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Updated: Jun 17, 2025

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Left Atrial Appendage Closure Compared With Oral Anticoagulants for Patients With Atrial Fibrillation: A Systematic
Angelo Oliva1,2,3, Anna Maria Ioppolo1, Mauro Chiarito2,3
1Cardiovascular Department Humanitas Gavazzeni Hospital Bergamo Italy.
Insights
Percutaneous left atrial appendage closure (LAAC) is as effective and safe as oral anticoagulants for preventing stroke in atrial fibrillation patients. LAAC demonstrated comparable efficacy to vitamin K antagonists (VKAs) and direct oral anticoagulants (DOACs) with potential bleeding benefits.
Area of Science:
- Cardiology
- Interventional Cardiology
- Medical Devices
Background:
- Atrial fibrillation necessitates anticoagulation to prevent cardioembolic events.
- Percutaneous left atrial appendage closure (LAAC) is an alternative to oral anticoagulation.
- Comparative data on LAAC versus oral anticoagulants are limited.
Conclusions:
- LAAC is a non-pharmacological alternative with similar efficacy and safety to oral anticoagulation for atrial fibrillation.
- Further prospective studies are needed to confirm these findings in larger patient populations.
Background:
Percutaneous left atrial appendage closure (LAAC) has been suggested as an alternative to long-term oral anticoagulation for nonvalvular atrial fibrillation, but comparative data remain scarce. We aimed to assess ischemic and bleeding outcomes of LAAC compared with vitamin K antagonists (VKAs) or direct oral anticoagulants (DOACs) for the prevention of cardioembolic events in patients with atrial fibrillation.
Methods And Results:
Embase and MEDLINE were searched for randomized trials comparing LAAC, VKAs, and DOACs. The primary efficacy end point was any stroke or systemic embolism. Treatment effects were calculated from a network meta-analysis and ranked according to the surface under the cumulative ranking curve. Seven trials and 73 199 patients were included. The risk of the primary end point was not statistically different between LAAC versus VKAs (odds ratio [OR], 0.92 [95% CI, 0.62-1.50]) and LAAC versus DOACs (OR, 1.11 [95% CI, 0.71-1.73]). LAAC and DOACs resulted in similar risk of major or minor (OR, 0.93 [95% CI, 0.61-1.42]) and major bleeding (OR, 0.92 [95% CI, 0.58-1.46]); however, after exclusion of procedural bleeding, bleeding risk was significantly lower in those undergoing LAAC. Both LAAC and DOACs reduced the risk of all-cause death compared with VKAs (LAAC versus VKAs: OR, 0.70 [95% CI, 0.53-0.91]; DOACs versus VKAs: OR, 0.90 [95% CI, 0.85-0.95], respectively). DOACs ranked as the best treatment for stroke or systemic embolism prevention (66.9%) and LAAC for reducing major bleeding (63.9%) and death (96.4%).
Conclusions:
As a nonpharmacological alternative to oral anticoagulation for atrial fibrillation, LAAC showed similar efficacy and safety compared with VKAs or DOACs. Prospective confirmation from larger studies is warranted.
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