ECMO Strikes Out in Patients with Acute Myocardial Infarction and Cardiogenic Shock

פוסט זה זמין גם ב: עברית

David J. Cohen, MD, MSc, reviewing 

A major randomized trial showed no mortality difference with extracorporeal membrane oxygenation versus supportive care alone.

Despite great strides in managing acute myocardial infarction (AMI), 30-day mortality rates remain at 40% to 50% when cardiogenic shock complicates AMI (AMI-CS). Several percutaneous devices can provide substantial, temporary circulatory support to vital organs (about 3–5 liters/minute of blood flow). Given their relative safety and ease of insertion, short-term circulatory support with these devices has been hypothesized to offer potential benefit in patients with AMI-CS as cardiac function recovers.

To assess whether this approach improves survival, investigators randomized 420 patients (mean age, 63 years; 19% women) with AMI-CS who were undergoing planned coronary revascularization (almost all with percutaneous coronary intervention) to mechanical circulatory support using extracorporeal membrane oxygenation (ECMO) or supportive care alone (NCT03637205. opens in new tab). About 78% of participants had undergone cardiopulmonary resuscitation before randomization.

The primary endpoint — all-cause mortality at 30 days — was virtually identical with ECMO (47.8%) and supportive care alone (49.0%). The ECMO group had higher rates of moderate-to-severe bleeding (23%, vs. 10% with supportive care alone) and vascular complications requiring treatment (11% vs. 4%, respectively). Findings were consistent across age and clinical subgroups.

COMMENT

These data are a sobering reminder that pathophysiologic principles do not necessarily predict clinical benefit. Despite providing near-normal cardiac output, ECMO did not improve survival in patients with AMI-CS. Potential explanations include high rates of bleeding and vascular complications with ECMO (potentially offsetting any benefit of circulatory support) and the fact that ECMO leads to increased cardiac afterload and ventricular volume overload, which may impair myocardial recovery. Several ongoing trials are testing whether a percutaneous microaxial left ventricular assist device (which does not increase afterload) can improve survival after AMI-CS. For now, though, we should temper enthusiasm for use of mechanical circulatory support in these patients, given its cost, associated complications, and uncertain benefit.

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