Microaxial Flow Pump or Standard Care in Infarct-Related Cardiogenic Shock
DanGer Shock trial design and results
Design
Multicentre randomised controlled trial
Treatment
Microaxial flow pump with standard care
Control
Standard care alone
Population
355 analysed patients with STEMI-related cardiogenic shock, median age 67
Follow-up
180 days
Primary endpoint
Death from any cause at 180 days
Result
Routine use of a microaxial flow pump reduced the risk of death from any cause at 180 days compared with standard care alone, among 179 and 176 patients respectively. Adverse events were more frequent in the pump group. Renal-replacement therapy was needed in 75 of 179 (41.9%) with the pump versus 47 of 176 (26.7%) with standard care — relative risk 1.98.
Secondary endpoints
Escalation to other mechanical support, renal replacement therapy, bleeding, limb ischaemia
The routine use of a microaxial flow pump with standard care in the treatment of patients with STEMI-related cardiogenic shock led to a lower risk of death from any cause at 180 days than standard care alone.
The trial authors, in the published abstract
How it has aged
The first mechanical support device to show a mortality benefit in cardiogenic shock, after IABP-SHOCK II and both ECMO trials (ECMO-CS, ECLS-SHOCK) came up empty. The complication rate is substantial and the population narrow — STEMI-related shock specifically.
Publications
Microaxial Flow Pump or Standard Care in Infarct-Related Cardiogenic Shock
Møller JE, Engstrøm T, Jensen LO, et al. Microaxial Flow Pump or Standard Care in Infarct-Related Cardiogenic Shock. N Engl J Med 2024 Apr 18;390(15):1382-1393.
Lower all-cause mortality at 180 days
More adverse events including bleeding and limb ischaemia