Department of Nuclear Medicine, University Hospital of Bordeaux, Bordeaux, France
Department of Nuclear Medicine, Centre Henri Becquerel, Rouen, France.
J Nucl Med. 2016 Nov;57(11):1760-1763. doi: 10.2967/jnumed.116.173294. Epub 2016 Jun 3.
Data from the literature show that the fetal absorbed dose from F-FDG administration to the pregnant mother ranges from 0.5E-2 to 4E-2 mGy/MBq. These figures were, however, obtained using different quantification techniques and with basic geometric anthropomorphic phantoms. The aim of this study was to refine the fetal dose estimates of published as well as new cases using realistic voxel-based phantoms.
The F-FDG doses to the fetus (n = 19; 5-34 wk of pregnancy) were calculated with new voxel-based anthropomorphic phantoms of the pregnant woman. The image-derived fetal time-integrated activity values were combined with those of the mothers' organs from the International Commission on Radiological Protection publication 106 and the dynamic bladder model with a 1-h bladder-voiding interval. The dose to the uterus was used as a proxy for early pregnancy (up to 10 wk). The time-integrated activities were entered into OLINDA/EXM 1.1 to derive the dose with the classic anthropomorphic phantoms of pregnant women, then into OLINDA/EXM 2.0 to assess the dose using new voxel-based phantoms.
The average fetal doses (mGy/MBq) with OLINDA/EXM 2.0 were 2.5E-02 in early pregnancy, 1.3E-02 in the late part of the first trimester, 8.5E-03 in the second trimester, and 5.1E-03 in the third trimester. The differences compared with the doses calculated with OLINDA/EXM 1.1 were +7%, +70%, +35%, and -8%, respectively.
Except in late pregnancy, the doses estimated with realistic voxelwise anthropomorphic phantoms are higher than the doses derived from old geometric phantoms. The doses remain, however, well below the threshold for any deterministic effects. Thus, pregnancy is not an absolute contraindication of a clinically justified F-FDG PET scan.
使用新的基于体素的人体模型来细化已发表和新案例的胎儿剂量估算。
使用新的基于体素的孕妇人体模型计算胎儿(n = 19;妊娠 5-34 周)的 F-FDG 剂量。将来自国际辐射防护委员会出版物 106 的母亲器官的图像衍生胎儿时间积分活动值与母亲器官的图像衍生胎儿时间积分活动值相结合,并使用具有 1 小时膀胱排空间隔的动态膀胱模型。将子宫剂量用作早孕(直至 10 周)的代理。将时间积分活动值输入 OLINDA/EXM 1.1 以从经典孕妇人体模型中得出剂量,然后输入 OLINDA/EXM 2.0 以使用新的基于体素的人体模型评估剂量。
OLINDA/EXM 2.0 的平均胎儿剂量(mGy/MBq)分别为早孕 2.5E-02,第一 trimester 末 1.3E-02,第二 trimester 8.5E-03,第三 trimester 5.1E-03。与 OLINDA/EXM 1.1 计算的剂量相比,差异分别为+7%、+70%、+35%和-8%。
除了妊娠晚期,基于真实体素的人体模型估算的剂量高于从旧的几何人体模型得出的剂量。然而,剂量仍然远低于任何确定性效应的阈值。因此,妊娠并不是临床合理的 F-FDG PET 扫描的绝对禁忌症。