Pregnancy outcomes following gestational exposure to papaverine: An observational comparative study

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Abstract

Aims: Papaverine is indicated for abdominal pain of various aetiologies. However, data on maternal and foetal safety following gestational exposure are lacking. The aim was to examine whether first trimester exposure to papaverine is associated with increased risk for major malformation and whether gestational exposure at any stage is associated with increased risk for preterm delivery, lower birthweight, small for gestational age, caesarean section (CS), lower Apgar score and perinatal death. Methods: A retrospective comparative study consisted of pregnant women treated with papaverine between February 2010 and October 2019 at a large tertiary center. The control group comprised of livebirth deliveries randomly selected from the institutional obstetric database. Results: The study group consisted of 498 pregnancies, which resulted in 537/544 (98.7%) live births, of whom 46/537 (8.6%) were exposed during the first trimester. The control group consisted of 498 pregnancies and 514 live births. Rate of major malformations did not differ between study group (2/46, 4.3%) and control (25/315, 4.9%, P =.67). Papaverine exposure was associated with higher rate of preterm delivery (22.3 vs. 10.3%, P

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Gueta, I., Braun, A., Gilan, A., Berlin, M., Kohn, E., Barchel, D., … Loebstein, R. (2021). Pregnancy outcomes following gestational exposure to papaverine: An observational comparative study. British Journal of Clinical Pharmacology, 87(10), 3910–3915. https://doi.org/10.1111/bcp.14809

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