Key result
Sepsis linked to ~46% higher absolute 30-day mortality in cardiogenic shock patients on MCS.
Why the study?
While microaxial flow pump support reduces mortality in STEMI-related cardiogenic shock, increased complications such as sepsis are observed, prompting investigation of the influence of sepsis on patient prognosis.
Does sepsis increase mortality in patients with cardiogenic shock following acute myocardial infarction receiving mechanical circulatory support via a microaxial flow pump?
Cohort (n=38)
Does sepsis increase mortality in patients with cardiogenic shock following acute myocardial infarction receiving mechanical circulatory support via a microaxial flow pump?
Absolute Event Rate: 53.9% vs 8.3%
p-value: p=0.014
Sepsis significantly increases the risk of 30-day and 365-day all-cause mortality in patients with cardiogenic shock following AMI supported by a microaxial flow pump.
Sepsis was associated with markedly higher mortality in MCS-treated cardiogenic shock; hypothesis-generating for prevention trials.
Background: Cardiogenic shock (CS) is characterized as a state of low cardiac output that is frequently associated with multisystem organ failure. For over two decades, revascularization of the culprit lesion remained the only interventional treatment option to improve outcomes in CS following acute myocardial infarction. However, recently published data provide evidence that the use of a microaxial flow pump for mechanical circulatory support (MCS) in STEMI-related cardiogenic shock significantly reduced mortality after 180 days. Increased rates of complications such as sepsis were observed under MCS. The present study aimed to investigate the influence of sepsis on prognoses in patients with CS receiving temporary MCS with a microaxial flow pump. Methods and Results: This retrospective cohort study included 38 patients who received a microaxial flow pump for CS between 2014 and 2017. All patients were analyzed for the presence of sepsis, defined as infection and an increase in the Sequential Organ Failure Assessment (SOFA) score of ≥2 points. Analyzed clinical outcomes included all-cause mortality after 30 and 365 days and changes in renal function. A total of 38 patients were included in the final analysis. The 30-day all-cause mortality was significantly higher in the sepsis group than in the no-sepsis group (53.9% vs. 8.3%, p = 0.014). The findings were consistent for mortality at 365 days (65.4% vs. 16.7%, p = 0.008). Conclusions: These results indicate that sepsis significantly increases the risk of all-cause mortality at 30 and 365 days among patients with CS following AMI and receiving MCS via a microaxial flow pump.
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Düsing et al. (2026) conducted a cohort in Cardiogenic shock following acute myocardial infarction (n=38). Sepsis vs. No sepsis was evaluated on 30-day all-cause mortality (p=0.014). Sepsis significantly increased 30-day all-cause mortality compared to no sepsis (53.9% vs. 8.3%, p=0.014) in patients with cardiogenic shock receiving mechanical circulatory support.
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