Key result
First-trimester beta-blockers show no increased risk for major congenital anomalies despite links to specific defects.
Why the study?
Data about risks of congenital anomalies in offspring associated with first-trimester β-blocker exposure have not been summarized.
Does first-trimester oral beta-blocker use increase the risk of congenital malformations in pregnant women?
Meta-Analysis
Does first-trimester oral beta-blocker use increase the risk of congenital malformations in pregnant women?
Odds Ratio: 1 (95% CI 0.91–1.1)
First-trimester beta-blocker exposure does not increase overall major congenital anomalies but is associated with increased risks of specific organ defects, including cardiovascular and neural tube defects.
Reassures on overall major anomaly risk with first-trimester beta-blockers; leaves open targeted study of specific organ defects.
β-blockers are commonly used during the first trimester of pregnancy. Data about risks of congenital anomalies in offspring have not been summarized. We performed a meta-analysis to determine teratogenicity of β-blockers in early pregnancy. A systematic literature search was performed using PubMed, EMBASE, Cochrane Clinical Trials, and hand search. Meta-analyses were performed using random-effects models based on odds ratios (ORs). Prespecified subgroup analyses were performed to explore heterogeneity. Randomized controlled trials or observational studies examining risks of congenital malformations associated with first trimester β-blocker exposure compared with no exposure were included. Thirteen population-based case-control or cohort studies were identified. Based on meta-analyses, first-trimester oral β-blocker use showed no increased odds of all or major congenital anomalies (OR=1.00; 95% confidence interval, 0.91-1.10; 5 studies). However, in analyses examining organ-specific malformations, increased odds of cardiovascular defects (OR=2.01; 95% confidence interval, 1.18-3.42; 4 studies), cleft lip/palate (OR=3.11; 95% confidence interval, 1.79-5.43; 2 studies), and neural tube defects (OR=3.56; 95% confidence interval, 1.19-10.67; 2 studies) were observed. The effects on severe hypospadias were nonsignificant (1 study). Causality is difficult to interpret given the small number of heterogeneous studies and possibility of biases. Given the frequency of this exposure in pregnancy, further research is needed.
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Yakoob et al. (2013) conducted a meta-analysis in Pregnancy. First-trimester oral β-blockers vs. No exposure was evaluated on All or major congenital anomalies (OR 1.00, 95% CI 0.91-1.10). First-trimester beta-blocker exposure showed no increased odds of all or major congenital anomalies (OR 1.00; 95% CI 0.91-1.10), though increased odds of specific organ defects were observed.
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