Abstract 4363412: Discontinuation of Beta-Blockers After Acute Coronary Syndrome: A Systematic Review and Meta-Analysis

Introduction: The optimal duration of beta-blocker (BB) therapy after myocardial infarction remains uncertain in patients without heart failure, especially given their frequent lifelong use and potential adverse effects. Research Question: To address this gap, we conducted a meta-analysis to evaluate the impact of BB discontinuation on clinical outcomes in patients with preserved left ventricular ejection fraction (LVEF). Methods: PubMed, Embase, and the Cochrane Central Register of Controlled Trials were systematically searched for studies enrolling patients with acute coronary syndrome (ACS) and preserved LVEF (≥50%), comparing BB discontinuation versus continuation. Outcomes of interest included all-cause mortality (ACM), major adverse cardiovascular events (MACE), cardiovascular (CV) death, non-CV death, cardiovascular hospitalisation, myocardial infarction, stroke, and unplanned revascularisation. Risk ratios (RR) and hazard ratios (HR) were pooled using random-effects models with 95% confidence intervals (CI). Statistical significance was defined as p < 0.05, and analyses were conducted using RStudio. Results: Six studies, including 144,661 patients, were analysed. The mean age ranged from 57 to 65 years. In four studies, BB were discontinued after 12 months, while in the remaining two, discontinuation occurred at 11 and 6 months, respectively. The prevalence of hypertension ranged from 23.8% to 42.6%. BB discontinuation was associated with increased risk of CV death (RR 1.30; 95% CI 1.14–1.48; p < 0.01; Figure 1A), non-CV death (RR 1.16; 95% CI 1.07–1.25; p < 0.01), and myocardial infarction (RR 1.11; 95% CI 1.03–1.19; p < 0.01; Figure 1B). However, when accounting for time-to-event data, there were no significant differences in ACM (HR 1.02; 95% CI 0.95–1.10; p = 0.54; Figure 1C) or MACE (HR 1.04; 95% CI 0.92–1.18; p = 0.53; Figure 1D). No differences were observed for stroke (HR 1.02; 95% CI 0.89–1.17; p = 0.74) or unplanned revascularisation (RR 0.95; 95% CI 0.86–1.06; p = 0.74). Conclusion: In this meta-analysis, discontinuing BB after ACS in patients with preserved LVEF was associated with higher risks of CV and non-CV death, as well as myocardial infarction. No differences were found in ACM or MACE. These results underscore the need for further studies to identify patient subgroups that may benefit most from continued therapy.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4363412
Primary Topic
Heart rate and cardiovascular health
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article
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article

Abstract 4363412: Discontinuation of Beta-Blockers After Acute Coronary Syndrome: A Systematic Review and Meta-Analysis

Liliam Takayama, Srijan Lal Shrestha, José Manuel Orenday-Barraza, George Wuni et al.
Circulation
Heart rate and cardiovascular health
article

Abstract 4363412: Discontinuation of Beta-Blockers After Acute Coronary Syndrome: A Systematic Review and Meta-Analysis

Liliam Takayama, Srijan Lal Shrestha, José Manuel Orenday-Barraza, George Wuni, Webster Donaldy, Sebastian Jaramillo, Camila Guida, G Ganesh, Christopher Chinnatambi
article en

Abstract

Introduction: The optimal duration of beta-blocker (BB) therapy after myocardial infarction remains uncertain in patients without heart failure, especially given their frequent lifelong use and potential adverse effects. Research Question: To address this gap, we conducted a meta-analysis to evaluate the impact of BB discontinuation on clinical outcomes in patients with preserved left ventricular ejection fraction (LVEF). Methods: PubMed, Embase, and the Cochrane Central Register of Controlled Trials were systematically searched for studies enrolling patients with acute coronary syndrome (ACS) and preserved LVEF (≥50%), comparing BB discontinuation versus continuation. Outcomes of interest included all-cause mortality (ACM), major adverse cardiovascular events (MACE), cardiovascular (CV) death, non-CV death, cardiovascular hospitalisation, myocardial infarction, stroke, and unplanned revascularisation. Risk ratios (RR) and hazard ratios (HR) were pooled using random-effects models with 95% confidence intervals (CI). Statistical significance was defined as p < 0.05, and analyses were conducted using RStudio. Results: Six studies, including 144,661 patients, were analysed. The mean age ranged from 57 to 65 years. In four studies, BB were discontinued after 12 months, while in the remaining two, discontinuation occurred at 11 and 6 months, respectively. The prevalence of hypertension ranged from 23.8% to 42.6%. BB discontinuation was associated with increased risk of CV death (RR 1.30; 95% CI 1.14–1.48; p < 0.01; Figure 1A), non-CV death (RR 1.16; 95% CI 1.07–1.25; p < 0.01), and myocardial infarction (RR 1.11; 95% CI 1.03–1.19; p < 0.01; Figure 1B). However, when accounting for time-to-event data, there were no significant differences in ACM (HR 1.02; 95% CI 0.95–1.10; p = 0.54; Figure 1C) or MACE (HR 1.04; 95% CI 0.92–1.18; p = 0.53; Figure 1D). No differences were observed for stroke (HR 1.02; 95% CI 0.89–1.17; p = 0.74) or unplanned revascularisation (RR 0.95; 95% CI 0.86–1.06; p = 0.74). Conclusion: In this meta-analysis, discontinuing BB after ACS in patients with preserved LVEF was associated with higher risks of CV and non-CV death, as well as myocardial infarction. No differences were found in ACM or MACE. These results underscore the need for further studies to identify patient subgroups that may benefit most from continued therapy.

CirculationVol. 152(Suppl_3)
New York City Health and Hospitals Corporation (US), Piedmont Athens Regional (US), Yale New Haven Hospital (US), Pontifícia Universidade Católica do Paraná (BR), Austral University (AR), Cooper University Hospital (US), Harlem Hospital Center (US), Instituto Dante Pazzanese de Cardiologia (BR)
Openalex Percentile: Top 51%
Heart rate and cardiovascular health
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