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Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
The Role of Ventricular Assist Devices in Patients with Ischemic vs. Non-Ischemic Cardiomyopathy
Eglė Rumbinaitė1, Dainius Karčiauskas2,3, Grytė Ramantauskaitė1
1Clinical Department of Cardiology, Lithuanian University of Health Sciences, LT-50161 Kaunas, Lithuania.
Insights
Preoperative right-sided pressures and renal dysfunction predict early mortality after HeartMate 3 left ventricular assist device (LVAD) implantation. Ischemic cardiomyopathy patients show better early recovery than dilated cardiomyopathy patients.
Area of Science:
- Cardiology
- Mechanical Circulatory Support
- Heart Failure Research
Background:
- The HeartMate 3 (HM3) left ventricular assist device (LVAD) improves outcomes in advanced heart failure (HF).
- The impact of heart failure etiology (ischemic cardiomyopathy [ICM] vs. dilated cardiomyopathy [DCM]) on HM3 LVAD outcomes needs further clarification.
Purpose of the Study:
- To assess early outcomes after HM3 LVAD implantation in ICM versus DCM patients.
- To identify preoperative predictors of mortality and hemodynamic instability post-HM3 LVAD implantation.
Main Methods:
- Retrospective single-center cohort study of 30 HM3 LVAD recipients (2017-2024).
- Patients stratified by HF etiology: ICM (n=17) and DCM (n=13).
- Analysis of preoperative clinical, echocardiographic, and right heart catheterization data; primary endpoint: 30-day survival.
Main Results:
- Elevated preoperative central venous pressure, right ventricular pressure, and pulmonary vascular resistance predicted mortality.
- Higher preoperative creatinine and longer cardiopulmonary bypass times were associated with non-survival.
- Postoperative vasopressor use correlated with elevated pre-implant systolic pulmonary artery pressure.
Conclusions:
- Preoperative right-sided pressures and renal dysfunction are key predictors of early mortality post-HM3 LVAD.
- Ischemic cardiomyopathy patients demonstrate superior early left ventricular recovery compared to DCM patients.
- Personalized preoperative risk stratification, especially for DCM patients with pulmonary hypertension, is crucial for optimizing HM3 LVAD outcomes.
Abstract:
Background: The HeartMate 3 (HM3) left ventricular assist device (LVAD) has demonstrated improved clinical outcomes in patients with advanced heart failure (HF). However, the influence of underlying HF etiology-ischemic cardiomyopathy (ICM) versus dilated cardiomyopathy (DCM)-on post-implantation outcomes remains insufficiently characterized. Objectives: This paper aims to evaluate early postoperative outcomes following HM3 LVAD implantation in patients with ICM versus DCM and to identify the preoperative hemodynamic and clinical predictors of early mortality and hemodynamic instability. Methods: We conducted a retrospective single-center cohort study of 30 patients who underwent HM3 LVAD implantation between 2017 and 2024. Patients were stratified by HF etiology (ICM, n = 17; DCM, n = 13), and preoperative clinical, echocardiographic, and right heart catheterization data were analyzed. The primary endpoint was 30-day postoperative survival. Secondary endpoints included postoperative hemodynamic stability and the need for vasopressor support. Results: Non-survivors (n = 13) demonstrated elevated central venous pressure (>16.5 mmHg), mean right ventricular pressure (>31.5 mmHg), and pulmonary vascular resistance (>7.5 Wood units), in addition to higher preoperative creatinine levels and longer cardiopulmonary bypass times. Vasopressor requirement postoperatively was associated with elevated pre-implant systolic pulmonary artery pressure. Conclusions: Preoperative right-sided pressures and renal dysfunction are strong predictors of early mortality following HM3 LVAD implantation. Patients with ICM exhibit greater early left ventricular recovery compared to those with DCM. These findings underscore the importance of comprehensive and personalized preoperative risk stratification-particularly in patients with DCM and pulmonary hypertension-to optimize postoperative outcomes and guide patient selection for durable LVAD support.
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