Selective serotonin reuptak inhibitor exposure during early pregnancy and the risk of fetal major malformations: Focus on paroxetine.

Objective. To analyze all studies reporting primary data on the rate of phetal malformations after early in utero exposure to paroxetine, investigated either specifically or jointly with other antidepressant medications. Data sources. Medical literature was identified through searches of Medline-PubMed, Toxnet, Embase, and the Cochrane Library. Search terms were pregnancy, antidepressants, SSRIs, paroxetine, and fetal malformations. Additional studies were identified from the reference lists of published articles. Data selection. Twenty-five articles reporting primary data on the rate of fetal structural malformations following exposure to paroxetine or selective serotonin reuptake inhibitors as a group during the first trimester of pregnancy were electronically or manually selected. Data synthesis. Studies on the teratogenic risk of paroxetine show a high degree of heterogeneity. Morehover, research studies performed with the same methodology and thus showing the same level of evidence report conflicting results. Conclusions. Given the inconsistency of the findings and limitations of the methodology of the published studies, the teratogenic potential of paroxetine that has been reported in some studies remains unproven. This relevant safety question is likely to remain unanswered until large, prospective studies are conducted. Such studies should be designed to include a control group of untreated mothers with similar psychiatric diagnosis so as to differentiate effects of drug exposure from impact of underlying mental disorder on the fetus. Moreover, further experimental studies are warranted to definitively assess clinical consequences of the impact on fetal development related to physiologic effects of prenatal paroxetine exposure on different maternal and fetal parameters.