Key result
Direct oral anticoagulants were associated with a significantly reduced risk of thromboembolic events compared to vitamin K antagonists in patients with atrial fibrillation and cardiac amyloidosis (OR 0.52).
Why the study?
Evidence comparing the safety and efficacy of direct oral anticoagulants with vitamin K antagonists in patients with atrial fibrillation and cardiac amyloidosis needed systematic review and synthesis.
Does DOAC therapy reduce thromboembolic events and major bleeding compared to VKAs in patients with atrial fibrillation and cardiac amyloidosis?
Meta-Analysis (n=1,579)
Does DOAC therapy reduce thromboembolic events and major bleeding compared to VKAs in patients with atrial fibrillation and cardiac amyloidosis?
Odds Ratio: 0.52 (95% CI 0.32–0.84)
DOACs are associated with a reduced risk of thromboembolic events compared to VKAs without increasing major bleeding in patients with atrial fibrillation and cardiac amyloidosis.
Background: This study aimed to systematically review and synthesize evidence comparing direct oral anticoagulants (DOACs) with vitamin K antagonists (VKAs) for anticoagulation in patients with atrial fibrillation (AF) and cardiac amyloidosis (CA). Methods: A comprehensive search of PubMed and EMBASE databases was conducted through January 2024 to identify studies comparing DOACs and VKAs in AF patients with CA. Eligible studies underwent rigorous screening and data extraction to evaluate safety and efficacy outcomes. Results: Four studies met the criteria. The first study reported similar embolic event rates between DOACs (3.9%) and VKAs (2.9%) per 100 patient years, while major bleeding rates were 5.21% and 3.74%, respectively. The second paper found stroke rates of 2% for DOACs and 4% for VKAs, with bleeding complications observed in 10% of DOAC patients compared to 20% in VKA patients. The third cohort demonstrated that DOACs were associated with significantly lower risks of stroke and major bleeding compared to VKAs. The last study reported embolic event rates of 1.6 and 2.0 per 100 patient years for DOACs and VKAs, respectively. In the pooled analysis, DOACs were associated with a reduced risk of thromboembolic events (odds ratio [OR] = 0.52; 95% confidence interval [CI]: 0.32-0.84), and no difference in major bleeding between the two groups (OR = 0.61, 95% CI: 0.25-1.51). Conclusions: Existing studies support the use of DOACs as a non-inferior therapeutic option compared to VKAs for preventing thromboembolism in patients with AF and cardiac amyloidosis. DOACs may also offer practical advantages, including reduced bleeding risks and ease of management, but further high-quality randomized controlled trials are needed to confirm these findings and guide clinical practice.
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Nong et al. (2025) conducted a meta-analysis in Atrial Fibrillation and Cardiac Amyloidosis (n=1,579). Direct oral anticoagulants (DOACs) vs. Vitamin K antagonists (VKAs) was evaluated on Thromboembolic events (OR 0.52, 95% CI 0.32-0.84). Direct oral anticoagulants were associated with a significantly reduced risk of thromboembolic events compared to vitamin K antagonists in patients with atrial fibrillation and cardiac amyloidosis (OR 0.52).
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