Watchman vs. Amulet for Left Atrial Appendage Closure: Current Evidence and Future Perspectives

Author:

Frazzetto Marco1ORCID,Sanfilippo Claudio1ORCID,Costa Giuliano1ORCID,Contrafatto Claudia1,Giacalone Chiara1ORCID,Scandura Salvatore1,Castania Giuseppe1,De Santis Jessica1,Sanfilippo Maria1,Di Salvo Maria Elena1,Tamburino Corrado1,Barbanti Marco23ORCID,Grasso Carmelo1ORCID

Affiliation:

1. Division of Cardiology, A.O.U. Policlinico “G. Rodolico San Marco”, 95123 Catania, Italy

2. Faculty of Medicine and Surgery, Università degli Studi di Enna “Kore”, 94100 Enna, Italy

3. Division of Cardiology, Ospedale Umberto I, ASP 4 di Enna, 94100 Enna, Italy

Abstract

Left atrial appendage closure (LAAC) is a crucial intervention for stroke prevention in patients with non-valvular atrial fibrillation who are unsuitable for long-term anticoagulation. Amulet and Watchman are the most implanted devices worldwide for performing LAAC, and the aim of this review is to provide a comprehensive comparison focusing on their efficacy, safety, and short- and long-term outcomes. The Watchman device, the first to gain FDA approval, has been extensively studied and demonstrates significant reductions in stroke and systemic embolism rates. The Amulet device, a newer alternative, promises enhanced design features for more efficient appendage sealing. Current data highlight that both devices offer similar efficacy and safety for LAAC. While the two devices differ in terms of intraprocedural complication rates, they offer similar short- to long-term outcomes in terms of peri-device leaks, device-related thrombosis, and mortality. Both devices are indicated for patients who are unable to tolerate OAC, given their similar risk and safety profiles. Newer clinical studies are directed at establishing the efficacy of both devices as the primary method for stroke prevention in AF as an alternative to OAC.

Publisher

MDPI AG

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