Key result
ECPELLA is linked to ~52% lower 30-day mortality vs. VA-ECMO in refractory cardiogenic shock.
Why the study?
Does ECPELLA reduce 30-day mortality in patients with refractory cardiogenic shock receiving VA-ECMO?
Population
326 patients with refractory cardiogenic shock, including those with cardiac arrest, who received VA-ECMO…
Comparison
Concomitant use of VA-ECMO and Impella (ECPELLA) vs VA-ECMO with or without intra-aortic balloon pump
Design
Cohort
Follow-up
30-day
Authors
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In patients with refractory cardiogenic shock, the combined use of VA-ECMO and Impella (ECPELLA) significantly improved 30-day survival compared to VA-ECMO alone or with IABP, despite an increased risk of complications.
Cohort (n=326)
No
Does ECPELLA reduce 30-day mortality in patients with refractory cardiogenic shock receiving VA-ECMO?
Hazard Ratio: 0.48 (95% CI 0.35–0.66)
p-value: p=<0.001
In patients with refractory cardiogenic shock, the combined use of VA-ECMO and Impella (ECPELLA) significantly improved 30-day survival compared to VA-ECMO alone or with IABP, despite an increased risk of complications.
Inamori et al. (2025) conducted a cohort in Refractory cardiogenic shock (n=326). ECPELLA (VA-ECMO and Impella) vs. VA-ECMO with or without IABP was evaluated on 30-day mortality (HR 0.48, 95% CI 0.35-0.66, p=<0.001). ECPELLA was associated with a significantly lower risk of 30-day mortality compared to VA-ECMO with or without IABP in patients with refractory cardiogenic shock (HR 0.48; 95% CI 0.35-0.66; p<0.001).
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