapies targeting the fungus. The antiparasitic drug bithionol has been recently identified as having potent fungicidal activity. In this study, we used a combined gene dosing and drug affinity responsive target stability (GD-DARTS) screen as well as protein modeling to identify a common drug binding site of bithionol within multiple NAD-dependent dehydrogenase drug targets. This combination genetic and proteomic method thus provides a powerful method for identifying novel fungicidal drug targets for further development. PMID:27486194
Zhang, Aizhen; Wen, Ning; Nurushev, Teamour; Burmeister, Jay; Chetty, Indrin J
2013-01-01
A commercial electron Monte Carlo (eMC) dose calculation algorithm has become available in Eclipse treatment planning system. The purpose of this work was to evaluate the eMC algorithm and investigate the clinical implementation of this system. The beam modeling of the eMC algorithm was performed for beam energies of 6, 9, 12, 16, and 20 MeV for a Varian Trilogy and all available applicator sizes in the Eclipse treatment planning system. The accuracy of the eMC algorithm was evaluated in a homogeneous water phantom, solid water phantoms containing lung and bone materials, and an anthropomorphic phantom. In addition, dose calculation accuracy was compared between pencil beam (PB) and eMC algorithms in the same treatment planning system for heterogeneous phantoms. The overall agreement between eMC calculations and measurements was within 3%/2 mm, while the PB algorithm had large errors (up to 25%) in predicting dose distributions in the presence of inhomogeneities such as bone and lung. The clinical implementation of the eMC algorithm was investigated by performing treatment planning for 15 patients with lesions in the head and neck, breast, chest wall, and sternum. The dose distributions were calculated using PB and eMC algorithms with no smoothing and all three levels of 3D Gaussian smoothing for comparison. Based on a routine electron beam therapy prescription method, the number of eMC calculated monitor units (MUs) was found to increase with increased 3D Gaussian smoothing levels. 3D Gaussian smoothing greatly improved the visual usability of dose distributions and produced better target coverage. Differences of calculated MUs and dose distributions between eMC and PB algorithms could be significant when oblique beam incidence, surface irregularities, and heterogeneous tissues were present in the treatment plans. In our patient cases, monitor unit differences of up to 7% were observed between PB and eMC algorithms. Monitor unit calculations were also preformed
Ulmer, W.; Schaffner, B.
2010-01-01
We have developed a model for proton depth dose and lateral distributions based on Monte Carlo calculations (GEANT4) and an integration procedure of the Bethe-Bloch equation (BBE). The model accounts for the transport of primary and secondary protons, the creation of recoil protons and heavy recoil nuclei as well as lateral scattering of these contributions. The buildup, which is experimentally observed in higher energy depth dose curves, is modeled by inclusion of two different origins: 1. S...
Calculation of mean dose deposited in expended volume around an ion path
Institute of Scientific and Technical Information of China (English)
LiuXiao－Wei; ZhangChun－Xiang
1998-01-01
Using the relation of radial dose distributioin which is inverse proportion to suqare of radial distance,and considering angular distribution of secondary electrons,an analytical formula of mean dose deposited in extended volume around an ion is given and the inactivation cross sections of heavy ions are calculated.The results are in reasonable agreement with experimental data.Compared to the numerical integral methods,the method using analytical formulae is straightforward and simple.
Dose rate calculations for the removal of the mixer pump from Tank 101 SY
International Nuclear Information System (INIS)
Plans are currently being made for the removal of the mixer pump in tank 101 SY. Because the pump is contaminated with radioactive waste, it is essential that those involved in the pump removal operation have an indication of the expected dose rates when the pump is removed. Calculations were made to determine the dose rates for removing the pump, inserting the pump into a shipping container and filling the shipping container with either steel or lead shot for shielding
Interpolation method for calculation of computed tomography dose from angular varying tube current
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The scope and magnitude of radiation dose from computed tomography (CT) examination has led to increased scrutiny and focus on accurate dose tracking. The use of tube current modulation (TCM) results complicates dose tracking by generating unique scans that are specific to the patient. Three methods of estimating the radiation dose from a CT examination that uses TCM are compared: using the average current for an entire scan, using the average current for each slice in the scan, and using an estimation of the angular variation of the dose contribution. To determine the impact of TCM on the radiation dose received, a set of angular weighting functions for each tissue of the body are derived by fitting a function to the relative dose contributions tabulated for the four principle exposure projections. This weighting function is applied to the angular tube current function to determine the organ dose contributions from a single rotation. Since the angular tube current function is not typically known, a method for estimating that function is also presented. The organ doses calculated using these three methods are compared to simulations that explicitly include the estimated TCM function. (authors)
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A flexible and interactive code, NEPTUN, has been written in FORTRAN IV for the PDP-10 computer to assess the impact on man of radionuclides in aquatic food chains. NEPTUN is based on an equilibrium model of the linear-chain type, and calculates aquatic food concentrations and doses to man. A decay term is included for the holdup time of the various food types. A total of seven food types can be selected, which include drinking water, freshwater and salt-water plants, inverebrates and fish. Thirty different diets can be implemented and five different dose factor files can be chosen. These include dose conversion factors for infants and adults based on ICRP 2 and ICRP 26 methodologies. All dose factors involve a dose commitment of 50 years, or equivalently, 50 years of chronic exposure. To date, only stochastic ICRP 26 dose caluclations have been implemented. The basic concentration factor file contains data for 211 different radionuclides; the dose factor files are less comprehensive. However, all files can be readily expanded. The output includes tables of concentrations and doses for individual radionuclides, as well as summaries for groups of radionuclides. Existing aquatic food chain models and the sources of currently-used generic concentration factors are briefly reviewed, and dose factors based on ICRP 2 and ICRP 26 methodologies are contrasted. (auth)
Organ doses from environmental exposures calculated using voxel phantoms of adults and children
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This paper presents effective and organ dose conversion coefficients for members of the public due to environmental external exposures, calculated using the ICRP adult male and female reference computational phantoms as well as voxel phantoms of a baby, two children and four adult individual phantoms-–one male and three female, one of them pregnant. Dose conversion coefficients are given for source geometries representing environmental radiation exposures, i.e. whole body irradiations from a volume source in air, representing a radioactive cloud, a plane source in the ground at a depth of 0.5 g cm–2, representing ground contamination by radioactive fall-out, and uniformly distributed natural sources in the ground. The organ dose conversion coefficients were calculated employing the Monte Carlo code EGSnrc simulating the photon transport in the voxel phantoms, and are given as effective and equivalent doses normalized to air kerma free-in-air at height 1 m above the ground in Sv Gy–1. The findings showed that, in general, the smaller the body mass of the phantom, the higher the dose. The difference in effective dose between an adult and an infant is 80–90% at 50 keV and less than 40% above 100 keV. Furthermore, dose equivalent rates for photon exposures of several radionuclides for the above environmental exposures were calculated with the most recent nuclear decay data. Data are shown for effective dose, thyroid, colon and red bone marrow. The results are expected to facilitate regulation of exposure to radiation, relating activities of radionuclides distributed in air and ground to dose of the public due to external radiation as well as the investigation of the radiological effects of major radiation accidents such as the recent one in Fukushima and the decision making of several committees. (paper)
Organ doses from environmental exposures calculated using voxel phantoms of adults and children
Petoussi-Henss, Nina; Schlattl, H.; Zankl, M.; Endo, A.; Saito, K.
2012-09-01
This paper presents effective and organ dose conversion coefficients for members of the public due to environmental external exposures, calculated using the ICRP adult male and female reference computational phantoms as well as voxel phantoms of a baby, two children and four adult individual phantoms--one male and three female, one of them pregnant. Dose conversion coefficients are given for source geometries representing environmental radiation exposures, i.e. whole body irradiations from a volume source in air, representing a radioactive cloud, a plane source in the ground at a depth of 0.5 g cm-2, representing ground contamination by radioactive fall-out, and uniformly distributed natural sources in the ground. The organ dose conversion coefficients were calculated employing the Monte Carlo code EGSnrc simulating the photon transport in the voxel phantoms, and are given as effective and equivalent doses normalized to air kerma free-in-air at height 1 m above the ground in Sv Gy-1. The findings showed that, in general, the smaller the body mass of the phantom, the higher the dose. The difference in effective dose between an adult and an infant is 80-90% at 50 keV and less than 40% above 100 keV. Furthermore, dose equivalent rates for photon exposures of several radionuclides for the above environmental exposures were calculated with the most recent nuclear decay data. Data are shown for effective dose, thyroid, colon and red bone marrow. The results are expected to facilitate regulation of exposure to radiation, relating activities of radionuclides distributed in air and ground to dose of the public due to external radiation as well as the investigation of the radiological effects of major radiation accidents such as the recent one in Fukushima and the decision making of several committees.
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The calculation of the collective dose and averted collective dose after applying countermeasures in an industrial environment has been divided in two parts. In the first part (Kis et al. 2002) separate Monte Carlo simulations of photon transport resulted in the air kermas per photon per unit area due to the industrial surfaces contaminated by 137Cs at specific points using the so-called local approach. In the local approach the air kerma rates due to specific intervention elements at the evaluation locations in the whole environment are determined (Gutierrez et al. 2000). In this way the collective and averted collective dose due to the radiation from a particular intervention element (e.g. the roof of a building) can be obtained. It can, therefore, provide a ranking of the specific intervention elements based on their contribution to collective dose as well. The deposition pattern and the long-term behaviour of deposited radionuclides vary widely in natural circumstances; therefore the number of the photons emitted from the various surfaces per unit area and time can differ significantly. This means the results of the Monte Carlo simulations have to be weighted according to the number of emitted photons so that the actual radiation field can be set up. For this purpose, a dose calculation code has been developed in the framework of the TEMAS project (Gutierrez et al. 2000) which allows to calculate collective doses for different environments. This code has been applied in the present work
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This is the first report to provide radiation doses, arising from inhalation of radon itself, in mice and rats. To quantify absorbed doses to organs and tissues in mice, rats, and humans, we computed the behavior of inhaled radon in their bodies on the basis of a physiologically based pharmacokinetic (PBPK) model. It was assumed that radon dissolved in blood entering the gas exchange compartment is transported to any tissue by the blood circulation to be instantaneously distributed according to a tissue/blood partition coefficient. The calculated concentrations of radon in the adipose tissue and red bone marrow following its inhalation were much higher than those in the others, because of the higher partition coefficients. Compared with a previous experimental data for rats and model calculation for humans, the present calculation was proved to be valid. Absorbed dose rates to organs and tissues were estimated to be within the range of 0.04-1.4 nGy (Bqm-3)-1 day-1 for all the species. Although the dose rates are not so high, it may be better to pay attention to the dose to the red bone marrow from the perspective of radiation protection. For more accurate dose assessment, it is necessary to update tissue/blood partition coefficients of radon that strongly govern the result of the PBPK modeling. (author)
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Even with state of the art treatment planning systems the photon dose calculation can be erroneous under certain circumstances. In these cases Monte Carlo methods promise a higher accuracy. We have used the photon transport code CHILD of the GSF-Forschungszentrum, which was developed to calculate dose in diagnostic radiation protection matters. The code was refined for application in radiotherapy for high energy photon irradiation and should serve for dose verification in individual cases. The irradiation phantom can be entered as any desired 3D matrix or be generated automatically from an individual CT database. The particle transport takes into account pair production, photo, and Compton effect with certain approximations. Efficiency is increased by the method of 'fractional photons'. The generated secondary electrons are followed by the unscattered continuous-slowing-down-approximation (CSDA). The developed Monte Carlo code Monaco Matrix was tested with simple homogeneous and heterogeneous phantoms through comparisons with simulations of the well known but slower EGS4 code. The use of a point source with a direction independent energy spectrum as simplest model of the radiation field from the accelerator head is shown to be sufficient for simulation of actual accelerator depth dose curves. Good agreement (<2%) was found for depth dose curves in water and in bone. With complex test phantoms and comparisons with EGS4 calculated dose profiles some drawbacks in the code were found. Thus, the implementation of the electron multiple-scattering should lead us to step by step improvement of the algorithm. (orig.)
Clinical implementation of full Monte Carlo dose calculation in proton beam therapy
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Paganetti, Harald; Jiang, Hongyu; Parodi, Katia; Slopsema, Roelf; Engelsman, Martijn [Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114 (United States)
2008-09-07
The goal of this work was to facilitate the clinical use of Monte Carlo proton dose calculation to support routine treatment planning and delivery. The Monte Carlo code Geant4 was used to simulate the treatment head setup, including a time-dependent simulation of modulator wheels (for broad beam modulation) and magnetic field settings (for beam scanning). Any patient-field-specific setup can be modeled according to the treatment control system of the facility. The code was benchmarked against phantom measurements. Using a simulation of the ionization chamber reading in the treatment head allows the Monte Carlo dose to be specified in absolute units (Gy per ionization chamber reading). Next, the capability of reading CT data information was implemented into the Monte Carlo code to model patient anatomy. To allow time-efficient dose calculation, the standard Geant4 tracking algorithm was modified. Finally, a software link of the Monte Carlo dose engine to the patient database and the commercial planning system was established to allow data exchange, thus completing the implementation of the proton Monte Carlo dose calculation engine ('DoC++'). Monte Carlo re-calculated plans are a valuable tool to revisit decisions in the planning process. Identification of clinically significant differences between Monte Carlo and pencil-beam-based dose calculations may also drive improvements of current pencil-beam methods. As an example, four patients (29 fields in total) with tumors in the head and neck regions were analyzed. Differences between the pencil-beam algorithm and Monte Carlo were identified in particular near the end of range, both due to dose degradation and overall differences in range prediction due to bony anatomy in the beam path. Further, the Monte Carlo reports dose-to-tissue as compared to dose-to-water by the planning system. Our implementation is tailored to a specific Monte Carlo code and the treatment planning system XiO (Computerized Medical
Calculation of radiation dose to the lens of the eye using Monte Carlo simulation
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The radiation dose to the lens of the eye of patients undergoing diagnostic and interventional radiological procedures of the lacrimal drainage system has been calculated using a Monte Carlo technique. The technique has also been suggested for the retrospective estimation of the lens dose; when applied to individual patients, good correlation is obtained. In such study, data is required for image acquisition frame numbers and fluoro on-time, mean exposure values for these parameters, and the ratio of lens-to-air dose (viz. the head factor, HF) derived for a standard adult head
SU-E-J-60: Efficient Monte Carlo Dose Calculation On CPU-GPU Heterogeneous Systems
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Purpose: It is well-known that the performance of GPU-based Monte Carlo dose calculation implementations is bounded by memory bandwidth. One major cause of this bottleneck is the random memory writing patterns in dose deposition, which leads to several memory efficiency issues on GPU such as un-coalesced writing and atomic operations. We propose a new method to alleviate such issues on CPU-GPU heterogeneous systems, which achieves overall performance improvement for Monte Carlo dose calculation. Methods: Dose deposition is to accumulate dose into the voxels of a dose volume along the trajectories of radiation rays. Our idea is to partition this procedure into the following three steps, which are fine-tuned for CPU or GPU: (1) each GPU thread writes dose results with location information to a buffer on GPU memory, which achieves fully-coalesced and atomic-free memory transactions; (2) the dose results in the buffer are transferred to CPU memory; (3) the dose volume is constructed from the dose buffer on CPU. We organize the processing of all radiation rays into streams. Since the steps within a stream use different hardware resources (i.e., GPU, DMA, CPU), we can overlap the execution of these steps for different streams by pipelining. Results: We evaluated our method using a Monte Carlo Convolution Superposition (MCCS) program and tested our implementation for various clinical cases on a heterogeneous system containing an Intel i7 quad-core CPU and an NVIDIA TITAN GPU. Comparing with a straightforward MCCS implementation on the same system (using both CPU and GPU for radiation ray tracing), our method gained 2-5X speedup without losing dose calculation accuracy. Conclusion: The results show that our new method improves the effective memory bandwidth and overall performance for MCCS on the CPU-GPU systems. Our proposed method can also be applied to accelerate other Monte Carlo dose calculation approaches. This research was supported in part by NSF under Grants CCF
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Stereotactic body radiotherapy (SBRT) is an effective technique in lung cancer treatment and several prerequisites are essential in order to achieve good local control. These include precise imaging of the lesion before irradiation and accurate dose calculation to account for density heterogeneities in lung tissue. Both aspects were investigated within the framework of the thesis: a new approach in imaging with a conventional electronic portal imaging device (EPID) was investigated and the performance and limits of a new Monte Carlo (MC) calculation algorithm commercially available were studied. More specifically, digitally reconstructed radiographs (DRR) of lung lesions were compared with MV portal images in a feasibility study to assess any displacement of the tumour. The precision of displacement results of three registration algorithms was tested when compared to a projection image of the tumour. The various algorithms were applied to test images, a lung simulation phantom and finally to patient data including 38 tumours and images of 113 fractions. Image guidance results of tested registration algorithms proved the accuracy in the lung phantom study whereas clinical patient data had successful registrations in about 59% of anterior-posterior (AP) and 46% of lateral projections, respectively. Excluding real patient data with a clinical target volume smaller than 10 cm3, successful registrations occurred in 90% of AP and 50% lateral projections. With respect to dose calculation accuracy, experimental verification of a commercial Monte Carlo-based planning system was performed for high-energy photon beams. Several simple and complex treatment cases were calculated and compared with measurements in different phantom types. Besides ion chamber measurements, radiochromic films were irradiated to gain 2D dose distributions which were compared to calculations applying the gamma-index criterion. The dose calculation accuracy of the Monte Carlo algorithm implemented in
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A common approach to implementing the Monte Carlo method for the calculation of brachytherapy radiation dose deposition is to use a phase space file containing information on particles emitted from a brachytherapy source. However, the loading of the phase space file during the dose calculation consumes a large amount of computer random access memory, imposing a higher requirement for computer hardware. In this study, we propose a method to parameterize the information (e.g., particle location, direction and energy) stored in the phase space file by using several probability distributions. This method was implemented for dose calculations of a commercial Ir-192 high dose rate source. Dose calculation accuracy of the parameterized source was compared to the results observed using the full phase space file in a simple water phantom and in a clinical breast cancer case. The results showed the parameterized source at a size of 200 kB was as accurate as the phase space file represented source of 1.1 GB. By using the parameterized source representation, a compact Monte Carlo job can be designed, which allows an easy setup for parallel computing in brachytherapy planning. (paper)
Zhang, M.; Zou, W.; Chen, T.; Kim, L.; Khan, A.; Haffty, B.; Yue, N. J.
2014-01-01
A common approach to implementing the Monte Carlo method for the calculation of brachytherapy radiation dose deposition is to use a phase space file containing information on particles emitted from a brachytherapy source. However, the loading of the phase space file during the dose calculation consumes a large amount of computer random access memory, imposing a higher requirement for computer hardware. In this study, we propose a method to parameterize the information (e.g., particle location, direction and energy) stored in the phase space file by using several probability distributions. This method was implemented for dose calculations of a commercial Ir-192 high dose rate source. Dose calculation accuracy of the parameterized source was compared to the results observed using the full phase space file in a simple water phantom and in a clinical breast cancer case. The results showed the parameterized source at a size of 200 kB was as accurate as the phase space file represented source of 1.1 GB. By using the parameterized source representation, a compact Monte Carlo job can be designed, which allows an easy setup for parallel computing in brachytherapy planning.
Dose calculation method with 60-cobalt gamma rays in total body irradiation
Scaff, L A M
2001-01-01
Physical factors associated to total body irradiation using sup 6 sup 0 Co gamma rays beams, were studied in order to develop a calculation method of the dose distribution that could be reproduced in any radiotherapy center with good precision. The method is based on considering total body irradiation as a large and irregular field with heterogeneities. To calculate doses, or doses rates, of each area of interest (head, thorax, thigh, etc.), scattered radiation is determined. It was observed that if dismagnified fields were considered to calculate the scattered radiation, the resulting values could be applied on a projection to the real size to obtain the values for dose rate calculations. In a parallel work it was determined the variation of the dose rate in the air, for the distance of treatment, and for points out of the central axis. This confirm that the use of the inverse square law is not valid. An attenuation curve for a broad beam was also determined in order to allow the use of absorbers. In this wo...
Effect of intravenous contrast on treatment planning system dose calculations in the lung
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Intravenous contrast-enhanced computed tomography is utilised in radiotherapy lung treatment planning to improve the delineation of the tumour volume and nodal areas. In the resultant CT images, the electron density is increased within the vascular structures of the lung and the overall density in the lung volume may also be increased. As yet, it is unclear whether the change in density affects the accuracy of dose calculations based on this CT data. Two investigations were undertaken. Firstly, contrast-enhancement was simulated using an anthropomorphic phantom. In the second investigation, bulk density corrections were performed in an existing patient dataset. In both investigations, treatment plans were generated using both pre- and post-contrast datasets. The numbers of monitor units calculated in each of the plans were compared, as were the resulting isodose curves, dose volume histograms and physical mean lung doses. The numbers of monitor units calculated from the contrast- and non contrast-enhanced datasets agreed within 2%. The isodose curves and dose volume histograms showed very minor differences in size and shape. With the introduction of contrast agent, the physical mean lung doses calculated remained below the limit recommended for an acceptable plan. These results indicate that the introduction of contrast agent has a minimal dosimetric impact upon lung cancer treatment plans
Mathematical knowledge and drug dosage calculation: Necessary clinical skills for the nurse
Directory of Open Access Journals (Sweden)
Athanasakis Efstratios
2013-01-01
Full Text Available When nurses perform their tasks, they manage situations where maths knowledge is required. Such a situation is the calculation of medication dosage. Aim: The literature review of papers relevant with the mathematical knowledge and drug calculation skills of nurses and nursing students. Material-Method: A search of published research and review articles from January 1989 until March 2012, has been conducted in Pubmed database. The search terms used were: nurses, mathematics skills, numeracy skills and medication dosology calculation skills. Results: Literature review showed that many studies focus in the mathematical knowledge and drug dosage calculation competency of nursing students. Results from these studies revealed that nursing students had poor mathematical knowledge and drug dosage calculation skills. In contrast with students, professional nurses are more likely to have sufficient skills in drug calculations. Apart from the papers analyzing calculation skills' assessment, several studies examined educational interventions in the context of calculation skills enhancement. Accuracy and proficiency in the dosage calculation of medications is a preventive factor of errors made at medication preparation and administration. Conclusion: Mathematical knowledge and drug dosage calculation abilities are interrelated concepts and essential clinical skills for the nurse. The fact that nursing students do not have adequate skills for calculating medications' dosage, might be an issue that schools of nursing education should focus in. Further research of the drug dosage calculation skills is considered essential.
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A systematic study of isodose distributions and dose uniformity in sample carriers of the Portuguese Gamma Irradiation Facility was carried out using the MCNP code. Each carrier can be loaded with 4 cardboard boxes (0.4x0.4x 0.4 m3 ). Each box was divided in eight equal cubes. Absorbed dose rate, gamma flux per energy interval and average gamma energy were calculated inside the eight cubes. For comparison purposes, boxes filled with air and 'dummy' boxes loaded with layers of folded and crumpled newspapers to reach the desired density were used. The contributions from source, irradiator structures, sample material and other origins (ceiling, floor and walls) for the total photon spectra were also calculated. The dose distribution in the irradiator depends on the material and its density. These results show that the MCNP is an important tool to perform a dose mapping of the irradiator for each material to be irradiated. The economic benefits of the knowledge of the dose mapping for each material are important because allow to save time utilisation of UTR, dosimeters and man power. The previous knowledge of the dose mapping permits to establish an appropriate irradiation planning, which results in good dose uniformity in the material and reducing previous experimental work. (author)
Noblet, C.; Chiavassa, S.; Smekens, F.; Sarrut, D.; Passal, V.; Suhard, J.; Lisbona, A.; Paris, F.; Delpon, G.
2016-05-01
In preclinical studies, the absorbed dose calculation accuracy in small animals is fundamental to reliably investigate and understand observed biological effects. This work investigated the use of the split exponential track length estimator (seTLE), a new kerma based Monte Carlo dose calculation method for preclinical radiotherapy using a small animal precision micro irradiator, the X-RAD 225Cx. Monte Carlo modelling of the irradiator with GATE/GEANT4 was extensively evaluated by comparing measurements and simulations for half-value layer, percent depth dose, off-axis profiles and output factors in water and water-equivalent material for seven circular fields, from 20 mm down to 1 mm in diameter. Simulated and measured dose distributions in cylinders of water obtained for a 360° arc were also compared using dose, distance-to-agreement and gamma-index maps. Simulations and measurements agreed within 3% for all static beam configurations, with uncertainties estimated to 1% for the simulation and 3% for the measurements. Distance-to-agreement accuracy was better to 0.14 mm. For the arc irradiations, gamma-index maps of 2D dose distributions showed that the success rate was higher than 98%, except for the 0.1 cm collimator (92%). Using the seTLE method, MC simulations compute 3D dose distributions within minutes for realistic beam configurations with a clinically acceptable accuracy for beam diameter as small as 1 mm.
