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Updated: Jan 31, 2026

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
Impella Support for Acute Myocardial Infarction Complicated by Cardiogenic Shock.
Benedikt Schrage1, Karim Ibrahim2, Tobias Loehn2
1University Heart Centre Hamburg, Department of General and Interventional Cardiology, Germany (B.S., R.T., S.B., D.W.).
The Impella device did not reduce 30-day mortality in acute myocardial infarction with cardiogenic shock (AMI-CS) patients compared to intra-aortic balloon pump (IABP) or medical therapy. Increased bleeding and vascular complications were observed with Impella use.
Area of Science:
- Cardiology
- Interventional Cardiology
- Mechanical Circulatory Support
Background:
- Percutaneous mechanical circulatory support (MCS) devices are increasingly used in acute myocardial infarction complicated by cardiogenic shock (AMI-CS).
- Evidence supporting the effectiveness of these devices, such as the Impella, remains limited.
- This study compares outcomes of Impella use versus intra-aortic balloon pump (IABP) and medical treatment in AMI-CS patients.
Purpose of the Study:
- To evaluate the outcomes of Impella device use in patients with AMI-CS.
- To compare the effectiveness of Impella against IABP and medical treatment in this patient population.
- To assess 30-day all-cause mortality in patients with AMI-CS treated with Impella.
Main Methods:
- Retrospective data collection from European tertiary care hospitals for AMI-CS patients treated with Impella.
- Matching 237 Impella patients with 237 patients from the IABP-SHOCK II trial based on key clinical parameters.
- Primary endpoint was 30-day all-cause mortality, with secondary assessment of bleeding and vascular complications.
Main Results:
- No significant difference in 30-day all-cause mortality between the Impella group (48.5%) and the matched IABP group (46.4%).
- Impella use was associated with significantly higher rates of severe or life-threatening bleeding (8.5% vs. 3.0%) and peripheral vascular complications (9.8% vs. 3.8%).
- Results remained consistent when limiting the analysis to IABP-treated patients as the control.
Conclusions:
- In this retrospective analysis, the Impella device did not demonstrate a reduction in 30-day mortality for AMI-CS patients compared to IABP or medical therapy.
- The study highlights an increased risk of bleeding and vascular complications with Impella use.
- A large randomized trial is necessary to definitively determine the effect of the Impella device on outcomes in AMI-CS patients.
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