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3-Year Outcomes From the Amplatzer Amulet Left Atrial Appendage Occluder Randomized Controlled Trial (Amulet IDE)

Dhanunjaya Lakkireddy, David E. Thaler, Christopher R. Ellis, Vijendra Swarup, Alok Gambhir, James Hermiller, Jens Erik Nielsen‐Kudsk, Stephen G. Worthley, Devi G. Nair, Boris Schmidt, Rodney Horton, Nigel Gupta, Jordan A. Anderson, Ryan Gage, Mohamad Alkhouli, Stephan Windecker

2023JACC: Cardiovascular Interventions37 citationsDOIOpen Access PDF

Abstract

BACKGROUND: The Amulet (Abbott) left atrial appendage occluder investigational device exemption trial is the largest randomized trial evaluating the safety and effectiveness of the Amulet left atrial appendage occluder compared with the Watchman 2.5 device (Boston Scientific) through 5 years. OBJECTIVES: This analysis evaluated the device effect on 3-year outcomes in the Amulet investigational device exemption trial. METHODS: The medication regimen and key clinical outcomes were reported through 3 years including: 1) the composite of ischemic stroke or systemic embolism (SE); 2) the composite of all strokes, SE, or cardiovascular (CV) death; 3) major bleeding; and 4) all-cause death and CV death. RESULTS: A total of 1,878 patients at 108 sites were randomized. A significantly higher percentage of patients were free of oral anticoagulation usage at 3 years with Amulet (96.2%) vs Watchman (92.5%) (P < 0.01). Clinical outcomes were comparable for the composite of ischemic stroke or SE (5.0% vs 4.6%; P = 0.69); the composite of all strokes, SE, or CV death (11.1% vs 12.7%; P = 0.31); major bleeding (16.1% vs 14.7%; P = 0.46); all-cause death (14.6% vs 17.9%; P = 0.08); and CV death (6.6% vs 8.5%; P = 0.14) for Amulet and Watchman, respectively. Through 3 years, device factors (device-related thrombus or peridevice leak ≥3 mm) preceded ischemic stroke events and CV deaths more frequently in Watchman compared with Amulet patients. CONCLUSIONS: The Amulet occluder demonstrated continued safety and effectiveness with over 96% free of oral anticoagulation usage through 3 years in a high-risk population compared to the Watchman device. (AMPLATZER Amulet LAA Occluder Trial [Amulet IDE]; NCT02879448).

Topics & Concepts

MedicineStroke (engine)ThrombusRandomized controlled trialEmbolismSurgeryClinical trialInternal medicineCardiologyEngineeringMechanical engineeringAtrial Fibrillation Management and OutcomesCardiovascular and Diving-Related ComplicationsCardiac pacing and defibrillation studies