Autoradiography-based, three-dimensional calculation of dose rate for murine, human-tumor xenografts
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A Fast Fourier Transform method for calculating the three-dimensional dose rate distribution for murine, human-tumour xenografts is outlined. The required input includes evenly-spaced activity slices which span the tumour. Numerical values in these slices are determined by quantitative 125I autoradiography. For the absorbed dose-rate calculation, we assume the activity from both 131I- and 90Y-labeled radiopharmaceuticals would be distributed as is measured with the 125I label. Two example cases are presented: an ovarian-carcinoma xenograft with an IgG 2ak monoclonal antibody and a neuroblastoma xenograft with meta-iobenzylguanidine (MIBG). (Author)
Applying graphics processor units to Monte Carlo dose calculation in radiation therapy
Directory of Open Access Journals (Sweden)
Bakhtiari M
2010-01-01
Full Text Available We investigate the potential in using of using a graphics processor unit (GPU for Monte-Carlo (MC-based radiation dose calculations. The percent depth dose (PDD of photons in a medium with known absorption and scattering coefficients is computed using a MC simulation running on both a standard CPU and a GPU. We demonstrate that the GPU′s capability for massive parallel processing provides a significant acceleration in the MC calculation, and offers a significant advantage for distributed stochastic simulations on a single computer. Harnessing this potential of GPUs will help in the early adoption of MC for routine planning in a clinical environment.
Comparison of gamma dose rate calculations for PWR spent fuel assemblies
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Gamma dose rate calculations from the U.S. Department of Energy and the French Commissariat a l'Energie Atomique et aux Energies Alternatives were compared for PWR spent fuel assembly models with UO2 fuel at 33 MWd/kg burnup and MOX fuel at 60 MWd/kg. Both sides used their reference physics codes in a three-step calculation procedure involving depleting fresh assemblies to obtain the discharge compositions, obtaining the isotopic gamma source after 30 years of simulated radioactive decay, and applying the source to heterogeneous 3-D transport models to tally the flux at one meter away from the axial midpoint through air. The fluxes were ultimately converted to dose rates with different energy-dependent conversion factors. This study was able to pinpoint the intermediate calculations that exhibited the largest sources of discrepancy between the two approaches. Most notably, the U.S. gamma source calculation accounts for Bremsstrahlung and adjusts its multi-group photon release rates to conserve energy. Despite these differences, very similar dose rates were calculated by both approaches. For the UO2 case, which was intended to benchmark a frequently-cited reference study, both the DOE and CEA calculated 30-year dose rates between 4.6 and 5.8 Sv/h with various conversion factors, which are roughly three times lower than the reference study's results. For the MOX case, the calculated dose rates ranged from 8.5 to 11 Sv/h. Given the same conversion factor, the largest difference between DOE and CEA values was about 1.5 Sv/h. (author)
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Han Tao; Followill, David; Repchak, Roman; Molineu, Andrea; Howell, Rebecca; Salehpour, Mohammad [Department of Radiation Physics, University of Texas MD Anderson Cancer Center, Houston, Texas 77030 (United States); Mikell, Justin [Department of Radiation Physics, the University of Texas MD Anderson Cancer Center, Houston, Texas 77030 (United States); University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas 77030 (United States); Mourtada, Firas [Department of Radiation Physics, the University of Texas MD Anderson Cancer Center, Houston, Texas 77030 (United States); Department of Radiation Oncology, Christiana Care Health System, Newark, Delaware 19713 (United States)
2013-05-15
Purpose: The novel deterministic radiation transport algorithm, Acuros XB (AXB), has shown great potential for accurate heterogeneous dose calculation. However, the clinical impact between AXB and other currently used algorithms still needs to be elucidated for translation between these algorithms. The purpose of this study was to investigate the impact of AXB for heterogeneous dose calculation in lung cancer for intensity-modulated radiation therapy (IMRT) and volumetric-modulated arc therapy (VMAT). Methods: The thorax phantom from the Radiological Physics Center (RPC) was used for this study. IMRT and VMAT plans were created for the phantom in the Eclipse 11.0 treatment planning system. Each plan was delivered to the phantom three times using a Varian Clinac iX linear accelerator to ensure reproducibility. Thermoluminescent dosimeters (TLDs) and Gafchromic EBT2 film were placed inside the phantom to measure delivered doses. The measurements were compared with dose calculations from AXB 11.0.21 and the anisotropic analytical algorithm (AAA) 11.0.21. Two dose reporting modes of AXB, dose-to-medium in medium (D{sub m,m}) and dose-to-water in medium (D{sub w,m}), were studied. Point doses, dose profiles, and gamma analysis were used to quantify the agreement between measurements and calculations from both AXB and AAA. The computation times for AAA and AXB were also evaluated. Results: For the RPC lung phantom, AAA and AXB dose predictions were found in good agreement to TLD and film measurements for both IMRT and VMAT plans. TLD dose predictions were within 0.4%-4.4% to AXB doses (both D{sub m,m} and D{sub w,m}); and within 2.5%-6.4% to AAA doses, respectively. For the film comparisons, the gamma indexes ({+-}3%/3 mm criteria) were 94%, 97%, and 98% for AAA, AXB{sub Dm,m}, and AXB{sub Dw,m}, respectively. The differences between AXB and AAA in dose-volume histogram mean doses were within 2% in the planning target volume, lung, heart, and within 5% in the spinal cord
Drug–Gene Interactions: Inherent Variability In Drug Maintenance Dose Requirements
Westervelt, Paul; Cho, Kihoon; Bright, David R.; Kisor, David F.
2014-01-01
The influence of genetics on pharmacokinetics can introduce variability among individual patients that may cause treatment failure, toxicity, or both. Such variability, specifically in clearance rates, can influence drug maintenance dosing regimens.
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Currently, national standards for diagnostic and therapeutic procedures using ionizing radiation are developed in the Czech Republic. The standards are divided into four main categories, three of them are clinical standards for procedures in diagnostic/interventional radiology, radiation therapy and nuclear medicine. The last one is a medical physics standard for dose assessment in diagnostic/interventional radiology and nuclear medicine. The diagnostic and interventional radiology part of the medical physics standard is discussed here. The medical physics standard for diagnostic and interventional radiology involves a computation of risk related quantities, it means an effective dose and a mean glandular dose (MGD). The standard is divided into seven separate articles concerning general radiography, mammography, panoramic radiography, intraoral radiography, computed tomography, fluoroscopy and interventional radiology. Each part contains a list of exposure parameters of a given patient and a list of given X ray machine parameters, which are required for an examination reconstruction and dose calculation. Detailed instructions on how to compute the effective dose or MGD from the given data follows. For the calculation, PCXMC program is recommended for radiography and fluoroscopy examinations and ImPACT spreadsheet with NRPB SR250 data is used for computed tomography. For mammography, a dose formalism suggested by Dance is used for the calculation of MGD. Directly measurable quantities used as an input for the calculations are incident air kerma Ki for mammography, weighted computed tomography kerma index CTKIw for computed tomography, entrance surface air kerma Ke or product of kerma and area PKL for general radiography, fluoroscopy and interventional radiology. These directly measurable dose quantities are based on kerma instead of absorbed dose, as recommended by IAEA and ICRU. The medical physics standard should help to implement this new 'kerma formalism' into
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Utilization of nuclear energy to produce or generate electricity is a growing practice in the world, since it represent an economic and safe option to replace fossil fuels. During operation of nuclear power plants, radioactive materials are produced. A small fraction of these material are released to environment in the form of liquid or gaseous effluents. Estimation of radiation doses causing by effluents release has three purposes. During design phase of a nuclear station it is useful to adapt the wastes treatment systems to acceptable limits. During licensing phase, the regulator organism verifies the design of nuclear station effectuating estimation of doses. Finally, during operation of a nuclear station, before every unload of radioactive effluents, radiation doses should be evaluate in order to fulfill technical specifications, which limit the release of radioactive materials to environment. 1. To perform calculations of individual doses due to liquid radioactive effluents unload in units 1 and 2 of Laguna Verde nuclear power plant (In licensing phase). 2. To perform a parametric study of the effect of unload recirculation over individual dose, since recirculation has two principal effects: thermodynamical effects in nuclear station and radioactivity concentration, the last can affect the fullfilment of dose limits. 3. To perform the calculation of collective doses causes by unloads of liquid effluents within a radius of 80 Kms. of nuclear station caused by unload of liquid radioactive effluents during normal operation of nuclear power plant and does not include doses caused during accident conditions. In Mexico the organism in charge of regulation of peaceful uses of nuclear energy is Comision Nacional de Seguridad Nuclear y Salvaguardias (CNSNS) and for Laguna Verde licensing, the regulations of country who manufactured the reactor was adopted, it is to say United States of America. In Appendix 'C' units used along this work are explained. Unless another
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Mathematical phantoms of the human body at various ages are employed with Monte Carlo radiation transport codes for calculation of photon specific absorbed fractions. The author has developed a pediatric phantom series based on the design of the adult phantom, but with explicit equations for each organ so that organ sizes and marrow distributions could be assigned properly. Since the phantoms comprise simple geometric shapes, predictive dose capability is limited when geometry is critical to the calculation. Hence, there is a demand for better phantom design in situations where geometry is critical, such as for external irradiation or for internal emitters with low energy photons. Recent advances in computerized axial tomography (CAT) present the potential for derivation of anatomical information, which is so critical to development of phantoms, and ongoing developmental work on compuer architecture to handle large arrays for Monte Carlo calculations should make complex-geometry dose calculations economically feasible within this decade
Dose calculation for accident situations at TRIGA research reactor using LEU fuel type
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The 14 MW TRIGA R.R. is a unique design of TRIGA conception. The core was fully converted in May 2006 to use LEU fuel instead of the HEU fuel type. The core contains 29 fuel assemblies, 8 control rods and beryllium reflector, associated instrumentation and controls. The U-235 enrichment for TRIGA - HEU fuel is 93.15 wt % and for TRIGA - LEU is 40.00 wt %. The differences between the two fuel types, as shown by the calculations, will results in a higher core inventory especially for heavy elements (i.e. actinides and transuranium elements), but modifications for noble gases, halogens and other volatile fission products are not so important. Dose calculations for an hypothetical accident scenario was considered and dose and radiological consequence calculations were performed. The results of the calculations and a discussion related on the differences between the consequences in the two cases are also presented. (authors)
Monte Carlo calculations of the depth-dose distribution in skin contaminated by hot particles
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Patau, J.-P. (Toulouse-3 Univ., 31 (France))
1991-01-01
Accurate computer programs were developed in order to calculate the spatial distribution of absorbed radiation doses in the skin, near high activity particles (''hot particles''). With a view to ascertaining the reliability of the codes the transport of beta particles was simulated in a complex configuration used for dosimetric measurements: spherical {sup 60}Co sources of 10-1000 {mu}m fastened to an aluminium support with a tissue-equivalent adhesive overlaid with 10 {mu}m thick aluminium foil. Behind it an infinite polystyrene medium including an extrapolation chamber was assumed. The exact energy spectrum of beta emission was sampled. Production and transport of secondary knock-on electrons were also simulated. Energy depositions in polystyrene were calculated with a high spatial resolution. Finally, depth-dose distributions were calculated for hot particles placed on the skin. The calculations will be continued for other radionuclides and for a configuration suited to TLD measurements. (author).
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Full text: Purpose: To discuss the findings of an investigation into uranium intake and to discuss the lessons learned from the subsequent bioassay monitoring and dose calculations. Method: An investigation was held to determine direct and root causes after elevated air concentration levels were reported during the execution of an ad-hoc task. A programme of bioassay monitoring (urine sampling and lung counts) was implemented for the involved staff and committed effective doses were calculated. Major findings of the investigation: a) Inadequate pre-task assessment led to hazards not being identified and subsequently proper control measures were not implemented; b) Inadequate localised control of contamination led to contamination of worker's clothes and faces and contamination of rest of area; c) Workers were complacent which led to a lapse in safety awareness and subsequently they removed their face masks during the task. Problems experienced with bioassay monitoring and dose calculations: a) Some bioassay samples were not taken or were given incorrectly; b) Calculating doses were difficult due to lack of information regarding date of intake; whether there were other possible intakes; and the physiochemical nature of the uranium; c) Weak correlation between predicted and actual bioassay data; d) Period between starting bioassay monitoring and the actual event was too long. Conclusions: a) Shortcomings in the control of contamination with protective clothing and during the execution of ad-hoc tasks; b) Identifying hazards and assessing it is extremely dependant on the skill and capabilities if the Radiation Protection Officers; c) Instructions to workers regarding sampling of urine and arrangements around the sampling should be very specific with only one person responsible for managing the process; d) Be aware of the psychological impact on the affected workers; e) 2 nd Independent dose calculation important for verifying doses; f) Detection capabilities and
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To investigate the radiation dose to the fetus using retrospective tube current modulation (TCM) data selected from archived clinical records. This paper describes the calculation of fetal doses using retrospective TCM data and Monte Carlo (MC) simulations. Three TCM schemes were adopted for use with three pregnant patient phantoms. MC simulations were used to model CT scanners, TCM schemes and pregnant patients. Comparisons between organ doses from TCM schemes and those from non-TCM schemes show that these three TCM schemes reduced fetal doses by 14, 18 and 25 %, respectively. These organ doses were also compared with those from ImPACT calculation. It is found that the difference between the calculated fetal dose and the ImPACT reported dose is as high as 46 %. This work demonstrates methods to study organ doses from various TCM protocols and potential ways to improve the accuracy of CT dose calculation for pregnant patients. (authors)
Measurements and calculations of neutron spectra and neutron dose distribution in human phantoms
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The measurement and calculation of the radiation field around and in a phantom, with regard to the neutron component and the contaminating gamma radiation, are essential for radiation protection and radiotherapy purposes. The final report includes the development of the simple detector system, automized detector measuring facilities and a computerized evaluating system. The results of the depth dose and neutron spectra experiments and calculations in a human phantom are given
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The characteristics of the epithermal neutron beam at BMRR were measured, calculated, and reported by R.G. Fairchild. This beam has already been used for animal irradiations. The authors anticipate that it will be used for clinical trials. Thermal and epithermal neutron flux densities distributions, and dose rate distributions, as a function of depth were measured in a lucite dog-head phantom. Monte Carlo calculations were performed and compared with the measured values
Calculation of energy spectra for the therapeutic electron beams from depth-dose curves
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In this note the algorithm for calculation of the electron energy spectrum from the depth-dose curve was tested by data on a 4 MeV linear accelerator with scanning beam. A Perspex phantom with cellulose triacetate dosimetric films was irradiated on a conveyor moving perpendicularly to the area of beam scanning, thus simulating irradiation by broad beam. Excellent agreement between measured and calculated spectra is claimed. (U.K.)
Real-time 3D dose calculation and display: a tool for plan optimization
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Purpose: Both human and computer optimization of treatment plans have advantages; humans are much better at global pattern recognition, and computers are much better at detailed calculations. A major impediment to human optimization of treatment plans by manipulation of beam parameters is the long time required for feedback to the operator on the effectiveness of a change in beam parameters. Our goal was to create a real-time dose calculation and display system that provides the planner with immediate (fraction of a second) feedback with displays of three-dimensional (3D) isodose surfaces, digitally reconstructed radiographs (DRRs), dose-volume histograms, and/or a figure of merit (FOM) (i.e., a single value plan score function). This will allow the experienced treatment planner to optimize a plan by adjusting beam parameters based on a direct indication of plan effectiveness, the FOM value, and to use 3D display of target, critical organs, DRRs, and isodose contours to guide changes aimed at improving the FOM value. Methods and Materials: We use computer platforms that contain easily utilized parallel processors and very tight coupling between calculation and display. We ported code running on a network of two workstations and an array of transputers to a single multiprocessor workstation. Our current high-performance graphics workstation contains four 150-MHz processors that can be readily used in a shared-memory multithreaded calculation. Results: When a 10 x 10-cm beam is moved, using an 8-mm dose grid, the full 3D dose matrix is recalculated using a Bentley-Milan-type dose calculation algorithm, and the 3D dose surface display is then updated, all in < 0.1 s. A 64 x 64-pixel DRR calculation can be performed in < 0.1 s. Other features, such as automated aperture calculation, are still required to make real-time feedback practical for clinical use. Conclusion: We demonstrate that real-time plan optimization using general purpose multiprocessor workstations is a
Woon, Y. L.; Heng, S. P.; Wong, J. H. D.; Ung, N. M.
2016-03-01
Inhomogeneity correction is recommended for accurate dose calculation in radiotherapy treatment planning since human body are highly inhomogeneous with the presence of bones and air cavities. However, each dose calculation algorithm has its own limitations. This study is to assess the accuracy of five algorithms that are currently implemented for treatment planning, including pencil beam convolution (PBC), superposition (SP), anisotropic analytical algorithm (AAA), Monte Carlo (MC) and Acuros XB (AXB). The calculated dose was compared with the measured dose using radiochromic film (Gafchromic EBT2) in inhomogeneous phantoms. In addition, the dosimetric impact of different algorithms on intensity modulated radiotherapy (IMRT) was studied for head and neck region. MC had the best agreement with the measured percentage depth dose (PDD) within the inhomogeneous region. This was followed by AXB, AAA, SP and PBC. For IMRT planning, MC algorithm is recommended for treatment planning in preference to PBC and SP. The MC and AXB algorithms were found to have better accuracy in terms of inhomogeneity correction and should be used for tumour volume within the proximity of inhomogeneous structures.
Investigations on the necessity of dose calculations for several planes of the target volume
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In radiotherapy planning, the shape of a target volume can at present be exactly delimited by means of computed tomography. A method often applied is to project the largest target volume scan on the plane of the central ray and to calculate the dose in this plane. This method does not allow to take into account any change of the target volume scan which will be mainly due to the body contours of the patient. The results of dose calculations made in several planes for pharyngeal and laryngeal tumors are presented. With this procedure, 33 out of 60 irradiation techniques for nine tumor sites meet the requirements with regard to the central ray plane. If several planes are regarded, this is only true for ten irradiation plans. If is therefore absolutely necessary to calculate the doses of several planes if the target volume has an irregular shape or if the body contours vary considerably. This is the only way to prevent a false treatment caused by possibly severe dose excesses or dose insufficiencies in radiotherapy. (orig.)
Calculation of organ doses in x-ray examinations of premature babies
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Lung disease represents one of the most life-threatening conditions in prematurely born children. In the evaluation of the neonatal chest, the primary and most important diagnostic study is the chest radiograph. Since prematurely born children are very sensitive to radiation, those radiographs may lead to a significant radiation detriment. Knowledge of the radiation dose is therefore necessary to justify the exposures. To calculate doses in the entire body and in specific organs, computational models of the human anatomy are needed. Using medical imaging techniques, voxel phantoms have been developed to achieve a representation as close as possible to the anatomical properties. In this study two voxel phantoms, representing prematurely born babies, were created from computed tomography- and magnetic resonance images: Phantom 1 (1910 g) and Phantom 2 (590 g). The two voxel phantoms were used in Monte Carlo calculations (MCNPX) to assess organ doses. The results were compared with the commercially available software package PCXMC in which the available mathematical phantoms can be downsized toward the prematurely born baby. The simple phantom-scaling method used in PCXMC seems to be sufficient to calculate doses for organs within the radiation field. However, one should be careful in specifying the irradiation geometry. Doses in organs that are wholly or partially outside the primary radiation field depend critically on the irradiation conditions and the phantom model
Optimization in radiotherapy treatment planning thanks to a fast dose calculation method
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This thesis deals with the radiotherapy treatments planning issue which need a fast and reliable treatment planning system (TPS). The TPS is composed of a dose calculation algorithm and an optimization method. The objective is to design a plan to deliver the dose to the tumor while preserving the surrounding healthy and sensitive tissues. The treatment planning aims to determine the best suited radiation parameters for each patient's treatment. In this thesis, the parameters of treatment with IMRT (Intensity modulated radiation therapy) are the beam angle and the beam intensity. The objective function is multi-criteria with linear constraints. The main objective of this thesis is to demonstrate the feasibility of a treatment planning optimization method based on a fast dose-calculation technique developed by (Blanpain, 2009). This technique proposes to compute the dose by segmenting the patient's phantom into homogeneous meshes. The dose computation is divided into two steps. The first step impacts the meshes: projections and weights are set according to physical and geometrical criteria. The second step impacts the voxels: the dose is computed by evaluating the functions previously associated to their mesh. A reformulation of this technique makes possible to solve the optimization problem by the gradient descent algorithm. The main advantage of this method is that the beam angle parameters could be optimized continuously in 3 dimensions. The obtained results in this thesis offer many opportunities in the field of radiotherapy treatment planning optimization. (author)
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It is reported in the literature that the material used in an embolization of an arteriovenous malformation (AVM) can attenuate the radiation beams used in stereotactic radiosurgery (SRS) up to 10% to 15%. The purpose of this work is to assess the dosimetric impact of this attenuating material in the SRS treatment of embolized AVMs, using Monte Carlo simulations assuming clinical conditions. A commercial Monte Carlo dose calculation engine was used to recalculate the dose distribution of 20 AVMs previously planned with a pencil beam dose calculation algorithm. Dose distributions were compared using the following metrics: average, minimal and maximum dose of AVM, and 2D gamma index. The effect in the obliteration rate was investigated using radiobiological models. It was found that the dosimetric impact of the embolization material is less than 1.0 Gy in the prescription dose to the AVM for the 20 cases studied. The impact in the obliteration rate is less than 4.0%. There is reported evidence in the literature that embolized AVMs treated with SRS have low obliteration rates. This work shows that there are dosimetric implications that should be considered in the final treatment decisions for embolized AVMs
FORTRAN Code for Glandular Dose Calculation in Mammography Using Sobol-Wu Parameters
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Mowlavi A A
2007-07-01
Full Text Available Background: Accurate computation of the radiation dose to the breast is essential to mammography. Various the thicknesses of breast, the composition of the breast tissue and other variables affect the optimal breast dose. Furthermore, the glandular fraction, which refers to the composition of the breasts, as partitioned between radiation-sensitive glandular tissue and the adipose tissue, also has an effect on this calculation. Fatty or fibrous breasts would have a lower value for the glandular fraction than dense breasts. Breast tissue composed of half glandular and half adipose tissue would have a glandular fraction in between that of fatty and dense breasts. Therefore, the use of a computational code for average glandular dose calculation in mammography is a more effective means of estimating the dose of radiation, and is accurate and fast. Methods: In the present work, the Sobol-Wu beam quality parameters are used to write a FORTRAN code for glandular dose calculation in molybdenum anode-molybdenum filter (Mo-Mo, molybdenum anode-rhodium filter (Mo-Rh and rhodium anode-rhodium filter (Rh-Rh target-filter combinations in mammograms. The input parameters of code are: tube voltage in kV, half-value layer (HVL of the incident x-ray spectrum in mm, breast thickness in cm (d, and glandular tissue fraction (g. Results: The average glandular dose (AGD variation against the voltage of the mammogram X-ray tube for d = 4 cm, HVL = 0.34 mm Al and g=0.5 for the three filter-target combinations, as well as its variation against the glandular fraction of breast tissue for kV=25, HVL=0.34, and d=4 cm has been calculated. The results related to the average glandular absorbed dose variation against HVL for kV = 28, d=4 cm and g= 0.6 are also presented. The results of this code are in good agreement with those previously reported in the literature. Conclusion: The code developed in this study calculates the glandular dose quickly, and it is complete and
Organ doses from medical x-ray examinations calculated using Monte Carlo techniques
Jones, D G
1985-01-01
Monte Carlo techniques were used to calculate the mean doses received by 20 organs during diagnostic X-ray examinations. Results are presented for 22 commonly used radiographic views and for 45 combinations of tube voltage and filtration ranging from 50 to 140 kVp and 1.5 to 4 mm of aluminium, respectively.
