Key result
The WATCHMAN left atrial appendage occlusion device was successfully implanted in all 5 patients with persistent or permanent atrial fibrillation without complications, with no flow leakage observed at 8 weeks.
Why the study?
Does left atrial appendage occlusion device implantation provide a safe alternative for stroke prevention in patients with atrial fibrillation who cannot tolerate anticoagulation?
Case Report (n=5)
Yes
Does left atrial appendage occlusion device implantation provide a safe alternative for stroke prevention in patients with atrial fibrillation who cannot tolerate anticoagulation?
Percutaneous left atrial appendage occlusion using the WATCHMAN device is feasible and safe in patients with persistent or permanent atrial fibrillation who cannot tolerate anticoagulation.
May support LAAO feasibility in anticoagulation-intolerant AF; leaves open stroke prevention efficacy pending larger trials.
PURPOSE: Atrial fibrillation (AF) is one of the major risk factors for ischemic stroke, and 90% of thromboembolisms in these patients arise from the left atrial appendage (LAA). Recently, it has been documented that an LAA occlusion device (OD) is not inferior to warfarin therapy, and that it reduces mortality and risk of stroke in patients with AF. MATERIALS AND METHODS: We implanted LAA-ODs in 5 Korean patients (all male, 59.8 ± 7.3 years old) with long-standing persistent AF or permanent AF via a percutaneous trans-septal approach. RESULTS: 1) The major reasons for LAA-OD implantation were high risk of recurrent stroke (80%), labile international neutralizing ratio with hemorrhage (60%), and 3/5 (60%) patients had a past history of failed cardioversion for rhythm control. 2) The mean LA size was 51.3 ± 5.0 mm and LAA size was 25.1 × 30.1 mm. We implanted the LAA-OD (28.8 ± 3.4 mm device) successfully in all 5 patients with no complications. 3) After eight weeks of anticoagulation, all patients switched from warfarin to anti-platelet agent after confirmation of successful LAA occlusion by trans-esophageal echocardiography. CONCLUSION: We report on our early experience with LAA-OD deployment in patients with 1) persistent or permanent AF who cannot tolerate anticoagulation despite significant risk of ischemic stroke, or 2) recurrent stroke in patients who are unable to maintain sinus rhythm.
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Kim et al. (2011) conducted a case report in Atrial Fibrillation (n=5). Left Atrial Appendage Occlusion Device (WATCHMAN) was evaluated on Successful device implantation without complications. The WATCHMAN left atrial appendage occlusion device was successfully implanted in all 5 patients with persistent or permanent atrial fibrillation without complications, with no flow leakage observed at 8 weeks.
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