AI Article Synopsis

  • The study investigates short-term mortality rates related to the ECPELLA treatment (veno-arterial extracorporeal membrane oxygenation combined with the Impella device) in patients with acute myocardial infarction complicated by cardiogenic shock (AMI-CS).
  • Data from the Japanese Registry for Percutaneous Ventricular Assist Devices (J-PVAD) revealed a 30-day mortality rate of 46.1% among 922 AMI-CS patients, with age over 80 and specific health factors significantly increasing risk.
  • The J-PVAD score helps predict mortality risk, showing that higher scores correlate with higher mortality; for instance, the score of 0 had a 20% mortality rate, while a score of

Article Abstract

Background: The short-term mortality associated with veno-arterial extracorporeal membrane oxygenation combined with the Impella device (termed ECPELLA) for acute myocardial infarction complicated by cardiogenic shock (AMI-CS) remains unclear.

Methods And Results: The Japanese Registry for Percutaneous Ventricular Assist Devices (J-PVAD) includes data on all patients treated with an Impella in Japan. We extracted data for 922 AMI-CS patients who underwent ECPELLA support and conducted an exploratory analysis focusing on 30-day mortality. The median age of patients was 69 years, and 83.8% were male. The overall 30-day mortality was 46.1%. Factors associated with mortality included age >80 years, in-hospital cardiac arrest, systolic blood pressure <90 mmHg, serum creatinine >1.5 mg/dL, and serum lactate >4.0 mmol/L. In patients aged >80 years with any of these factors, mortality was significantly higher than in those without, ranging from 57.5% to 64.9%. The J-PVAD score assigns 1 point per predictor, with a C-statistic of 0.620 (95% confidence interval 0.586-0.654). The 30-day mortality was 20.0% for a J-PVAD score of 0, increasing to 70.0% for a score of 5.

Conclusions: The J-PVAD data indicate high short-term mortality in AMI-CS patients treated with ECPELLA, particularly among older patients. Further studies are needed to validate this risk stratification in this patient subset.

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Source
http://dx.doi.org/10.1253/circj.CJ-24-0522DOI Listing

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