Cardiothoracic & vascular anesthesia

Levosimendan in Patients with Low Cardiac Output Syndrome After Cardiac Surgery: A Substudy of the Multicenter Randomized CHEETAH Trial

J Cardiothorac Vasc AnesthPublished Secondary analysis of the CHEETAH randomised trial

Authors' conclusion

Among patients requiring hemodynamic support after cardiac surgery with CPB, perioperative levosimendan infusion did not affect long-term survival (1-5 years) compared with placebo.

Study context

Population
Adults requiring hemodynamic support for cardiac index <2.5 L/min/m² after cardiac surgery with cardiopulmonary bypass (CPB), tertiary hospital
Participants
134 adults
Comparison
Levosimendan vs placebo, in addition to standard inotropic care
Primary endpoint
Long-term mortality (1-5 years) after randomisation
Follow-up
5 years
Methodological detailssingle-centre subanalysis, multicentre randomised trial, placebo-controlled
  • Single-centre subanalysis
  • Multicentre randomised trial
  • Placebo-controlled

Primary result

As reported in the abstract

Long-term mortality (5 years) · 1-5 years

No significant between-group difference in long-term mortality (5 years)

HR 1.59; 95% CI 0.81 to 3.11

p = 0.17

Secondary outcomes

Mean pulmonary artery pressure · 4 to 6 hours after randomisation · lower with levosimendan

P = 0.019

Other secondary outcomes (hemodynamics, inotropic support, acute kidney injury (AKI), RRT, mechanical ventilation duration, intensive care unit (ICU) and hospital stay, 30-day mortality)

No significant differences

Original publication

Levosimendan in Patients with Low Cardiac Output Syndrome After Cardiac Surgery: A Substudy of the Multicenter Randomized CHEETAH Trial. J Cardiothorac Vasc Anesth. Published 10 October 2024. doi:10.1053/j.jvca.2024.10.003

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