Key result
Direct oral anticoagulants showed comparable rates of cardiovascular death or thromboembolic events to vitamin K antagonists (RR 0.67; 95% CI 0.42-1.08; p=0.10) but significantly reduced major bleeding.
Why the study?
DOACs could provide an alternative to VKAs, but their safety and efficacy needed systematic review in patients with AF undergoing bioprosthetic heart valve replacement or valve repair.
Do DOACs reduce thromboembolic and bleeding events compared to VKAs in patients with atrial fibrillation and surgically implanted bioprosthetic heart valves or valve repairs?
Meta-Analysis (n=1,857)
Do DOACs reduce thromboembolic and bleeding events compared to VKAs in patients with atrial fibrillation and surgically implanted bioprosthetic heart valves or valve repairs?
Answers are grounded in this paper and cite their sources.
DOACs provide a safe and effective alternative to VKAs in patients with AF and bioprosthetic heart valves or repairs, significantly reducing major bleeding and thromboembolic stroke.
Aims: Oral anticoagulation with direct oral anticoagulants (DOAC) could provide an alternative to vitamin K antagonists (VKA) for patients with atrial fibrillation (AF) undergoing bioprosthetic heart valve replacement or valve repair. Methods and results: The aim of this meta-analysis was to review the safety and efficacy of DOAC in patients with surgical implanted bioprosthetic heart valves or valve repairs and AF including data from six clinical trials with a total of 1,857 patients. The efficacy and safety data of DOAC and VKA were pooled to perform random-effects meta-analyses using the Mantel–Haenszel method with pooled risk ratios (RR) and 95% confidence interval (CI). A trial sequential analysis (TSA) was performed to assess statistical robustness. Death caused by cardiovascular cause or thromboembolic events were comparable (RR 0.67, 95% CI: 0.42–1.08; p = 0.10) as DOAC significantly reduced the risk for major bleeding (RR 0.55, 95% CI: 0.35–0.88; p = 0.01) and thromboembolic stroke or systemic embolism rates (RR 0.54, 95% CI: 0.32–0.90; p = 0.02). Rates for intracranial bleeding and hemorrhagic stroke (RR 0.27, 95% CI: 0.07–0.99; p = 0.05) show a trend toward fewer events in the DOAC group. Outcomes for major or minor bleeding events and all-cause mortality were comparable for DOAC and VKA. Conclusion: Cumulative data analysis reveals that DOAC may provide an effective and safe alternative to VKA in patients with AF after surgically implanted bioprosthetic heart valves or repair with AF. Within a relatively heterogeneous study population, this meta-analysis shows a risk reduction of major bleedings and thromboembolic stroke or systemic embolisms for DOAC.
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Gerfer et al. (2022) conducted a meta-analysis in Atrial fibrillation with bioprosthetic heart valve replacement or valve repair (n=1,857). Direct oral anticoagulants (DOAC) vs. Vitamin K antagonists (VKA) was evaluated on Death caused by cardiovascular cause or thromboembolic events (RR 0.67, 95% CI 0.42-1.08, p=0.10). Direct oral anticoagulants showed comparable rates of cardiovascular death or thromboembolic events to vitamin K antagonists (RR 0.67; 95% CI 0.42-1.08; p=0.10) but significantly reduced major bleeding.
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