Po-03-196 long-term clinical outcomes of peri-device leak in patients undergoing left atrial appendage occlusion in the amulet ide trial

The Amulet IDE trial is a global, randomized (1:1) trial of the Amplatzer ™ Amulet™ LAA occluder (Abbott) versus the Watchman™ device (Boston Scientific) in patients with non-valvular AF. Patients with a peri-device leak (PDL)> 3mm have shown to be at increased risk for stroke or systemic embolism (SSE) at 18 months. However, longer-term clinical implications from PDL are unclear.
Source: Heart Rhythm - Category: Cardiology Authors: Source Type: research
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