Levosimendan pre-treatment improves outcomes in patients undergoing coronary artery bypass graft surgery

Br J Anaesth. 2009 Feb;102(2):198-204. doi: 10.1093/bja/aen367.

Abstract

Background: The calcium sensitizer levosimendan has anti-ischaemic effects mediated via the opening of sarcolemmal and mitochondrial ATP-sensitive potassium channels. These properties suggest potential application in clinical situations where cardioprotection would be beneficial, such as cardiac surgery. We thus decided to investigate whether pharmacological pre-treatment with levosimendan reduces intensive care unit (ICU) length of stay in patients undergoing elective myocardial revascularization under cardiopulmonary bypass.

Methods: One hundred and six patients undergoing elective coronary artery bypass grafting were randomly assigned in a double-blind manner to receive levosimendan or placebo. Levosimendan (24 microg kg(-1)) or placebo was administered as a slow i.v. bolus over a 10 min period before the initiation of bypass.

Results: Tracheal intubation time and the length of ICU stay were significantly reduced in the levosimendan group (P<0.01). The number of patients needing inotropic support for >12 h was significantly higher in the control group (18.0% vs 3.8%; P=0.021). Compared with control patients, levosimendan-treated patients had lower postoperative troponin I concentrations (P<0.0001) and a higher cardiac power index (P<0.0001).

Conclusions: Pre-treatment with levosimendan in patients undergoing surgical myocardial revascularization resulted in less myocardial injury, a reduction in tracheal intubation time, less requirement for inotropic support, and a shorter length of ICU stay.

Trial registration: ClinicalTrials.gov NCT00610350.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • Cardiopulmonary Bypass
  • Cardiotonic Agents / administration & dosage
  • Cardiotonic Agents / therapeutic use*
  • Coronary Artery Bypass*
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Hemodynamics / drug effects
  • Humans
  • Hydrazones / administration & dosage
  • Hydrazones / therapeutic use*
  • Infusions, Intravenous
  • Intensive Care Units
  • Intraoperative Care / methods
  • Intubation, Intratracheal
  • Length of Stay
  • Male
  • Middle Aged
  • Prospective Studies
  • Pyridazines / administration & dosage
  • Pyridazines / therapeutic use*
  • Simendan
  • Time Factors
  • Treatment Outcome
  • Troponin I / blood

Substances

  • Biomarkers
  • Cardiotonic Agents
  • Hydrazones
  • Pyridazines
  • Troponin I
  • Simendan

Associated data

  • ClinicalTrials.gov/NCT00610350