Beneficial effects of levosimendan to wean patients from VA-ECMO: a systematic review and meta-analysis

Minerva Cardiol Angiol. 2023 Oct;71(5):564-574. doi: 10.23736/S2724-5683.22.06054-9. Epub 2022 Jun 10.

Abstract

Introduction: Patients with refractory cardiogenic shock can benefit from veno-arterial extracorporeal membrane oxygenation (VA-ECMO). The use of levosimendan in VA-ECMO patients may facilitate weaning and enhance survival.

Evidence acquisition: MEDLINE, Scopus, Web of Science, and Cochrane were searched from inception to October 10th, 2021. Eligible clinical trials and observational studies reporting the use of levosimendan in VA-ECMO were searched. Two reviewers extracted data and independently assessed the risk of bias. To integrate the data, a random-effect model was applied. The success of weaning from VA-ECMO was the primary outcome.

Evidence synthesis: Ten observational studies, including a total of 987 patients, were identified. Levosimendan was associated with successful weaning (362/448) compared with controls (328/539) (OR 2.37, 95% CI 1.71-3.28; P=0.01) and reduced mortality (144/433 vs. 258/507) (nine studies, OR 0.53, 95% CI 0.36-0.78; P=0.01) compared with control.

Conclusions: Levosimendan was associated with successful weaning and increased survival in VA-ECMO patients. Randomized trials should confirm these findings.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Extracorporeal Membrane Oxygenation* / adverse effects
  • Humans
  • Shock, Cardiogenic / drug therapy
  • Shock, Cardiogenic / etiology
  • Simendan / therapeutic use

Substances

  • Simendan