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医用回旋加速器设施规划与调试的强制性要求。

Mandatory Requirements for Planning and Commissioning of Medical Cyclotron Facility.

作者信息

Kumar Rajeev, Tandon Pankaj, Deep Kamal

机构信息

Department of Nuclear Medicine, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India.

Radiological Safety Division, Atomic Energy Regulatory Board, Mumbai, Maharashtra, India.

出版信息

Indian J Nucl Med. 2024 Jul-Aug;39(4):243-250. doi: 10.4103/ijnm.ijnm_102_23. Epub 2024 Nov 18.

DOI:10.4103/ijnm.ijnm_102_23
PMID:39790829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11708802/
Abstract

Over the last 15 years, there has been substantial growth in the installation of medical cyclotrons. This is mainly due to the increased demand for the production of positron emission tomography radiopharmaceuticals. In every country, there is a regulatory body that regulates the uses of medical cyclotron intending to protect occupational workers, the public, and the environment. It regulates the entire stages of such facilities, which mainly controls regulatory activities such as construction, commissioning, operation, and decommissioning. This article primarily highlights the key practices for planning and installation of a medical cyclotron facility (MCF). It also covers the particular aspects that should be considered in the early stages of project planning and provides information for best practices and challenges. If these aspects are properly addressed, then it ensures the safe operation of the MCF. The texts also elaborate on the necessary requirements for effective planning of the MCF, such as layout and space considerations, workload plan and maximum research capacity of the institute and equipment, shielding requirements, water cooling circuit, storage of radioactive components, management of radioactive waste from medical cyclotron and radiochemistry laboratory, construction and commissioning project management, exhaust system and filtration options, plans for staffing and training, and combination of equipment safety systems and building safety systems.

摘要

在过去15年中,医用回旋加速器的安装数量大幅增长。这主要是由于对正电子发射断层扫描放射性药物生产的需求增加。在每个国家,都有一个监管机构来规范医用回旋加速器的使用,旨在保护职业工作人员、公众和环境。它对这类设施的整个阶段进行监管,主要控制诸如建设、调试、运行和退役等监管活动。本文主要强调医用回旋加速器设施(MCF)规划和安装的关键做法。它还涵盖了项目规划早期阶段应考虑的特定方面,并提供了最佳实践和挑战的信息。如果这些方面得到妥善解决,就能确保MCF的安全运行。本文还阐述了MCF有效规划的必要要求,如布局和空间考虑、工作量计划以及研究所和设备的最大研究能力、屏蔽要求、水冷回路、放射性组件的储存、医用回旋加速器和放射化学实验室的放射性废物管理、建设和调试项目管理、排气系统和过滤选项、人员配备和培训计划,以及设备安全系统和建筑安全系统的结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/ca8f1883a9e5/IJNM-39-243-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/4312038d627a/IJNM-39-243-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/227e4ff230ef/IJNM-39-243-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/a87331d96236/IJNM-39-243-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/ca8f1883a9e5/IJNM-39-243-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/4312038d627a/IJNM-39-243-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/227e4ff230ef/IJNM-39-243-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/a87331d96236/IJNM-39-243-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839b/11708802/ca8f1883a9e5/IJNM-39-243-g004.jpg

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本文引用的文献

1
Practical experience and challenges in the operation of medical cyclotron.医用回旋加速器运行中的实践经验与挑战
Nucl Med Commun. 2017 Jan;38(1):10-14. doi: 10.1097/MNM.0000000000000598.
2
Regulatory requirements for designing PET-CT facility in India.印度PET-CT设备设计的监管要求。
Indian J Nucl Med. 2010 Apr;25(2):39-43. doi: 10.4103/0972-3919.72684.