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Updated: Mar 19, 2026

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
Retrospective analysis of circulatory support with the Impella CP® device in patients with therapy refractory
K Lackermair1, S Sattler2, B C Huber1
1Department of Cardiology, Munich University Clinic, Ludwig-Maximilians University, Munich, Germany.
Insights
The Impella CP® device offers feasible and safe left ventricular support in severe cardiogenic shock (CS). Survival rates in CS patients treated with Impella CP® appear improved compared to predicted mortality.
Area of Science:
- Cardiology
- Mechanical Circulatory Support
Background:
- Cardiogenic shock (CS) requires rapid left ventricular support.
- The Impella CP® device offers circulatory support up to 4.0 L/min.
- Systematic analysis of Impella CP® use in CS is lacking.
Purpose of the Study:
- To analyze the feasibility and safety of Impella CP® in severe, refractory CS.
- To evaluate 30-day survival rates in patients treated with Impella CP®.
- To compare outcomes based on CS aetiology and use of extracorporeal life support (ECLS).
Main Methods:
- Retrospective analysis of 28 consecutive CS patients treated with Impella CP®.
- Mortality estimation using the SAPS II Score.
- Assessment of 30-day survival, CS aetiologies, and impact of additional ECLS.
Main Results:
- Acute coronary syndrome (ACS) was the most common aetiology (15 patients).
- 30-day survival was 36% (18 deaths), compared to an estimated mortality of 87.1% (SAPS II Score 73±14).
- ACS-CS patients showed a trend towards better survival; ECLS did not significantly alter survival. Vascular complications occurred in 3 patients; haemolysis was common.
Conclusions:
- Impella CP® application is feasible and safe in severely ill CS patients.
- Observed 30-day survival suggests an improvement compared to predicted mortality.
- Further investigation into Impella CP® efficacy in specific CS aetiologies is warranted.
Background:
In cardiogenic shock (CS) the Impella CP® device provides a fast available left ventricular circulatory support of up to 4.0L/min. However, the use of the Impella CP® device was not systematically analysed yet.
Methods:
We performed a retrospective analysis of 28 consecutive patients suffering from severe therapy refractory CS treated with Impella CP®. Mortality was estimated using the SAPS II-Score. Primary outcome was 30-day survival. We compared the different aetiologies of CS and the effect of additional extracorporeal life support (ECLS).
Results:
Aetiology of CS was acute coronary syndrome (ACS) in 15 patients, 9 patients received additional therapy with ECLS. SAPS II was 73±14, representing an estimated mortality of 87.1%. 18 patients deceased representing a 30-day survival of 36%. Comparing the different aetiologies, ACS-CS patients show a trend towards better survival. Additional therapy with ECLS did not change 30-day survival. In 3 cases, vascular complication needing surgical treatment occurred. All other patients showed no relevant complications except for the commonly seen haemolysis with consecutive need of transfusion.
Conclusion:
Our data could demonstrate that the Impella CP® application in these severely diseased patients is feasible and safe. Compared to the estimated mortality, the 30-day survival seems to be improved.
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