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Updated: Feb 26, 2026

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
Comparative Efficacy and Safety of Vasopressors and Inotropes in Acute Myocardial Infarction-Related Cardiogenic
Ahmed Osman Hassan Ali1, Farrukh Ameer2, Ahmad A Ibrahim3
1Critical Care, Dr. Soliman Fakeeh Hospital, Riyadh, SAU.
Abstract:
This systematic review and network meta-analysis evaluated the comparative efficacy and safety of vasopressors and inotropes in patients with cardiogenic shock complicating acute myocardial infarction. Electronic databases were searched from inception to December 2025 for randomized controlled trials (RCTs) and observational studies that compared norepinephrine, epinephrine, dopamine, dobutamine, milrinone, and levosimendan. The primary outcome was all-cause mortality, and the secondary outcomes included arrhythmia and refractory shock. Data were synthesized using a frequentist random-effects network meta-analysis. The certainty of evidence was assessed using the GRADE framework. In total, 14 studies (N = 5,157) were included, comprising six RCTs and eight observational studies. The network geometry was connected via bridging observational data. In the modern era (post-2000), no single agent significantly reduced mortality compared with others. Milrinone and dobutamine were equivalent in terms of in-hospital mortality (odds ratio (OR) = 0.90, 95% confidence interval (CI) 0.69-1.19; high certainty). Norepinephrine was associated with a lower arrhythmic risk than dopamine and was superior to epinephrine, which significantly increased the risk of refractory shock (OR = 8.24, 95% CI = 1.61-42.18; moderate certainty) and mortality (OR = 1.63 vs. norepinephrine). Historical studies have shown large effect sizes that have diminished over time (the Proteus phenomenon). Norepinephrine is the preferred vasopressor due to its safety profile; however, the choice of inotrope between milrinone and dobutamine should be guided by patient physiology rather than survival expectations. Future research requires large-scale trials to detect modest mortality benefits in patients with diabetes.
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