Dose calculation algorithms for radiation therapy with an MRI-Integrated radiation device
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Image-guided adaptive radiation therapy (IGART) aims at improving therapy outcome on the basis of more precise knowledge of the anatomical and physiological situation during treatment. By integration of magnetic resonance imaging (MRI), better differentiation is possible between the target volume to be irradiated and healthy surrounding tissues. In addition, changes that occur either between or during treatment fractions can be taken into account. On the basis of this information, a better conformation of radiation dose to the target volume may be achieved, which may in turn improve prognosis and reduce radiation side effects. This requires a precise calculation of radiation dose in a magnetic field that is present in these integrated irradiation devices. Real-time adaptation of the treatment plan is aimed at for which fast dose calculation is needed. Kernel-based methods are good candidates to achieve short calculation times; however, they presently only exist for radiation therapy in the absence of magnetic fields. This work suggests and investigates two approaches towards kernel-based dose calculation algorithms. One of them is integrated into treatment plan optimisation and applied to four clinical cases.
Mashouf, Shahram; Lechtman, Eli; Beaulieu, Luc; Verhaegen, Frank; Keller, Brian M; Ravi, Ananth; Pignol, Jean-Philippe
2013-09-21
The American Association of Physicists in Medicine Task Group No. 43 (AAPM TG-43) formalism is the standard for seeds brachytherapy dose calculation. But for breast seed implants, Monte Carlo simulations reveal large errors due to tissue heterogeneity. Since TG-43 includes several factors to account for source geometry, anisotropy and strength, we propose an additional correction factor, called the inhomogeneity correction factor (ICF), accounting for tissue heterogeneity for Pd-103 brachytherapy. This correction factor is calculated as a function of the media linear attenuation coefficient and mass energy absorption coefficient, and it is independent of the source internal structure. Ultimately the dose in heterogeneous media can be calculated as a product of dose in water as calculated by TG-43 protocol times the ICF. To validate the ICF methodology, dose absorbed in spherical phantoms with large tissue heterogeneities was compared using the TG-43 formalism corrected for heterogeneity versus Monte Carlo simulations. The agreement between Monte Carlo simulations and the ICF method remained within 5% in soft tissues up to several centimeters from a Pd-103 source. Compared to Monte Carlo, the ICF methods can easily be integrated into a clinical treatment planning system and it does not require the detailed internal structure of the source or the photon phase-space. PMID:23965939
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A method used for the radioactive inventory calculation and dose evaluation of the CIRENE fuel clusters and ECO fuel elements irradiated in the RB-3 reactor is discussed in this paper with particular regard to the processed problem dependent nuclear data libraries. 8 refs, 1 fig., 1 tab
DEFF Research Database (Denmark)
Grandjean, Philippe; Budtz-Joergensen, Esben
2013-01-01
follow-up of a Faroese birth cohort were used. Serum-PFC concentrations were measured at age 5 years, and serum antibody concentrations against tetanus and diphtheria toxoids were obtained at ages 7 years. Benchmark dose results were calculated in terms of serum concentrations for 431 children with...
Personal radiation doses in PET/CT facility: measurements vs. calculations.
Hippeläinen, E; Nikkinen, P; Ihalainen, T; Uusi-Simola, J; Savolainen, S
2008-01-01
The estimation of shielding requirement of a new positron emission tomography (PET) facility is essential. Because of penetrating annihilation photons, not only radiation safety in the vicinity of patients should be considered, but also rooms adjacent to uptake and imaging rooms should be taken into account. Before installing a PET/CT camera to nuclear medicine facilities of Helsinki University Central Hospital (HUCH), a typical PET imaging day was simulated using phantoms. Phantoms were filled with 300 +/- 36 MBq of (18)F isotope and dose rates were measured at 12 central locations in the laboratory. In addition to measurements, dose rates were also calculated using guidelines of AAPM Task Group 108. The relationship between the measured and calculated dose rates was found to be good and statistically significant, using Pearson's correlation test. The evaluated monthly doses were compared with personal dosemeter readings. AAPM's report gives practical tools for evaluation of radiation shielding. Calculations can be carried out successfully for existing hospital complexes too. However, calculations should be carried out carefully, because especially doors, windows and partitions can easily cause underestimation of shielding requirements as shown in this work. PMID:18713782
Dose rate calculations from radioactive vascular stents: DPK versus exact MC approach
International Nuclear Information System (INIS)
Vascular stents activated with radioactive isotopes are planned to be used in clinical practice to prevent restenosis in human coronary arteries after balloon angioplasty. Medical stents are cylindrical meshes and their complex geometry is usually treated for energy dose calculation with approximate dose point kernel (DPK) approach. The important point missed in the DPK approach is the absence of the stent material and, hence, the absence of energy absorption inside the stent. We have performed a comparison between DPK and exact Monte Carlo calculations for some simplified stent models. It appears that DPK approximation significantly overestimates pike dose values especially for the case of γ-emitting sources. We suggest DPK kernel normalization, which minimizes the difference at relatively far distances, while significant discrepancies near the stent surface still remain. (orig.)
Ulmer, W
2010-01-01
We have developed a model for proton depth dose and lateral distributions based on Monte Carlo calculations (GEANT4) and an integration procedure of the Bethe-Bloch equation (BBE). The model accounts for the transport of primary and secondary protons, the creation of recoil protons and heavy recoil nuclei as well as lateral scattering of these contributions. The buildup, which is experimentally observed in higher energy depth dose curves, is modeled by inclusion of two different origins: 1. Secondary reaction protons with a contribution of ca. 65 % of the buildup (for monoenergetic protons). 2. Landau tails as well as Gaussian type of fluctuations for range straggling effects. All parameters of the model for initially monoenergetic proton beams have been obtained from Monte Carlo calculations or checked by them. Furthermore, there are a few parameters, which can be obtained by fitting the model to measured depth dose curves in order to describe individual characteristics of the beamline - the most important b...
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The ANISN code has been used in this study to evaluate the attenuation of neutron beams of various spectra incident normally on slabs of different kinds of concrete. Spectra of the most common sources (Am-Be and Cf-252) and those of giant resonance neutrons, produced at electron accelerators, were studied. The concretes examined had densities between 2.1 and 4.64 g.cm-3. The calculation were made in terms of the deep dose equivalent index, the effective dose equivalent and the ambient dose equivalent. Values of attenuation length in the various materials were derived from the attenuation curves. The results found should allow for useful evaluations in every day practice for health physicist
Suitability of point kernel dose calculation techniques in brachytherapy treatment planning
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Lakshminarayanan Thilagam
2010-01-01
Full Text Available Brachytherapy treatment planning system (TPS is necessary to estimate the dose to target volume and organ at risk (OAR. TPS is always recommended to account for the effect of tissue, applicator and shielding material heterogeneities exist in applicators. However, most brachytherapy TPS software packages estimate the absorbed dose at a point, taking care of only the contributions of individual sources and the source distribution, neglecting the dose perturbations arising from the applicator design and construction. There are some degrees of uncertainties in dose rate estimations under realistic clinical conditions. In this regard, an attempt is made to explore the suitability of point kernels for brachytherapy dose rate calculations and develop new interactive brachytherapy package, named as BrachyTPS, to suit the clinical conditions. BrachyTPS is an interactive point kernel code package developed to perform independent dose rate calculations by taking into account the effect of these heterogeneities, using two regions build up factors, proposed by Kalos. The primary aim of this study is to validate the developed point kernel code package integrated with treatment planning computational systems against the Monte Carlo (MC results. In the present work, three brachytherapy applicators commonly used in the treatment of uterine cervical carcinoma, namely (i Board of Radiation Isotope and Technology (BRIT low dose rate (LDR applicator and (ii Fletcher Green type LDR applicator (iii Fletcher Williamson high dose rate (HDR applicator, are studied to test the accuracy of the software. Dose rates computed using the developed code are compared with the relevant results of the MC simulations. Further, attempts are also made to study the dose rate distribution around the commercially available shielded vaginal applicator set (Nucletron. The percentage deviations of BrachyTPS computed dose rate values from the MC results are observed to be within plus/minus 5
Individual Dose Calculations with Use of the Revised Techa River Dosimetry System TRDS-2009D
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Degteva, M. O.; Shagina, N. B.; Tolstykh, E. I.; Vorobiova, M. I.; Anspaugh, L. R.; Napier, Bruce A.
2009-10-23
An updated deterministic version of the Techa River Dosimetry System (TRDS-2009D) has been developed to estimate individual doses from external exposure and intake of radionuclides for residents living on the Techa River contaminated as a result of radioactive releases from the Mayak plutonium facility in 1949–1956. The TRDS-2009D is designed as a flexible system that uses, depending on the input data for an individual, various elements of system databases to provide the dosimetric variables requested by the user. Several phases are included in the computation schedule. The first phase includes calculations with use of a common protocol for all cohort members based on village-average-intake functions and external dose rates; individual data on age, gender and history of residence are included in the first phase. This phase results in dose estimates similar to those obtained with system TRDS-2000 used previously to derive risks of health effects in the Techa River Cohort. The second phase includes refinement of individual internal doses for those persons who have had body-burden measurements or exposure parameters specific to the household where he/she lived on the Techa River. The third phase includes summation of individual doses from environmental exposure and from radiological examinations. The results of TRDS-2009D dose calculations have demonstrated for the ETRC members on average a moderate increase in RBM dose estimates (34%) and a minor increase (5%) in estimates of stomach dose. The calculations for the members of the ETROC indicated similar small changes for stomach, but significant increase in RBM doses (400%). Individual-dose assessments performed with use of TRDS-2009D have been provided to epidemiologists for exploratory risk analysis in the ETRC and ETROC. These data provide an opportunity to evaluate the possible impact on radiogenic risk of such factors as confounding exposure (environmental and medical), changes in the Techa River source
Effect of Kidney Function on Drug Kinetics and Dosing in Neonates, Infants, and Children
F. Rodieux (Frederique); M. Wilbaux (Melanie); J.N. van den Anker (John); M. Pfister (Marc)
2015-01-01
textabstractNeonates, infants, and children differ from adults in many aspects, not just in age, weight, and body composition. Growth, maturation and environmental factors affect drug kinetics, response and dosing in pediatric patients. Almost 80 % of drugs have not been studied in children, and dos
Dose calculations using artificial neural networks: A feasibility study for photon beams
Vasseur, Aurélien; Makovicka, Libor; Martin, Éric; Sauget, Marc; Contassot-Vivier, Sylvain; Bahi, Jacques
2008-04-01
Direct dose calculations are a crucial requirement for Treatment Planning Systems. Some methods, such as Monte Carlo, explicitly model particle transport, others depend upon tabulated data or analytic formulae. However, their computation time is too lengthy for clinical use, or accuracy is insufficient, especially for recent techniques such as Intensity-Modulated Radiotherapy. Based on artificial neural networks (ANNs), a new solution is proposed and this work extends the properties of such an algorithm and is called NeuRad. Prior to any calculations, a first phase known as the learning process is necessary. Monte Carlo dose distributions in homogeneous media are used, and the ANN is then acquired. According to the training base, it can be used as a dose engine for either heterogeneous media or for an unknown material. In this report, two networks were created in order to compute dose distribution within a homogeneous phantom made of an unknown material and within an inhomogeneous phantom made of water and TA6V4 (titanium alloy corresponding to hip prosthesis). All NeuRad results were compared to Monte Carlo distributions. The latter required about 7 h on a dedicated cluster (10 nodes). NeuRad learning requires between 8 and 18 h (depending upon the size of the training base) on a single low-end computer. However, the results of dose computation with the ANN are available in less than 2 s, again using a low-end computer, for a 150×1×150 voxels phantom. In the case of homogeneous medium, the mean deviation in the high dose region was less than 1.7%. With a TA6V4 hip prosthesis bathed in water, the mean deviation in the high dose region was less than 4.1%. Further improvements in NeuRad will have to include full 3D calculations, inhomogeneity management and input definitions.
Dose calculations using artificial neural networks: A feasibility study for photon beams
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Vasseur, Aurelien [University of Franche-Comte, IRMA/CREST Femto-ST, Portes du Jura, 4 place Tharradin, BP 71427, 25211 Montbeliard Cedex (France); University of Franche-Comte, AND/LIFC, rue Engel Gros, 90016 Belfort (France)], E-mail: aurelien.vasseur@gmail.com; Makovicka, Libor; Martin, Eric [University of Franche-Comte, IRMA/CREST Femto-ST, Portes du Jura, 4 place Tharradin, BP 71427, 25211 Montbeliard Cedex (France); Sauget, Marc [University of Franche-Comte, IRMA/CREST Femto-ST, Portes du Jura, 4 place Tharradin, BP 71427, 25211 Montbeliard Cedex (France); University of Franche-Comte, AND/LIFC, rue Engel Gros, 90016 Belfort (France); Contassot-Vivier, Sylvain; Bahi, Jacques [University of Franche-Comte, AND/LIFC, rue Engel Gros, 90016 Belfort (France)
2008-04-15
Direct dose calculations are a crucial requirement for Treatment Planning Systems. Some methods, such as Monte Carlo, explicitly model particle transport, others depend upon tabulated data or analytic formulae. However, their computation time is too lengthy for clinical use, or accuracy is insufficient, especially for recent techniques such as Intensity-Modulated Radiotherapy. Based on artificial neural networks (ANNs), a new solution is proposed and this work extends the properties of such an algorithm and is called NeuRad. Prior to any calculations, a first phase known as the learning process is necessary. Monte Carlo dose distributions in homogeneous media are used, and the ANN is then acquired. According to the training base, it can be used as a dose engine for either heterogeneous media or for an unknown material. In this report, two networks were created in order to compute dose distribution within a homogeneous phantom made of an unknown material and within an inhomogeneous phantom made of water and TA6V4 (titanium alloy corresponding to hip prosthesis). All NeuRad results were compared to Monte Carlo distributions. The latter required about 7 h on a dedicated cluster (10 nodes). NeuRad learning requires between 8 and 18 h (depending upon the size of the training base) on a single low-end computer. However, the results of dose computation with the ANN are available in less than 2 s, again using a low-end computer, for a 150x1x150 voxels phantom. In the case of homogeneous medium, the mean deviation in the high dose region was less than 1.7%. With a TA6V4 hip prosthesis bathed in water, the mean deviation in the high dose region was less than 4.1%. Further improvements in NeuRad will have to include full 3D calculations, inhomogeneity management and input definitions.
Calculation of mean central dose in interstitial brachytherapy using Delaunay triangulation
International Nuclear Information System (INIS)
In 1997 the ICRU published Report 58 'Dose and Volume Specification for Reporting Interstitial Therapy' with the objective of addressing the problem of absorbed dose specification for reporting contemporary interstitial therapy. One of the concepts proposed in that report is 'mean central dose'. The fundamental goal of the mean central dose (MCD) calculation is to obtain a single, readily reportable and intercomparable value which is representative of dose in regions of the implant 'where the dose gradient approximates a plateau'. Delaunay triangulation (DT) is a method used in computational geometry to partition the space enclosed by the convex hull of a set of distinct points P into a set of nonoverlapping cells. In the three-dimensional case, each point of P becomes a vertex of a tetrahedron and the result of the DT is a set of tetrahedra. All treatment planning for interstitial brachytherapy inherently requires that the location of the radioactive sources, or dwell positions in the case of HDR, be known or digitized. These source locations may be regarded as a set of points representing the implanted volume. Delaunay triangulation of the source locations creates a set of tetrahedra without manual intervention. The geometric centers of these tetrahedra define a new set of points which lie 'in between' the radioactive sources and which are distributed uniformly over the volume of the implant. The arithmetic mean of the dose at these centers is a three dimensional analog of the two-dimensional triangulation and inspection methods proposed for calculating MCD in ICRU 58. We demonstrate that DT can be successfully incorporated into a computerized treatment planning system and used to calculate the MCD
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The U.S. Department of Energy (DOE) is currently considering design options for preclosure facilities in a license application for a geologic repository for spent nuclear fuel and high-level radioactive waste at Yucca Mountain, Nevada. The Center for Nuclear Waste Regulatory Analyses (CNWRA) developed the PCSA Tool Version 3.0.0 software for the U.S. Nuclear Regulatory Commission (NRC) to aid in the regulatory review of a potential DOE license application. The objective of this paper is to demonstrate PCSA Tool modeling capabilities (i.e., a generic two-compartment, mass-balance model) for estimating radionuclide concentrations in air and radiological dose consequences to indoor workers in a control room from potential leakage of radioactively contaminated air from an adjacent handling area. The presented model computes internal and external worker doses from inhalation and submersion in a finite cloud of contaminated air in the control room and augments previous capabilities for assessing indoor worker dose. As a complement to the example event sequence frequency analysis in the companion paper, example consequence calculations are presented in this paper for the postulated event sequence. In conclusion: this paper presents a model for estimating radiological doses to indoor workers for the leakage of airborne radioactive material from handling areas. Sensitivity of model results to changes in various input parameters was investigated via illustrative example calculations. Indoor worker dose estimates were strongly dependent on the duration of worker exposure and the handling-area leakage flow rate. In contrast, doses were not very sensitive to handling-area exhaust ventilation flow rates. For the presented example, inhalation was the dominant radiological dose pathway. The two companion papers demonstrate independent analysis capabilities of the regulator for performing confirmatory calculations of frequency and consequence, which assist the assessment of worker
GPU-based fast Monte Carlo dose calculation for proton therapy
Jia, Xun; Schümann, Jan; Paganetti, Harald; Jiang, Steve B.
2012-12-01
Accurate radiation dose calculation is essential for successful proton radiotherapy. Monte Carlo (MC) simulation is considered to be the most accurate method. However, the long computation time limits it from routine clinical applications. Recently, graphics processing units (GPUs) have been widely used to accelerate computationally intensive tasks in radiotherapy. We have developed a fast MC dose calculation package, gPMC, for proton dose calculation on a GPU. In gPMC, proton transport is modeled by the class II condensed history simulation scheme with a continuous slowing down approximation. Ionization, elastic and inelastic proton nucleus interactions are considered. Energy straggling and multiple scattering are modeled. Secondary electrons are not transported and their energies are locally deposited. After an inelastic nuclear interaction event, a variety of products are generated using an empirical model. Among them, charged nuclear fragments are terminated with energy locally deposited. Secondary protons are stored in a stack and transported after finishing transport of the primary protons, while secondary neutral particles are neglected. gPMC is implemented on the GPU under the CUDA platform. We have validated gPMC using the TOPAS/Geant4 MC code as the gold standard. For various cases including homogeneous and inhomogeneous phantoms as well as a patient case, good agreements between gPMC and TOPAS/Geant4 are observed. The gamma passing rate for the 2%/2 mm criterion is over 98.7% in the region with dose greater than 10% maximum dose in all cases, excluding low-density air regions. With gPMC it takes only 6-22 s to simulate 10 million source protons to achieve ˜1% relative statistical uncertainty, depending on the phantoms and energy. This is an extremely high efficiency compared to the computational time of tens of CPU hours for TOPAS/Geant4. Our fast GPU-based code can thus facilitate the routine use of MC dose calculation in proton therapy.
Organ dose calculation in CT based on scout image data and automatic image registration
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Kortesniemi, Mika; Salli, Eero; Seuri, Raija [HUS Helsinki Medical Imaging Center, Univ. of Helsinki, Helsinki (Finland)], E-mail: mika.kortesniemi@hus.fi
2012-10-15
Background Computed tomography (CT) has become the main contributor of the cumulative radiation exposure in radiology. Information on cumulative exposure history of the patient should be available for efficient management of radiation exposures and for radiological justification. Purpose To develop and evaluate automatic image registration for organ dose calculation in CT. Material and Methods Planning radiograph (scout) image data describing CT scan ranges from 15 thoracic CT examinations (9 men and 6 women) and 10 abdominal CT examinations (6 men and 4 women) were co-registered with the reference trunk CT scout image. 2-D affine transformation and normalized correlation metric was used for image registration. Longitudinal (z-axis) scan range coordinates on the reference scout image were converted into slice locations on the CT-Expo anthropomorphic male and female models, following organ and effective dose calculations. Results The average deviation of z-location of studied patient images from the corresponding location in the reference scout image was 6.2 mm. The ranges of organ and effective doses with constant exposure parameters were from 0 to 28.0 mGy and from 7.3 to 14.5 mSv, respectively. The mean deviation of the doses for fully irradiated organs (inside the scan range), partially irradiated organs and non-irradiated organs (outside the scan range) was 1%, 5%, and 22%, respectively, due to image registration. Conclusion The automated image processing method to registrate individual chest and abdominal CT scout radiograph with the reference scout radiograph is feasible. It can be used to determine the individual scan range coordinates in z-direction to calculate the organ dose values. The presented method could be utilized in automatic organ dose calculation in CT for radiation exposure tracking of the patients.
Organ dose calculation in CT based on scout image data and automatic image registration
International Nuclear Information System (INIS)
Background Computed tomography (CT) has become the main contributor of the cumulative radiation exposure in radiology. Information on cumulative exposure history of the patient should be available for efficient management of radiation exposures and for radiological justification. Purpose To develop and evaluate automatic image registration for organ dose calculation in CT. Material and Methods Planning radiograph (scout) image data describing CT scan ranges from 15 thoracic CT examinations (9 men and 6 women) and 10 abdominal CT examinations (6 men and 4 women) were co-registered with the reference trunk CT scout image. 2-D affine transformation and normalized correlation metric was used for image registration. Longitudinal (z-axis) scan range coordinates on the reference scout image were converted into slice locations on the CT-Expo anthropomorphic male and female models, following organ and effective dose calculations. Results The average deviation of z-location of studied patient images from the corresponding location in the reference scout image was 6.2 mm. The ranges of organ and effective doses with constant exposure parameters were from 0 to 28.0 mGy and from 7.3 to 14.5 mSv, respectively. The mean deviation of the doses for fully irradiated organs (inside the scan range), partially irradiated organs and non-irradiated organs (outside the scan range) was 1%, 5%, and 22%, respectively, due to image registration. Conclusion The automated image processing method to registrate individual chest and abdominal CT scout radiograph with the reference scout radiograph is feasible. It can be used to determine the individual scan range coordinates in z-direction to calculate the organ dose values. The presented method could be utilized in automatic organ dose calculation in CT for radiation exposure tracking of the patients
Exposure Dose Calculation In Some Serious Accident Cases For Irradiation Facility SVST-Co60/B
International Nuclear Information System (INIS)
Two serious accidents which could happen to SVST-Co60/B irradiator are assumed: the source racks are jammed and could not return to the storage position and a source pencil is knocked out on the production maze by a tote-box. By using MCNP code the calculation of exposure doses in the approach zone and the residential area outside the facility for two above-mentioned cases has been carried out and its results for both cases show that the exposure doses in the approach zone are higher than the limit dose (>100 mSv/h) but the exposure doses in the residential area are still in safe range (-2 mSv/h). (author)
Calculation of annual radiation doses to human organs due to consumption of marine fish
International Nuclear Information System (INIS)
The annual radiation doses have been estimated from the analysis of 40 K, 137 Cs, 226 Ra, 228 Ra radionuclides in the marine fish of the Bay of Bengal for ten different organs of man including, red marrow, lung, thyroid, lower large intestine, upper large intestine, small intestine, muscle, stomach, gonads and bone surface. The lowest dose is calculated in thyroid as 2.7x10 -9 Sv/y and the highest in bone surface as 1.1x10-7 Sv/y. The dose due to 226Ra is highest (1.2x10-7 Sv/y) in the whole body while the lowest dose is delivered by 40K (3.6x10-8 Sv/yil)
Dosimetric validation of Acuros XB with Monte Carlo methods for photon dose calculations
International Nuclear Information System (INIS)
Purpose: The dosimetric accuracy of the recently released Acuros XB advanced dose calculation algorithm (Varian Medical Systems, Palo Alto, CA) is investigated for single radiation fields incident on homogeneous and heterogeneous geometries, and a comparison is made to the analytical anisotropic algorithm (AAA). Methods: Ion chamber measurements for the 6 and 18 MV beams within a range of field sizes (from 4.0x4.0 to 30.0x30.0 cm2) are used to validate Acuros XB dose calculations within a unit density phantom. The dosimetric accuracy of Acuros XB in the presence of lung, low-density lung, air, and bone is determined using BEAMnrc/DOSXYZnrc calculations as a benchmark. Calculations using the AAA are included for reference to a current superposition/convolution standard. Results: Basic open field tests in a homogeneous phantom reveal an Acuros XB agreement with measurement to within ±1.9% in the inner field region for all field sizes and energies. Calculations on a heterogeneous interface phantom were found to agree with Monte Carlo calculations to within ±2.0%(σMC=0.8%) in lung (ρ=0.24 g cm-3) and within ±2.9%(σMC=0.8%) in low-density lung (ρ=0.1 g cm-3). In comparison, differences of up to 10.2% and 17.5% in lung and low-density lung were observed in the equivalent AAA calculations. Acuros XB dose calculations performed on a phantom containing an air cavity (ρ=0.001 g cm-3) were found to be within the range of ±1.5% to ±4.5% of the BEAMnrc/DOSXYZnrc calculated benchmark (σMC=0.8%) in the tissue above and below the air cavity. A comparison of Acuros XB dose calculations performed on a lung CT dataset with a BEAMnrc/DOSXYZnrc benchmark shows agreement within ±2%/2mm and indicates that the remaining differences are primarily a result of differences in physical material assignments within a CT dataset. Conclusions: By considering the fundamental particle interactions in matter based on theoretical interaction cross sections, the Acuros XB algorithm is
Dose calculations of brachytherapy with compensations of gamma-ray absorption
International Nuclear Information System (INIS)
A dose-distribution calculation system for the brachytherapy was developed with a personal-computer (NEC PC-9800 series). The operating system, MS-DOS ver. 2.1, was used and the programs were written by the compiler BASIC and the assembler. The followings are the features of the system. The system can be realized with low cost compared to a commercially available mini-computer system. And the system has high performances in the speed of calculation and data-transfer without the lack of accuracy. Moreover the gamma rays absorption within sources and their containers are considered in the calculation of the table-data. (author)
Mathematical child phantom for the calculation of dose to the organs at risk
International Nuclear Information System (INIS)
In order to calculate the doses received by the organs of 530 children treated by radiation for cancer between 1945 and 1969 at the G. Roussy Institute, we have developed a computer program for organ location calculation. To calculate the location of each child's organs of interest at the time of the treatment, only two parameters are necessary; sex and height or sex and age when the height at the time of the treatment is unknown. The algorithm is based on the metric studies of growth known as auxology. Each organ is located by one point representing its center. The model has been checked on 100 healthy children
Mathematical child phantom for the calculation of dose to the organs at risk
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Francois, P.; Beurtheret, C.; Dutreix, A.; De Vathaire, F.
