整机18F-FDG PET/CT:更多选择,提升临床扫描效率。

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Jie Xiao, Shuguang Chen, Xiaoguang Hou, Haojun Yu, Siwei Liu, Taoying Gu, Guobing Liu, Qi Ge, Jingyi Wang, Hongcheng Shi
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引用次数: 0

摘要

背景:本研究旨在基于理论模型和单一中心的临床经验,通过优化扫描策略,使全身(TB) 18F-FDG PET/CT系统的临床扫描效率最大化。结果:本前瞻性研究包括两部分。第一部分涉及模拟实验,使用理论模型在四种临床扫描场景中最大化患者吞吐量和/或最小化放射性示踪剂活性:固定工作时间,预定放射性示踪剂活性,为固定数量的患者整合各种注射活性方案,以及在固定工作时间内将动态扫描纳入常规静态扫描。针对这些情况,提出了最优扫描策略。第二部分通过在实际临床环境下进行的高通量测试验证了估计的吞吐量结果,固定工作时间为8小时。在固定工作时间为8小时下,全活性、半活性、1/3活性和1/10活性注射方案的理论患者吞吐量分别为60、48、43、30例患者。相应的实际临床吞吐量分别为60、49、48、28例。对于总18F-FDG活性为37,000至148,000 MBq(1至4 Ci), 1/3活性注射方案产生了最高的患者吞吐量,范围为52至72例。策略性地结合各种注射活性方案可以减少放射性示踪剂活性的消耗。此外,在常规静态扫描全活度、半活度和1/3活度之后以及在1/10活度之前进行全活度动态扫描,被证明是更经济的策略。结论:针对TB 18F-FDG PET/CT系统的典型临床场景,提出了优化的扫描策略,可以提高临床扫描效率,适应不同的临床需求。这些策略使中心能够在保持诊断质量的同时平衡吞吐量和活动效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Total-body <sup>18</sup>F-FDG PET/CT: more choices to promote clinical scanning efficiency.

Total-body <sup>18</sup>F-FDG PET/CT: more choices to promote clinical scanning efficiency.

Total-body <sup>18</sup>F-FDG PET/CT: more choices to promote clinical scanning efficiency.

Total-body 18F-FDG PET/CT: more choices to promote clinical scanning efficiency.

Background: The study aims to maximize clinical scan efficiency for Total-body (TB) 18F-FDG PET/CT systems by optimizing scan strategies based on theoretical models and clinical experience from a single center.

Results: This prospective study include two parts. The first part involved simulation experiments using theoretical models to maximize patient throughput and/or minimizing radiotracer activity across four clinical scanning scenarios: fixed working time, predetermined radiotracer activity, integration of various injection activity regimens for a fixed number of patients, and incorporation of dynamic scans into routine static scans within a fixed working time. The optimal scan strategies for these scenarios were then proposed. The second part validated the estimated throughput results through high-throughput tests performed in the real clinical settings with an fixed working time of 8 h. Under a fixed working time of 8 h, the theoretical patient throughput for full-activity, half-activity, 1/3-activity, and 1/10-activity injection regimens was 60, 48, 43, 30 patients, respectively. The corresponding real clinical throughput achieved was 60, 49, 48, 28 patients. For a total 18F-FDG activity of 37,000 to 148,000 MBq (1 to 4 Ci), the 1/3-activity injection regimen yielded the highest patient throughput, ranging 52 to 72 patients. Strategically combining various injection activity regimens could reduce radiotracer activity consumption. Additionally, placing full-activity dynamic scans after routine static scans for full-activity, half-activity, and 1/3-activity, and before 1/10 activity, proved to ba more economical strategies.

Conclusions: Optimized scan strategies for typical clinical scenarios of TB 18F-FDG PET/CT systems were proposed, which could promote clinical scan efficiency and accommodate diverse clinical requirements. These strategies enable centers to balance throughput and activity efficiency while maintaining diagnostic quality.

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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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