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静脉注射18F-FDG注射液后冲洗注射器对残留剂量及肝脏标准化摄取值的影响
引用本文:郝振亮,王俊清,任超,赵晓斌.静脉注射18F-FDG注射液后冲洗注射器对残留剂量及肝脏标准化摄取值的影响[J].中国医学影像技术,2019,35(7):1091-1094.
作者姓名:郝振亮  王俊清  任超  赵晓斌
作者单位:民航总医院放射科, 北京 100123,中国医学科学院北京协和医院核医学科, 北京 100730,中国医学科学院北京协和医院核医学科, 北京 100730,首都医科大学附属北京天坛医院核医学科, 北京 100070
基金项目:国家自然科学基金(81527805)。
摘    要:目的 探讨PET/CT检查时静脉注射18F-FDG注射液后冲洗注射器对放射性药物残留剂量以及肝脏标准化摄取值(SUV)的影响。方法 收集接受PET/CT检查的50例患者,根据注药方式分为对照组(n=25)和实验组(n=25)。采用23G头皮针建立静脉通路,注射18F-FDG注射液后,对照组直接用5 ml生理盐水冲洗管道;实验组先用1 ml生理盐水冲洗管道,然后用2 ml生理盐水冲洗注射器,最后用剩余2 ml再次冲洗管道。比较2组间18F-FDG注射后残留剂量以及肝脏SUV平均值(SUVmean)和SUV最大值(SUVmax)的差异。结果 实验组总残留剂量(0.22±0.08)mCi]、注射器内残留剂量(0.19±0.07)mCi]和静脉通道内残留剂量(0.03±0.02)mCi]均小于对照组(P均<0.01)。实验组与对照组肝脏3个不同层面(第二肝门层面、门静脉左支层面、第一肝门层面)的SUVmean和SUVmax差异均无统计学意义(P均>0.05)。结论 冲洗注射器能减少18F-FDG注射液残留量。注射器内少量放射性药物残留尚不足以引起肝脏SUV变化,但进一步规范18F-FDG注射操作流程仍属必要。

关 键 词:氟脱氧葡萄糖F18  注射器  残留量  标准化摄取值  正电子发射体层摄影术
收稿时间:2019/1/12 0:00:00
修稿时间:2019/5/28 0:00:00

Impact of syringe saline flush after injection of 18F-FDG on residual dose and standardized uptake value of liver
HAO Zhenliang,WANG Junqing,REN Chao and ZHAO Xiaobin.Impact of syringe saline flush after injection of 18F-FDG on residual dose and standardized uptake value of liver[J].Chinese Journal of Medical Imaging Technology,2019,35(7):1091-1094.
Authors:HAO Zhenliang  WANG Junqing  REN Chao and ZHAO Xiaobin
Institution:Department of Radiology, Civil Aviation General Hospital, Beijing 100123, China,Department of Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China,Department of Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China and Department of Nuclear Medicine, Beijing Tiantan Hospital, Capital Medical University, Beijing 100070, China
Abstract:Objective To investigate the impact of saline flush for syringe after 18F-FDG injection on the residual dose of 18F-FDG and the standardized uptake value (SUV) of liver during PET/CT examination. Methods A total of 50 patients who underwent PET/CT examination were enrolled and divided into control group (n=25) and experimental group (n=25) according to different injection methods. Device system of the vein passage was established with 23 gauge scalp needle. In control group, the intravenous line was directly flushed with 5 ml physiological saline after 18F-FDG injection, while in experimental group, firstly the intravenous line was flushed with 1 ml saline, then the syringe was flushed with 2 ml saline, finally the intravenous line was flushed again with the residual 2 ml saline. The residual dose of 18F-FDG and SUVmean and SUVmax of liver were compared between the two groups. Results The total residual dose (0.22±0.08]mCi), syringe residual dose (0.19±0.07]mCi) and intravenous channel residual dose (0.03±0.02]mCi) in the experimental group were all lower than those in control group (all P<0.01). There was no significant difference of SUVmean nor SUVmax between experimental group and control group at 3 different levels of the liver (level of the second liver porta, level of the left portal vein and level of the first liver porta, all P>0.05). Conclusion Flushing the syringe can reduce residual dose of 18F-FDG injection. A small amount of radiopharmaceuticals retention in the syringe may not affect SUV for liver, but further standardization of the operation process of 18F-FDG injection is still necessary.
Keywords:fludeoxyglucose F 18  syringes  residual dose  standardized uptake value  positron-emission tomography
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