Key result
Beta-blockers reduce arrhythmias in pregnant women with LQTS but are linked to fetal growth restriction.
Why the study?
Beta-blocker therapy is foundational for managing long QT syndrome, but its use during pregnancy introduces potential fetal risks.
Does beta-blocker therapy reduce arrhythmic events in pregnant women with Long QT syndrome?
Systematic Review
Does beta-blocker therapy reduce arrhythmic events in pregnant women with Long QT syndrome?
Beta-blocker therapy is highly effective in reducing maternal arrhythmic events in pregnant women with Long QT syndrome, but necessitates individualized selection and close monitoring due to associated fetal risks like growth restriction.
Supports individualized beta-blocker use in pregnant LQTS with fetal monitoring; confirms maternal benefit while extending evidence on growth risks.
Long QT syndrome (LQTS) presents significant challenges for pregnant women due to the elevated risk of arrhythmic events. Beta-blocker therapy is a cornerstone of treatment in managing LQTS, but its use during pregnancy introduces potential fetal risks. This systematic review synthesizes the evidence on the efficacy and safety of beta-blocker therapy in pregnant women with LQTS. A systematic review was conducted to assess studies on beta-blocker use in pregnant women diagnosed with LQTS. We reviewed observational studies and case reports to evaluate maternal cardiac outcomes, fetal safety, and the need for postpartum management. Studies were selected based on inclusion criteria focused on LQTS, beta-blocker therapy during pregnancy, and associated maternal and fetal outcomes. Our review showed that beta-blocker therapy significantly reduced arrhythmic events in pregnant women with LQTS, particularly in symptomatic carriers. Multiple studies demonstrated that the continuation of beta-blocker therapy throughout pregnancy and the postpartum period minimized maternal cardiac risks. However, beta-blocker use was associated with fetal risks such as intrauterine growth restriction (IUGR), lower birth weight, and, in some cases, bradycardia. Atenolol, in particular, was linked to significant fetal growth restrictions, while other beta-blockers, such as propranolol and metoprolol, showed more variable effects on fetal outcomes. Despite these concerns, some studies reported favorable postnatal growth recovery in infants exposed to beta-blockers in utero. Beta-blocker use must be carefully managed due to potential fetal risks. Regular monitoring, individualized treatment plans, and appropriate selection of beta-blocker type are essential to optimizing both maternal and fetal outcomes. Further research is necessary to refine treatment protocols and reduce fetal risks associated with beta-blocker therapy during pregnancy.
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Alrabadi et al. (2024) conducted a systematic review in Long QT syndrome (LQTS) in pregnancy. Beta-blocker therapy was evaluated on Maternal cardiac outcomes and fetal safety. Beta-blocker therapy significantly reduced arrhythmic events in pregnant women with LQTS, but was associated with fetal risks such as intrauterine growth restriction and lower birth weight.
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