Respiratory Trials·org

Cardiology in critical care · Mechanical support in cardiogenic shock

DanGer Shock randomised trial

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
  • Confined to STEMI-related cardiogenic shock