Levosimendan neither improves nor worsens mortality in patients with cardiogenic shock due to ST-elevation myocardial infarction

Vasc Health Risk Manag. 2010 Sep 7:6:657-63. doi: 10.2147/vhrm.s8856.

Abstract

Background: The aim of this study was to evaluate the effect of levosimendan on mortality in cardiogenic shock (CS) after ST elevation myocardial infarction (STEMI).

Methods and results: Data were obtained prospectively from the SCAAR (Swedish Coronary Angiography and Angioplasty Register) and the RIKS-HIA (Register of Information and Knowledge about Swedish Heart Intensive Care Admissions) about 94 consecutive patients with CS due to STEMI. Patients were classified into levosimendan-mandatory and levosimendan-contraindicated cohorts. Inotropic support with levosimendan was mandatory in all patients between January 2004 and December 2005 (n = 46). After the SURVIVE and REVIVE II studies were presented, levosimendan was considered contraindicated and was not used in consecutive patients between December 2005 and December 2006 (n = 48). The cohorts were similar with respect to pre-treatment characteristics and concomitant medications. There was no difference in the incidence of new-onset atrial fibrillation, in-hospital cardiac arrest and length of stay at the coronary care unit. There was no difference in adjusted mortality at 30 days and at one year.

Conclusion: The use of levosimendan neither improves nor worsens mortality in patients with CS due to STEMI. Well-designed randomized clinical trials are needed to define the role of inotropic therapy in the treatment of CS.

Keywords: heart failure; inotropic agents; myocardial infarction; pharmacology; shock.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aged
  • Atrial Fibrillation / etiology
  • Cardiotonic Agents / therapeutic use*
  • Chi-Square Distribution
  • Cohort Studies
  • Electrocardiography
  • Female
  • Heart Arrest / etiology
  • Humans
  • Hydrazones / therapeutic use*
  • Length of Stay
  • Male
  • Myocardial Infarction / complications
  • Myocardial Infarction / drug therapy*
  • Myocardial Infarction / mortality
  • Myocardial Revascularization
  • Proportional Hazards Models
  • Pyridazines / therapeutic use*
  • Sex Factors
  • Shock, Cardiogenic / drug therapy*
  • Shock, Cardiogenic / etiology
  • Shock, Cardiogenic / mortality
  • Simendan
  • Statistics, Nonparametric

Substances

  • Cardiotonic Agents
  • Hydrazones
  • Pyridazines
  • Simendan