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September 25, 2014BMC Pregnancy and Childbirth41 citationsOpen Access

Increased risk of severe congenital heart defects in offspring exposed to selective serotonin-reuptake inhibitors in early pregnancy – an epidemiological study using validated EUROCAT data

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TKTanja Majbrit KnudsenAHAnne Vinkel HansenEGEster Garne

Key Result

Maternal use of selective serotonin-reuptake inhibitors during the first trimester increased the risk of severe congenital heart defects in offspring by four times (AOR 4.03).

Study Design

Type

Cohort (n=72,280)

Structured PICO

Does maternal use of selective serotonin-reuptake inhibitors during early pregnancy increase the risk of severe congenital heart defects in offspring?

P
Population
72,280 registered pregnancies in Funen, Denmark in the period 1995-2008
I
Intervention
Selective serotonin-reuptake inhibitors (SSRIs) used during first trimester
C
Comparator
No SSRI use during first trimester
O
Outcome
Severe congenital heart defects (CHD) in offspringhard clinical

Maternal use of SSRIs during the first trimester is associated with a four-fold increased risk of severe congenital heart defects in offspring, though not septal defects.

Main Result

Effect estimate: AOR 4.03 (95% CI 1.75-9.26)

Absolute Event Rate: 0.71% vs 0.17%

Limitations

  • Limited size of the study population resulting in lack of statistical power for specific diagnoses and interactions.
  • Risk of misclassification of exposure since prescription redemption does not guarantee medication consumption.
  • Lack of information on important potential confounders due to reliance on administrative registers.
  • Grouping of CHD diagnoses with heterogeneous etiology may dilute the studied association.

Abstract

BACKGROUND: Previous studies suggest a possible association between maternal use of selective serotonin-reuptake inhibitors (SSRIs) during early pregnancy and congenital heart defects (CHD). The purpose of this study was to verify this association by using validated data from the Danish EUROCAT Register, and secondary, to investigate whether the risk differs between various socioeconomic groups. METHODS: We conducted a cohort study based on Danish administrative register data linked with the Danish EUROCAT Register, which includes all CHD diagnosed in live births, fetal deaths and in pregnancies terminated due to congenital anomalies. The study population consisted of all registered pregnancies (n = 72,280) in Funen, Denmark in the period 1995-2008. SSRI-use was assessed using The Danish National Prescription Registry, information on marital status, maternal educational level, income, and country of origin from Statistics Denmark was used as indicators of socioeconomic situation, and the CHD were studied in subgroups defined by EUROCAT. Logistic Regression was used to investigate the association between redeemed prescriptions for SSRIs and CHD. RESULTS: The risk of severe CHD in the offspring of the 845 pregnant women who used SSRIs during first trimester increased four times (AOR 4.03 (95% CI 1.75-9.26)). We found no increased risk of septal defects. Socioeconomic position did not modify the association between maternal SSRI-use during pregnancy and severe CHD. CONCLUSION: This study, which is based on data with high case ascertainment, suggests that maternal use of SSRIs during first trimester increases the risk of severe CHD, but does not support findings from previous studies, based on administrative register data, regarding an increased risk of septal defects. The study was unable to document an interaction between socioeconomic status and maternal SSRI-use on the risk of severe CHD.

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Cite This Study

Knudsen et al. (2014) conducted a cohort in Pregnancy (n=72,280). Selective serotonin-reuptake inhibitors (SSRIs) vs. Unexposed (no SSRI prescription during the exposure window) was evaluated on Severe congenital heart defects (AOR 4.03, 95% CI 1.75-9.26). Maternal use of selective serotonin-reuptake inhibitors during the first trimester increased the risk of severe congenital heart defects in offspring by four times (AOR 4.03).

synapsesocial.com/papers/6a10beed8102eb4b66ee4ce7https://doi.org/10.1186/1471-2393-14-333
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