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Levosimendan in patients with cardiogenic shock complicating myocardial infarction: A meta-analysis
1Department of Intensive Care Medicine, 3rd Hospital of HeBei Medical University, Shi Jiazhuang, China; Department of Anaesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Insights
Levosimendan improved hemodynamic function in patients with myocardial infarction and cardiac shock. However, this systematic review found no significant survival benefit, indicating a need for further research on its clinical efficacy.
Area of Science:
- Cardiology
- Pharmacology
- Critical Care Medicine
Background:
- Cardiac shock is a primary cause of mortality in acute myocardial infarction patients.
- Identifying effective treatments for cardiogenic shock is crucial for improving patient outcomes.
Purpose of the Study:
- To systematically review and meta-analyze the clinical outcomes of levosimendan in patients with cardiogenic shock complicating myocardial infarction.
- To compare levosimendan's efficacy against control groups regarding mortality and other clinical parameters.
Main Methods:
- A comprehensive search of multiple databases (PubMed, EMBASE, Cochrane, CNKI) was conducted up to May 2016.
- Included randomized and non-randomized clinical trials involving adult patients with cardiogenic shock post-myocardial infarction.
- Primary outcome was mortality; secondary outcomes included hemodynamic parameters, organ function scores, and length of ICU stay.
Main Results:
- Thirteen studies with 648 patients were analyzed.
- Levosimendan showed a nonsignificant trend towards reduced mortality (RR=0.82 [0.65-1.01], P=0.07).
- Significant improvements were observed in pulmonary arterial pressure (PAP) and end-systolic volume (ESV) reduction, and increases in cardiac index (CI), cardiac power index (CPI), ejection fraction (EF), mean blood pressure (MBP), and mixed venous oxygen saturation (SvO2).
Conclusions:
- Levosimendan effectively improves hemodynamic parameters and cardiac function in patients with cardiogenic shock complicating myocardial infarction.
- Current evidence does not demonstrate a significant survival benefit of levosimendan in this patient population.
- Further research may be warranted to clarify levosimendan's role in managing cardiogenic shock.
Purpose:
Cardiac shock is the leading cause of death in patients with acute myocardial infarction. The objective of this systematic review and meta-analysis was to evaluate whether levosimendan, compared to any type of control, is associated with improved clinical outcomes in patients with cardiogenic shock complicating myocardial infarction.
Materials And Methods:
The PubMed, EMBASE, Cochrane Central Register, and China National Knowledge Information databases were searched for pertinent studies published up until 1 May 2016. Randomized and non-randomized clinical trials comparing levosimendan to standard therapy or placebo, in adult patients with cardiogenic shock complicating myocardial infarction, and reporting at least one outcome of interest were included. The primary outcome was mortality, whereas secondary outcomes were length of ICU stay, SOFA score, cardiac index (CI), cardiac power index (CPI), ejection fraction (EF), end-systolic volume (ESV), mean blood pressure (MBP), pulmonary arterial pressure (PAP), mixed venous oxygen saturation (SvO2), pulmonary artery occlusion pressure (PAOP) and glomerular filtration rate (GFR). We pooled risk ratio (RR) and 95% confidence interval (CI) using fixed and random effects models.
Results:
Thirteen studies comprising a total of 648 patients were included in the analysis. There was a nonsignificant reduction in mortality with levosimendan compared to the controls (RR=0.82 [0.65-1.01], P for effect=0.07, I2=0%). In the levosimendan group PAP and ESV were significantly reduced, while CI, CPI, EF, MBP and SvO2 were significantly increased. No differences in SOFA score, ICU days, PAOP or GFR were noted.
Conclusions:
Levosimendan can improve hemodynamic parameters and cardiac function when compared with a control group, with no evidence of benefit in terms of survival.
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