1988-05-01
In order to calculate the doses received by the organs of 530 children treated by radiation for cancer between 1945 and 1969 at the G. Roussy Institute, we have developed a computer program for organ location calculation. To calculate the location of each child's organs of interest at the time of the treatment, only two parameters are necessary; sex and height or sex and age when the height at the time of the treatment is unknown. The algorithm is based on the metric studies of growth known as auxology. Each organ is located by one point representing its center. The model has been checked on 100 healthy children.
Dose Finding of Small-Molecule Oncology Drugs: Optimization throughout the Development Life Cycle.
Jänne, Pasi A; Kim, Geoffrey; Shaw, Alice T; Sridhara, Rajeshwari; Pazdur, Richard; McKee, Amy E
2016-06-01
In the current era of rapid marketing approval for promising new products in oncology, dose finding and optimization for small-molecule oncology drugs occurs throughout the development cycle and into the postmarketing setting. Many trials that support a regulatory application have high rates of dose reductions and discontinuations, which may result in postmarketing requirements (PMR) to study alternate doses or dosing schedules. Kinase inhibitors particularly have been susceptible to this problem, and among the 31 approved drugs of this class, the approvals of eight have included such PMRs and/or commitments. Thus, the current paradigm for dose finding and optimization could be improved. Newer strategies for dose finding rather than traditional 3 + 3 designs should be considered where feasible, and dose optimization should be continued after phase I and throughout development. Such strategies will increase the likelihood of a right dose for the right drug at the time of regulatory approval. Clin Cancer Res; 22(11); 2613-7. ©2016 AACR SEE ALL ARTICLES IN THIS CCR FOCUS SECTION, "NEW APPROACHES FOR OPTIMIZING DOSING OF ANTICANCER AGENTS". PMID:27250931
Modelling lateral beam quality variations in pencil kernel based photon dose calculations
Nyholm, T.; Olofsson, J.; Ahnesjö, A.; Karlsson, M.
2006-08-01
Standard treatment machines for external radiotherapy are designed to yield flat dose distributions at a representative treatment depth. The common method to reach this goal is to use a flattening filter to decrease the fluence in the centre of the beam. A side effect of this filtering is that the average energy of the beam is generally lower at a distance from the central axis, a phenomenon commonly referred to as off-axis softening. The off-axis softening results in a relative change in beam quality that is almost independent of machine brand and model. Central axis dose calculations using pencil beam kernels show no drastic loss in accuracy when the off-axis beam quality variations are neglected. However, for dose calculated at off-axis positions the effect should be considered, otherwise errors of several per cent can be introduced. This work proposes a method to explicitly include the effect of off-axis softening in pencil kernel based photon dose calculations for arbitrary positions in a radiation field. Variations of pencil kernel values are modelled through a generic relation between half value layer (HVL) thickness and off-axis position for standard treatment machines. The pencil kernel integration for dose calculation is performed through sampling of energy fluence and beam quality in sectors of concentric circles around the calculation point. The method is fully based on generic data and therefore does not require any specific measurements for characterization of the off-axis softening effect, provided that the machine performance is in agreement with the assumed HVL variations. The model is verified versus profile measurements at different depths and through a model self-consistency check, using the dose calculation model to estimate HVL values at off-axis positions. A comparison between calculated and measured profiles at different depths showed a maximum relative error of 4% without explicit modelling of off-axis softening. The maximum relative error
Liu, Han; Zhuang, Tingliang; Stephans, Kevin; Videtic, Gregory; Raithel, Stephen; Djemil, Toufik; Xia, Ping
2015-01-01
For patients with medically inoperable early-stage non-small cell lung cancer (NSCLC) treated with stereotactic body radiation therapy, early treatment plans were based on a simpler dose calculation algorithm, the pencil beam (PB) calculation. Because these patients had the longest treatment follow-up, identifying dose differences between the PB calculated dose and Monte Carlo calculated dose is clinically important for understanding of treatment outcomes. Previous studies found significant dose differences between the PB dose calculation and more accurate dose calculation algorithms, such as convolution-based or Monte Carlo (MC), mostly for three-dimensional conformal radiotherapy (3D CRT) plans. The aim of this study is to investigate whether these observed dose differences also exist for intensity-modulated radiotherapy (IMRT) plans for both centrally and peripherally located tumors. Seventy patients (35 central and 35 peripheral) were retrospectively selected for this study. The clinical IMRT plans that were initially calculated with the PB algorithm were recalculated with the MC algorithm. Among these paired plans, dosimetric parameters were compared for the targets and critical organs. When compared to MC calculation, PB calculation overestimated doses to the planning target volumes (PTVs) of central and peripheral tumors with different magnitudes. The doses to 95% of the central and peripheral PTVs were overestimated by 9.7% ± 5.6% and 12.0% ± 7.3%, respectively. This dose overestimation did not affect doses to the critical organs, such as the spinal cord and lung. In conclusion, for NSCLC treated with IMRT, dose differences between the PB and MC calculations were different from that of 3D CRT. No significant dose differences in critical organs were observed between the two calculations. PMID:26699560
Tandon, Vishal; Kang, Woo Seok; Robbins, Tremaan A; Spencer, Abigail J; Kim, Ernest S; McKenna, Michael J; Kujawa, Sharon G; Fiering, Jason; Pararas, Erin E L; Mescher, Mark J; Sewell, William F; Borenstein, Jeffrey T
2016-03-01
The anatomical and pharmacological inaccessibility of the inner ear is a major challenge in drug-based treatment of auditory disorders. This also makes pharmacokinetic characterization of new drugs with systemic delivery challenging, because efficacy is coupled with how efficiently a drug can reach its target. Direct delivery of drugs to cochlear fluids bypasses pharmacokinetic barriers and helps to minimize systemic toxicity, but anatomical barriers make administration of multiple doses difficult without an automated delivery system. Such a system may be required for hair-cell regeneration treatments, which will likely require timed delivery of several drugs. To address these challenges, we have developed a micropump for controlled, automated inner-ear drug delivery with the ultimate goal of producing a long-term implantable/wearable delivery system. The current pump is designed to be used with a head mount for guinea pigs in preclinical drug characterization experiments. In this system, we have addressed several microfluidic challenges, including maintaining controlled delivery at safe, low flow rates and delivering drug without increasing the volume of fluid in the cochlea. By integrating a drug reservoir and all fluidic components into the microfluidic structure of the pump, we have made the drug delivery system robust compared to previous systems that utilized separate, tubing-connected components. In this study, we characterized the pump's unique infuse-withdraw and on-demand dosing capabilities on the bench and in guinea pig animal models. For the animal experiments, we used DNQX, a glutamate receptor antagonist, as a physiological indicator of drug delivery. DNQX suppresses compound action potentials (CAPs), so we were able to infer the distribution and spreading of the DNQX over time by measuring the changes in CAPs in response to stimuli at several characteristic frequencies. PMID:26778829
International Nuclear Information System (INIS)
After an accidental release of radionuclides to the inhabited environment the external gamma irradiation from deposited radioactivity contributes significantly to the radiation exposure of the population for extended periods. For evaluating this exposure pathway, three main model requirements are needed: (i) to calculate the air kerma value per photon emitted per unit source area, based on Monte Carlo (MC) simulations; (ii) to describe the distribution and dynamics of radionuclides on the diverse urban surfaces; and (iii) to combine all these elements in a relevant urban model to calculate the resulting doses according to the actual scenario. This paper provides an overview about the different approaches to calculate photon transport in urban areas and about several dose calculation codes published. Two types of Monte Carlo simulations are presented using the global and the local approaches of photon transport. Moreover, two different philosophies of the dose calculation, the 'location factor method' and a combination of relative contamination of surfaces with air kerma values are described. The main features of six codes (ECOSYS, EDEM2M, EXPURT, PARATI, TEMAS, URGENT) are highlighted together with a short model-model features intercomparison
A Monte Carlo evaluation of RapidArc dose calculations for oropharynx radiotherapy.
Gagne, I M; Ansbacher, W; Zavgorodni, S; Popescu, C; Beckham, W A
2008-12-21
RapidArc, recently released by Varian Medical Systems, is a novel extension of IMRT in which an optimized 3D dose distribution may be delivered in a single gantry rotation of 360 degrees or less. The purpose of this study was to investigate the accuracy of the analytical anisotropic algorithm (AAA), the sole algorithm for photon dose calculations of RapidArc treatment plans. The clinical site chosen was oropharynx and the associated nodes involved. The VIMC-Arc system, which utilizes BEAMnrc and DOSXYZnrc for particle transport through the linac head and patient CT phantom, was used as a benchmarking tool. As part of this study, the dose for a single static aperture, typical for RapidArc delivery, was calculated by the AAA, MC and compared with the film. This film measurement confirmed MC modeling of the beam aperture in water. It also demonstrated that the AAA dosimetric error can be as high as 12% near isolated leaf edges and up to 5% at the leaf end. The composite effect of these errors in a full RapidArc calculation in water involving a C-shaped target and the associated organ at risk produced a 1.5% overprediction of the mean target dose. In our cohort of six patients, the AAA was found, on average, to overestimate the PTV60 coverage at the 95% level in the presence of air cavities by 1.0% (SD = 1.1%). Removing the air cavities from the target volumes reduced these differences by about a factor of 2. The dose to critical structures was also overestimated by the AAA. The mean dose to the spinal cord was higher by 1.8% (SD = 0.8%), while the effective maximum dose (D2%) was only 0.2% higher (SD = 0.6%). The mean dose to the parotid glands was overestimated by approximately 9%. This study has shown that the accuracy of the AAA for RapidArc dose calculations, performed at a resolution of 2.5 mm or better, is adequate for clinical use. PMID:19033640
CALDoseX: a software tool for absorbed dose calculations in diagnostic radiology
International Nuclear Information System (INIS)
Conversion coefficients (CCs) between absorbed dose to organs and tissues at risk and measurable quantities commonly used in X-ray diagnosis have been calculated for the last 30 years mostly with mathematical MIRD5-type phantoms, in which organs are represented by simple geometrical bodies, like ellipsoids, tori, truncated cylinders, etc. In contrast, voxel-based phantoms are true to nature representations of human bodies. The purpose of this study is therefore to calculate CCs for common examinations in X-ray diagnosis with the recently developed MAX06 (Male Adult voXel) and FAX06 (Female Adult voXel) phantoms for various projections and different X-ray spectra and to make these CCs available to the public through a software tool, called CALDoseX (CALculation of Dose for X-ray diagnosis). (author)
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The normal tissue complication probability (NTCP) is a predictor of radiobiological effect for organs at risk (OAR). The calculation of the NTCP is based on the dose-volume-histogram (DVH) which is generated by the treatment planning system after calculation of the 3D dose distribution. Including the NTCP in the objective function for intensity modulated radiation therapy (IMRT) plan optimization would make the planning more effective in reducing the postradiation effects. However, doing so would lengthen the total planning time. The purpose of this work is to establish a method for NTCP determination, independent of a DVH calculation, as a quality assurance check and also as a mean of improving the treatment planning efficiency. In the study, the CTs of ten randomly selected prostate patients were used. IMRT optimization was performed with a PINNACLE3 V 6.2b planning system, using planning target volume (PTV) with margins in the range of 2 to 10 mm. The DVH control points of the PTV and OAR were adapted from the prescriptions of Radiation Therapy Oncology Group protocol P-0126 for an escalated prescribed dose of 82 Gy. This paper presents a new model for the determination of the rectal NTCP (RNTCP). The method uses a special function, named GVN (from Gy, Volume, NTCP), which describes the RNTCP if 1 cm3 of the volume of intersection of the PTV and rectum (Rint) is irradiated uniformly by a dose of 1 Gy. The function was 'geometrically' normalized using a prostate-prostate ratio (PPR) of the patients' prostates. A correction of the RNTCP for different prescribed doses, ranging from 70 to 82 Gy, was employed in our model. The argument of the normalized function is the Rint, and parameters are the prescribed dose, prostate volume, PTV margin, and PPR. The RNTCPs of another group of patients were calculated by the new method and the resulting difference was <±5% in comparison to the NTCP calculated by the PINNACLE3 software where Kutcher's dose-response model for
A 3D Lagrangian particle model for direct plume gamma dose rate calculations
International Nuclear Information System (INIS)
A fully 3D Lagrangian particle model has been presented for calculating the direct gamma dose rates due to a radionuclide plume in the atmosphere. A continuous release of radionuclides into the atmosphere was simulated by liberating a series of puffs (each containing 100 Lagrangian particles). These puffs were released with a constant time lag between the successive puffs. The Lagrangian particle trajectories were tracked for about 25 h in a turbulent atmosphere, with a specified wind field. The atmosphere turbulent/stability characteristics like wind velocity fluctuations, eddy lifetime, etc, were obtained from the reported data in the published literature. For calculating the direct plume gamma dose rates, a point isotropic source formula has been used with appropriate attenuation and build-up factors for the air medium. Each Lagrangian particle represented a point source whose radioactive strength was calculated from the known release rate. The dose rates at ground due to the radionuclide plume were calculated by adding the contribution from each Lagrangian particle in the domain. The numerically calculated dose rates were compared with the numerical results reported in the literature. An excellent comparison was observed for downwind distances up to about 20 km. However, for distances exceeding 20 km, the numerical data were below the reported results for the Gaussian plume model. This discrepancy was due to the vertical wind shear. It is concluded that a Gaussian plume model can be used for the concentration calculations provided the lateral dispersion parameter, σy, includes the effect of wind shear, for distances exceeding 20 km. (author)
Calculation of nanoparticle capture efficiency in magnetic drug targeting
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The implant assisted magnetic targeted drug delivery system of Aviles, Ebner and Ritter, which uses high gradient magnetic separation (HGMS) is considered. In this 2D model large ferromagnetic particles are implanted as seeds to aid collection of multiple domain nanoparticles (radius ∼200nm). Here, in contrast, single domain magnetic nanoparticles (radius in 20-100 nm) are considered and the Langevin function is used to describe the magnetization. Simulations based on this model were performed using the open source C++ finite volume library OpenFOAM. The simulations indicate that use of the Langevin function predicts greater collection efficiency than might be otherwise expected
Dosimetric evaluation of photon dose calculation under jaw and MLC shielding
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Purpose: The accuracy of photon dose calculation algorithms in out-of-field regions is often neglected, despite its importance for organs at risk and peripheral dose evaluation. The present work has assessed this for the anisotropic analytical algorithm (AAA) and the Acuros-XB algorithms implemented in the Eclipse treatment planning system. Specifically, the regions shielded by the jaw, or the MLC, or both MLC and jaw for flattened and unflattened beams have been studied.Methods: The accuracy in out-of-field dose under different conditions was studied for two different algorithms. Measured depth doses out of the field, for different field sizes and various distances from the beam edge were compared with the corresponding AAA and Acuros-XB calculations in water. Four volumetric modulated arc therapy plans (in the RapidArc form) were optimized in a water equivalent phantom, PTW Octavius, to obtain a region always shielded by the MLC (or MLC and jaw) during the delivery. Doses to different points located in the shielded region and in a target-like structure were measured with an ion chamber, and results were compared with the AAA and Acuros-XB calculations. Photon beams of 6 and 10 MV, flattened and unflattened were used for the tests.Results: Good agreement between calculated and measured depth doses was found using both algorithms for all points measured at depth greater than 3 cm. The mean dose differences (±1SD) were −8%± 16%, −3%± 15%, −16%± 18%, and −9%± 16% for measurements vs AAA calculations and −10%± 14%, −5%± 12%, −19%± 17%, and −13%± 14% for Acuros-XB, for 6X, 6 flattening-filter free (FFF), 10X, and 10FFF beams, respectively. The same figures for dose differences relative to the open beam central axis dose were: −0.1%± 0.3%, 0.0%± 0.4%, −0.3%± 0.3%, and −0.1%± 0.3% for AAA and −0.2%± 0.4%, −0.1%± 0.4%, −0.5%± 0.5%, and −0.3%± 0.4% for Acuros-XB. Buildup dose was overestimated with AAA, while Acuros-XB gave
Reassessment and reinforcement of nuclear decay database used for dose calculation
International Nuclear Information System (INIS)
A nuclear decay database of ICRP Publ.38 has been used for calculating dose coefficients for intake of radionuclides and effective dose rates for submersion. Publ.38 were compiled from decay data sets of the Evaluated Nuclear Structure Data File (ENSDF), which were prepared in the 1970's. It is very important to update the database by taking the recent revision of the ENSDF into account. This paper presents a comprehensive study on a reassessment and reinforcement of the nuclear decay database of Publ.38. For all 820 radionuclides listed in Publ.38, half-lives, branching ratios of the decay modes, and energies and intensities of radiations emitted were calculated from decay data sets of the ENSDF, the latest version in 1997, and compared with those of Publ.38. In most nuclides, the calculated values from the ENSDF were in good agreement with those of Publ.38. However, significant differences in the half-lives and the total energies of radiations were found in several nuclides, notably in 60Fe, 79Se, 80Sr, 108mAg, 126Ba, 202Pb, and 231Th. It was shown that internal dose coefficients of 202Pb calculated using the two decay data differ by a factor of two as a result of revision in the decay data sets. The results suggest that the nuclear decay data of Publ.38 are still adequate for dose calculation in most nuclides but the update of the data is required for several ones. Nuclear decay data for dose calculation were compiled from the ENSDF for 204 nuclides that are not listed in Publ.38. The compiled data involve 162 nuclides with half-lives ≥10 min, 28 daughters and 14 nuclides that are important in fusion reactor facilities. Analysis of the decay data sets was performed to check their self-consistency and possible revisions were made for their format and syntax errors, level schemes, normalization records, and so on . The revised data sets were processed by the EDISTR code to compile the decay data of Publ.38 form. The data were presented as a data book, JAERI Data
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Purpose: The objective of this work is to assess the sensitivity of Monte Carlo (MC) dose calculations to uncertainties in human tissue composition for a range of low photon energy brachytherapy sources: 125I, 103Pd, 131Cs, and an electronic brachytherapy source (EBS). The low energy photons emitted by these sources make the dosimetry sensitive to variations in tissue atomic number due to the dominance of the photoelectric effect. This work reports dose to a small mass of water in medium Dw,m as opposed to dose to a small mass of medium in medium Dm,m. Methods: Mean adipose, mammary gland, and breast tissues (as uniform mixture of the aforementioned tissues) are investigated as well as compositions corresponding to one standard deviation from the mean. Prostate mean compositions from three different literature sources are also investigated. Three sets of MC simulations are performed with the GEANT4 code: (1) Dose calculations for idealized TG-43-like spherical geometries using point sources. Radial dose profiles obtained in different media are compared to assess the influence of compositional uncertainties. (2) Dose calculations for four clinical prostate LDR brachytherapy permanent seed implants using 125I seeds (Model 2301, Best Medical, Springfield, VA). The effect of varying the prostate composition in the planning target volume (PTV) is investigated by comparing PTV D90 values. (3) Dose calculations for four clinical breast LDR brachytherapy permanent seed implants using 103Pd seeds (Model 2335, Best Medical). The effects of varying the adipose/gland ratio in the PTV and of varying the elemental composition of adipose and gland within one standard deviation of the assumed mean composition are investigated by comparing PTV D90 values. For (2) and (3), the influence of using the mass density from CT scans instead of unit mass density is also assessed. Results: Results from simulation (1) show that variations in the mean compositions of tissues affect low energy
Monte Carlo calculations of the impact of a hip prosthesis on the dose distribution
International Nuclear Information System (INIS)
Because of the ageing of the population, an increasing number of patients with hip prostheses are undergoing pelvic irradiation. Treatment planning systems (TPS) currently available are not always able to accurately predict the dose distribution around such implants. In fact, only Monte Carlo simulation has the ability to precisely calculate the impact of a hip prosthesis during radiotherapeutic treatment. Monte Carlo phantoms were developed to evaluate the dose perturbations during pelvic irradiation. A first model, constructed with the DOSXYZnrc usercode, was elaborated to determine the dose increase at the tissue-metal interface as well as the impact of the material coating the prosthesis. Next, CT-based phantoms were prepared, using the usercode CTCreate, to estimate the influence of the geometry and the composition of such implants on the beam attenuation. Thanks to a program that we developed, the study was carried out with CT-based phantoms containing a hip prosthesis without metal artefacts. Therefore, anthropomorphic phantoms allowed better definition of both patient anatomy and the hip prosthesis in order to better reproduce the clinical conditions of pelvic irradiation. The Monte Carlo results revealed the impact of certain coatings such as PMMA on dose enhancement at the tissue-metal interface. Monte Carlo calculations in CT-based phantoms highlighted the marked influence of the implant's composition, its geometry as well as its position within the beam on dose distribution
International Nuclear Information System (INIS)
Full text: The neutron-capture therapy with use of gadolinium-containing pharmacological preparations is one of perspective and not enough investigated directions of application of neutron irradiation in medicine. At definition of the absorbed dose of neutron-capture therapy one of important questions is definition of concentration gadolinium and pharmacokinetics in irradiated tumour. In the given study has been investigated pharmacokinetics of gadolinium-containing preparation 'Magnevist' at intratumoral injection in inoculated tumours of sarcoma C180 at mice. For 'Magnevist' detection its property of radioopacity has been used. In experiments to mice with inoculated tumours C180 the various doses of 'Magnevist' (0.1, 0.2, 0.3 and 0.4 ml) were injected into tumour centre. X-ray images were made before 'Magnevist' injection (control) and after preparation injection every 5 minutes within one hour. It has been shown that at dose 0.1 ml 'Magnevist' eliminated from tumour within 10 minutes. At higher doses of preparation more slow elimination of 'Magnevist' from injection site was observed. Obtained results allow with sufficient accuracy to calculate the time of presence of optimum concentration of 'Magnevist' in tumour at intratumoral injection. It in turn gives the chance to calculate precisely the absorbed dose at irradiation by beam of epi-thermal neutrons. (author)
PCXMC, a Monte Carlo program for calculating patient doses in medical x-ray examinations
International Nuclear Information System (INIS)
PCXMC is a Monte Carlo program for calculating patients' organ doses and effective doses in medical x-ray examinations. The organs and tissues considered in the program are: active bone marrow, adrenals, brain, breasts, colon (upper and lower large intestine), extrathoracic airways, gall bladder, heart, kidneys, liver, lungs, lymph nodes, muscle, oesophagus, oral mucosa, ovaries, pancreas, prostate, salivary glands, skeleton, skin, small intestine, spleen, stomach, testicles, thymus, thyroid, urinary bladder and uterus. The program calculates the effective dose with both the present tissue weighting factors of ICRP Publication 103 (2007) and the old tissue weighting factors of ICRP Publication 60 (1991). The anatomical data are based on the mathematical hermaphrodite phantom models of Cristy and Eckerman (1987), which describe patients of six different ages: new-born, 1, 5, 10, 15-year-old and adult patients. Some changes are made to these phantoms in order to make them more realistic for external irradiation conditions and to enable the calculation of the effective dose according to the new ICRP Publication 103 tissue weighting factors. The phantom sizes are adjustable to mimic patients of an arbitrary weight and height. PCXMC allows a free adjustment of the x-ray beam projection and other examination conditions of projection radiography and fluoroscopy
Evolution of calculation models for the proton-therapy dose planning software
International Nuclear Information System (INIS)
This work was achieved in collaboration between the Institut Curie Proton-therapy Center of Orsay (ICPO), the DOSIsoft company and the CREATIS laboratory, in order to develop a new dose calculation model for the new ICPO treatment room. A new accelerator and gantry room from the IBA company were installed during the up-grade project of the proton-therapy center, with the intention of enlarging the cancer localizations treated at ICPO. Developing a package of methods and new dose calculation algorithms to adapt them to the new specific characteristics of the delivered beams by the IBA system is the first goal of this PhD work. They all aim to be implemented in the DOSIsoft treatment planning software, Isogray. First, the double scattering technique is treated in taking into account major differences between the IBA system and the ICPO fixed beam lines passive system. Secondly, a model is explored for the scanned beams modality. The second objective of this work is improving the Ray-Tracing and Pencil-Beam dose calculation models already in use. For the double scattering and uniform scanning techniques, the patient personalized collimator at the end of the beam line causes indeed a patient dose distribution contamination. A reduction method of that phenomenon was set up for the passive beam system. An analytical model was developed which describes the contamination function with parameters validated through Monte-Carlo simulations on the GATE platform. It allows us to apply those methods to active scanned beams. (author)
Dosimetric evaluation of Acuros XB Advanced Dose Calculation algorithm in heterogeneous media
International Nuclear Information System (INIS)
A study was realised to evaluate and determine relative figures of merit of a new algorithm for photon dose calculation when applied to inhomogeneous media. The new Acuros XB algorithm implemented in the Varian Eclipse treatment planning system was compared against a Monte Carlo method (VMC++), and the Analytical Anisotropic Algorithm (AAA). The study was carried out in virtual phantoms characterized by simple geometrical structures. An insert of different material and density was included in a phantom built of skeletal-muscle and HU = 0 (setting 'A'): Normal Lung (lung, 0.198 g/cm3); Light Lung (lung, 0.035 g/cm3); Bone (bone, 1.798 g/cm3); another phantom (setting 'B') was built of adipose material and including thin layers of bone (1.85 g/cm3), adipose (0.92 g/cm3), cartilage (1.4745 g/cm3), air (0.0012 g/cm3). Investigations were performed for 6 and 15 MV photon beams, and for a large (13 × 13 cm2) and a small (2.8 × 13 cm2) field. Results are provided in terms of depth dose curves, transverse profiles and Gamma analysis (3 mm/3% and 2 mm/2% distance to agreement/dose difference criteria) in planes parallel to the beam central axis; Monte Carlo simulations were assumed as reference. Acuros XB gave an average gamma agreement, with a 3 mm/3% criteria, of 100%, 86% and 100% for Normal Lung, Light Lung and Bone settings, respectively, and dose to medium calculations. The same figures were 86%, 11% and 100% for AAA, where only dose rescaled to water calculations are possible. In conclusion, Acuros XB algorithm provides a valid and accurate alternative to Monte Carlo calculations for heterogeneity management
Patient-specific Monte Carlo dose calculations for 103Pd breast brachytherapy
Miksys, N.; Cygler, J. E.; Caudrelier, J. M.; Thomson, R. M.
