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With the recent FDA approval of the Watchman device, clinicians can consider left atrial appendage (LAA) occlusion to prevent stroke in patients with nonvalvular atrial fibrillation (AF). These researchers performed a patient-level meta-analysis of the two large studies (PROTECT-AF and PREVAIL) that formed the basis for the FDA approval, combined with two nonrandomized, continuing-access registries of these trials.
The meta-analysis covered 1877 LAA occlusion patients and 382 patients receiving warfarin alone. LAA occlusion recipients were treated with aspirin and warfarin for ≥45 days after device implantation. All patients were considered at high risk for stroke (estimated annual risk for stroke if untreated, 5.7%–7.6%).
Mean follow-up rang…