Effects of levosimendan without loading dose on systolic and diastolic function in patients with end-stage heart failure

Cardiol J. 2011;18(5):532-7. doi: 10.5603/cj.2011.0009.

Abstract

Background: Levosimendan (L) is used in clinical practice for the treatment of severe heart failure (HF); it has inotropic and vasodilatory effects, without increasing myocardial oxygen consumption. In acute HF, levosimendan improves hemodynamic parameters; previous studies have demonstrated that it has favorable effects on left ventricular (LV) diastolic function. The aim of our study was to evaluate the effect of on LV long-axis function that represents the earlier marker of diastolic dysfunction.

Methods: We enrolled 41 patients (age 62 ± 12 years) admitted to our Department for acute HF, NYHA class IV and severe LV dysfunction. Twenty-six patients were treated with L (0.1 μg/kg/min ev for 24 h without loading dose) and 15 patients were treated with standard therapy (C). We evaluated clinical, blood exams and echocardiographic parameters at baseline and one week after L or C treatment.

Results: Baseline demographic, clinical and biochemical data were similar in both groups. After one week, the L group had shown a significant improvement in NYHA class and a reduction of pro-B-type natriuretic peptide (pro-BNP). In echocardiographic study, we observed an improvement in LV longitudinal function (p 〈 0.05) and LV ejection fraction (p 〈 0.05) with a reduction of E/E' (p 〈 0.05) in the L group. We divided the L group into ischemic and non- -ischemic patients and we demonstrated a significant increase in systolic function in the former. No differences were found between subgroups in diastolic function.

Conclusions: L therapy, without loading dose, improves NYHA class and ventricular function in patients with acute HF; we believe that these prolonged hemodynamic effects are due to active metabolities of L.

MeSH terms

  • Aged
  • Biomarkers / blood
  • Cardiotonic Agents / metabolism
  • Cardiotonic Agents / therapeutic use*
  • Chi-Square Distribution
  • Diastole / drug effects
  • Female
  • Heart Failure / diagnostic imaging
  • Heart Failure / drug therapy*
  • Heart Failure / physiopathology
  • Hemodynamics / drug effects
  • Humans
  • Hydrazones / metabolism
  • Hydrazones / therapeutic use*
  • Italy
  • Male
  • Middle Aged
  • Natriuretic Peptide, Brain / blood
  • Pyridazines / metabolism
  • Pyridazines / therapeutic use*
  • Severity of Illness Index
  • Simendan
  • Systole / drug effects
  • Treatment Outcome
  • Ultrasonography
  • Ventricular Dysfunction, Left / diagnostic imaging
  • Ventricular Dysfunction, Left / drug therapy*
  • Ventricular Dysfunction, Left / physiopathology
  • Ventricular Function, Left / drug effects*

Substances

  • Biomarkers
  • Cardiotonic Agents
  • Hydrazones
  • Pyridazines
  • Natriuretic Peptide, Brain
  • Simendan