Why the study?
Despite the withdrawal of the HeartWare Ventricular Assist Device (HVAD), hundreds of patients remain supported by it, and their long-term management remains under debate.
Does the HeartMate 3 LVAD improve 5-year survival and reduce major adverse events compared to the HeartWare LVAD in patients requiring mechanical circulatory support?
Does the HeartMate 3 LVAD improve 5-year survival and reduce major adverse events compared to the HeartWare LVAD in patients requiring mechanical circulatory support?
The HeartMate 3 LVAD demonstrates superior 5-year survival and significantly lower rates of stroke and pump thrombosis compared to the HeartWare device in a real-world multicenter registry.
Despite the withdrawal of the HeartWare Ventricular Assist Device (HVAD), hundreds of patients are still supported with this continuous-flow pump, and the long-term management of these patients is still under debate. This study aims to analyse 5 years survival and freedom from major adverse events in patients supported by HVAD and HeartMate3 (HM3). From 2010 to 2022, the MIRAMACS Italian Registry enrolled all-comer patients receiving a LVAD support at seven Cardiac Surgery Centres. Out of 447 LVAD implantation, 214 (47.9%) received HM3 and 233 (52.1%) received HVAD. Cox-regression analysis adjusted for major confounders showed an increased risk for mortality (HR 1.5 [1.2-1.9]; p = 0.031), for both ischemic stroke (HR 2.08 [1.06-4.08]; p = 0.033) and haemorrhagic stroke (HR 2.6 [1.3-4.9]; p = 0.005), and for pump thrombosis (HR 25.7 [3.5-188.9]; p < 0.001) in HVAD patients. The propensity-score matching analysis (130 pairs of HVAD vs. HM3) confirmed a significantly lower 5 years survival (81.25% vs. 64.1%; p 0.02), freedom from haemorrhagic stroke (90.5% vs. 70.1%; p < 0.001) and from pump thrombosis (98.5% vs. 74.7%; p < 0.001) in HVAD cohort. Although similar perioperative outcome, patients implanted with HVAD developed a higher risk for mortality, haemorrhagic stroke and thrombosis during 5 years of follow-up compared to HM3 patients.
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Francica et al. (2023) studied this question.
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