Abstract

Continuous-flow left ventricular assist devices (CF-LVADs) have markedly improved outcomes in patients with heart failure. The HeartMate II (HM II) was the first CF-LVAD approved in the U.S. as a bridge to transplant (BTT) or as a definitive therapy (DT). However, LVAD thrombosis is a major complication associated with the use of these devices.

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