Document Detail


Levosimendan is superior to enoximone in refractory cardiogenic shock complicating acute myocardial infarction.
MedLine Citation:
PMID:  18664782     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: Cardiogenic shock is the leading cause of death in patients hospitalized for acute myocardial infarction. The objectives were to investigate the effects of levosimendan, a novel inodilator, compared with the phosphodiesterase-III inhibitor enoximone in refractory cardiogenic shock complicating acute myocardial infarction, on top of current therapy. DESIGN: Prospective, randomized, controlled single-center clinical trial. SETTING: Medical and coronary intensive care unit in a university hospital. PATIENTS: Thirty-two patients with refractory cardiogenic shock for at least 2 hrs requiring additional therapy. INTERVENTIONS: Infusion of either levosimendan (12 microg/kg over 10 min, followed by 0.1 microg/kg/min over 50 min, and of 0.2 microg/kg/min for the next 23 hrs) or enoximone (fractional loading dose of 0.5 mg/kg, followed by 2-10 microg/kg/min continuously) after initiation of current therapy, always including revascularization, intra-aortic balloon pump counterpulsation, and inotropes. MEASUREMENTS AND MAIN RESULTS: Survival rate at 30 days was significantly higher in the levosimendan-treated group (69%, 11 of 16) compared with the enoximone group (37%, 6 of 16, p = 0.023). Invasive hemodynamic parameters during the first 48 hrs were comparable in both groups. Levosimendan induced a trend toward higher cardiac index, cardiac power index, left ventricular stroke work index, and mixed venous oxygen saturation. In addition, lower cumulative values for catecholamines at 72 hrs and for clinical signs of inflammation were seen in the levosimendan-treated patients. Multiple organ failure leading to death occurred exclusively in the enoximone group (4 of 16 patients). CONCLUSIONS: In severe and refractory cardiogenic shock complicating acute myocardial infarction, levosimendan, added to current therapy, may contribute to improved survival compared with enoximone.
Authors:
Joerg T Fuhrmann; Alexander Schmeisser; Matthias R Schulze; Carsten Wunderlich; Steffen P Schoen; Thomas Rauwolf; Christof Weinbrenner; Ruth H Strasser
Publication Detail:
Type:  Journal Article; Randomized Controlled Trial    
Journal Detail:
Title:  Critical care medicine     Volume:  36     ISSN:  1530-0293     ISO Abbreviation:  Crit. Care Med.     Publication Date:  2008 Aug 
Date Detail:
Created Date:  2008-07-30     Completed Date:  2008-08-25     Revised Date:  2009-08-18    
Medline Journal Info:
Nlm Unique ID:  0355501     Medline TA:  Crit Care Med     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2257-66     Citation Subset:  AIM; IM    
Affiliation:
Department of Internal Medicine and Cardiology, Heart Center Dresden-University Hospital, University of Technology, Dresden, Germany. joerg.fuhrmann@lycos.de
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MeSH Terms
Descriptor/Qualifier:
Aged
Cardiotonic Agents / therapeutic use*
Coronary Care Units
Enoximone / therapeutic use*
Female
Hemodynamics
Hospital Mortality
Humans
Hydrazones / therapeutic use*
Kaplan-Meiers Estimate
Male
Middle Aged
Myocardial Infarction / complications*,  diagnosis
Phosphodiesterase Inhibitors / therapeutic use*
Pyridazines / therapeutic use*
Shock, Cardiogenic / drug therapy*,  etiology,  mortality
Chemical
Reg. No./Substance:
0/Cardiotonic Agents; 0/Hydrazones; 0/Phosphodiesterase Inhibitors; 0/Pyridazines; 131741-08-7/simendan; 77671-31-9/Enoximone
Comments/Corrections
Comment In:
Crit Care Med. 2008 Aug;36(8):2450-1   [PMID:  18664796 ]
Crit Care Med. 2009 Mar;37(3):1181-2   [PMID:  19237968 ]
Crit Care Med. 2009 Mar;37(3):1182   [PMID:  19237971 ]
Crit Care Med. 2009 Sep;37(9):2678; author reply 2678-9   [PMID:  19687655 ]
Erratum In:
Crit Care Med. 2008 Oct;36(10):2966

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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