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IDAC-Dose 2.2,一款基于国际辐射防护委员会(ICRP)最新成人和儿童参考计算体模的诊断核医学内照射剂量软件。

IDAC-Dose 2.2, an internal dosimetry software for diagnostic nuclear medicine based on the latest ICRP adult and paediatric reference computational phantoms.

作者信息

Andersson Martin, Eckerman Keith, Mattsson Sören

机构信息

Department of Radiation Physics, Sahlgrenska Cancer Center, Medical Radiation Physics, Department of Translational Medicine, University of Gothenburg, Lund University, Skåne University Hospital, Malmö, Malmö, SE-205 02, Sweden.

Center for Radiation Protection Knowledge, Oak Ridge National Laboratory, Oak Ridge, TN, USA.

出版信息

EJNMMI Phys. 2025 Jun 13;12(1):56. doi: 10.1186/s40658-025-00774-z.

DOI:10.1186/s40658-025-00774-z
PMID:40512410
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12165913/
Abstract

BACKGROUND

For patients investigated with radiopharmaceuticals, it is important to be able to perform valid calculations of the absorbed dose in organs and tissues. An internal dosimetry computer program, IDAC-Dose2.1, has been updated to be based on the ICRP specific absorbed fractions and computational framework of internal dose assessment for 12 adult and paediatric reference individuals given in ICRP Publication 133 and 155. The updated dosimetry software intended for nuclear medicine is named IDAC-Dose2.2. The calculations are based on radionuclide decay scheme of ICRP Publication 107. Biokinetic models can be based on up to 83 different source regions irradiating 48 target tissues, defining the effective dose as presented in ICRP Publications 60 and 103. The computer program was validated against another ICRP dosimetry software, DCAL ver. 2022, that employs the same computational framework and is used for occupational and environmental intakes of radionuclides. IDAC-Dose2.2 calculates absorbed doses to the 2 adult and 10 paediatric,15-yrs, 10-yrs, 5-yrs, 1-yr, 100 days (infant) and 0 day (new-born), sex specific ICRP reference phantoms. It has an additional sub-module which can interpolate the calculated absorbed dose and effective dose to an arbitrary age between 0 and 20 years (20 years = adult) or an arbitrary weight of 3.5-73 kg for male and 3.5-64 kg for female instead of only using the 6 fixed phantoms ages.

RESULTS

IDAC-Dose2.2 was applied on three frequently used radiopharmaceuticals: intravenously administered 2-[F]FDG, orally administered Tc-pertechnetate and I-iodide. Using the tissue weighting factors from ICRP Publication 103, the effective dose per administered activity was estimated for 2-[F]FDG: 0.017mSv/MBq, 0.020 mSv/MBq, 0.029 mSv/MBq, 0.044 mSv/MBq, 0.075 mSv/MBq, 0.16 mSv/MBq 0.16 mSv/MBq for adult, 15-, 10-, 5-, 1-year old, 100 days (infant) and 0 day (newborn), respectively. Effective dose of 0.034 mSv/MBq was also calculated for 2-[F]FDG to a reference person of 8-years old. For the same three radiopharmaceuticals, S-values were generated for all phantoms in IDAC-Dose2.2 and validated against the dosimetry program DCAL, showing identical results.

CONCLUSIONS

The internal dosimetry program IDAC-Dose was updated to include all 12 specific sets of absorbed fractions of the ICRP adult and paediatric reference phantoms and applied to three radiopharmaceuticals for validation against DCAL and to generate improved absorbed dose estimations for preadults in diagnostic nuclear medicine. The sub-module for age or weight interpolation of absorbed doses follows the ICRP computational framework used for members of the public. IDAC-Dose2.2 will used by the ICRP for absorbed and effective dose calculations in diagnostic nuclear medicine. The results from other software, which uses the same primer data (e.g. ICRP SAF values or decay data) could deviate from those of IDAC-Dose 2.2 and published ICRP dose values if the software do not follow the ICRP computational framework for internal dosimetry. IDAC-Dose2.2 is a free software for research and available at http://www.idac-dose.org . The online version can be operated directly through a web browser and the standalone version is an executable file, which is downloaded and installed directly on the local computer.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/915549c1023c/40658_2025_774_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/886850c3c319/40658_2025_774_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/e1ce87020cd5/40658_2025_774_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/91c6f13017ea/40658_2025_774_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/915549c1023c/40658_2025_774_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/886850c3c319/40658_2025_774_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/e1ce87020cd5/40658_2025_774_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/91c6f13017ea/40658_2025_774_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2294/12165913/915549c1023c/40658_2025_774_Fig4_HTML.jpg
摘要

背景

对于使用放射性药物进行检查的患者,能够对器官和组织中的吸收剂量进行有效的计算非常重要。一个内部剂量学计算机程序IDAC-Dose2.1已更新,以基于国际辐射防护委员会(ICRP)第133号和第155号出版物中给出的12名成人和儿童参考个体的特定吸收分数以及内部剂量评估的计算框架。更新后的用于核医学的剂量学软件名为IDAC-Dose2.2。计算基于ICRP第107号出版物的放射性核素衰变方案。生物动力学模型可以基于多达83个不同的源区域对48个靶组织进行照射,按照ICRP第60号和第103号出版物中的定义来确定有效剂量。该计算机程序已针对另一个ICRP剂量学软件DCAL ver. 2022进行了验证,DCAL ver. 2022采用相同的计算框架,用于放射性核素的职业和环境摄入量计算。IDAC-Dose2.2可计算2名成人以及10名儿童(15岁、10岁、5岁、1岁、100天(婴儿)和0天(新生儿))、按性别区分的ICRP参考体模的吸收剂量。它有一个额外的子模块,可以将计算出的吸收剂量和有效剂量内插到0至20岁(20岁=成人)之间的任意年龄,或者男性3.5至73千克、女性3.5至64千克的任意体重,而不是仅使用6个固定的体模年龄。

结果

IDAC-Dose2.2应用于三种常用的放射性药物:静脉注射的2-[F]FDG、口服的高锝酸盐和碘化物。使用ICRP第103号出版物中的组织权重因子,估计每给药活度的有效剂量,对于2-[F]FDG,成人、15岁、10岁、5岁、1岁、100天(婴儿)和0天(新生儿)分别为0.017mSv/MBq、0.020 mSv/MBq、0.029 mSv/MBq、0.044 mSv/MBq、0.075 mSv/MBq、0.16 mSv/MBq、0.16 mSv/MBq。还计算出2-[F]FDG对一名8岁参考人的有效剂量为0.034 mSv/MBq。对于相同的三种放射性药物,在IDAC-Dose2.2中为所有体模生成了S值,并与剂量学程序DCAL进行了验证,结果相同。

结论

内部剂量学程序IDAC-Dose已更新,纳入了ICRP成人和儿童参考体模的所有12组特定吸收分数集,并应用于三种放射性药物,以与DCAL进行验证,并为诊断核医学中的儿童生成改进的吸收剂量估计值。吸收剂量的年龄或体重内插子模块遵循用于公众成员的ICRP计算框架。ICRP将使用IDAC-Dose2.2进行诊断核医学中的吸收剂量和有效剂量计算。如果其他软件不遵循ICRP内部剂量学计算框架,使用相同原始数据(如ICRP特定吸收分数值或衰变数据)的软件结果可能会与IDAC-Dose 2.2和已发布的ICRP剂量值不同。IDAC-Dose2.2是一款免费的研究软件,可在http://www.idac-dose.org获取。在线版本可直接通过网络浏览器操作,独立版本是一个可执行文件,可直接下载并安装在本地计算机上。

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