Key result
Beta-blockers linked to ~40% lower mortality after post-PCI STEMI with preserved LVEF.
Why the study?
The role of prophylactic beta-blocker therapy in patients treated with primary PCI for STEMI who have mildly reduced or preserved LVEF remains a subject of debate.
Does prophylactic beta-blocker therapy reduce all-cause mortality in patients undergoing primary PCI for STEMI with preserved LVEF (≥40%)?
Meta-Analysis (n=28,736)
Does prophylactic beta-blocker therapy reduce all-cause mortality in patients undergoing primary PCI for STEMI with preserved LVEF (≥40%)?
Relative Risk: 0.6 (95% CI 0.43–0.85)
p-value: p=0.003
Prophylactic beta-blocker therapy in post-PCI STEMI patients with preserved LVEF is associated with reduced all-cause mortality, though this finding is limited by high heterogeneity and conflicting results between observational studies and open-label RCTs.
May warrant consideration in post-PCI STEMI with preserved LVEF; leaves open need for confirmatory RCTs on cardiovascular outcomes.
The role of prophylactic beta-blocker therapy in patients treated with primary percutaneous coronary intervention (PCI) for ST-elevation myocardial infarction (STEMI) who have mildly reduced or preserved left ventricular ejection fraction (LVEF) remains a subject of debate. This systematic review and meta-analysis aimed to evaluate the efficacy of beta-blocker therapy versus no beta-blocker therapy in this specific patient population. We searched PubMed, National Institutes of Health (NIH), Elsevier, Google Scholar, and ClinicalTrials.gov for studies published between 2014 and 2024. Eligible studies included randomized controlled trials (RCTs) and observational studies comparing beta-blockers with no beta-blockers in patients undergoing PCI for STEMI with an LVEF ≥ 40%. The primary outcome was all-cause mortality; secondary outcomes included cardiovascular mortality, reinfarction, and hospitalization for heart failure or stroke. Effect sizes were calculated as relative risk (RR) with 95% confidence intervals (CI). Our search yielded 187 articles, from which six studies (four observational and two RCTs) met the inclusion criteria, encompassing a pooled cohort of 28,736 patients (mean age: 63.5 years; 83% male). Of these, 13,650 (47.5%) received beta-blockers at hospital discharge. The meta-analysis of five studies (18,459 patients) indicated that beta-blocker use was associated with a significant reduction in all-cause mortality. However, heterogeneity was high; sensitivity analysis removing one influential RCT reduced I² to 55% and strengthened the significance. Subgroup analysis for cardiovascular mortality (four studies, 14,784 patients) showed a significant risk reduction in two observational studies but no significant effect in two RCTs. No significant differences were observed for reinfarction or hospitalization for heart failure or stroke. The quality of evidence from RCTs was deemed low due to their open-label design. In conclusion, while beta-blocker therapy may reduce all-cause mortality in post-PCI STEMI patients with preserved LVEF, its effect on cardiovascular mortality is inconsistent between study types. High-quality, blinded RCTs are warranted to definitively establish efficacy in this population.
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Affas et al. (2025) conducted a meta-analysis in ST-elevation myocardial infarction with preserved left ventricular ejection fraction (n=28,736). Beta-blocker therapy vs. No beta-blocker therapy was evaluated on All-cause mortality (RR 0.60, 95% CI 0.43-0.85, p=0.003). Prophylactic beta-blocker therapy reduced all-cause mortality by 40% (RR 0.60) compared to no beta-blockers in post-PCI STEMI patients with preserved LVEF, though driven by observational data.
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