2016-04-01
This work retrospectively investigates patient-specific Monte Carlo (MC) dose calculations for 103Pd permanent implant breast brachytherapy, exploring various necessary assumptions for deriving virtual patient models: post-implant CT image metallic artifact reduction (MAR), tissue assignment schemes (TAS), and elemental tissue compositions. Three MAR methods (thresholding, 3D median filter, virtual sinogram) are applied to CT images; resulting images are compared to each other and to uncorrected images. Virtual patient models are then derived by application of different TAS ranging from TG-186 basic recommendations (mixed adipose and gland tissue at uniform literature-derived density) to detailed schemes (segmented adipose and gland with CT-derived densities). For detailed schemes, alternate mass density segmentation thresholds between adipose and gland are considered. Several literature-derived elemental compositions for adipose, gland and skin are compared. MC models derived from uncorrected CT images can yield large errors in dose calculations especially when used with detailed TAS. Differences in MAR method result in large differences in local doses when variations in CT number cause differences in tissue assignment. Between different MAR models (same TAS), PTV {{D}90} and skin {{D}1~\\text{c{{\\text{m}}3}}} each vary by up to 6%. Basic TAS (mixed adipose/gland tissue) generally yield higher dose metrics than detailed segmented schemes: PTV {{D}90} and skin {{D}1~\\text{c{{\\text{m}}3}}} are higher by up to 13% and 9% respectively. Employing alternate adipose, gland and skin elemental compositions can cause variations in PTV {{D}90} of up to 11% and skin {{D}1~\\text{c{{\\text{m}}3}}} of up to 30%. Overall, AAPM TG-43 overestimates dose to the PTV ({{D}90} on average 10% and up to 27%) and underestimates dose to the skin ({{D}1~\\text{c{{\\text{m}}3}}} on average 29% and up to 48%) compared to the various MC models derived using the post-MAR CT images studied
Comparison of the Calculated and Measured Dose under Lead Blocks in Radiation Therapy Photon Beams
International Nuclear Information System (INIS)
Depth dose data for irregularly shaped fields cannot be previously prepared as they usually are for circular and square fields in photon beams of linacs and Cobalt-60 units. Thus we apply a computer program for that purpose, each time inserting the specific field shape into the computer by a digitizer. The program is based on the implementation of the well known Clarkson's method, exactly as described by Khan(1). The method also allows to calculate the dose under blocks in various depths. In order to verify the validity of the program we compared the calculated dose with that one measured in a waterlike phantom made of white polystyrene (PTW's raw water). The calculation also allows to evaluate the contribution of the scatter radiation to the total dose under the blocks. The dose under two lead blocks was measured within a field of 25x25cm2 as measured on the level of isocenter. The size of blocks as compared to the open field is shown in fig.2. The depths of measurements were dmax, 5cm, 10cm and 20 cm (point B in fig2.). The results are expressed in % with respect to the reference point in dmax (point A in fig.2) and are shown in table 1 (Cobalt gamma rays), in table 2 (6MV X rays) and in table 3 (18MV X rays). The fractions shown in brackets represent the contribution of the scattered radiation to the dose under blocks. The results show that the calculation is in excellent agreement with the measurement for small blocks, it somewhat underestimates the dose for large blocks and small depths, but it is satisfactory for the depths greater than 5 cm. The results also show that the contribution of the scattered radiation is essentially higher under small blocks and that it generally increases with the depth. The maximum difference in no case exceeded 2.5 % of the dose in the reference point. From the point of view of radiation protection, this difference can be considered as negligible. On the other hand, from the point of view of radiotherapy the obtained accuracy is
Clouvas, A; Antonopoulos-Domis, M; Silva, J
2000-01-01
The dose rate conversion factors D/sub CF/ (absorbed dose rate in air per unit activity per unit of soil mass, nGy h/sup -1/ per Bq kg/sup -1/) are calculated 1 m above ground for photon emitters of natural radionuclides uniformly distributed in the soil. Three Monte Carlo codes are used: 1) The MCNP code of Los Alamos; 2) The GEANT code of CERN; and 3) a Monte Carlo code developed in the Nuclear Technology Laboratory of the Aristotle University of Thessaloniki. The accuracy of the Monte Carlo results is tested by the comparison of the unscattered flux obtained by the three Monte Carlo codes with an independent straightforward calculation. All codes and particularly the MCNP calculate accurately the absorbed dose rate in air due to the unscattered radiation. For the total radiation (unscattered plus scattered) the D/sub CF/ values calculated from the three codes are in very good agreement between them. The comparison between these results and the results deduced previously by other authors indicates a good ag...
Adjustment of a Korean Voxel Phantom and Its Effect on Monte Carlo Dose Calculations
International Nuclear Information System (INIS)
Many different voxel models have been developed for use in the calculation of the radiation doses to organs and tissues in the human body. Most of these voxel models are constructed from the CT and MR images of individuals. The organs and tissues are, however, not always discernable on CT and MR images, making it difficult to segment some organs and tissues. Furthermore, these models do not represent the average radiation workers in Korea because the height, weight, and organ masses are different from those of the average Korean workers. This paper compares two Korean voxel models (VKH-Man, HDRK-Man), which have been constructed from the same data set of serially-sectioned color images, in terms of calculated organs doses. The HDRK-Man has been developed by adjusting the VKH Man to the data of the 'Reference Korean'. In this study, organs doses were calculated with these developed models and the calculated values were compared each other to see the effect of the adjustment
Adjustment of a Korean Voxel Phantom and Its Effect on Monte Carlo Dose Calculations
Energy Technology Data Exchange (ETDEWEB)
Jeong, Jong Hwi; Choi, Sang Hyoun; Cho, Sung Koo [Hanyang University, Seoul (Korea, Republic of); Lee, Choon Sik [University of Florida, Gainesville (United States); Chung, Min Suk; Kim, Chan Hyeong [Ajou University School of Medicine, Suwon (Korea, Republic of)
2007-07-01
Many different voxel models have been developed for use in the calculation of the radiation doses to organs and tissues in the human body. Most of these voxel models are constructed from the CT and MR images of individuals. The organs and tissues are, however, not always discernable on CT and MR images, making it difficult to segment some organs and tissues. Furthermore, these models do not represent the average radiation workers in Korea because the height, weight, and organ masses are different from those of the average Korean workers. This paper compares two Korean voxel models (VKH-Man, HDRK-Man), which have been constructed from the same data set of serially-sectioned color images, in terms of calculated organs doses. The HDRK-Man has been developed by adjusting the VKH Man to the data of the 'Reference Korean'. In this study, organs doses were calculated with these developed models and the calculated values were compared each other to see the effect of the adjustment.
Application of a Monte Carlo linac model in routine verifications of dose calculations
International Nuclear Information System (INIS)
The analysis of some parameters of interest in Radiotherapy Medical Physics based on an experimentally validated Monte Carlo model of an Elekta Precise lineal accelerator, was performed for 6 and 15 Mv photon beams. The simulations were performed using the EGSnrc code. As reference for simulations, the optimal beam parameters values (energy and FWHM) previously obtained were used. Deposited dose calculations in water phantoms were done, on typical complex geometries commonly are used in acceptance and quality control tests, such as irregular and asymmetric fields. Parameters such as MLC scatter, maximum opening or closing position, and the separation between them were analyzed from calculations in water. Similarly simulations were performed on phantoms obtained from CT studies of real patients, making comparisons of the dose distribution calculated with EGSnrc and the dose distribution obtained from the computerized treatment planning systems (TPS) used in routine clinical plans. All the results showed a great agreement with measurements, finding all of them within tolerance limits. These results allowed the possibility of using the developed model as a robust verification tool for validating calculations in very complex situation, where the accuracy of the available TPS could be questionable. (Author)
Results of 1 year of clinical experience with independent dose calculation software for VMAT fields
Directory of Open Access Journals (Sweden)
Juan Fernando Mata Colodro
2014-01-01
Full Text Available It is widely accepted that a redundant independent dose calculation (RIDC must be included in any treatment planning verification procedure. Specifically, volumetric modulated arc therapy (VMAT technique implies a comprehensive quality assurance (QA program in which RIDC should be included. In this paper, the results obtained in 1 year of clinical experience are presented. Eclipse from Varian is the treatment planning system (TPS, here in use. RIDC were performed with the commercial software; Diamond ® (PTW which is capable of calculating VMAT fields. Once the plan is clinically accepted, it is exported via Digital Imaging and Communications in Medicine (DICOM to RIDC, together with the body contour, and then a point dose calculation is performed, usually at the isocenter. A total of 459 plans were evaluated. The total average deviation was -0.3 ± 1.8% (one standard deviation (1SD. For higher clearance the plans were grouped by location in: Prostate, pelvis, abdomen, chest, head and neck, brain, stereotactic radiosurgery, lung stereotactic body radiation therapy, and miscellaneous. The highest absolute deviation was -0.8 ± 1.5% corresponding to the prostate. A linear fit between doses calculated by RIDC and by TPS produced a correlation coefficient of 0.9991 and a slope of 1.0023. These results are very close to those obtained in the validation process. This agreement led us to consider this RIDC software as a valuable tool for QA in VMAT plans.
International Nuclear Information System (INIS)
The dose rate conversion factors dot DCF (absorbed dose rate in air per unit activity per unit of soil mass, nGy h-1 per Bq kg-1) are calculated 1 m above ground for photon emitters of natural radionuclides uniformly distributed in the soil. Three Monte Carlo codes are used: (1) The MCNP code of Los Alamos; (2) The GEANT code of CERN; and (3) a Monte Carlo code developed in the Nuclear Technology Laboratory of the Aristotle University of Thessaloniki. The accuracy of the Monte Carlo results is tested by the comparison of the unscattered flux obtained by the three Monte Carlo codes with an independent straightforward calculation. All codes and particularly the MCNP calculate accurately the absorbed dose rate in air due to the unscattered radiation. For the total radiation (unscattered plus scattered) the dot DCF values calculated from the three codes are in very good agreement between them. The comparison between these results and the results deduced previously by other authors indicates a good agreement (less than 15% of difference) for photon energies above 1,500 keV. Antithetically, the agreement is not as good (difference of 20--30%) for the low energy photons
Monte Carlo calculation of synchrotron x-ray beam dose profiles in a lung phantom
International Nuclear Information System (INIS)
Full text: Recent advances in synchrotron generated X-ray beams with high fluence rate permit investigation of the application of an array of closely spaced, parallel or converging microplanar beams in radiotherapy. The proposed technique takes advantage of the hypothesized repair mechanism of capillary cells between alternate microbeam zones, which regenerates the lethally irradiated endothelial cells. The lateral and depth doses of 100 keV microplanar beams are investigated for different beam dimensions and spacings in a tissue, lung and tissue/lung/tissue phantom. The EGS4 Monte Carlo code is used to calculate dose profiles at different depth and bundles of beams (up to 20x20 cm square cross section). The maximum dose on the beam axis (peak) and the minimum interbeam dose (valley) are compared at different depths, bundles, heights, widths and beam spacings. Relatively high peak to valley ratios are observed in the lung region, suggesting an ideal environment for microbeam radiotherapy. For a single field, the ratio at the tissue/lung interface will set the maximum dose to the target volume. However, in clinical application, several fields would be involved allowing much greater doses to be applied for the elimination of cancer cells. We conclude therefore that multifield microbeam therapy has the potential to achieve useful therapeutic ratios for the treatment of lung cancer
International Nuclear Information System (INIS)
The objective of this study was to estimate doses in the physician and the nurse assistant at different positions during interventional radiology procedures. In this study, effective doses obtained for the physician and at points occupied by other workers were normalised by air kerma-area product (KAP). The simulations were performed for two X-ray spectra (70 kVp and 87 kVp) using the radiation transport code MCNPX (version 2.7.0), and a pair of anthropomorphic voxel phantoms (MASH/FASH) used to represent both the patient and the medical professional at positions from 7 cm to 47 cm from the patient. The X-ray tube was represented by a point source positioned in the anterior posterior (AP) and posterior anterior (PA) projections. The CC can be useful to calculate effective doses, which in turn are related to stochastic effects. With the knowledge of the values of CCs and KAP measured in an X-ray equipment, at a similar exposure, medical professionals will be able to know their own effective dose. - Highlights: ► This study presents a series of simulations to determine scatter-dose in IR. ► Irradiation of the worker is non-uniform and a part of his body is shielded. ► With the CCs it is possible to estimate the occupational doses in the CA examination. ► Protection of medical personnel in IR is an important issue of radiological protection
An analytic linear accelerator source model for GPU-based Monte Carlo dose calculations
Tian, Zhen; Li, Yongbao; Folkerts, Michael; Shi, Feng; Jiang, Steve B.; Jia, Xun
2015-10-01
Recently, there has been a lot of research interest in developing fast Monte Carlo (MC) dose calculation methods on graphics processing unit (GPU) platforms. A good linear accelerator (linac) source model is critical for both accuracy and efficiency considerations. In principle, an analytical source model should be more preferred for GPU-based MC dose engines than a phase-space file-based model, in that data loading and CPU-GPU data transfer can be avoided. In this paper, we presented an analytical field-independent source model specifically developed for GPU-based MC dose calculations, associated with a GPU-friendly sampling scheme. A key concept called phase-space-ring (PSR) was proposed. Each PSR contained a group of particles that were of the same type, close in energy and reside in a narrow ring on the phase-space plane located just above the upper jaws. The model parameterized the probability densities of particle location, direction and energy for each primary photon PSR, scattered photon PSR and electron PSR. Models of one 2D Gaussian distribution or multiple Gaussian components were employed to represent the particle direction distributions of these PSRs. A method was developed to analyze a reference phase-space file and derive corresponding model parameters. To efficiently use our model in MC dose calculations on GPU, we proposed a GPU-friendly sampling strategy, which ensured that the particles sampled and transported simultaneously are of the same type and close in energy to alleviate GPU thread divergences. To test the accuracy of our model, dose distributions of a set of open fields in a water phantom were calculated using our source model and compared to those calculated using the reference phase-space files. For the high dose gradient regions, the average distance-to-agreement (DTA) was within 1 mm and the maximum DTA within 2 mm. For relatively low dose gradient regions, the root-mean-square (RMS) dose difference was within 1.1% and the maximum
Effect of Kidney Function on Drug Kinetics and Dosing in Neonates, Infants, and Children.
Rodieux, Frederique; Wilbaux, Melanie; van den Anker, Johannes N; Pfister, Marc
2015-12-01
Neonates, infants, and children differ from adults in many aspects, not just in age, weight, and body composition. Growth, maturation and environmental factors affect drug kinetics, response and dosing in pediatric patients. Almost 80% of drugs have not been studied in children, and dosing of these drugs is derived from adult doses by adjusting for body weight/size. As developmental and maturational changes are complex processes, such simplified methods may result in subtherapeutic effects or adverse events. Kidney function is impaired during the first 2 years of life as a result of normal growth and development. Reduced kidney function during childhood has an impact not only on renal clearance but also on absorption, distribution, metabolism and nonrenal clearance of drugs. 'Omics'-based technologies, such as proteomics and metabolomics, can be leveraged to uncover novel markers for kidney function during normal development, acute kidney injury, and chronic diseases. Pharmacometric modeling and simulation can be applied to simplify the design of pediatric investigations, characterize the effects of kidney function on drug exposure and response, and fine-tune dosing in pediatric patients, especially in those with impaired kidney function. One case study of amikacin dosing in neonates with reduced kidney function is presented. Collaborative efforts between clinicians and scientists in academia, industry, and regulatory agencies are required to evaluate new renal biomarkers, collect and share prospective pharmacokinetic, genetic and clinical data, build integrated pharmacometric models for key drugs, optimize and standardize dosing strategies, develop bedside decision tools, and enhance labels of drugs utilized in neonates, infants, and children. PMID:26138291
DEFF Research Database (Denmark)
Christensen, Erik R.; Kusk, Kresten Ole; Nyholm, Niels
2009-01-01
We derive equations for the effective concentration giving 10% inhibition (EC10) with 95% confidence limits for probit (log-normal), Weibull, and logistic dose -responsemodels on the basis of experimentally derived median effective concentrations (EC50s) and the curve slope at the central point (50......% inhibition). For illustration, data from closed, freshwater algal assays are analyzed using the green alga Pseudokirchneriella subcapitata with growth rate as the response parameter. Dose-response regressions for four test chemicals (tetraethylammonium bromide, musculamine, benzonitrile, and 4......-4-(trifluoromethyl)phenoxy-phenol) with ranges of representative slopes at 50% response (0.54-2.62) and EC50s (2.20-357 mg/L) were selected. Reference EC50s and EC10s with 95% confidence limits using probit or Weibull models are calculated by nonlinear regression on the whole dataset using a dose - response...
International Nuclear Information System (INIS)
A large group of workers in many fields are exposed to ionizing radiation, this type of exposure is called occupational exposure to radiation. It is important to monitor this exposure periodically and take the necessary protection measures to minimize this exposure to as low as reasonably achievable. This work presents a detailed analysis of occupational exposure data during the period 1990 to 1999 for the monitored workers in Syria. The types of work for these worker have been classified into five main groups, and further classification for monitored workers have been done according to the practices, using the national dose record for monitored workers; the numbers of monitored workers were determined each year and the collective doses and average annual doses were calculated for each practice. Explanations for causes of exposure were given in addition to suggestions and recommendation for reduction of these exposures to as low as reasonably achievable. (author)
Calculation of absorbed dose of anchorage-dependent cells from internal beta-rays irradiation
International Nuclear Information System (INIS)
Objective: To elicit the formula of internal dosimetry in anchorage-dependent cells by beta-emitting radionuclides from uniformly distributed volume sources. Methods: By means of the definition of absorbed dose and the MIRD (Medical International Radiation Dose) scheme the formula of internal dosimetry was reasonably deduced. Firstly, studying the systems of suspension culture cells. Then, taking account of the speciality of the systems of the anchorage-dependent cells and the directions of irradiation, the absorbed dose of anchorage -dependent cells was calculated by the accumulated radioactivity, beta-ray energy, and the volume of the cultured systems. Results: The formula of internal dosimetry of suspension culture cells and anchorage-dependent cells were achieved. At the same time, the formula of internal dosimetry of suspension culture cells was compared with that of MIRD and was confirmed accurate. Conclusion: The formula of internal dosimetry is concise, reliable and accurate
Fogliata, Antonella; Nicolini, Giorgia; Clivio, Alessandro; Vanetti, Eugenio; Mancosu, Pietro; Cozzi, Luca
2011-03-01
A new algorithm, Acuros® XB Advanced Dose Calculation, has been introduced by Varian Medical Systems in the Eclipse planning system for photon dose calculation in external radiotherapy. Acuros XB is based on the solution of the linear Boltzmann transport equation (LBTE). The LBTE describes the macroscopic behaviour of radiation particles as they travel through and interact with matter. The implementation of Acuros XB in Eclipse has not been assessed; therefore, it is necessary to perform these pre-clinical validation tests to determine its accuracy. This paper summarizes the results of comparisons of Acuros XB calculations against measurements and calculations performed with a previously validated dose calculation algorithm, the Anisotropic Analytical Algorithm (AAA). The tasks addressed in this paper are limited to the fundamental characterization of Acuros XB in water for simple geometries. Validation was carried out for four different beams: 6 and 15 MV beams from a Varian Clinac 2100 iX, and 6 and 10 MV 'flattening filter free' (FFF) beams from a TrueBeam linear accelerator. The TrueBeam FFF are new beams recently introduced in clinical practice on general purpose linear accelerators and have not been previously reported on. Results indicate that Acuros XB accurately reproduces measured and calculated (with AAA) data and only small deviations were observed for all the investigated quantities. In general, the overall degree of accuracy for Acuros XB in simple geometries can be stated to be within 1% for open beams and within 2% for mechanical wedges. The basic validation of the Acuros XB algorithm was therefore considered satisfactory for both conventional photon beams as well as for FFF beams of new generation linacs such as the Varian TrueBeam.
SU-E-T-416: VMAT Dose Calculations Using Cone Beam CT Images: A Preliminary Study
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Yu, S; Sehgal, V; Kuo, J; Daroui, P; Ramsinghani, N; Al-Ghazi, M [University of California, Orange, CA (United States)
2014-06-01
Purpose: Cone beam CT (CBCT) images have been used routinely for patient positioning throughout the treatment course. However, use of CBCT for dose calculation is still investigational. The purpose of this study is to assess the utility of CBCT images for Volumetric Modulated Arc Therapy (VMAT) plan dose calculation. Methods: A CATPHAN 504 phantom (The Phantom Laboratory, Salem, NY) was used to compare the dosimetric and geometric accuracy between conventional CT and CBCT (in both full and half fan modes). Hounsfield units (HU) profiles at different density areas were evaluated. A C shape target that surrounds a central avoidance structure was created and a VMAT plan was generated on the CT images and copied to the CBCT phantom images. Patient studies included three brain patients, and one head and neck (H'N) patient. VMAT plans generated on the patients treatment planning CT was applied to CBCT images obtained during the first treatment. Isodose distributions and dosevolume- histograms (DVHs) were compared. Results: For the phantom study, the HU difference between CT and CBCT is within 100 (maximum 96 HU for Teflon CBCT images in full fan mode). The impact of these differences on the calculated dose distributions was clinically insignificant. In both phantom and patient studies, target DVHs based on CBCT images were in excellent agreement with those based on planning CT images. Mean, Median, near minimum (D98%), and near maximum (D2%) doses agreed within 0-2.5%. A slightly larger discrepancy is observed in the patient studies compared to that seen in the phantom study, (0-1% vs. 0 - 2.5%). Conclusion: CBCT images can be used to accurately predict dosimetric results, without any HU correction. It is feasible to use CBCT to evaluate the actual dose delivered at each fraction. The dosimetric consequences resulting from tumor response and patient geometry changes could be monitored.
