New Fetal Dose Estimates from 18F-FDG Administered During Pregnancy: Standardization of Dose Calculations and Estimations with Voxel-Based Anthropomorphic Phantoms

被引:18
作者
Zanotti-Fregonara, Paolo [1 ]
Chastan, Mathieu [2 ]
Edet-Sanson, Agathe [2 ]
Ekmekcioglu, Ozgul [3 ]
Erdogan, Ezgi Basak [3 ]
Hapdey, Sebastien [2 ]
Hindie, Elif [1 ]
Stabin, Michael G. [4 ]
机构
[1] Univ Hosp Bordeaux, Dept Nucl Med, Bordeaux, France
[2] Ctr Henri Becquerel, Dept Nucl Med, Rouen, France
[3] Istanbul Univ, Cerrahpasa Med Fac, Dept Nucl Med, Istanbul, Turkey
[4] Vanderbilt Univ, Dept Radiol & Radiol Sci, Nashville, TN USA
关键词
PET; radiation safety; radiobiology/dosimetry; F-18-FDG; pregnancy; dosimetry; PERSONAL-COMPUTER SOFTWARE; FDG-PET/CT; GLUCOSE; PRETERM;
D O I
10.2967/jnumed.116.173294
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Data from the literature show that the fetal absorbed dose from F-18-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. Methods: The F-18-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. Results: 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. Conclusion: 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-18-FDG PET scan.
引用
收藏
页码:1760 / 1763
页数:4
相关论文
共 25 条
  • [1] Placental glucose transfer and fetal growth
    Baumann, MU
    Deborde, S
    Illsley, NP
    [J]. ENDOCRINE, 2002, 19 (01) : 13 - 22
  • [2] Benveniste H, 2003, J NUCL MED, V44, P1522
  • [3] Hodgkin's Disease Staging by FDG PET/CT in a Pregnant Woman
    Calais J.
    Hapdey S.
    Tilly H.
    Vera P.
    Chastan M.
    [J]. Nuclear Medicine and Molecular Imaging, 2014, 48 (3) : 244 - 246
  • [4] POSITRON EMISSION TOMOGRAPHY STUDY OF HUMAN-BRAIN FUNCTIONAL-DEVELOPMENT
    CHUGANI, HT
    PHELPS, ME
    MAZZIOTTA, JC
    [J]. ANNALS OF NEUROLOGY, 1987, 22 (04) : 487 - 497
  • [5] Clement C. H., 2008, Annals of the ICRP, V38, P1, DOI 10.1016/j.icrp.2008.08.003
  • [6] An unknown pregnancy at term detected by a FDG-PET/CT study in a patient with Hodgkin's lymphoma: A case report
    Erdogan, E. B.
    Ekmekcioglu, O.
    Vatankulu, B.
    Ergul, N.
    Demir, M.
    Sonmezoglu, K.
    [J]. REVISTA ESPANOLA DE MEDICINA NUCLEAR E IMAGEN MOLECULAR, 2015, 34 (03): : 201 - 202
  • [7] *ICRP, 2003, ICRP PUBL, V89
  • [8] Cerebral metabolic rate for glucose during the first six months of life: An FDG positron emission tomography study
    Kinnala, A
    SuhonenPolvi, H
    Aarimaa, T
    Kero, P
    Korvenranta, H
    Ruotsalainen, U
    Bergman, J
    Haaparanta, M
    Solin, O
    Nuutila, P
    Wegelius, U
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1996, 74 (03): : F153 - F157
  • [9] THE BLOOD-BRAIN-BARRIER GLUCOSE-TRANSPORTER IS CONSERVED IN PRETERM AND TERM NEWBORN-INFANTS
    MANTYCH, GJ
    SOTELOAVILA, C
    DEVASKAR, SU
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (01) : 46 - 49
  • [10] Cerebral glucose transport and metabolism in preterm human infants
    Powers, WJ
    Rosenbaum, JL
    Dence, CS
    Markham, J
    Videen, TO
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (06) : 632 - 638