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In the manufacturer-sponsored MOMENTUM-3 trial, investigators enrolled patients with advanced heart failure who were deemed eligible for a left ventricular assist device (LVAD) as destination therapy or as a bridge to transplantation. A total of 1028 patients (median age, 62; 81% men; mean left ventricular ejection fraction, 17%) were randomized to a fully magnetically levitated centrifugal-flow left ventricular assist device (LVAD; HeartMate 3) or a traditional axial-flow device (HeartMate 2). Interim analyses found markedly lower risks for pump thrombosis and lower risks for nondisabling strokes with the magnetically levitated device than with the axial-flow device (NEJM JW Cardiol Apr 2018 and N Engl J Med 2018; 378:1386). Now, the MOMEN…