Literature DB >> 25830592

Pregnancy outcome following maternal exposure to mirtazapine: a multicenter, prospective study.

Ursula Winterfeld1, Gil Klinger, Alice Panchaud, Sally Stephens, Judy Arnon, Heli Malm, Bernke Te Winkel, Maurizio Clementi, Alessandra Pistelli, Eva Maňáková, Georgios Eleftheriou, Paul Merlob, Yusuf C Kaplan, Thierry Buclin, Laura E Rothuizen.   

Abstract

This multicenter, observational prospective cohort study addresses the risk associated with exposure to mirtazapine during pregnancy. Pregnancy outcomes after exposure to mirtazapine were compared with 2 matched control groups: (1) exposure to any selective serotonin reuptake inhibitor (SSRI, control subjects with a psychiatric condition) and (2) no exposure to medication known to be teratogenic or any antidepressant (general control subjects). Data were collected by members of the European Network of Teratology Information Services between 1995 and 2011. Observations from 357 exposed pregnancies were compared with 357 pregnancies from each control group. The rate of major birth defects between the mirtazapine and the SSRI group did not differ significantly (4.5% vs 4.2%; odds ratio [OR], 1.1; 95% confidence interval [95% CI], 0.5-2.3; P = 0.9). A trend toward a higher rate of birth defects in the mirtazapine group compared with general control subjects (4.5% vs 1.9%; OR, 2.4; 95% CI, 0.9-6.3; P = 0.08) reached statistical significance after exclusion of chromosomal or genetic anomalies (4.1% vs 1.3%; OR, 3.3; 95% CI, 1.04-10.3; P = 0.03), but this difference became again nonsignificant if cases of exposure not comprising the first trimester were excluded from the analysis (3.4% vs 1.9%; OR, 1.8; 95% CI, 0.6-5.0; P = 0.26). The crude miscarriage rate did not differ significantly between the mirtazapine, the SSRI, and the general control groups (12.1% vs 12.0% vs 9.3%; P = 0.44). However, a higher rate of elective pregnancy termination was observed in the mirtazapine group compared with SSRI and general control subjects (7.8% vs 3.4% vs 5.6%; P = 0.03). This study did not observe a statistically significant difference in the rate of major birth defects after first-trimester exposure between mirtazapine, SSRI-exposed, and nonexposed pregnancies. A marginally higher rate of birth defects was, however, observed in the mirtazapine and SSRI groups compared with the low rate of birth defects in our general control subjects. Overall pregnancy outcome after mirtazapine exposure was similar to that of the SSRI-exposed control group.

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Year:  2015        PMID: 25830592     DOI: 10.1097/JCP.0000000000000309

Source DB:  PubMed          Journal:  J Clin Psychopharmacol        ISSN: 0271-0749            Impact factor:   3.153


  7 in total

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3.  Pregnancy outcomes in women on metformin for diabetes or other indications among those seeking teratology information services.

Authors:  Alice Panchaud; Valentin Rousson; Thierry Vial; Nathalie Bernard; David Baud; Emmanuelle Amar; Marco De Santis; Alessandra Pistelli; Anne Dautriche; Frederique Beau-Salinas; Matteo Cassina; Hannah Dunstan; Anneke Passier; Yusuf Cem Kaplan; Mine Kadioglu Duman; Eva Maňáková; Georgios Eleftheriou; Gil Klinger; Ursula Winterfeld; Laura E Rothuizen; Thierry Buclin; Chantal Csajka; Sonia Hernandez-Diaz
Journal:  Br J Clin Pharmacol       Date:  2018-01-14       Impact factor: 4.335

Review 4.  Depression and Anxiety During Pregnancy: Evaluating the Literature in Support of Clinical Risk-Benefit Decision-Making.

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7.  Mirtazapine exposure in pregnancy and fetal safety: A nationwide cohort study.

Authors:  Anne Ostenfeld; Tonny Studsgaard Petersen; Lars Henning Pedersen; Hanne Brix Westergaard; Ellen Christine Leth Løkkegaard; Jon Traerup Andersen
Journal:  Acta Psychiatr Scand       Date:  2022-04-01       Impact factor: 7.734

  7 in total

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