SU-E-T-416: VMAT Dose Calculations Using Cone Beam CT Images: A Preliminary Study
International Nuclear Information System (INIS)
Purpose: Cone beam CT (CBCT) images have been used routinely for patient positioning throughout the treatment course. However, use of CBCT for dose calculation is still investigational. The purpose of this study is to assess the utility of CBCT images for Volumetric Modulated Arc Therapy (VMAT) plan dose calculation. Methods: A CATPHAN 504 phantom (The Phantom Laboratory, Salem, NY) was used to compare the dosimetric and geometric accuracy between conventional CT and CBCT (in both full and half fan modes). Hounsfield units (HU) profiles at different density areas were evaluated. A C shape target that surrounds a central avoidance structure was created and a VMAT plan was generated on the CT images and copied to the CBCT phantom images. Patient studies included three brain patients, and one head and neck (H'N) patient. VMAT plans generated on the patients treatment planning CT was applied to CBCT images obtained during the first treatment. Isodose distributions and dosevolume- histograms (DVHs) were compared. Results: For the phantom study, the HU difference between CT and CBCT is within 100 (maximum 96 HU for Teflon CBCT images in full fan mode). The impact of these differences on the calculated dose distributions was clinically insignificant. In both phantom and patient studies, target DVHs based on CBCT images were in excellent agreement with those based on planning CT images. Mean, Median, near minimum (D98%), and near maximum (D2%) doses agreed within 0-2.5%. A slightly larger discrepancy is observed in the patient studies compared to that seen in the phantom study, (0-1% vs. 0 - 2.5%). Conclusion: CBCT images can be used to accurately predict dosimetric results, without any HU correction. It is feasible to use CBCT to evaluate the actual dose delivered at each fraction. The dosimetric consequences resulting from tumor response and patient geometry changes could be monitored
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Gomes, Renato G.; Rebello, Wilson F.; Vellozo, Sergio O.; Junior, Luis M., E-mail: renatoguedes@ime.eb.br, E-mail: rebello@ime.eb.br, E-mail: vellozo@cbpf.br, E-mail: luisjrmoreira@hotmail.com [Instituto Militar de Engenharia (IME), Janeiro, RJ (Brazil); Vital, Helio C., E-mail: vital@ctex.eb.br [Centro Tecnologico do Exercito (CTEx), Barra de Guaratiba, RJ (Brazil); Rusin, Tiago, E-mail: tiago.rusin@mma.gov.br [Ministerio do Meio Ambiente, Brasilia, DF (Brazil); Silva, Ademir X., E-mail: ademir@con.ufrj.br [Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ (Brazil)
2013-07-01
MCNPX simulations have been performed in order to calculate dose rates as well as spectra along the four experimental channels of the gamma irradiating facility at the Technology Center of the Brazilian Army (CTEx). Safety, operational and research requirements have led to the need to determine both the magnitude and spectra of the leaking gamma fluxes. The CTEx experimental facility is cavity type with a moveable set of 28 horizontally positioned rods, filled with Cesium-137 chloride and doubly encased in stainless steel that yields an approximately plane 42 kCi-source that provides a maximum dose rate of about 1.5 kG/h into two irradiating chambers. The channels are intended for irradiation tests outside facility. They would allow larger samples to be exposed to lower gamma dose rates under controlled conditions. Dose rates have been calculated for several positions inside the channels as well as at their exits. In addition, for purposes related to the safety of operators and personnel, the angles submitted by the exiting beams have also been evaluated as they spread when leaving the channels. All calculations have been performed by using a computational model of the CTEx facility that allows its characteristics and operation to be accurately simulated by using the Monte Carlo Method. Virtual dosimeters filled with Fricke (ferrous sulfate) were modeled and positioned throughout 2 vertical channels (top and bottom) and 2 horizontal ones (front and back) in order to map dose rates and gamma spectrum distributions. The calculations revealed exiting collimated beams in the order of tenths of Grays per minute as compared to the maximum 25 Gy / min dose rate in the irradiator chamber. In addition, the beams leaving the two vertical channels were found to exhibit a widespread cone-shaped distribution with aperture angle ranging around 85 deg. The data calculated in this work are intended for use in the design of optimized experiments (better positioning of samples and
GPU-based Monte Carlo radiotherapy dose calculation using phase-space sources
International Nuclear Information System (INIS)
A novel phase-space source implementation has been designed for graphics processing unit (GPU)-based Monte Carlo dose calculation engines. Short of full simulation of the linac head, using a phase-space source is the most accurate method to model a clinical radiation beam in dose calculations. However, in GPU-based Monte Carlo dose calculations where the computation efficiency is very high, the time required to read and process a large phase-space file becomes comparable to the particle transport time. Moreover, due to the parallelized nature of GPU hardware, it is essential to simultaneously transport particles of the same type and similar energies but separated spatially to yield a high efficiency. We present three methods for phase-space implementation that have been integrated into the most recent version of the GPU-based Monte Carlo radiotherapy dose calculation package gDPM v3.0. The first method is to sequentially read particles from a patient-dependent phase-space and sort them on-the-fly based on particle type and energy. The second method supplements this with a simple secondary collimator model and fluence map implementation so that patient-independent phase-space sources can be used. Finally, as the third method (called the phase-space-let, or PSL, method) we introduce a novel source implementation utilizing pre-processed patient-independent phase-spaces that are sorted by particle type, energy and position. Position bins located outside a rectangular region of interest enclosing the treatment field are ignored, substantially decreasing simulation time with little effect on the final dose distribution. The three methods were validated in absolute dose against BEAMnrc/DOSXYZnrc and compared using gamma-index tests (2%/2 mm above the 10% isodose). It was found that the PSL method has the optimal balance between accuracy and efficiency and thus is used as the default method in gDPM v3.0. Using the PSL method, open fields of 4 × 4, 10 × 10 and 30 × 30 cm
GPU-based Monte Carlo radiotherapy dose calculation using phase-space sources.
Townson, Reid W; Jia, Xun; Tian, Zhen; Graves, Yan Jiang; Zavgorodni, Sergei; Jiang, Steve B
2013-06-21
A novel phase-space source implementation has been designed for graphics processing unit (GPU)-based Monte Carlo dose calculation engines. Short of full simulation of the linac head, using a phase-space source is the most accurate method to model a clinical radiation beam in dose calculations. However, in GPU-based Monte Carlo dose calculations where the computation efficiency is very high, the time required to read and process a large phase-space file becomes comparable to the particle transport time. Moreover, due to the parallelized nature of GPU hardware, it is essential to simultaneously transport particles of the same type and similar energies but separated spatially to yield a high efficiency. We present three methods for phase-space implementation that have been integrated into the most recent version of the GPU-based Monte Carlo radiotherapy dose calculation package gDPM v3.0. The first method is to sequentially read particles from a patient-dependent phase-space and sort them on-the-fly based on particle type and energy. The second method supplements this with a simple secondary collimator model and fluence map implementation so that patient-independent phase-space sources can be used. Finally, as the third method (called the phase-space-let, or PSL, method) we introduce a novel source implementation utilizing pre-processed patient-independent phase-spaces that are sorted by particle type, energy and position. Position bins located outside a rectangular region of interest enclosing the treatment field are ignored, substantially decreasing simulation time with little effect on the final dose distribution. The three methods were validated in absolute dose against BEAMnrc/DOSXYZnrc and compared using gamma-index tests (2%/2 mm above the 10% isodose). It was found that the PSL method has the optimal balance between accuracy and efficiency and thus is used as the default method in gDPM v3.0. Using the PSL method, open fields of 4 × 4, 10 × 10 and 30 × 30 cm
The calculation of radial dose from heavy ions: predictions of biological action cross sections
Katz, R.; Cucinotta, F. A.; Zhang, C. X.; Wilson, J. W. (Principal Investigator)
1996-01-01
The track structure model of heavy ion cross sections was developed by Katz and co-workers in the 1960s. In this model the action cross section is evaluated by mapping the dose-response of a detector to gamma rays (modeled from biological target theory) onto the radial dose distribution from delta rays about the path of the ion. This is taken to yield the radial distribution of probability for a "hit" (an interaction leading to an observable end-point). Radial integration of the probability yields the cross section. When different response from ions of different Z having the same stopping power is observed this model may be indicated. Since the 1960s there have been several developments in the computation of the radial dose distribution, in the measurement of these distributions, and in new radiobiological data against which to test the model. The earliest model, by Butts and Katz made use of simplified delta ray distribution functions, of simplified electron range-energy relations, and neglected angular distributions. Nevertheless it made possible the calculation of cross sections for the inactivation of enzymes and viruses, and allowed extension to tracks in nuclear emulsions and other detectors and to biological cells. It set the pattern for models of observable effects in the matter through which the ion passed. Here we outline subsequent calculations of radial dose which make use of improved knowledge of the electron emission spectrum, the electron range-energy relation, the angular distribution, and some considerations of molecular excitation, of particular interest both close to the path of the ion and the outer limits of electron penetration. These are applied to the modeling of action cross sections for the inactivation of several strains of E-coli and B. subtilis spores where extensive measurements in the "thin-down" region have been made with heavy ion beams. Such calculations serve to test the radial dose calculations at the outer limit of electron
Monte Carlo calculations for doses in organs and tissues to oral radiography
International Nuclear Information System (INIS)
Using the MIRD 5 phantom and Monte Carlo technique, organ doses in patients undergoing external dental examination were calculated taking into account the different x-ray beam geometries and the various possible positions of x-ray source with regard to the head of the patient. It was necessary to introduce in the original computer program a new source description specific for dental examinations. To have a realistic evaluation of organ doses during dental examination it was necessary to introduce a new region in the phantom heat which characterizes the teeth and salivary glands. The attenuation of the x-ray beam by the lead shield of the radiographic film was also introduced in the calculation. (author)
X/Qs and unit dose calculations for Central Waste Complex interim safety basis effort
International Nuclear Information System (INIS)
The objective for this problem is to calculate the ground-level release dispersion factors (X/Q) and unit doses for onsite facility and offsite receptors at the site boundary and at Highway 240 for plume meander, building wake effect, plume rise, and the combined effect. The release location is at Central Waste Complex Building P4 in the 200 West Area. The onsite facility is located at Building P7. Acute ground level release 99.5 percentile dispersion factors (X/Q) were generated using the GXQ. The unit doses were calculated using the GENII code. The dimensions of Building P4 are 15 m in W x 24 m in L x 6 m in H
Deterministic Partial Differential Equation Model for Dose Calculation in Electron Radiotherapy
Duclous, Roland; Frank, Martin
2009-01-01
Treatment with high energy ionizing radiation is one of the main methods in modern cancer therapy that is in clinical use. During the last decades, two main approaches to dose calculation were used, Monte Carlo simulations and semi-empirical models based on Fermi-Eyges theory. A third way to dose calculation has only recently attracted attention in the medical physics community. This approach is based on the deterministic kinetic equations of radiative transfer. Starting from these, we derive a macroscopic partial differential equation model for electron transport in tissue. This model involves an angular closure in the phase space. It is exact for the free-streaming and the isotropic regime. We solve it numerically by a newly developed HLLC scheme based on [BerCharDub], that exactly preserves key properties of the analytical solution on the discrete level. Several numerical results for test cases from the medical physics literature are presented.
A method for calculation of dose per unit concentration values for aquatic biota
International Nuclear Information System (INIS)
A dose per unit concentration database has been generated for application to ecosystem assessments within the FASSET framework. Organisms are represented by ellipsoids of appropriate dimensions, and the proportion of radiation absorbed within the organisms is calculated using a numerical method implemented in a series of spreadsheet-based programs. Energy-dependent absorbed fraction functions have been derived for calculating the total dose per unit concentration of radionuclides present in biota or in the media they inhabit. All radionuclides and reference organism dimensions defined within FASSET for marine and freshwater ecosystems are included. The methodology has been validated against more complex dosimetric models and compared with human dosimetry based on ICRP 72. Ecosystem assessments for aquatic biota within the FASSET framework can now be performed simply, once radionuclide concentrations in target organisms are known, either directly or indirectly by deduction from radionuclide concentrations in the surrounding medium
GPU-based fast Monte Carlo simulation for radiotherapy dose calculation
Jia, Xun; Graves, Yan Jiang; Folkerts, Michael; Jiang, Steve B
2011-01-01
Monte Carlo (MC) simulation is commonly considered to be the most accurate dose calculation method in radiotherapy. However, its efficiency still requires improvement for many routine clinical applications. In this paper, we present our recent progress towards the development a GPU-based MC dose calculation package, gDPM v2.0. It utilizes the parallel computation ability of a GPU to achieve high efficiency, while maintaining the same particle transport physics as in the original DPM code and hence the same level of simulation accuracy. In GPU computing, divergence of execution paths between threads can considerably reduce the efficiency. Since photons and electrons undergo different physics and hence attain different execution paths, we use a simulation scheme where photon transport and electron transport are separated to partially relieve the thread divergence issue. High performance random number generator and hardware linear interpolation are also utilized. We have also developed various components to hand...
Vojtyla, P
2005-01-01
The radiological impact of emissions of radioactive substances from accelerator facilities is characterized by a dominant contribution of the external exposure from short-lived radionuclides in the plume. Ventilation outlets of accelerator facilities are often at low emission heights and receptors reside very close to stacks. Simplified exposure models are not appropriate and integration of the dose kernel over the radioactive plume is required. By using Monte Carlo integration with certain biasing, the integrand can be simplified substantially and an optimum spatial resolution can be achieved. Moreover, long-term releases can be modeled by sampling real weather situations. The mathematical formulation does not depend on any particular atmospheric dispersion model and the applicable code parts can be designed separately, which is another advantage. The obtained results agree within ±10% with results calculated for the semi-infinite cloud model by using detailed particle transport codes and human phantoms.
Barapatre, Nirav; Symvoulidis, Panagiotis; Möller, Winfried; Prade, Friedrich; Deliolanis, Nikolaos C; Hertel, Sebastian; Winter, Gerhard; Yildirim, Ali Ö; Stoeger, Tobias; Eickelberg, Oliver; Ntziachristos, Vasilis; Schmid, Otmar
2015-01-01
Administration of drugs via inhalation is an attractive route for pulmonary and systemic drug delivery. The therapeutic outcome of inhalation therapy depends not only on the dose of the lung-delivered drug, but also on its bioactivity and regional distribution. Fluorescence imaging has the potential to monitor these aspects already during preclinical development of inhaled drugs, but quantitative methods of analysis are lacking. In this proof-of-concept study, we demonstrate that Cryoslicing Imaging allows for 3D quantitative fluorescence imaging on ex vivo murine lungs. Known amounts of fluorescent substance (nanoparticles or fluorophore-drug conjugate) were instilled in the lungs of mice. The excised lungs were measured by Cryoslicing Imaging. Herein, white light and fluorescence images are obtained from the face of a gradually sliced frozen organ block. A quantitative representation of the fluorescence intensity throughout the lung was inferred from the images by accounting for instrument noise, tissue autofluorescence and out-of-plane fluorescence. Importantly, the out-of-plane fluorescence correction is based on the experimentally determined effective light attenuation coefficient of frozen murine lung tissue (10.0 ± 0.6 cm(-1) at 716 nm). The linear correlation between pulmonary total fluorescence intensity and pulmonary fluorophore dose indicates the validity of this method and allows direct fluorophore dose assessment. The pulmonary dose of a fluorescence-labeled drug (FcγR-Alexa750) could be assessed with an estimated accuracy of 9% and the limit of detection in ng regime. Hence, Cryoslicing Imaging can be used for quantitative assessment of dose and 3D distribution of fluorescence-labeled drugs or drug carriers in the lungs of mice. PMID:25262414
Radiation doses from radiation sources of neutrons and photons by different computer calculation
International Nuclear Information System (INIS)
In the present paper the calculation technique aspects of dose rate from neutron and photon radiation sources are covered with reference both to the basic theoretical modeling of the MERCURE-4, XSDRNPM-S and MCNP-3A codes and from practical point of view performing safety analyses of irradiation risk of two transportation casks. The input data set of these calculations -regarding the CEN 10/200 HLW container and dry PWR spent fuel assemblies shipping cask- is frequently commented as for as connecting points of input data and understanding theoric background are concerned
Preliminary Calculations of Shutdown Dose Rate for the CTS Diagnostics System
DEFF Research Database (Denmark)
Klinkby, Esben Bryndt; Nonbøl, Erik; Lauritzen, Bent
2015-01-01
focus on supplying input which affect the system design. Examples include: - Heatloads on plasma facing mirrors and preliminary stress and thermal analysis - Port plug cooling requirements and it's dependence on system design (in particular blanket cut-out) - Shutdown dose-rate calculations (relative...... a direct and unshielded view to the plasma, the first mirror will be subject to significant radiation and among the first tasks in the CTS design, is to determine whether the mirror will need active cooling. At present the CTS is in the conceptual design phase and the related neutronics calculations...
Methodology for calculation of doses to man and implementation in Pandora
International Nuclear Information System (INIS)
This report describes methods and data for calculation of doses to man to be used in safety assessments of repositories for nuclear fuel. The methods are based on the latest recommendations from the ICRP; the EU and the national radiation protection authorities. Equations are given for calculation of doses from ingestion of contaminated water and food, inhalation of contaminated air and external exposure from radionuclides in the ground. With the exception of the exposure from food ingestion, the equations are the same used in previous safety assessments. A general equation is suggested for estimation of the exposure from food ingestion, in which the annual demand of carbon is used instead of the annual ingestion of different food-stuffs, which was earlier applied. The report contains tables with recommended values for physiological characteristics such as water intake, food intake and inhalation rates, based on information summarised in an Appendix. Furthermore, tables are given with recommended age dependent dose conversion factors for ingestion and inhalation for a number of nuclides of interest for safety assessments. The most recently published dose conversion factors for external exposure from contaminated ground are also given. An overview of the implementation of the methodology in Pandora, which is the tool that SKB and Posiva currently use for biosphere modelling, is also provided. The work presented in the report is a result from a joint project commissioned by SKB and Posiva
Methodology for calculation of doses to man and implementation in Pandora
Energy Technology Data Exchange (ETDEWEB)
Avila, Rodolfo [Facilia AB, Bromma (Sweden); Bergstroem, Ulla [Swepro Project Management AB, Solna (Sweden)
2006-07-15
This report describes methods and data for calculation of doses to man to be used in safety assessments of repositories for nuclear fuel. The methods are based on the latest recommendations from the ICRP; the EU and the national radiation protection authorities. Equations are given for calculation of doses from ingestion of contaminated water and food, inhalation of contaminated air and external exposure from radionuclides in the ground. With the exception of the exposure from food ingestion, the equations are the same used in previous safety assessments. A general equation is suggested for estimation of the exposure from food ingestion, in which the annual demand of carbon is used instead of the annual ingestion of different food-stuffs, which was earlier applied. The report contains tables with recommended values for physiological characteristics such as water intake, food intake and inhalation rates, based on information summarised in an Appendix. Furthermore, tables are given with recommended age dependent dose conversion factors for ingestion and inhalation for a number of nuclides of interest for safety assessments. The most recently published dose conversion factors for external exposure from contaminated ground are also given. An overview of the implementation of the methodology in Pandora, which is the tool that SKB and Posiva currently use for biosphere modelling, is also provided. The work presented in the report is a result from a joint project commissioned by SKB and Posiva.
International Nuclear Information System (INIS)
In its recent recommendations the ICRP adopted two voxel models of an adult male and an adult female to be used for the forthcoming update of organ dose conversion coefficients. These voxel models are representative of an average population, i.e. they resemble the ICRP reference anatomical data with respect to their external dimensions and their organ masses and were constructed for this purpose. They will be used as the standard human models for the computation of dose conversion coefficients in occupational protection as well as for the protection of the patient and the general public. Using these new models, conversion coefficients for environmental exposures were computed. Two source geometries were simulated, exposure from a radioactive cloud and from ground contamination, by taking into account the precise angular and energy distributions of the gamma rays. The organ dose conversion coefficients were calculated using the Monte Carlo code EGSnrc simulating the photon transport in the voxel models. Furthermore, new nuclear decay data have been released by the ICRP. These have been used in order to calculate dose equivalent rates for photon exposures of several radionuclides for the above environmental exposures. (author)
Ulmer, W.; Schaffner, B.
2011-03-01
We have developed a model for proton depth dose and lateral distributions based on Monte Carlo calculations (GEANT4) and an integration procedure of Bethe-Bloch equation (BBE). The model accounts for the transport of primary and secondary protons, the creation of recoil protons and heavy recoil nuclei as well as lateral scattering of these contributions. The buildup, which is experimentally observed in higher energy depth dose curves, is modeled by an inclusion of two different origins: (1) secondary reaction protons with a contribution of ca. 65% of the buildup (for monoenergetic protons). (2) Landau tails as well as Gaussian type of fluctuations for range straggling effects. All parameters of the model for initially monoenergetic proton beams have been obtained from Monte Carlo calculations or checked by them. Furthermore, there are a few parameters, which can be obtained by fitting the model to the measured depth dose curves in order to describe individual characteristics of the beamline—the most important being the initial energy spread. We find that the free parameters of the depth dose model can be predicted for any intermediate energy from a couple of measured curves.
Fast CPU-based Monte Carlo simulation for radiotherapy dose calculation
Ziegenhein, Peter; Pirner, Sven; Kamerling, Cornelis Ph; Oelfke, Uwe
2015-08-01
Monte-Carlo (MC) simulations are considered to be the most accurate method for calculating dose distributions in radiotherapy. Its clinical application, however, still is limited by the long runtimes conventional implementations of MC algorithms require to deliver sufficiently accurate results on high resolution imaging data. In order to overcome this obstacle we developed the software-package PhiMC, which is capable of computing precise dose distributions in a sub-minute time-frame by leveraging the potential of modern many- and multi-core CPU-based computers. PhiMC is based on the well verified dose planning method (DPM). We could demonstrate that PhiMC delivers dose distributions which are in excellent agreement to DPM. The multi-core implementation of PhiMC scales well between different computer architectures and achieves a speed-up of up to 37× compared to the original DPM code executed on a modern system. Furthermore, we could show that our CPU-based implementation on a modern workstation is between 1.25× and 1.95× faster than a well-known GPU implementation of the same simulation method on a NVIDIA Tesla C2050. Since CPUs work on several hundreds of GB RAM the typical GPU memory limitation does not apply for our implementation and high resolution clinical plans can be calculated.
Effects of the difference in tube voltage of the CT scanner on dose calculation
Rhee, Dong Joo; Kim, Sung-Woo; Moon, Young Min; Kim, Jung Ki; Jeong, Dong Hyeok
2015-01-01
Computed Tomography (CT) measures the attenuation coefficient of an object and converts the value assigned to each voxel into a CT number. In radiation therapy, CT number, which is directly proportional to the linear attenuation coefficient, is required to be converted to electron density for radiation dose calculation for cancer treatment. However, if various tube voltages were applied to take the patient CT image without applying the specific CT number to electron density conversion curve, ...
