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Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
Prophylactic Impella CP versus VA-ECMO in Patients Undergoing Complex High-Risk Indicated PCI
Deborah M F van den Buijs1,2, Adriaan Wilgenhof3, Paul Knaapen1
1Amsterdam Universitair Medisch Centrum, Vrije Universiteit Medisch Centrum, Amsterdam, Netherlands.
This study found no significant difference in outcomes for patients with complex high-risk indicated percutaneous coronary intervention (CHIP) using Impella CP or veno-arterial extracorporeal membrane oxygenation (VA-ECMO) for mechanical circulatory support.
Area of Science:
- Cardiology
- Interventional Cardiology
- Mechanical Circulatory Support
Background:
- Complex high-risk indicated percutaneous coronary intervention (CHIP) requires mechanical circulatory support (MCS) to prevent hemodynamic instability.
- Limited comparative data exist for different MCS devices in CHIP patients declined for surgery.
Purpose of the Study:
- To compare the efficacy and safety of Impella CP versus veno-arterial extracorporeal membrane oxygenation (VA-ECMO) in CHIP patients.
- To evaluate major adverse cardiac events (MACE) and mortality rates between the two MCS devices.
Main Methods:
- Retrospective analysis of a multicenter observational study.
- Inclusion of CHIP patients supported by Impella CP or VA-ECMO who were declined surgery.
- Evaluation of periprocedural hemodynamic instability, MACE, and mortality (in-hospital and 30-day).
Main Results:
- No significant difference in periprocedural hemodynamic instability between Impella CP (3.7%) and VA-ECMO (14.3%).
- Similar rates of Major Adverse Cardiac Events (MACE) for Impella CP (30.7%) and VA-ECMO (21.4%).
- No significant differences in in-hospital or 30-day mortality between the two support systems.
Conclusions:
- Both Impella CP and VA-ECMO provide comparable hemodynamic support in CHIP patients.
- The choice between Impella CP and VA-ECMO does not significantly impact MACE or mortality outcomes in this patient cohort.
- Further research may explore specific patient subgroups that could benefit more from one device over the other.
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