4.2 Article

Outcomes in patients with smaller body surface area after HeartMate 3 left ventricular assist device implantation

期刊

ARTIFICIAL ORGANS
卷 46, 期 3, 页码 460-470

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WILEY
DOI: 10.1111/aor.14065

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left ventricular assist devices; outcomes; small body size

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This study investigated clinical outcomes in patients with small body size following HM3 LVAD implantation, showing comparable survival and incidence of adverse events between small and large BSA groups, with lower pump speed and flow in the small BSA group, as well as no cases of confirmed pump thrombosis.
Background Due to anatomic and physiologic concerns, prior generations of the left ventricular assist devices (LVAD) have frequently been denied to patients with small body size. However, outcomes in patients with small body surface area (BSA) following HeartMate 3 (HM3) LVAD implantation remain relatively unknown. Methods A cohort of 220 patients implanted at a single center was divided into two groups: BSA <= 1.8 m(2) (small BSA, n = 37) and BSA >1.8 m(2) (large BSA, n = 183). We investigated baseline characteristics and clinical outcomes including survival and incidence of adverse events. Results Small BSA patients were older (60 vs. 57 years), more likely female (60% vs. 20%), had a lower body mass index (24 vs. 32 kg/m(2)), lower incidence of diabetes (32% vs. 51%), history of stroke (5% vs. 19%), and left ventricular thrombus (0% vs. 11%). They had smaller left ventricular end diastolic diameter (64.8 vs. 69.3 mm). Pump speed and pump flows at discharge were lower in the small BSA group. Survival at 1 year and 2 years was 86% versus 87% and 86% versus 79% for small versus large BSA groups (p = 0.408), respectively. The rates of adverse events were similar between groups and there were no cases of confirmed pump thrombosis. The incidence of readmissions for low flow alarms was higher in the small BSA group (0.55 vs. 0.24 EPPY). Conclusions These findings demonstrate comparable outcomes in patients with small body size and suggest that this parameter should not be an exclusion criterion on patients who are otherwise candidates for HM3 LVAD implantation.

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