Laffon Eric, Cazeau Anne-Laure, Monet Antoine, de Clermont Henri, Fernandez Philippe, Marthan Roger, Ducassou Dominique
CHU de Bordeaux, Service de Médecine Nucléaire, F-33600 Pessac, France.
J Nucl Med Technol. 2008 Dec;36(4):200-2. doi: 10.2967/jnmt.107.049627. Epub 2008 Nov 13.
This work addresses the issue of using (18)F-FDG PET in patients with renal failure.
A model analysis has been developed to compare tissue (18)F-FDG uptake in a patient who has normal renal function with uptake in a theoretic limiting case that assumes tracer plasma decay is tracer physical decay and is trapped irreversibly.
This comparison has allowed us to propose, in the limiting case, that the usually injected activity be lowered by a factor of 3. We also proposed that the PET static acquisition be obtained at about 160 min after tracer injection. These 2 proposals were aimed at obtaining a similar patient radiation dose and similar tissue (18)F-FDG uptake.
In patients with arbitrary renal failure (i.e., between the 2 extremes of normal function and the theoretic limiting case), we propose that the injected activity be lowered (without exceeding a factor of 3) and that the acquisition be started between 45 and 160 min after tracer injection, depending on the severity of renal failure. Furthermore, the model also shows that the more severe the renal failure is, the more overestimated is the standardized uptake value, unless the renal failure indirectly impairs tissue sensitivity to insulin and hence glucose metabolism.
本研究探讨了肾衰竭患者使用(18)F-FDG PET的问题。
已开发出一种模型分析方法,用于比较肾功能正常患者的组织(18)F-FDG摄取情况与理论极限情况下的摄取情况,该理论极限情况假设示踪剂血浆衰变即示踪剂物理衰变且被不可逆地滞留。
通过这种比较,我们在极限情况下提出,通常注射的活度应降低3倍。我们还提议在示踪剂注射后约160分钟进行PET静态采集。这两个提议旨在使患者接受相似的辐射剂量并使组织(18)F-FDG摄取情况相似。
对于任意肾衰竭患者(即介于正常功能和理论极限情况这两个极端之间),我们建议降低注射活度(不超过3倍),并根据肾衰竭的严重程度在示踪剂注射后45至160分钟之间开始采集。此外,该模型还表明,肾衰竭越严重,标准化摄取值被高估得就越多,除非肾衰竭间接损害组织对胰岛素的敏感性从而影响葡萄糖代谢。