Exposure to Thioguanine During 117 Pregnancies in Women With Inflammatory Bowel Disease
- PMID: 36521000
- PMCID: PMC10155742
- DOI: 10.1093/ecco-jcc/jjac183
Exposure to Thioguanine During 117 Pregnancies in Women With Inflammatory Bowel Disease
Abstract
Background: Safety of thioguanine in pregnant patients with inflammatory bowel disease [IBD] is sparsely recorded. This study was aimed to document the safety of thioguanine during pregnancy and birth.
Methods: In this multicentre case series, IBD patients treated with thioguanine during pregnancy were included. Data regarding disease and medication history, pregnancy course, obstetric complications, and neonatal outcomes were collected.
Results: Data on 117 thioguanine-exposed pregnancies in 99 women were collected. Most [78%] had Crohn's disease and the mean age at delivery was 31 years. In 18 pregnancies [15%], IBD flared. Obstetric and infectious complications were seen in 15% [n = 17] and 7% [n = 8] of pregnancies, respectively. Ten pregnancies [8.5%] resulted in a first trimester miscarriage, one in a stillbirth at 22 weeks of gestational age and one in an induced abortion due to trisomy 21. In total, 109 neonates were born from 101 singleton pregnancies and four twin pregnancies. One child was born with a congenital abnormality [cleft palate]. In the singleton pregnancies, 10 children were born prematurely and 10 were born small for gestational age. Screening for myelosuppresion was performed in 16 neonates [14.7%]; two had anaemia in umbilical cord blood. All outcomes were comparable to either the general Dutch population or to data from three Dutch cohort studies on the use of conventional thiopurines in pregnant IBD patients.
Conclusion: In this large case series, the use of thioguanine during pregnancy is not associated in excess with adverse maternal or neonatal outcomes.
Keywords: Inflammatory bowel disease; pregnancy; thioguanine.
© The Author(s) 2022. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation.
Conflict of interest statement
FC, MAdB, CJJM, EMvA, RHC, CSH, MCV, ALMW, MLS, BJ, IA, PJB, GJT, LW, MWMDL, PGAvB, MK, MGVMR, FH, MEB, WAvD, JW, MMPJAvdV and HJCB have nothing to declare. MS has received an unrestricted research grant from TEVA. DPvA served as speaker, adviser, and/or principal investigator for Dr Falk, Ferring, Galapagos/Gilead, and Takeda, and received research grants from Janssen and Dr Falk. AAvB served as speaker, adviser, and/or principal investigator for AbbVie, Arandal, Arena Pharmaceuticals/Pfizer, Celgene, Ferring, Galapagos/Gilead, Janssen/Johnson and Johnson, Merck Sharpe & Dohme, Pfizer, Receptos, Roche, Takeda, TEVA, Bristol Myers Squibb, and received research grants from TEVA, Eurostars funding, ZonMW, and Pfizer. FDMvS served as adviser for Takeda, Galapagos, and Dr Falk. LPLG has served as a speaker for AbbVie and Boston, and received a grant from Ferring to develop e-learning about therapeutic drug monitoring. JPK has served as an adviser for AbbVie and Janssen/Johnson & Johnson. PWJM has served as a speaker for Janssen, Galapagos, and Takeda, and received research grants from Galapagos and Takeda. NKdB has served as a speaker for AbbVie and MSD, has served as consultant and principal investigator for TEVA Pharma BV and Takeda, and received unrestricted research grants from Dr. Falk, TEVA Pharma BV, MLDS, and Takeda.
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