{"title":"[Evaluation of Residual Ratio and Optimization of Residual Setting in Automated Infusion Device for <sup>18</sup>F-florbetapir Administration].","authors":"Ryu Emura, Ayana Tanji, Kouki Suzuki, Yuka Nakamura, Masayoshi Ikeda, Katsuya Seki, Hirotaro Nakanishi, Shigeru Kiryu","doi":"10.6009/jjrt.26-1656","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>This study aimed to quantify residual radioactivity in medical devices used during <sup>18</sup>F-florbetapir administration with the UG-02 automated infusion device and to identify the optimal residual setting for accurate dose calculation.</p><p><strong>Methods: </strong>We analyzed 52 amyloid positron emission tomography (PET) examinations performed at our institution. After radiotracer administration, residual radioactivity was measured in the drug vial, infusion circuit, route, residual solution, and individual circuit components. Administration rates and residual ratios were calculated after decay correction to the injection time. Residual ratios estimated by the UG-02 system were compared with measured values, and the optimal residual setting was determined using least-squares optimization. Statistical analyses were performed using paired t-tests, with statistical significance set at P<0.05.</p><p><strong>Results: </strong>The mean administered dose was 348.0±33.3 MBq, whereas the mean residual activity was 93.1±12.6 MBq, corresponding to an administration rate of 77.8% and a residual ratio of 22.2%. The infusion circuit exhibited the highest residual ratio (18.0%), primarily attributable to the air vent filter (13.5%) and infusion set (4.0%). The UG-02 system significantly overestimated the residual ratio in the drug vial compared with the measured value (1.5% vs. 0.9%, P<0.01). The optimal residual setting was 16.1%, reducing the relative error of the displayed dose from 17.1% to 0.08%.</p><p><strong>Conclusion: </strong>This study characterized residual distribution within the UG-02 automated infusion system and identified an optimal residual setting for <sup>18</sup>F-florbetapir administration. Implementing this setting improves dose calculation accuracy, reduces underdosing risk, and may contribute to improving the quantitative reliability of amyloid PET imaging.</p>","PeriodicalId":74309,"journal":{"name":"Nihon Hoshasen Gijutsu Gakkai zasshi","volume":"82 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nihon Hoshasen Gijutsu Gakkai zasshi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6009/jjrt.26-1656","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: This study aimed to quantify residual radioactivity in medical devices used during 18F-florbetapir administration with the UG-02 automated infusion device and to identify the optimal residual setting for accurate dose calculation.
Methods: We analyzed 52 amyloid positron emission tomography (PET) examinations performed at our institution. After radiotracer administration, residual radioactivity was measured in the drug vial, infusion circuit, route, residual solution, and individual circuit components. Administration rates and residual ratios were calculated after decay correction to the injection time. Residual ratios estimated by the UG-02 system were compared with measured values, and the optimal residual setting was determined using least-squares optimization. Statistical analyses were performed using paired t-tests, with statistical significance set at P<0.05.
Results: The mean administered dose was 348.0±33.3 MBq, whereas the mean residual activity was 93.1±12.6 MBq, corresponding to an administration rate of 77.8% and a residual ratio of 22.2%. The infusion circuit exhibited the highest residual ratio (18.0%), primarily attributable to the air vent filter (13.5%) and infusion set (4.0%). The UG-02 system significantly overestimated the residual ratio in the drug vial compared with the measured value (1.5% vs. 0.9%, P<0.01). The optimal residual setting was 16.1%, reducing the relative error of the displayed dose from 17.1% to 0.08%.
Conclusion: This study characterized residual distribution within the UG-02 automated infusion system and identified an optimal residual setting for 18F-florbetapir administration. Implementing this setting improves dose calculation accuracy, reduces underdosing risk, and may contribute to improving the quantitative reliability of amyloid PET imaging.
目的:本研究旨在定量UG-02自动输注器给药期间使用的医疗器械中的残留放射性,并确定准确计算剂量的最佳残留设置。方法:我们分析了在我院进行的52例淀粉样正电子发射断层扫描(PET)检查。放射性示踪剂给药后,在药瓶、输注回路、路径、残留溶液和单个回路元件中测量残留放射性。对注射时间进行衰减校正后计算给药率和残留比。将UG-02系统估算的残差比与实测值进行比较,采用最小二乘优化法确定残差最优设置。结果:平均给药剂量为348.0±33.3 MBq,平均残留活性为93.1±12.6 MBq,给药率为77.8%,残留比为22.2%。输液回路的残留率最高(18.0%),主要是由排气过滤器(13.5%)和输液器(4.0%)造成的。与实测值相比,UG-02系统明显高估了药瓶中的残留比(1.5% vs. 0.9%)。结论:本研究表征了UG-02自动输注系统中的残留分布,并确定了18F-florbetapir给药的最佳残留设置。实施这种设置可以提高剂量计算的准确性,减少剂量不足的风险,并可能有助于提高淀粉样蛋白PET成像的定量可靠性。