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Abstract 4366123: Impella Use in AMI-Related Cardiogenic Shock is Associated with Increased Mortality and Complications Compared to Intra-Aortic Balloon Pump: A Propensity-Matched Real-World Analysis
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Background:
Mechanical circulatory support is often employed in acute myocardial infarction (AMI) complicated by cardiogenic shock. While Impella and IABP are widely used, real-world data comparing their safety and effectiveness remain limited.
Research Question:
Does use of the Impella (axial-flow percutaneous ventricular assist device) device in AMI-related cardiogenic shock result in improved or worsened clinical outcomes compared to IABP (intra-aortic balloon pump)?
Methods:
We conducted a retrospective cohort study using the TriNetX US Collaborative Network including adult patients (≥18 years) with AMI and cardiogenic shock between January 1, 2018, and January 1, 2025. Patients were categorized based on the receipt of Impella (n=3,787) or IABP (n=3,787) within one month of AMI diagnosis. Propensity score matching (1:1) was applied to balance baseline characteristics. The primary outcome was 90-day all-cause mortality. Secondary outcomes included ischemic stroke, intracranial bleeding, reinfarction, ventricular arrhythmias, sepsis, GI bleeding, device-related embolization, acute kidney injury, and limb ischemia. Statistical analyses included risk difference (RD), risk ratio (RR), hazard ratio (HR), and log-rank p-values for survival.
Results:
Following matching, mean age was 70 years and 69% were male in both cohorts. Impella was associated with significantly higher mortality (36.7% vs 27.2%; RD +9.5% [95% CI 7.4–11.6], p<0.001; RR 1.35 [1.26–1.44]; HR 1.57 [1.45–1.71], p<0.001). Impella use also resulted in higher risk of intracranial bleeding (1.3% vs 0.7%; RD +0.6% [0.2–1.1], p=0.006; RR 1.92 [1.20–3.08]; HR 2.16 [1.34–3.46], p=0.001), sepsis (11.7% vs 9.7%; RD +2.0% [0.6–3.4], p=0.005; RR 1.21 [1.06–1.38]; HR 1.37 [1.19–1.57], p<0.001), major GI bleeding (6.4% vs 5.7%; HR 1.27 [1.05–1.52], p=0.012), and acute kidney injury (35.9% vs 33.7%; HR 1.21 [1.12–1.30], p<0.001). Ventricular arrhythmias were also more frequent in the Impella group (22.9% vs 21.8%; HR 1.18 [1.07–1.30], p=0.001). There were no significant differences in ischemic stroke, device-related embolization, or limb ischemia.
Conclusion:
In AMI complicated by cardiogenic shock, Impella use was associated with increased 90-day mortality and higher incidence of intracranial bleeding, sepsis, and renal injury compared to IABP. These findings support cautious application of Impella in this high-risk population and highlight the need for further prospective trials.
Ovid Technologies (Wolters Kluwer Health)
Title: Abstract 4366123: Impella Use in AMI-Related Cardiogenic Shock is Associated with Increased Mortality and Complications Compared to Intra-Aortic Balloon Pump: A Propensity-Matched Real-World Analysis
Description:
Background:
Mechanical circulatory support is often employed in acute myocardial infarction (AMI) complicated by cardiogenic shock.
While Impella and IABP are widely used, real-world data comparing their safety and effectiveness remain limited.
Research Question:
Does use of the Impella (axial-flow percutaneous ventricular assist device) device in AMI-related cardiogenic shock result in improved or worsened clinical outcomes compared to IABP (intra-aortic balloon pump)?
Methods:
We conducted a retrospective cohort study using the TriNetX US Collaborative Network including adult patients (≥18 years) with AMI and cardiogenic shock between January 1, 2018, and January 1, 2025.
Patients were categorized based on the receipt of Impella (n=3,787) or IABP (n=3,787) within one month of AMI diagnosis.
Propensity score matching (1:1) was applied to balance baseline characteristics.
The primary outcome was 90-day all-cause mortality.
Secondary outcomes included ischemic stroke, intracranial bleeding, reinfarction, ventricular arrhythmias, sepsis, GI bleeding, device-related embolization, acute kidney injury, and limb ischemia.
Statistical analyses included risk difference (RD), risk ratio (RR), hazard ratio (HR), and log-rank p-values for survival.
Results:
Following matching, mean age was 70 years and 69% were male in both cohorts.
Impella was associated with significantly higher mortality (36.
7% vs 27.
2%; RD +9.
5% [95% CI 7.
4–11.
6], p<0.
001; RR 1.
35 [1.
26–1.
44]; HR 1.
57 [1.
45–1.
71], p<0.
001).
Impella use also resulted in higher risk of intracranial bleeding (1.
3% vs 0.
7%; RD +0.
6% [0.
2–1.
1], p=0.
006; RR 1.
92 [1.
20–3.
08]; HR 2.
16 [1.
34–3.
46], p=0.
001), sepsis (11.
7% vs 9.
7%; RD +2.
0% [0.
6–3.
4], p=0.
005; RR 1.
21 [1.
06–1.
38]; HR 1.
37 [1.
19–1.
57], p<0.
001), major GI bleeding (6.
4% vs 5.
7%; HR 1.
27 [1.
05–1.
52], p=0.
012), and acute kidney injury (35.
9% vs 33.
7%; HR 1.
21 [1.
12–1.
30], p<0.
001).
Ventricular arrhythmias were also more frequent in the Impella group (22.
9% vs 21.
8%; HR 1.
18 [1.
07–1.
30], p=0.
001).
There were no significant differences in ischemic stroke, device-related embolization, or limb ischemia.
Conclusion:
In AMI complicated by cardiogenic shock, Impella use was associated with increased 90-day mortality and higher incidence of intracranial bleeding, sepsis, and renal injury compared to IABP.
These findings support cautious application of Impella in this high-risk population and highlight the need for further prospective trials.
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