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Impact of COVID-19 on Patients Supported with a Left Ventricular Assist Device
Jack Zakrzewski1, Laura Coyle2, Tracy Aicher2
1From the Department of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Insights
Patients with left ventricular assist devices (LVAD) face severe coronavirus disease-19 (COVID-19) risks. This study found increased mortality and complications in LVAD patients with COVID-19, highlighting vulnerability in this population.
Area of Science:
- Cardiology
- Infectious Diseases
- Critical Care Medicine
Background:
- Patients requiring left ventricular assist device (LVAD) support often have advanced heart failure.
- The impact of coronavirus disease-19 (COVID-19) on LVAD patients is not well-defined.
- LVAD patients may be at higher risk for severe COVID-19 outcomes.
Purpose of the Study:
- To describe the clinical course and outcomes of COVID-19 in patients with LVADs.
- To identify factors associated with mortality in LVAD patients hospitalized with COVID-19.
- To examine the postoperative course of LVAD implantation in patients with prior COVID-19 infection.
Main Methods:
- Retrospective review of medical records at a single center.
- Inclusion of 28 LVAD patients diagnosed with COVID-19 between March 2020 and March 2021.
- Inclusion of six patients with prior COVID-19 infection who underwent LVAD implantation.
Main Results:
- Nine out of 28 (32%) LVAD patients with COVID-19 died during the study period.
- Five patients (18%) died during their initial COVID-19 hospitalization; two (7%) had suspected pump thrombosis.
- Mechanical ventilation and intensive care unit admission were associated with increased mortality.
- All six patients with prior COVID-19 experienced complicated postoperative courses, with three (50%) suffering ischemic strokes and one (17%) 30-day mortality.
Conclusions:
- Left ventricular assist device patients are at increased risk of morbidity and mortality from COVID-19.
- COVID-19 infection poses significant challenges for LVAD patients, both medically and post-surgically.
- Further research is needed to understand and mitigate these risks.
Abstract:
Patients on left ventricular assist device (LVAD) support may be susceptible to severe disease and complications from coronavirus disease-19 (COVID-19). The purpose of this study was to describe the clinical course of COVID-19 in LVAD patients. A retrospective review was performed at our center; 28 LVAD patients who developed COVID-19 between March 2020 and March 2021, and six patients with a prior COVID-19 infection who underwent LVAD implantation, were identified and examined. Of the 28 patients, nine (32%) died during the study period, five (18%) during their index hospitalization for COVID-19. Two patients (7%) presented with suspected pump thrombosis. In a nonadjusted binary regression logistic analysis, admission to the intensive care unit (unadjusted odds ratio, 7.6 [CI, 1.2-48], P = 0.03), and the need for mechanical ventilation (unadjusted odds ratio 14 [CI, 1.3-159], P = 0.03) were associated with mortality. The six patients who previously had COVID-19 and subsequently received a LVAD were on intra-aortic balloon pump and inotropic support at time of surgery. All six experienced a complicated and prolonged postoperative course. Three patients (50%) suffered from ischemic stroke, and there was one (17%) 30 day mortality. We observed an increased risk of morbidity and mortality in LVAD patients with COVID-19.
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