Analyse of the international recommendations on the calculation of absorbed dose in the biota
International Nuclear Information System (INIS)
This paper evaluates the recommendations of ICRP which has as objective the environmental radioprotection. It was analysed the recommendations 26, 60, 91, 103 and 108 of the ICRP. The ICRP-103 defined the concept of animal and plant of reference (APR) to be used in the RAP based on the calculation of absorbed dose based on APR concept. This last view allows to build a legal framework of environmental protection with a etic, moral and scientific visualization, more defensible than the anthropomorphic concept
International Nuclear Information System (INIS)
Because of superior soft tissue contrast, the use of magnetic resonance imaging (MRI) as a complement to computed tomography (CT) in the target definition procedure for radiotherapy is increasing. To keep the workflow simple and cost effective and to reduce patient dose, it is natural to strive for a treatment planning procedure based entirely on MRI. In the present study, we investigate the dose calculation accuracy for different treatment regions when using bulk density assignments on MRI data and compare it to treatment planning that uses CT data. MR and CT data were collected retrospectively for 40 patients with prostate, lung, head and neck, or brain cancers. Comparisons were made between calculations on CT data with and without inhomogeneity corrections and on MRI or CT data with bulk density assignments. The bulk densities were assigned using manual segmentation of tissue, bone, lung, and air cavities. The deviations between calculations on CT data with inhomogeneity correction and on bulk density assigned MR data were small. The maximum difference in the number of monitor units required to reach the prescribed dose was 1.6%. This result also includes effects of possible geometrical distortions. The dose calculation accuracy at the investigated treatment sites is not significantly compromised when using MRI data when adequate bulk density assignments are made. With respect to treatment planning, MRI can replace CT in all steps of the treatment workflow, reducing the radiation exposure to the patient, removing any systematic registration errors that may occur when combining MR and CT, and decreasing time and cost for the extra CT investigation
Specific absorbed fractions and S-factors for calculating absorbed dose to embryo and fetus
International Nuclear Information System (INIS)
The variation of specific absorbed fractions from maternal tissues to embryo/fetus is investigated for four different target masses and geometries. S-factors are calculated for selected radionuclides assumed to be distributed uniformly in fetal tissues represented by spheres from 1 mg to 4 kg. As an example, the dose to fetal tissues for iodine-131 and iron-59 is estimated based on human biokinetic data for various stages of pregnancy. 24 references, 4 tables
International Nuclear Information System (INIS)
Purpose: Brachytherapy is a standard option of care for prostate cancer patients but may be improved by dynamic dose calculation based on localized seed positions. The American Brachytherapy Society states that the major current limitation of intraoperative treatment planning is the inability to localize the seeds in relation to the prostate. An image-guidance system was therefore developed to localize seeds for dynamic dose calculation. Methods: The proposed system is based on transrectal ultrasound (TRUS) and mobile C-arm fluoroscopy, while using a simple fiducial with seed-like markers to compute pose from the nonencoded C-arm. Three or more fluoroscopic images and an ultrasound volume are acquired and processed by a pipeline of algorithms: (1) seed segmentation, (2) fiducial detection with pose estimation, (3) seed matching with reconstruction, and (4) fluoroscopy-to-TRUS registration. Results: The system was evaluated on ten phantom cases, resulting in an overall mean error of 1.3 mm. The system was also tested on 37 patients and each algorithm was evaluated. Seed segmentation resulted in a 1% false negative rate and 2% false positive rate. Fiducial detection with pose estimation resulted in a 98% detection rate. Seed matching with reconstruction had a mean error of 0.4 mm. Fluoroscopy-to-TRUS registration had a mean error of 1.3 mm. Moreover, a comparison of dose calculations between the authors’ intraoperative method and an independent postoperative method shows a small difference of 7% and 2% forD90 and V100, respectively. Finally, the system demonstrated the ability to detect cold spots and required a total processing time of approximately 1 min. Conclusions: The proposed image-guidance system is the first practical approach to dynamic dose calculation, outperforming earlier solutions in terms of robustness, ease of use, and functional completeness
Calculating N fertilizer doses for oil-seed rape using plant and soil data
MAKOWSKI, DAVID; Maltas, Alexandra; Morison, Muriel; Reau, Raymond
2005-01-01
International audience We evaluated the economic and environmental interests of a balance-sheet method recently developed for calculating N fertilizer doses for oil-seed rape. The evaluation was performed using simple models of yield, grain oil content, and residual soil mineral nitrogen responses to applied N. The models were fitted to 53 fertilizer trials carried out in France between 1993 and 1999. The results show that the use of the balance-sheet method decreases the variability of fa...
G-dose and range: user friendly modules for dosimetry, shielding and range calculations
International Nuclear Information System (INIS)
An interactive multimedia tool, Nuclides.net, has been developed at the Institute for Transuranium Elements. The product is aimed at both students and professionals for reference data on radionuclides and computations based on internationally evaluated data. Based on the latest Internet technology Nuclides.net is ideally suited for education and training purposes in the nuclear related fields, such as radiation protection. Professionals can do calculations quickly and reliably using qualified radionuclide data. The Nuclides.net 'integrated environment' is a suite of computer programs ranging from a powerful user-friendly interface, which allows the user to navigate the nuclides chart and explore the properties of nuclides, to various computational modules. Among them, the G- D.O.S.E. dosimetry and shielding module allows the user to calculate gamma dose rates from point sources of single nuclide and mixtures. The user can alternatively obtain a dose rate through a given shield material and thickness, or a shield thickness of material required to obtain a given dose. More than 3000 nuclides are available in the Nuclides.net database for dosimetry calculation. In addition, the user has a choice of 10 shield materials. A results details window shows the contribution of each gamma-line or x-ray to the total dose rate, detailing the calculation of the mass absorption of the absorption coefficient, the interpolation of the build-up factors from the tabulated N.I.S.T. values and the calculation mass absorption coefficients. In its future new edition, to be released by mid-2006, a R.A.N.G.E. module, based on the S.R.I.M. engine (see. www.SRIM.org), has been added. Through an intuitive interface, the user can perform range and stopping powers of charge particles - electrons, protons, or any ions - in matter. The user can used predefined target or create his owns to fit best his needs. This module complements perfectly the R.A.N.G.E. module for radioprotection calculations
E. Konoz; Amir H. M. Sarrafi; Ardalani, S.
2011-01-01
Parallel artificial membrane permeation assays (PAMPA) have been extensively utilized to determine the drug permeation potentials. In the present work, the permeation of miscellaneous drugs measured as flux by PAMPA (logF) of 94 drugs, are predicted by quantitative structure property relationships modeling based on a variety of calculated theoretical descriptors, which screened and selected by genetic algorithm (GA) variable subset selection procedure. These descriptors were used as inputs fo...
Evaluation of on-board kV cone beam CT (CBCT)-based dose calculation
Yang, Yong; Schreibmann, Eduard; Li, Tianfang; Wang, Chuang; Xing, Lei
2007-02-01
On-board CBCT images are used to generate patient geometric models to assist patient setup. The image data can also, potentially, be used for dose reconstruction in combination with the fluence maps from treatment plan. Here we evaluate the achievable accuracy in using a kV CBCT for dose calculation. Relative electron density as a function of HU was obtained for both planning CT (pCT) and CBCT using a Catphan-600 calibration phantom. The CBCT calibration stability was monitored weekly for 8 consecutive weeks. A clinical treatment planning system was employed for pCT- and CBCT-based dose calculations and subsequent comparisons. Phantom and patient studies were carried out. In the former study, both Catphan-600 and pelvic phantoms were employed to evaluate the dosimetric performance of the full-fan and half-fan scanning modes. To evaluate the dosimetric influence of motion artefacts commonly seen in CBCT images, the Catphan-600 phantom was scanned with and without cyclic motion using the pCT and CBCT scanners. The doses computed based on the four sets of CT images (pCT and CBCT with/without motion) were compared quantitatively. The patient studies included a lung case and three prostate cases. The lung case was employed to further assess the adverse effect of intra-scan organ motion. Unlike the phantom study, the pCT of a patient is generally acquired at the time of simulation and the anatomy may be different from that of CBCT acquired at the time of treatment delivery because of organ deformation. To tackle the problem, we introduced a set of modified CBCT images (mCBCT) for each patient, which possesses the geometric information of the CBCT but the electronic density distribution mapped from the pCT with the help of a BSpline deformable image registration software. In the patient study, the dose computed with the mCBCT was used as a surrogate of the 'ground truth'. We found that the CBCT electron density calibration curve differs moderately from that of pCT. No
Tian, Zhen; Folkerts, Michael; Shi, Feng; Jiang, Steve B; Jia, Xun
2015-01-01
Monte Carlo (MC) simulation is considered as the most accurate method for radiation dose calculations. Accuracy of a source model for a linear accelerator is critical for the overall dose calculation accuracy. In this paper, we presented an analytical source model that we recently developed for GPU-based MC dose calculations. A key concept called phase-space-ring (PSR) was proposed. It contained a group of particles that are of the same type and close in energy and radial distance to the center of the phase-space plane. The model parameterized probability densities of particle location, direction and energy for each primary photon PSR, scattered photon PSR and electron PSR. For a primary photon PSRs, the particle direction is assumed to be from the beam spot. A finite spot size is modeled with a 2D Gaussian distribution. For a scattered photon PSR, multiple Gaussian components were used to model the particle direction. The direction distribution of an electron PSRs was also modeled as a 2D Gaussian distributi...
GPU-based ultra fast dose calculation using a finite pencil beam model
Gu, Xuejun; Men, Chunhua; Pan, Hubert; Majumdar, Amitava; Jiang, Steve B
2009-01-01
Online adaptive radiation therapy (ART) is an attractive concept that promises the ability to deliver an optimal treatment in response to the inter-fraction variability in patient anatomy. However, it has yet to be realized due to technical limitations. Fast dose deposit coefficient calculation is a critical component of the online planning process that is required for plan optimization of intensity modulated radiation therapy (IMRT). Computer graphics processing units (GPUs) are well-suited to provide the requisite fast performance for the data-parallel nature of dose calculation. In this work, we develop a dose calculation engine based on a finite-size pencil beam (FSPB) algorithm and a GPU parallel computing framework. The developed framework can accommodate any FSPB model. We test our implementation on a case of a water phantom and a case of a prostate cancer patient with varying beamlet and voxel sizes. All testing scenarios achieved speedup ranging from 200~400 times when using a NVIDIA Tesla C1060 card...
Production and Application of the Dose Calculation Program which used MS EXCEL and Bit System
International Nuclear Information System (INIS)
The medical diagnostic examination using ionizing radiation has improved the patients' life and brought revolution in medical examination along with the mechanical development. However, the development of medical imaging systems has also been the reason to increase the patients' exposure for ionizing radiation. ICRP recommends that each country adopts diagnostic reference levels depending on regional and national situations. The Korea Food and Drug Administration suggested the dosimetry measurement guideline for patients in 2007. Nonetheless, in reality, it is hard to know the skin dose of the patients when applying a x-ray since there is no radiation dosimeter in most of clinical situation. Therefore, this study sets a program based on the bit system to figure out easily the skin dose of a patients using MS Excel program in the PC setting. The results showed 10% better outcome.
Energy Technology Data Exchange (ETDEWEB)
Heinzelman, K M; Mansfield, W G
2010-04-27
This document evaluates the expected radiation dose due to the consumption of several specific food classes (dairy, meat, produce, etc.) contaminated with specific radionuclides, and relates concentration levels in food to the detection abilities of typical aboratory analysis/measurement methods. The attached charts present the limiting organ dose as a function of the radionuclide concentration in a particular food class, and allow the user to compare these concentrations and doses to typical analytical detection apabilities. The expected radiation dose depends on several factors: the age of the individual; the radionuclide present in the food; the concentration of the radionuclide in the food; and the amount of food consumed. Food consumption rates for individuals of various ges were taken from the 1998 United States Food and Drug Administration (FDA) document, Accidental Radioactive Contamination of HUman Food and Animal Feeds: Recommendations for State and Local Agencies. In that document, the FDA defines the erived Intervention Level (DIL), which is the concentration of a particular radionuclide in food that if consumed could result in an individual receiving a radiation dose exceeding the Protection Action Guide (PAG) thresholds for intervention. This document also resents odified, food class specific DIL, which is calculated using a somewhat modified version of the FDA's procedure. This document begins with an overview of the FDA's DIL calculation, followed by a description of the food class specific DIL calculations, and finally charts of the radiation dose per radioactivity concentration for several food class/radionuclide combinations.
International Nuclear Information System (INIS)
A new method for estimating radiation doses to UK critical groups is proposed for discussion. Amongst others, the Food Standards Agency (FSA) and the Scottish Environment Protection Agency (SEPA) undertake surveillance of UK food and the environment as a check on the effect of discharges of radioactive wastes. Discharges in gaseous and liquid form are made under authorisation by the Environment Agency and SEPA under powers in the Radioactive Substance Act. Results of surveillance by the FSA and SEPA are published in the Radioactivity in Food and the Environment (RIFE) report series. In these reports, doses to critical groups are normally estimated separately for gaseous and liquid discharge pathways. Simple summation of these doses would tend to overestimate doses actually received. Three different methods of combining the effects of both types of discharge in an integrated assessment are considered and ranked according to their ease of application, transparency, scientific rigour and presentational issues. A single integrated assessment method is then chosen for further study. Doses are calculated for surveillance data for the calendar year 2000 and compared with those from the existing RIFE method
Dose distribution calculation for in-vivo X-ray fluorescence scanning
International Nuclear Information System (INIS)
In-vivo X-ray fluorescence constitutes a useful and accurate technique, worldwide established for constituent elementary distribution assessment. Actually, concentration distributions of arbitrary user-selected elements can be achieved along sample surface with the aim of identifying and simultaneously quantifying every constituent element. The method is based on the use of a collimated X-ray beam reaching the sample. However, one common drawback for considering the application of this technique for routine clinical examinations was the lack of information about associated dose delivery. This work presents a complete study of the dose distribution resulting from an in-vivo X-ray fluorescence scanning for quantifying biohazard materials on human hands. Absorbed dose has been estimated by means of dosimetric models specifically developed to this aim. In addition, complete dose distributions have been obtained by means of full radiation transport calculations in based on stochastic Monte Carlo techniques. A dedicated subroutine has been developed using the Penelope 2008 main code also integrated with dedicated programs -Mat Lab supported- for 3 dimensional dose distribution visualization. The obtained results show very good agreement between approximate analytical models and full descriptions by means of Monte Carlo simulations. (Author)
Dose distribution calculation for in-vivo X-ray fluorescence scanning
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Figueroa, R. G. [Universidad de la Frontera, Departamento de Ciencias Fisicas, Av. Francisco Salazar 1145, Temuco 4811230, Araucania (Chile); Lozano, E. [Instituto Nacional del Cancer, Unidad de Fisica Medica, Av. Profesor Zanartu 1010, Santiago (Chile); Valente, M., E-mail: figueror@ufro.cl [Consejo Nacional de Investigaciones Cientificas y Tecnicas, Av. Ravadavia 1917, C1033AAJ, Buenos Aires (Argentina)
2013-08-01
In-vivo X-ray fluorescence constitutes a useful and accurate technique, worldwide established for constituent elementary distribution assessment. Actually, concentration distributions of arbitrary user-selected elements can be achieved along sample surface with the aim of identifying and simultaneously quantifying every constituent element. The method is based on the use of a collimated X-ray beam reaching the sample. However, one common drawback for considering the application of this technique for routine clinical examinations was the lack of information about associated dose delivery. This work presents a complete study of the dose distribution resulting from an in-vivo X-ray fluorescence scanning for quantifying biohazard materials on human hands. Absorbed dose has been estimated by means of dosimetric models specifically developed to this aim. In addition, complete dose distributions have been obtained by means of full radiation transport calculations in based on stochastic Monte Carlo techniques. A dedicated subroutine has been developed using the Penelope 2008 main code also integrated with dedicated programs -Mat Lab supported- for 3 dimensional dose distribution visualization. The obtained results show very good agreement between approximate analytical models and full descriptions by means of Monte Carlo simulations. (Author)
Calculation of multi-dimensional dose distribution in medium due to proton beam incidence
International Nuclear Information System (INIS)
The method of analyzing the multi-dimensional dose distribution in a medium due to proton beam incidence is presented to obtain the reliable and simplified method from clinical viewpoint, especially for the medical treatment of cancer. The heavy ion beam being taken out of an accelerator has to be adjusted to fit cancer location and size, utilizing a modified range modulator, a ridge filter, a bolus and a special scanning apparatus. The precise calculation of multi-dimensional dose distribution of proton beam is needed to fit treatment to a limit part. The analytical formulas consist of those for the fluence distribution in a medium, the divergence of flying range, the energy distribution itself, the dose distribution in side direction and the two-dimensional dose distribution. The fluence distribution in polystyrene in case of the protons with incident energy of 40 and 60 MeV, the energy distribution of protons at the position of a Bragg peak for various values of incident energy, the depth dose distribution in polystyrene in case of the protons with incident energy of 40 and 60 MeV and average energy of 100 MeV, the proton fluence and dose distribution as functions of depth for the incident average energy of 250 MeV, the statistically estimated percentage errors in the proton fluence and dose distribution, the estimated minimum detectable tumor thickness as a function of the number of incident protons for the different incident spectra with average energy of 250 MeV, the isodose distribution in a plane containing the central axis in case of the incident proton beam of 3 mm diameter and 40 MeV and so on are presented as the analytical results, and they are evaluated. (Nakai, Y.)
An algorithm for the calculation of dose distributions from dynamic wedges
International Nuclear Information System (INIS)
The Clinac 2100C of Varian has the option of a dynamic wedge. The control of the dynamic wedge is done by means of a segmentation table, which specifies a number of asymmetric fields with corresponding numbers of monitor units. Advantages of this dynamic wedge are the possibility to have more wedge angles and an increased flexibility of operation; a disadvantage is that the measurement of the data needed for a planning system may be time consuming. For the calculation of the dose distribution, we have developed an algorithm which eradicates this disadvantage because it only uses measured data from square fields of the open beam: central axis depth-doses, profiles and Peak Scatter Factors. It is based on a previously developed method which separates the dose into three factors: depth-dose, boundary distribution and envelope profile, and computes the dose of irregular field as well. Depth-dose and boundary distribution are computed by convolution of a field intensity with 'scatter' and 'boundary' pencil beam kernels respectively. For a rectangular field, the field intensity is computed by a weighted sum of intensity matrices, derived from the segmentation table. The matrix elements are equal to 1 within the asymmetric fields and equal to an effective transmission factor under the jaws. The weighting factors in the sum take into account the number of monitor units and the collimator scatter back to the monitor. For an irregular field, the blocked parts of the field are modified, taking into account the transmission through the blocks. This algorithm has been implemented in CADPLAN (Varian-Dosetek) and has been compared with measurements. The results are in good agreement with the international requirements on dose accuracy
International Nuclear Information System (INIS)
Purpose: To retrospectively re-calculate dose distributions for selected head and neck cancer patients, earlier treated with HDR 192Ir brachytherapy, using Monte Carlo (MC) simulations and compare results to distributions from the planning system derived using TG43 formalism. To study differences between dose to medium (as obtained with the MC code) and dose to water in medium as obtained through (1) ratios of stopping powers and (2) ratios of mass energy absorption coefficients between water and medium. Methods: The MC code Algebra was used to calculate dose distributions according to earlier actual treatment plans using anonymized plan data and CT images in DICOM format. Ratios of stopping power and mass energy absorption coefficients for water with various media obtained from 192-Ir spectra were used in toggling between dose to water and dose to media. Results: Differences between initial planned TG43 dose distributions and the doses to media calculated by MC are insignificant in the target volume. Differences are moderate (within 4–5 % at distances of 3–4 cm) but increase with distance and are most notable in bone and at the patient surface. Differences between dose to water and dose to medium are within 1-2% when using mass energy absorption coefficients to toggle between the two quantities but increase to above 10% for bone using stopping power ratios. Conclusion: MC predicts target doses for head and neck cancer patients in close agreement with TG43. MC yields improved dose estimations outside the target where a larger fraction of dose is from scattered photons. It is important with awareness and a clear reporting of absorbed dose values in using model based algorithms. Differences in bone media can exceed 10% depending on how dose to water in medium is defined
Energy Technology Data Exchange (ETDEWEB)
Carlsson Tedgren, A [Linkoping University, Linkoping, Linkoping (Sweden); Persson, M; Nilsson, J [Karolinska hospital, Stockholm, Stockholm (Sweden)
2014-06-15
Purpose: To retrospectively re-calculate dose distributions for selected head and neck cancer patients, earlier treated with HDR 192Ir brachytherapy, using Monte Carlo (MC) simulations and compare results to distributions from the planning system derived using TG43 formalism. To study differences between dose to medium (as obtained with the MC code) and dose to water in medium as obtained through (1) ratios of stopping powers and (2) ratios of mass energy absorption coefficients between water and medium. Methods: The MC code Algebra was used to calculate dose distributions according to earlier actual treatment plans using anonymized plan data and CT images in DICOM format. Ratios of stopping power and mass energy absorption coefficients for water with various media obtained from 192-Ir spectra were used in toggling between dose to water and dose to media. Results: Differences between initial planned TG43 dose distributions and the doses to media calculated by MC are insignificant in the target volume. Differences are moderate (within 4–5 % at distances of 3–4 cm) but increase with distance and are most notable in bone and at the patient surface. Differences between dose to water and dose to medium are within 1-2% when using mass energy absorption coefficients to toggle between the two quantities but increase to above 10% for bone using stopping power ratios. Conclusion: MC predicts target doses for head and neck cancer patients in close agreement with TG43. MC yields improved dose estimations outside the target where a larger fraction of dose is from scattered photons. It is important with awareness and a clear reporting of absorbed dose values in using model based algorithms. Differences in bone media can exceed 10% depending on how dose to water in medium is defined.
DeSilva, Mary Bachman; Hamer, Davidson H.; Keyi, Xu; Wilson, Ira B.; Sabin, Lora
2016-01-01
Adherence to antiretroviral medications is usually expressed in terms of the proportion of doses taken. However, the timing of doses taken may also be an important dimension to overall adherence. Little is known about whether patients who mistime doses are also more likely to skip doses. Using data from the completed Adherence for Life randomized controlled trial, we created visual and statistical models to capture and analyze dose timing data collected longitudinally with electronic drug monitors (EDM). From scatter plots depicting dose time versus calendar date, we identified dominant patterns of dose taking and calculated key features [slope of line over calendar date; residual mean standard error (RMSE)]. Each was assessed for its ability to categorize subjects with ‘suboptimal’ (EDM data, with ~300 to 400 observations/subject. While regression line slopes did not predict ‘sub-optimal’ adherence (AROC 0.51, 95 % CI 0.26–0.75), the variability in dose timing (RMSE) was strongly predictive (AROC 0.79, 95 % CI 0.62–0.97). Compared with the lowest quartile of RMSE (minimal dose time variability), each successive quartile roughly doubled the odds of ‘sub-optimal’ adherence (OR 2.1, 95 % CI 1.3–3.4). Patterns of dose timing and mistiming are strongly related to overall adherence behavior. Notably, individuals who skip doses are more likely to mistime doses, with the degree of risk positively correlated with the extent of dose timing variability. PMID:25893658
Gill, Christopher J; DeSilva, Mary Bachman; Hamer, Davidson H; Keyi, Xu; Wilson, Ira B; Sabin, Lora
2015-11-01
Adherence to antiretroviral medications is usually expressed in terms of the proportion of doses taken. However, the timing of doses taken may also be an important dimension to overall adherence. Little is known about whether patients who mistime doses are also more likely to skip doses. Using data from the completed Adherence for Life randomized controlled trial, we created visual and statistical models to capture and analyze dose timing data collected longitudinally with electronic drug monitors (EDM). From scatter plots depicting dose time versus calendar date, we identified dominant patterns of dose taking and calculated key features [slope of line over calendar date; residual mean standard error (RMSE)]. Each was assessed for its ability to categorize subjects with 'sub-optimal' (EDM data, with ~300 to 400 observations/subject. While regression line slopes did not predict 'sub-optimal' adherence (AROC 0.51, 95 % CI 0.26-0.75), the variability in dose timing (RMSE) was strongly predictive (AROC 0.79, 95 % CI 0.62-0.97). Compared with the lowest quartile of RMSE (minimal dose time variability), each successive quartile roughly doubled the odds of 'sub-optimal' adherence (OR 2.1, 95 % CI 1.3-3.4). Patterns of dose timing and mistiming are strongly related to overall adherence behavior. Notably, individuals who skip doses are more likely to mistime doses, with the degree of risk positively correlated with the extent of dose timing variability. PMID:25893658
International Nuclear Information System (INIS)
The Human Respiratory Tract Model proposed by the ICRP Publication 66 accounts for the morphology and physiology of the respiratory tract. The ICRP 66 presents deposition fraction in the respiratory tract regions considering reference values from Caucasian man. However, in order to obtain a more accurate assessment of intake and dose the ICRP recommends the use of specific information when they are available. The application of parameters from Brazilian population in the deposition and in the clearance model shows significant variations in the deposition fractions and in the fraction of inhaled activity transferred to blood. The main objective of this study is to evaluate the influence in dose calculation to each region of the respiratory tract when physiological parameters from Brazilian population are applied in the model. The purpose of the dosimetric model is to evaluate dose to each tissues of respiratory tract that are potentially risk from inhaled radioactive materials. The committed equivalent dose, H.T., is calculated by the product of the total number of transformations of the radionuclide in tissue source S over a period of fifty years after incorporation and of the energy absorbed per unit mass in the target tissue T, for each radiation emitted per transformation in tissue source S. The dosimetric model of Human Respirator y Tract was implemented in the software Excel for Windows (version 2000) and H.T. was determined in two stages. First it was calculated the number of total transformations, US, considering the fractional deposition of activity in each source tissue and then it was calculated the total energy absorbed per unit mass S.E.E., in the target tissue. It was assumed that the radionuclide emits an alpha particle with average energy of 5.15 MeV. The variation in the fractional deposition in the compartments of the respiratory tract in changing the physiological parameters from Caucasian to Brazilian adult man causes variation in the number of
Energy Technology Data Exchange (ETDEWEB)
Strange, D. L.; Bander, T. J.
