American Journal of Obstetrics & Gynecology
Volume 193, Issue 6 , Pages 2004-2009, December 2005

Citalopram use in pregnancy: Prospective comparative evaluation of pregnancy and fetal outcome

  • Anna Sivojelezova, BSc

      Affiliations

    • The Motherisk Program, Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children
    • Department of Pharmaceutical Sciences, University of Toronto, Ontario, Canada
    • Corresponding Author InformationReprint requests: Anna Sivojelezova, BSc, The Motherisk Program, Division of Clinical Pharmacology/Toxicology, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada.
  • ,
  • Samar Shuhaiber, MSc

      Affiliations

    • The Motherisk Program, Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children
  • ,
  • Lorig Sarkissian, BSc

      Affiliations

    • The Motherisk Program, Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children
  • ,
  • Adrienne Einarson, RN

      Affiliations

    • The Motherisk Program, Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children
  • ,
  • Gideon Koren, MD

      Affiliations

    • The Motherisk Program, Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children
    • Department of Pharmaceutical Sciences, University of Toronto, Ontario, Canada

Received 3 February 2005; received in revised form 1 April 2005; accepted 2 May 2005.

Objective

Citalopram is a selective serotonin reuptake inhibitor indicated for depression. The safety of this medication in pregnancy has not been fully established. The purpose of this study was to investigate whether citalopram is associated with an increased incidence of adverse pregnancy outcomes.

Study design

Pregnant women who contacted the Motherisk Program, a Teratogen Information Center in Toronto, Ontario, with regard to the safety of citalopram in pregnancy were enrolled in the study. The exposed women were matched to a disease-matched group of women and a nonteratogenic group. All women were matched for age (± 2 years) and gestational age at time of first call to the Motherisk (± 2 weeks). A structured telephone follow-up interview was conducted following the expected date of confinement.

Results

The total number of pregnant women enrolled in this study was 396 (132 women in each group). A total of 125 women took citalopram at least in the first trimester. Seventy-one (54%) women continued to take the drug throughout pregnancy. One hundred fourteen women (86%) had live births, 14 (11%) had spontaneous abortions, 2 (1.5%) had elective terminations, and 2 (1.5%) experienced stillbirths. Fetal survival rates, mean birth weights, and duration of pregnancy were not statistically different among the 3 groups. Of 108 live-born infants whose mothers were exposed to citalopram in the first trimester, there was 1 (0.9%) male infant born with a major malformation. There was a relative risk of 4.2 (95% confidence interval 1.71-10.26) in neonates exposed to citalopram close to term to be admitted to special-care nurseries as compared with the unexposed infants.

Conclusion

Citalopram use during the period of embryogenesis in pregnancy is not associated with an apparent major teratogenic risk. Late pregnancy use of citalopram is associated with increased risk of poor neonatal adaptation syndrome, recently described with other selective serotonin reuptake inhibitors.

Key words: Citalopram, Selective serotonin reuptake inhibitor, Pregnancy outcome, Poor neonatal adaptation

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 Supported in part by the Research Leadership for Better Pharmacotherapy During Pregnancy and Lactation.Gideon Koren is a Senior Scientist of the Canadian Institutes for Health Research and holder of the Ivey Chair in Molecular Toxicology, The University of Western Ontario.

PII: S0002-9378(05)00656-3

doi:10.1016/j.ajog.2005.05.012

American Journal of Obstetrics & Gynecology
Volume 193, Issue 6 , Pages 2004-2009, December 2005