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每次核医学检查中技术人员所接受的辐射剂量:锝-99m、镓-67、碘-131放射性示踪剂与氟-18氟脱氧葡萄糖之间的比较。

Radiation dose to technicians per nuclear medicine procedure: comparison between technetium-99m, gallium-67, and iodine-131 radiotracers and fluorine-18 fluorodeoxyglucose.

作者信息

Chiesa C, De Sanctis V, Crippa F, Schiavini M, Fraigola C E, Bogni A, Pascali C, Decise D, Marchesini R, Bombardieri E

机构信息

Unita' PET, Divisione Medicina Nucleare, Istituto Nazionale Tumori, Milano, Italy.

出版信息

Eur J Nucl Med. 1997 Nov;24(11):1380-9. doi: 10.1007/s002590050164.

Abstract

The aim of this study was to determine the non-extremity gamma dose received by a technician while performing an ordinary nuclear medicine procedure or a static (i.e. without blood sampling) fluorine-18 fluorodeoxyglucose (FDG) positron emission tomography (PET) study. The dose per patient was measured by means of a commercial electronic pocket Geiger Mueller dosimeter, worn in the upper left pocket of the overalls. This was previously tested by exposure to known point sources of technetium-99m, gallium-67, iodine-131 and fluorine-18 in the air. A further test was performed with 99mTc, 131I and 18F sources inserted in a water phantom to simulate the condition of high scattering degradation of the primary radiation due to the patient's tissues. Subsequently, the dose was measured by two technicians for a total of 314 clinical cases, covering the most common nuclear medicine procedures, including 44 static, two-level FDG PET studies with repositioning of the patient on the couch between the transmission and the emission scan and seven whole-body PET studies. The dose read by the dosimeter was corrected for environmental background and for detector efficiency measured with sources in the air. For a limited subset of cases, the time spent close to patients was also measured. Doses were then estimated by a crude non-absorbing point source approximation and by using experimental dose rates. A comparison between experimental and estimated doses, as well as with previously published data, completed the work. For most of the conventional procedures, the measured dose per procedure proved to be within the range 0.2-0.4 microSv, except for equilibrium angiocardioscintigraphy (1.0+/-0.5 microSv) and 99mTc-sestamibi single-photon emission tomography (1. 7+/-1.0 microSv). Comparison with data published in the last 20 years shows that our values are generally lower. The current more favourable working conditions are a result of technological improvements (for instance two-head gamma cameras capable of whole-body studies), and safer shielding and distance from patients. Two-level PET gave 11.5+/-4.4 microSv and whole-body PET 5.9+/-1.2 microSv. In a subset of patients these values could be subdivided into the separate contributions from each phase of the procedure. They were: 0.11+/-0.04 microSv for daily quality assurance, 2.9+/-3.0 microSv for two transmission scans, 0.3+/-0.1 microSv for syringe preparation, 2.8+/-1.8 microSv for injection and escorting the patient to the waiting room, 1.7+/-1.5 microSv for a whole-body emission scan, 7.7+/-5.2 microSv for two emission scans, and 0.8+/-0. 2 microSv for patient departure. The higher value from PET by comparison with conventional procedures is attributable to the higher specific gamma constant of 18F, as well as the longer time required for accurate positioning.

摘要

本研究的目的是确定技术人员在进行普通核医学检查或静态(即不进行血液采样)氟-18氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)检查时所接受的非肢体伽马剂量。通过佩戴在工作服左上口袋的商用电子袖珍盖革-米勒剂量计测量每位患者的剂量。该剂量计先前已通过暴露于空气中已知的锝-99m、镓-67、碘-131和氟-18点源进行了测试。还进行了进一步测试,将99mTc、131I和18F源插入水体模中,以模拟由于患者组织导致的原发射线高散射衰减情况。随后,两名技术人员对总共314例临床病例进行了剂量测量,涵盖了最常见的核医学检查,包括44例静态、两级FDG PET检查(在透射扫描和发射扫描之间患者在检查床上重新定位)以及7例全身PET检查。剂量计读取的剂量针对环境本底以及用空气中的源测量的探测器效率进行了校正。对于有限的一部分病例,还测量了靠近患者的时间。然后通过粗略的非吸收点源近似法和使用实验剂量率来估算剂量。实验剂量与估算剂量之间的比较,以及与先前发表的数据的比较,完成了这项工作。对于大多数传统检查,每次检查测量的剂量被证明在0.2 - 0.4微希沃特范围内,平衡心血管闪烁显像(1.0±0.5微希沃特)和99mTc - 司他比单光子发射断层扫描(1.7±1.0微希沃特)除外。与过去20年发表的数据比较表明,我们的值通常更低。当前更有利的工作条件是技术改进(例如能够进行全身检查的双头伽马相机)以及更安全的屏蔽和与患者保持距离的结果。两级PET检查的剂量为11.5±4.4微希沃特,全身PET检查的剂量为5.9±1.2微希沃特。在一部分患者中,这些值可以细分为检查每个阶段的单独贡献。它们分别是:日常质量保证为0.11±0.04微希沃特,两次透射扫描为2.9±3.0微希沃特,注射器准备为0.3±0.1微希沃特,注射并护送患者到候诊室为2.8±1.8微希沃特,全身发射扫描为1.7±1.5微希沃特,两次发射扫描为7.7±5.2微希沃特,患者离开为0.8±0.2微希沃特。与传统检查相比,PET检查剂量较高归因于18F的比伽马常数较高以及精确定位所需的时间较长。

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