Key result
β-blocker therapy did not significantly reduce the primary composite outcome of all-cause death and myocardial infarction (HR 0.88) compared to no β-blockers in patients with chronic CAD undergoing PCI.
Why the study?
The outcome benefits of beta-blockers in chronic coronary artery disease have not been fully assessed.
Does β-blocker therapy reduce the composite of all-cause death and MI in patients with chronic CAD after PCI?
Cohort (n=3,075)
Yes
Does β-blocker therapy reduce the composite of all-cause death and MI in patients with chronic CAD after PCI?
Routine β-blocker therapy does not improve clinical outcomes in patients with chronic CAD undergoing PCI, though a mortality benefit may exist for those with prior MI or revascularization.
BACKGROUND AND OBJECTIVES: The outcome benefits of β-blockers in chronic coronary artery disease (CAD) have not been fully assessed. We evaluated the prognostic impact of β-blockers on patients with chronic CAD after percutaneous coronary intervention (PCI). METHODS: A total of 3,075 patients with chronic CAD were included from the Grand Drug-Eluting Stent registry. We analyzed β-blocker prescriptions, including doses and types, in each patient at 3-month intervals from discharge. After propensity score matching, 1,170 pairs of patients (β-blockers vs. no β-blockers) were derived. Primary outcome was defined as a composite endpoint of all-cause death and myocardial infarction (MI). We further analyzed the outcome benefits of different doses (low-, medium-, and high-dose) and types (conventional or vasodilating) of β-blockers. RESULTS: During a median (interquartile range) follow-up of 3.1 (3.0-3.1) years, 134 (5.7%) patients experienced primary outcome. Overall, β-blockers demonstrated no significant benefit in primary outcome (hazard ratio [HR], 0.88; 95% confidence interval [CI], 0.63-1.24), all-cause death (HR, 0.87; 95% CI, 0.60-1.25), and MI (HR, 1.25; 95% CI, 0.49-3.15). In subgroup analysis, β-blockers were associated with a lower risk of all-cause death in patients with previous MI and/or revascularization (HR, 0.38; 95% CI, 0.14-0.99) (p for interaction=0.045). No significant associations were found for the clinical outcomes with different doses and types of β-blockers. CONCLUSIONS: Overall, β-blocker therapy was not associated with better clinical outcomes in patients with chronic CAD undergoing PCI. Limited mortality benefit of β-blockers may exist for patients with previous MI and/or revascularization. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03507205.
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Park et al. (2022) conducted a cohort in Chronic coronary artery disease (CAD) after percutaneous coronary intervention (PCI) (n=3,075). β-blockers vs. No β-blockers was evaluated on Composite of all-cause death and myocardial infarction (MI) (HR 0.88, 95% CI 0.63-1.24, p=0.500). β-blocker therapy did not significantly reduce the primary composite outcome of all-cause death and myocardial infarction (HR 0.88) compared to no β-blockers in patients with chronic CAD undergoing PCI.
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