Evidence map›Paper›PMID 25888213›Full record

ArticleBMJ (Clinical research ed.)2015

Selective serotonin reuptake inhibitors and venlafaxine in early pregnancy and risk of birth defects: population based cohort study and sibling design.

Kari Furu, Helle Kieler, Bengt Haglund, Anders Engeland, Randi Selmer, Olof Stephansson, Unnur Anna Valdimarsdottir, Helga Zoega, Miia Artama, Mika Gissler and 2 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in BMJ (Clinical research ed.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 63 papers, 11 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 11 pooled it
19.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 11 syntheses or guidelines pooled it, 185 citations in OpenAlex.

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  14. Observational
  15. Neuromodulation for Headache Management in Pregnancy.Current pain and headache reports · 2025
    Review
  16. Depression Treatment in Pregnancy: Is It Safe, or Is It Not?International journal of environmental research and public health · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Review

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 6 countries.

Kari FuruDepartment of Pharmacoepidemiology, Division of Epidemiology, Norwegian Institute of Public Health, PB 4404 Nydalen, NO 0403 Oslo, Norway kari.furu@fhi.no.
Helle KielerDepartment of Medicine Solna, Centre for Pharmacoepidemiology, Karolinska Institutet Stockholm, Sweden.
Bengt HaglundDepartment of Medicine Solna, Centre for Pharmacoepidemiology, Karolinska Institutet Stockholm, Sweden.
Anders EngelandDepartment of Pharmacoepidemiology, Division of Epidemiology, Norwegian Institute of Public Health, PB 4404 Nydalen, NO 0403 Oslo, Norway Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Randi SelmerDepartment of Pharmacoepidemiology, Division of Epidemiology, Norwegian Institute of Public Health, PB 4404 Nydalen, NO 0403 Oslo, Norway.
Olof StephanssonDepartment of Medicine Solna, Centre for Pharmacoepidemiology, Karolinska Institutet Stockholm, Sweden Department of Women's and Children's Health, Division of Obstetrics and Gynecology, Karolinska Institutet, Stockholm, Sweden.
Unnur Anna ValdimarsdottirCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland Department of Epidemiology, Harvard T H Chan School of Public Health, Boston, MA, USA.
Helga ZoegaCentre of Public Health Sciences, Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.
Miia ArtamaDepartment of Medical Genetics, University of Helsinki, Helsinki, Finland Department of Child Psychiatry, University of Turku, Turku, Finland.
Mika GisslerTHL National Institute for Health and Welfare, Helsinki, Finland Nordic School of Public Health, Gothenburg, Sweden.
Heli MalmTeratology Information Service, HUSLAB and Helsinki University Central Hospital, Helsinki, Finland Department of Clinical Pharmacology, Helsinki University, Helsinki, Finland.
Mette NørgaardDepartment of Clinical Epidemiology, Institute of Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark.
Karolinska Institutet · SENorwegian Institute of Public Health · NOUniversity of Iceland · ISAarhus University Hospital · DKHelsinki University Hospital · FINordic School of Public Health · SEUniversity of Bergen · NOUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess whether use of specific selective serotonin reuptake inhibitors (SSRIs) or venlafaxine in early pregnancy is associated with an increased risk of birth defects, with emphasis on cardiovascular birth defects even when accounting for lifestyle or other familial confounding.

designMulticountry population based cohort study, including sibling controlled design.

settingNordic population (Denmark, Finland, Iceland, Norway, and Sweden) identified from nationwide health registers at different periods in 1996-2010. POPULATION: The full study cohort included women giving birth to 2.3 million live singletons. The sibling cohort included 2288 singleton live births. The sibling controlled analyses included sibling pairs who were discordant for exposure to SSRIs or venlafaxine and birth defects.

main outcome measurePrevalence of birth defects, including subtypes of cardiac defects. Odds ratio of birth defects from logistic and conditional logistic regression.

resultsAmong 36,772 infants exposed to any SSRI in early pregnancy, 3.7% (n=1357) had a birth defect compared with 3.1% of 2,266,875 unexposed infants, yielding a covariate adjusted odds ratio of 1.13 (95% confidence interval 1.06 to 1.20). In the sibling controlled analysis the adjusted odds ratio decreased to 1.06 (0.91 to 1.24). The odds ratios for any cardiac birth defect with use of any SSRI or venlafaxine were 1.15 (95% confidence interval 1.05 to 1.26) in the covariate adjusted analysis and 0.92 (0.72 to 1.17) in the sibling controlled analysis. For atrial and ventricular septal defects the covariate adjusted odds ratio was 1.17 (1.05 to 1.31). Exposure to any SSRI or venlafaxine increased the prevalence of right ventricular outflow tract obstruction defects, with a covariate adjusted odds ratio of 1.48 (1.15 to 1.89). In the sibling controlled analysis the adjusted odds ratio decreased to 0.56 (0.21 to 1.49) for any exposure to SSRIs or venlafaxine and right ventricular outflow tract obstruction defects.

conclusionsIn this large Nordic study no substantial increase was found in prevalence of overall cardiac birth defects among infants exposed to SSRIs or venlafaxine in utero. Although the prevalence of septal defects and right ventricular outflow tract defects was higher in exposed infants, the lack of an association in the sibling controlled analyses points against a teratogenic effect of these drugs.

Indexed as

AdultCohort StudiesContraindicationsCyclohexanolsDepressive DisorderFemaleHeart Defects, CongenitalHumansInfant, NewbornLogistic ModelsOdds RatioPopulation SurveillancePregnancyPregnancy ComplicationsScandinavian and Nordic CountriesSelective Serotonin Reuptake InhibitorsCyclohexanolsSelective Serotonin Reuptake InhibitorsVenlafaxine Hydrochloride

Identifiers

PMID25888213
PMCPMC4410618
OpenAlexW1849790101

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.