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Levosimendan for postoperative subclinical heart failure after noncardiac surgery: a randomized, double-blinded, phase III trial

  • Christian Reiterer
  • , Barbara Kabon
  • , Alexander Taschner
  • , Alexandra Graf
  • , Nikolas Adamowitsch
  • , Katharina Horvath
  • , David Emler
  • , Oliver Zotti
  • , Nicole Hantakova
  • , Beatrix Hochreiter
  • , Melanie Fraunschiel
  • , Theresa Clement
  • , Edith Fleischmann

Research output: Journal article (peer-reviewed)Journal article

Abstract

The effect of Levosimendan on postoperative natriuretic peptides in noncardiac surgical patients remains unknown. Thus, this study evaluates the effect of a perioperative levosimendan administration on postoperative N-terminal brain pro natriuretic peptide (NT-proBNP) concentrations. In this prospective, double-blinded, parallel group, placebo-controlled, phase III trial 115 patients were assigned to perioperative single-dose of 12.5 mg of levosimendan and 115 to placebo between October 2020 through November 2023 (clinicaltrials.gov: NCT04329624). The primary outcome was postoperative maximum NT-proBNP concentration within the first 3 postoperative days. 228 patients completed the trial. Postoperative maximum NT-proBNP concentrations did not differ significantly between the groups (effect estimate: -64.51 ng.L-1; 95% CI -332.66 to 195.56; p = 0.61). Here, we show that perioperative levosimendan administration did not lead to a significantly lower release in postoperative NT-proBNP after noncardiac surgery.

Original languageEnglish
Article number5847
Pages (from-to)5847
JournalNature Communications
Volume16
Issue number1
DOIs
Publication statusPublished - Dec 2025

Keywords

  • Humans
  • Simendan/therapeutic use
  • Male
  • Natriuretic Peptide, Brain/blood
  • Female
  • Double-Blind Method
  • Aged
  • Heart Failure/drug therapy
  • Middle Aged
  • Peptide Fragments/blood
  • Postoperative Complications/drug therapy
  • Prospective Studies
  • Cardiotonic Agents/therapeutic use

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