1981-04-01
The MILDOS Computer Code estimates impacts from radioactive emissions from uranium milling facilities. These impacts are presented as dose commitments to individuals and the regional population within an 80 km radius of the facility. Only airborne releases of radioactive materials are considered: releases to surface water and to groundwater are not addressed in MILDOS. This code is multi-purposed and can be used to evaluate population doses for NEPA assessments, maximum individual doses for predictive 40 CFR 190 compliance evaluations, or maximum offsite air concentrations for predictive evaluations of 10 CFR 20 compliance. Emissions of radioactive materials from fixed point source locations and from area sources are modeled using a sector-averaged Gaussian plume dispersion model, which utilizes user-provided wind frequency data. Mechanisms such as deposition of particulates, resuspension. radioactive decay and ingrowth of daughter radionuclides are included in the transport model. Annual average air concentrations are computed, from which subsequent impacts to humans through various pathways are computed. Ground surface concentrations are estimated from deposition buildup and ingrowth of radioactive daughters. The surface concentrations are modified by radioactive decay, weathering and other environmental processes. The MILDOS Computer Code allows the user to vary the emission sources as a step function of time by adjustinq the emission rates. which includes shutting them off completely. Thus the results of a computer run can be made to reflect changing processes throughout the facility's operational lifetime. The pathways considered for individual dose commitments and for population impacts are: • Inhalation • External exposure from ground concentrations • External exposure from cloud immersion • Ingestioo of vegetables • Ingestion of meat • Ingestion of milk • Dose commitments are calculated using dose conversion factors, which are ultimately based
SU-F-19A-01: APBI Brachytherapy Treatment Planning: The Impact of Heterogeneous Dose Calculations
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Purpose: To quantify the difference in dose to PTV-EVAL and OARs (skin and rib) as calculated by (TG43) and heterogeneous calculations (CCC). Methods: 25 patient plans (5 Contura and 20 SAVI) were selected for analysis. Clinical dose distributions were computed with a commercially available treatment planning algorithm (TG43-D-(w,w)) and then recomputed with a pre-clinical collapsed cone convolution algorithm (CCCD-( m,m)). PTV-EVAL coverage (V90%, V95%), and rib and skin maximum dose were compared via percent difference. Differences in dose to normal tissue (V150cc, V200cc of PTV-EVAL) were also compared. Changes in coverage and maximum dose to organs at risk are reported in percent change, (100*(TG43 − CCC) / TG43)), and changes in maximum dose to normal tissue are absolute change in cc (TG43 − CCC). Results: Mean differences in V90, V95, V150, and V200 for the SAVI cases were −0.2%, −0.4%, −0.03cc, and −0.14cc, respectively, with maximum differences of −0.78%, −1.7%, 1.28cc, and 1.01cc, respectively. Mean differences in the 0.1cc dose to the rib and skin were −1.4% and −0.22%, respectively, with maximum differences of −4.5% and 16%, respectively. Mean differences in V90, V95, V150, and V200 for the Contura cases were −1.2%, −2.1%, −1.8cc, and −0.59cc, respectively, with maximum differences of −2.0%, −3.16%, −2.9cc, and −0.76cc, respectively. Mean differences in the 0.1cc dose to the rib and skin were −2.6% and −3.9%, respectively, with maximum differences of −3.2% and −5.7%, respectively. Conclusion: The effects of translating clinical knowledge based on D-(w,w) to plans reported in D-(m,m) are minimal (2% or less) on average, but vary based on the type and placement of the device, source, and heterogeneity information
Dual-energy CT-based material extraction for tissue segmentation in Monte Carlo dose calculations
Bazalova, Magdalena; Carrier, Jean-François; Beaulieu, Luc; Verhaegen, Frank
2008-05-01
Monte Carlo (MC) dose calculations are performed on patient geometries derived from computed tomography (CT) images. For most available MC codes, the Hounsfield units (HU) in each voxel of a CT image have to be converted into mass density (ρ) and material type. This is typically done with a (HU; ρ) calibration curve which may lead to mis-assignment of media. In this work, an improved material segmentation using dual-energy CT-based material extraction is presented. For this purpose, the differences in extracted effective atomic numbers Z and the relative electron densities ρe of each voxel are used. Dual-energy CT material extraction based on parametrization of the linear attenuation coefficient for 17 tissue-equivalent inserts inside a solid water phantom was done. Scans of the phantom were acquired at 100 kVp and 140 kVp from which Z and ρe values of each insert were derived. The mean errors on Z and ρe extraction were 2.8% and 1.8%, respectively. Phantom dose calculations were performed for 250 kVp and 18 MV photon beams and an 18 MeV electron beam in the EGSnrc/DOSXYZnrc code. Two material assignments were used: the conventional (HU; ρ) and the novel (HU; ρ, Z) dual-energy CT tissue segmentation. The dose calculation errors using the conventional tissue segmentation were as high as 17% in a mis-assigned soft bone tissue-equivalent material for the 250 kVp photon beam. Similarly, the errors for the 18 MeV electron beam and the 18 MV photon beam were up to 6% and 3% in some mis-assigned media. The assignment of all tissue-equivalent inserts was accurate using the novel dual-energy CT material assignment. As a result, the dose calculation errors were below 1% in all beam arrangements. Comparable improvement in dose calculation accuracy is expected for human tissues. The dual-energy tissue segmentation offers a significantly higher accuracy compared to the conventional single-energy segmentation.
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By the help of a Monte-Carlo program the dose that single organs, organ groups and bigger or smaller parts of body would receive on an average, caused by an irradiation definitely fixed by the geometry of irradiation and photon energy, can be determined. Thus the phantom in connection with the Monte-Carlo program can be used for several considerations as for example - calculation of dose from occupational exposures - calculation of dose from diagnostic procedures - calculation of dose from radiotherapy procedures. (orig.)
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Estimating uncertainties on doses from bioassay data is of interest in epidemiology studies that estimate cancer risk from occupational exposures to radionuclides. Bayesian methods provide a logical framework to calculate these uncertainties. However, occupational exposures often consist of many intakes, and this can make the Bayesian calculation computationally intractable. This paper describes a novel strategy for increasing the computational speed of the calculation by simplifying the intake pattern to a single composite intake, termed as complex intake regime (CIR). In order to assess whether this approximation is accurate and fast enough for practical purposes, the method is implemented by the Weighted Likelihood Monte Carlo Sampling (WeLMoS) method and evaluated by comparing its performance with a Markov Chain Monte Carlo (MCMC) method. The MCMC method gives the full solution (all intakes are independent), but is very computationally intensive to apply routinely. Posterior distributions of model parameter values, intakes and doses are calculated for a representative sample of plutonium workers from the United Kingdom Atomic Energy cohort using the WeLMoS method with the CIR and the MCMC method. The distributions are in good agreement: posterior means and Q 0.025 and Q 0.975 quantiles are typically within 20 %. Furthermore, the WeLMoS method using the CIR converges quickly: a typical case history takes around 10-20 min on a fast workstation, whereas the MCMC method took around 12-hr. The advantages and disadvantages of the method are discussed. (authors)
Application of Monte Carlo method for dose calculation in thyroid follicle
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The Monte Carlo method is an important tool to simulate radioactive particles interaction with biologic medium. The principal advantage of the method when compared with deterministic methods is the ability to simulate a complex geometry. Several computational codes use the Monte Carlo method to simulate the particles transport and they have the capacity to simulate energy deposition in models of organs and/or tissues, as well models of cells of human body. Thus, the calculation of the absorbed dose to thyroid's follicles (compound of colloid and follicles' cells) have a fundamental importance to dosimetry, because these cells are radiosensitive due to ionizing radiation exposition, in particular, exposition due to radioisotopes of iodine, because a great amount of radioiodine may be released into the environment in case of a nuclear accidents. In this case, the goal of this work was use the code of particles transport MNCP4C to calculate absorbed doses in models of thyroid's follicles, for Auger electrons, internal conversion electrons and beta particles, by iodine-131 and short-lived iodines (131, 132, 133, 134 e 135), with diameters varying from 30 to 500 μm. The results obtained from simulation with the MCNP4C code shown an average percentage of the 25% of total absorbed dose by colloid to iodine- 131 and 75% to short-lived iodine's. For follicular cells, this percentage was of 13% to iodine-131 and 87% to short-lived iodine's. The contributions from particles with low energies, like Auger and internal conversion electrons should not be neglected, to assessment the absorbed dose in cellular level. Agglomerative hierarchical clustering was used to compare doses obtained by codes MCNP4C, EPOTRAN, EGS4 and by deterministic methods. (author)
Estimated Visualization of Dose Calculation with GEANT4 in Medical Linac
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Geant4 is a toolkit used to simulate the pass age of particles through matter. Recently, it has been used in many medical physics applications. In radiotherapy, positron emission tomography, and magnetic resonance tomography, Geant4 has been applied to accurately simulate the propagation of particles and the interaction of particles, not only with medical devices, but also with patient's phantoms.1,2 Many researchers try to use patient's image data to calculate the dose. The use of DICOM images files to simulate is desired. We construct detector with parameterized volume for Geant4 simulations, which can be applied to simulations using DICOM data as the input.We try to apply this code to the patient's DICOM images to simulate the propagation and interaction of the particles. So we can calculate the absorbed dose of the patient. In this study, the used visualization tool is called gMocren. The purpose of the present paper is to verify a volume visualization tool that simultaneously displays both the complex patient data and the simulated dose distribution with real patient's DICOM data. We applied a volume visualization tool for GEANT4 simulation. We developed to create the each voxel's dose tables of the every slices and review the distribution with DICOM file, gMocren is very convenience tool but provide only qualitative analysis. We need more enhanced functions to display contour like RTP and utility program to create dose table in every points.
Image reconstruction and the effect on dose calculation for hip prostheses
International Nuclear Information System (INIS)
High atomic number inserts, such as hip prostheses and dental fillings, cause streak artifacts on computed tomography (CT) images when filtered back-projection (FBP) methods are used. These streak artifacts severely degrade our ability to differentiate the tumor volume. Also, incorrect Hounsfield numbers yield incorrect electron density information that may lead to erroneous dose calculations, and, as a result, compromise clinical outcomes. The aim of this research was to evaluate the dosimetric consequences of artifacts during radiotherapy planning of a prostate patient containing a hip prosthesis. The CT numbers corresponding to an iron prosthesis were inserted into the right femoral head of an existing CT image set. This artifact-free image was used as the standard image set. CT projections through the image set formed the sinogram, from which filtered back projection and iterative deblurring methods were used to create reconstructed image sets. These reconstructed image sets contained artifacts. Prostate treatment plans were then calculated using a Monte Carlo system for the standard and reconstructed CT image sets. Close to the prosthesis, the CT numbers between the reconstructed and standard image sets differed substantially. However, because the CT number differences covered only a small area, the dose distributions on the reconstructed and standard image sets were not significantly different. The dose-volume histograms for the prostate, rectum, and bladder were virtually identical. Our results indicate that even though CT image artifacts restrict our ability to differentiate tumors and critical structures, the dose distributions for a prostate plan containing a hip prosthesis, calculated on both artifact-free image sets and image sets containing artifacts, are not significantly different
Diego Azcona, Juan; Barbés, Benigno; Wang, Lilie; Burguete, Javier
2016-01-01
This paper presents a method to obtain the pencil-beam kernels that characterize a megavoltage photon beam generated in a flattening filter free (FFF) linear accelerator (linac) by deconvolution from experimental measurements at different depths. The formalism is applied to perform independent dose calculations in modulated fields. In our previous work a formalism was developed for ideal flat fluences exiting the linac’s head. That framework could not deal with spatially varying energy fluences, so any deviation from the ideal flat fluence was treated as a perturbation. The present work addresses the necessity of implementing an exact analysis where any spatially varying fluence can be used such as those encountered in FFF beams. A major improvement introduced here is to handle the actual fluence in the deconvolution procedure. We studied the uncertainties associated to the kernel derivation with this method. Several Kodak EDR2 radiographic films were irradiated with a 10 MV FFF photon beam from two linacs from different vendors, at the depths of 5, 10, 15, and 20cm in polystyrene (RW3 water-equivalent phantom, PTW Freiburg, Germany). The irradiation field was a 50mm diameter circular field, collimated with a lead block. The 3D kernel for a FFF beam was obtained by deconvolution using the Hankel transform. A correction on the low dose part of the kernel was performed to reproduce accurately the experimental output factors. Error uncertainty in the kernel derivation procedure was estimated to be within 0.2%. Eighteen modulated fields used clinically in different treatment localizations were irradiated at four measurement depths (total of fifty-four film measurements). Comparison through the gamma-index to their corresponding calculated absolute dose distributions showed a number of passing points (3%, 3mm) mostly above 99%. This new procedure is more reliable and robust than the previous one. Its ability to perform accurate independent dose calculations was
TH-A-19A-06: Site-Specific Comparison of Analytical and Monte Carlo Based Dose Calculations
Energy Technology Data Exchange (ETDEWEB)
Schuemann, J; Grassberger, C; Paganetti, H [Massachusetts General Hospital and Harvard Medical School, Boston, MA (United States); Dowdell, S [Illawarra Shoalhaven Local Health District, Wollongong (Australia)
2014-06-15
Purpose: To investigate the impact of complex patient geometries on the capability of analytical dose calculation algorithms to accurately predict dose distributions and to verify currently used uncertainty margins in proton therapy. Methods: Dose distributions predicted by an analytical pencilbeam algorithm were compared with Monte Carlo simulations (MCS) using TOPAS. 79 complete patient treatment plans were investigated for 7 disease sites (liver, prostate, breast, medulloblastoma spine and whole brain, lung and head and neck). A total of 508 individual passively scattered treatment fields were analyzed for field specific properties. Comparisons based on target coverage indices (EUD, D95, D90 and D50) were performed. Range differences were estimated for the distal position of the 90% dose level (R90) and the 50% dose level (R50). Two-dimensional distal dose surfaces were calculated and the root mean square differences (RMSD), average range difference (ARD) and average distal dose degradation (ADD), the distance between the distal position of the 80% and 20% dose levels (R80- R20), were analyzed. Results: We found target coverage indices calculated by TOPAS to generally be around 1–2% lower than predicted by the analytical algorithm. Differences in R90 predicted by TOPAS and the planning system can be larger than currently applied range margins in proton therapy for small regions distal to the target volume. We estimate new site-specific range margins (R90) for analytical dose calculations considering total range uncertainties and uncertainties from dose calculation alone based on the RMSD. Our results demonstrate that a reduction of currently used uncertainty margins is feasible for liver, prostate and whole brain fields even without introducing MC dose calculations. Conclusion: Analytical dose calculation algorithms predict dose distributions within clinical limits for more homogeneous patients sites (liver, prostate, whole brain). However, we recommend
Benchmark calculations of neutron dose rates at transport and storage casks
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The application of numerical calculations methods for demonstration of sufficient radiation shielding of radioactive waste transport and storage casks requires a validation based on appropriate measurements of gamma and neutron sources. The results of the comparison of measured data and calculations using the Monte Carlo program MCNP show deviations dependent on the loading of the cask within the standard deviation which is dominated by the measuring method. Considering the neutrons scattered at the salt MCNP (in case of disposal in the salt) tends to underestimate the nominal values, but still within the double standard deviation. This accuracy is not reached with MAVRIC. Based on AHE (active handling experiments) data benchmark calculations were performed that can be used as reference value. The total accuracy results from the accuracy of the source term and the measurement of the neutron dose rate with a deviation of 15%.
Ding, George X.; Duggan, Dennis M.; Coffey, Charles W.; Shokrani, Parvaneh; Cygler, Joanna E.
2006-06-01
The purpose of this study is to present our experience of commissioning, testing and use of the first commercial macro Monte Carlo based dose calculation algorithm for electron beam treatment planning and to investigate new issues regarding dose reporting (dose-to-water versus dose-to-medium) as well as statistical uncertainties for the calculations arising when Monte Carlo based systems are used in patient dose calculations. All phantoms studied were obtained by CT scan. The calculated dose distributions and monitor units were validated against measurements with film and ionization chambers in phantoms containing two-dimensional (2D) and three-dimensional (3D) type low- and high-density inhomogeneities at different source-to-surface distances. Beam energies ranged from 6 to 18 MeV. New required experimental input data for commissioning are presented. The result of validation shows an excellent agreement between calculated and measured dose distributions. The calculated monitor units were within 2% of measured values except in the case of a 6 MeV beam and small cutout fields at extended SSDs (>110 cm). The investigation on the new issue of dose reporting demonstrates the differences up to 4% for lung and 12% for bone when 'dose-to-medium' is calculated and reported instead of 'dose-to-water' as done in a conventional system. The accuracy of the Monte Carlo calculation is shown to be clinically acceptable even for very complex 3D-type inhomogeneities. As Monte Carlo based treatment planning systems begin to enter clinical practice, new issues, such as dose reporting and statistical variations, may be clinically significant. Therefore it is imperative that a consistent approach to dose reporting is used.
Gu, Xuejun; Jelen, Urszula; Li, Jinsheng; Jia, Xun; Jiang, Steve B.
2011-01-01
Targeting at the development of an accurate and efficient dose calculation engine for online adaptive radiotherapy, we have implemented a finite size pencil beam (FSPB) algorithm with a 3D-density correction method on GPU. This new GPU-based dose engine is built on our previously published ultrafast FSPB computational framework. Dosimetric evaluations against Monte Carlo dose calculations are conducted on 10 IMRT treatment plans (5 head-and-neck cases and 5 lung cases). For all cases, there i...
International Nuclear Information System (INIS)
The purpose of this study is to present our experience of commissioning, testing and use of the first commercial macro Monte Carlo based dose calculation algorithm for electron beam treatment planning and to investigate new issues regarding dose reporting (dose-to-water versus dose-to-medium) as well as statistical uncertainties for the calculations arising when Monte Carlo based systems are used in patient dose calculations. All phantoms studied were obtained by CT scan. The calculated dose distributions and monitor units were validated against measurements with film and ionization chambers in phantoms containing two-dimensional (2D) and three-dimensional (3D) type low- and high-density inhomogeneities at different source-to-surface distances. Beam energies ranged from 6 to 18 MeV. New required experimental input data for commissioning are presented. The result of validation shows an excellent agreement between calculated and measured dose distributions. The calculated monitor units were within 2% of measured values except in the case of a 6 MeV beam and small cutout fields at extended SSDs (>110 cm). The investigation on the new issue of dose reporting demonstrates the differences up to 4% for lung and 12% for bone when 'dose-to-medium' is calculated and reported instead of 'dose-to-water' as done in a conventional system. The accuracy of the Monte Carlo calculation is shown to be clinically acceptable even for very complex 3D-type inhomogeneities. As Monte Carlo based treatment planning systems begin to enter clinical practice, new issues, such as dose reporting and statistical variations, may be clinically significant. Therefore it is imperative that a consistent approach to dose reporting is used
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The fluence to effective-dose and organ-absorbed-dose conversion coefficients for charged pions and muons were calculated based on the instructions given in ICRP Publication 103. For the calculation, the particle motions in the ICRP/ICRU adult reference computational phantoms were simulated using the PHITS code for four idealized irradiation geometries as well as those closely representing the geometrical simulations of cosmic-ray muon exposure. Cosmic-ray pion and muon dose rates over a wide altitude range were estimated using the calculated dose conversion coefficients. The results of the calculation indicate that the assumption of the isotropic irradiation geometry is suitable to be utilized in the dose estimations for cosmic-ray pions and muons. It is also found from the calculation that the introduction of ICRP103 gives little impact on the pion and muon dosimetries, since the radiation weighting factors assigned to those particles are maintained in the issue. (author)
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multidetector CT system were calculated. This data was found to depend strongly on CT acquisition mode and exposure parameters as well as patient age and sex. The effective dose from a pediatric CT scan performed in axial mode was always considerably lower compared to the corresponding scan performed in helical mode, due to the additional tissue regions exposed to the primary beam in helical examinations as a result of z overscanning
Calculating tumor trajectory and dose-of-the-day using cone-beam CT projections
Energy Technology Data Exchange (ETDEWEB)
Jones, Bernard L., E-mail: bernard.jones@ucdenver.edu; Westerly, David; Miften, Moyed [Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, Colorado 80045 (United States)
2015-02-15
Purpose: Cone-beam CT (CBCT) projection images provide anatomical data in real-time over several respiratory cycles, forming a comprehensive picture of tumor movement. The authors developed and validated a method which uses these projections to determine the trajectory of and dose to highly mobile tumors during each fraction of treatment. Methods: CBCT images of a respiration phantom were acquired, the trajectory of which mimicked a lung tumor with high amplitude (up to 2.5 cm) and hysteresis. A template-matching algorithm was used to identify the location of a steel BB in each CBCT projection, and a Gaussian probability density function for the absolute BB position was calculated which best fit the observed trajectory of the BB in the imager geometry. Two modifications of the trajectory reconstruction were investigated: first, using respiratory phase information to refine the trajectory estimation (Phase), and second, using the Monte Carlo (MC) method to sample the estimated Gaussian tumor position distribution. The accuracies of the proposed methods were evaluated by comparing the known and calculated BB trajectories in phantom-simulated clinical scenarios using abdominal tumor volumes. Results: With all methods, the mean position of the BB was determined with accuracy better than 0.1 mm, and root-mean-square trajectory errors averaged 3.8% ± 1.1% of the marker amplitude. Dosimetric calculations using Phase methods were more accurate, with mean absolute error less than 0.5%, and with error less than 1% in the highest-noise trajectory. MC-based trajectories prevent the overestimation of dose, but when viewed in an absolute sense, add a small amount of dosimetric error (<0.1%). Conclusions: Marker trajectory and target dose-of-the-day were accurately calculated using CBCT projections. This technique provides a method to evaluate highly mobile tumors using ordinary CBCT data, and could facilitate better strategies to mitigate or compensate for motion during
GPU-based ultra fast dose calculation using differential convolution/superposition algorithm
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Background: Dose calculation plays a key role in treatment planning for radiotherapy, its performance and accuracy are crucial to the quality of treatment plans. Differential convolution/superposition algorithm is considered as an accurate algorithm for photon dose calculation; however, improvement on its computational efficiency is still desirable for such purpose as real time treatment planning. Purpose: The goal of this work is to boost the performance of differential convolution/superposition algorithm by devising a graphics processing unit (GPU) implementation so as to make the method practical for daily usage. Methods: In this work, we implemented a GPU-based version of the differential convolution/superposition algorithm, by which the most time-consuming parts are implemented on GPU. In order to fully utilize the GPU computing power, the algorithm is modified to match the GPU hardware architecture. Results: Compared with the algorithm completely running on CPU, the GPU-based algorithm can speed up 30-60 times on a Tesla C1060 with higher values corresponding to larger field size. Finally, we use γ index to analyze the accuracy of calculation results, no matter one field or multi-field, homogeneous phantom or inhomogeneous phantom, the GPU implementation has the same accuracy as the CPU implementation. Conclusions: GPU is a useful solution for satisfying the increasing demands on computation speed and accuracy of dose calculation. The GPU-based differential convolution/superposition can be feasible and cost-efficient for satisfying the increasing demands for either computation speed or accuracy by advanced radiation therapy technologies. (authors)
Comparison of CT number calibration techniques for CBCT-based dose calculation
Energy Technology Data Exchange (ETDEWEB)
Dunlop, Alex [The Royal Marsden NHS Foundation Trust, Joint Department of Physics, Institute of Cancer Research, London (United Kingdom); The Royal Marsden Hospital, Sutton, Surrey, Downs Road (United Kingdom); McQuaid, Dualta; Ni