Key result
Continuing OAC after recurrence-free AF ablation is linked to ~42% higher thromboembolic and bleeding events.
Why the study?
Although recent randomized trials suggest OAC discontinuation may be feasible in selected patients after successful AF ablation, real-world evidence on the net clinical benefit of continued OAC across thromboembolic risk strata remained limited.
Does continued oral anticoagulation reduce the composite of stroke/systemic embolism and major bleeding compared with discontinuation in patients free of atrial fibrillation recurrence at 12 months after catheter ablation?
Cohort (n=6,717)
Yes
Does continued oral anticoagulation reduce the composite of stroke/systemic embolism and major bleeding compared with discontinuation in patients free of atrial fibrillation recurrence at 12 months after catheter ablation?
In patients remaining free of atrial fibrillation recurrence 12 months after catheter ablation, continuing oral anticoagulation was associated with a higher risk of the composite of thromboembolism and major bleeding compared with discontinuation, particularly in lower-risk patients with a CHA2DS2-VA score of 1–2.
Background Current guidelines recommend individual oral anticoagulant (OAC) decision after catheter ablation for atrial fibrillation (AF) based on stroke risk. However, recent randomized trials suggest that OAC discontinuation following successful ablation may be feasible in selected patients. Real-world evidence on the net clinical benefit of continued OAC across thromboembolic risk strata remains limited. Methods Using the Korean National Health Insurance Service database, we identified patients who underwent catheter ablation for AF and remained free of recurrence through 12 months post-procedure (landmark analysis). Patients were classified as OAC continuation (n=2,946) or discontinuation (n=3,771) based on OAC use at the 12-month landmark. Overlap weighting (OW) was applied using a propensity score model with 32 covariates. The primary outcome was a composite of stroke/systemic embolism and major bleeding. Outcomes were analyzed overall and by CHA2DS2-VA subgroup (score 1–2 vs. ≥3). Results After applying overlap weighting using a propensity score model incorporating 32 covariates, adequate balance across all variables was achieved (all standardised mean differences <0.1 after weighting). In the overall OW-adjusted cohort, OAC continuation was associated with significantly higher rates of the primary composite outcome compared with discontinuation (1.34 vs. 0.94 events/100 person-years (PY); HR 1.42, 95% CI 1.12–1.80; P=0.004). This was driven by increased risks of stroke/systemic embolism (0.70 vs. 0.47/100 PY; HR 1.49, 95% CI 1.07–2.07; P=0.018) and major bleeding (0.78 vs. 0.52/100 PY; HR 1.46, 95% CI 1.07–1.99; P=0.016). Among patients with CHA2DS2-VA score 1–2, OAC continuation was associated with substantially higher risks of the composite outcome (1.20 vs. 0.52/100 PY; HR 2.27, 95% CI 1.62–3.18; P <0.001). In contrast, among patients with CHA2DS2-VA score ≥3, no significant difference was observed for any outcome (HR 1.01, 95% CI 0.74–1.39; P=0.946). Conclusion In patients free of AF recurrence at 12 months after catheter ablation, continued OAC was not associated with net clinical benefit, particularly among lower-risk patients (CHA2DS2-VA 1–2). These findings support individualized OAC decision-making guided by thromboembolic risk stratification following successful AF ablation.
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Lee et al. (2026) conducted a cohort in Atrial fibrillation post-catheter ablation (n=6,717). Oral anticoagulant (OAC) continuation vs. Oral anticoagulant (OAC) discontinuation was evaluated on Composite of stroke/systemic embolism and major bleeding (HR 1.42, 95% CI 1.12-1.80, p=0.004). OAC continuation after recurrence-free AF ablation had higher rates of stroke/systemic embolism and major bleeding than discontinuation (HR 1.42; 95% CI 1.12–1.80; P=0.004).
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