Intravenous levosimendan vs. dobutamine in acute decompensated heart failure patients on beta-blockers

Eur J Heart Fail. 2010 Apr;12(4):404-10. doi: 10.1093/eurjhf/hfq032.

Abstract

Aims: The aim of this study is to compare the effects of a 24 h intravenous infusion of levosimendan and a 48 h infusion of dobutamine on invasive haemodynamics in patients with acutely decompensated chronic NYHA class III-IV heart failure. All patients were receiving optimal oral therapy including a beta-blocker.

Methods and results: This was a multinational, randomized, double-blind, phase IV study in 60 patients; follow-up was 1 month. There was a significant increase in cardiac index and a significant decrease in pulmonary capillary wedge pressure (PCWP) at 24 and 48 h for both dobutamine and levosimendan. The improvement in cardiac index with levosimendan was not significantly different from dobutamine at 24 h (P = 0.07), but became significant at 48 h (0.44 +/- 0.56 vs. 0.66 +/- 0.63 L/min/m(2); P = 0.04). At 24 h, the reduction in the mean change in PCWP from baseline was similar for levosimendan and dobutamine, however, at 48 h the difference was more marked for levosimendan (-3.6 +/- 7.6 vs. -8.3 +/- 6.7 mmHg; P = 0.02). No difference was observed between the groups for change in NYHA class, beta-blocker use, hospitalizations, treatment discontinuations or rescue medication use. Reduction in B-type natriuretic peptide (BNP) was significantly greater with levosimendan at 48 h (P = 0.03). According to physician's assessment, the improvement in fatigue (P = 0.01) and dyspnoea (P = 0.04) was in favour of dobutamine treatment, and hypotension was significantly more frequent with levosimendan (P = 0.007). No increase in atrial fibrillation or ventricular tachycardia was seen in either group.

Conclusion: A 24 h levosimendan infusion achieved haemodynamic and neurohormonal improvement that was at least comparable at 24 h and superior at 48 h to a 48 h dobutamine infusion.

Publication types

  • Clinical Trial, Phase IV
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / administration & dosage
  • Adrenergic beta-Agonists / therapeutic use
  • Adrenergic beta-Antagonists / therapeutic use*
  • Aged
  • Analysis of Variance
  • Antihypertensive Agents / therapeutic use*
  • Cardiotonic Agents / administration & dosage
  • Cardiotonic Agents / therapeutic use
  • Confidence Intervals
  • Dobutamine / administration & dosage
  • Dobutamine / therapeutic use*
  • Double-Blind Method
  • Female
  • Heart Failure / drug therapy*
  • Heart Failure / pathology
  • Heart Failure / physiopathology
  • Hemodynamics
  • Humans
  • Hydrazones / administration & dosage
  • Hydrazones / therapeutic use*
  • Male
  • Myocardial Perfusion Imaging
  • Natriuretic Peptide, Brain / blood
  • Natriuretic Peptide, Brain / drug effects
  • Odds Ratio
  • Perfusion
  • Pulmonary Wedge Pressure
  • Pyridazines / administration & dosage
  • Pyridazines / therapeutic use*
  • Simendan
  • Vasodilator Agents / administration & dosage
  • Vasodilator Agents / therapeutic use

Substances

  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Antihypertensive Agents
  • Cardiotonic Agents
  • Hydrazones
  • Pyridazines
  • Vasodilator Agents
  • Natriuretic Peptide, Brain
  • Simendan
  • Dobutamine