Key result
Interrupting VKA during AF ablation is linked to ~38% higher thromboembolic and bleeding risk versus uninterrupted VKA.
Why the study?
Small series suggested uninterrupted VKA is safer than interrupted VKA during AF ablation, but a larger meta-analysis was needed to evaluate safety.
Does uninterrupted Vitamin K antagonist therapy reduce thromboembolic and bleeding complications compared to interrupted therapy in patients undergoing atrial fibrillation ablation?
Meta-Analysis (n=26,275)
Does uninterrupted Vitamin K antagonist therapy reduce thromboembolic and bleeding complications compared to interrupted therapy in patients undergoing atrial fibrillation ablation?
Uninterrupted Vitamin K antagonist therapy is safer than an interrupted strategy for peri-procedural anticoagulation during atrial fibrillation ablation.
Answers are grounded in this paper and cite their sources.
May favor uninterrupted VKA during AF ablation to lower complications; reinforces consensus but needs RCT confirmation.
Introduction Vitamin K antagonists(VKA) are still a widely used method of anticoagulation as a periprocedural strategy for atrial fibrillation(AF) ablation. Several small series have suggested that the uninterrupted (u) VKA strategy is safer than interrupted (iVKA). A meta-analysis with a larger sample size can offer different insights about the safety of both administration regimens. Objective To evaluate the thromboembolic and bleeding events with uVKA and iVKA strategies in a network meta-analysis. Methods A literature search yielded 47 studies that included patients undergoing AF ablation with different anticoagulation strategies. DOACS, uVKA, and iVKA and reported thromboembolic and bleeding complications. A network meta-analysis was used to pool effect sizes among the 3 anticoagulation regimens, with odds ratios (OR) with 95% confidence intervals (CI), and a pairwise meta-analysis using a random effects model. Results A total of 13.303 patients on VKA (uVKA: 9.781; iVKA: 3.522) were compared using 12.972 patients on DOACs. The network analysis showed that both thromboembolic and bleeding complications were higher in patients treated with iVKA than uVKA (OR = 1.38, 95% CI: 1.01–1.87, I² = 0%), and (OR = 1.37, 95% CI: 0.99–1.88, I² = 0%), respectively (Figure1). Conclusions Our network meta analysis shows that administration of interrupted VKA is inferior to uninterrupted VKA in terms of both bleeding and thromboembolic complications. The data supports uVKA as a strategy of choice for periablation anticoagulation.
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Makdah et al. (2025) conducted a meta-analysis in Atrial fibrillation (n=26,275). Uninterrupted Vitamin K Antagonists (uVKA) vs. Interrupted Vitamin K Antagonists (iVKA) was evaluated on Thromboembolic complications (OR 1.38, 95% CI 1.01-1.87). Interrupted VKA during atrial fibrillation ablation was associated with higher thromboembolic (OR 1.38; 95% CI 1.01-1.87) and bleeding (OR 1.37; 95% CI 0.99-1.88) complications than uninterrupted VKA.
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