Related Experiment Video
Updated: Aug 5, 2026

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
Percutaneous left ventricular assist device in cardiogenic shock associated with and without acute myocardial
Roopeessh Vempati1, John Gallagher2, Haidar Hajeh3
1Department of Internal Medicine, Trinity Health Oakland Hospital, Pontiac, MI, USA.
Insights
Patients with cardiogenic shock (CS) due to acute myocardial infarction (AMI-CS) treated with percutaneous left ventricular assist devices (pLVAD) had higher mortality and heart failure exacerbations compared to non-AMI CS patients. These findings highlight key outcome differences in CS management.
Area of Science:
- Cardiology
- Mechanical Circulatory Support
- Critical Care Medicine
Background:
- Percutaneous left ventricular assist devices (pLVAD) are increasingly utilized for cardiogenic shock (CS).
- Outcomes may vary between acute myocardial infarction-related CS (AMI-CS) and non-AMI CS due to distinct pathophysiologies.
- Understanding these differences is crucial for optimizing patient care.
Purpose of the Study:
- To compare outcomes of pLVAD use in patients with AMI-CS versus non-AMI CS.
- To identify specific differences in mortality and morbidity between these two patient groups.
- To inform clinical decision-making regarding mechanical circulatory support in CS.
Main Methods:
- Utilized the USA TriNetX Network (2016-2024) to identify adult CS patients treated with pLVAD.
- Defined AMI-CS by myocardial infarction within seven days of pLVAD implantation.
- Excluded patients with recent coronary artery bypass graft (CABG) and used propensity matching to create balanced cohorts (n=2,026 each).
Main Results:
- AMI-CS patients experienced higher 30-day (HR 1.19), 90-day (HR 1.13), and 180-day (HR 1.14) mortality compared to non-AMI CS.
- Heart failure exacerbations (HR 1.21) and pulmonary edema (HR 1.23) were significantly more common in the AMI-CS group.
- Rates of stroke, arrhythmias, cardiac arrest, acute kidney injury, bleeding, vascular complications, and hemodialysis were comparable between groups.
Conclusions:
- Patients with AMI-CS treated with pLVAD demonstrate significantly higher mortality rates.
- AMI-CS is associated with increased heart failure-related morbidity, including exacerbations and pulmonary edema.
- These findings underscore the need for tailored management strategies for CS patients based on underlying etiology.
Background:
Percutaneous left ventricular assist devices (pLVAD, such as Impella), are increasingly used for cardiogenic shock (CS). Outcomes may differ between acute myocardial infarction-related CS (AMI-CS) and non-AMI CS due to differing pathophysiology and trajectories.
Methods:
Using the USA TriNetX Network (2016-2024), we identified adults with CS treated withpLVAD. AMI-CS was defined by MI within seven days of implantation; non-AMI CS included all patients with CS not attributable to acute MI, representing heterogeneous etiologies such as decompensated cardiomyopathy, myocarditis, valvular failure, pulmonary vascular causes, and arrhythmic shock. Patients with recent coronary artery bypass graft (CABG) were excluded. Propensity matching produced two balanced cohorts (n = 2,026 each).
Results:
Among 6,873 AMI-CS and 4,521 non-AMI CS patients, matched groups were similar (mean age 63 years, 26% female). AMI-CS had higher mortality at 30 days (hazard ratio [HR] 1.19, p = 0.002), 90 days (HR 1.13, p = 0.02), and 180 days (HR 1.14, p = 0.007). Heart failure (HF) exacerbations (HR 1.21, p < 0.001) and pulmonary edema (HR 1.23, p = 0.005) were also more common in AMI-CS. Stroke, ventricular arrhythmias, cardiac arrest, acute kidney injury, major bleeding, vascular complications, and hemodialysis were comparable.
Conclusion:
AMI-CS patients supported with pLVAD experienced higher mortality and greater HF-related morbidity than non-AMI CS.
Related Concept Videos
Cardiomyopathy V: Interprofessional Care
Acute Coronary Syndrome III: Diagnostic Studies
