β-blocker therapy at discharge was associated with a significantly lower risk of all-cause death in patients with acute coronary syndrome undergoing PCI (HR 0.33; 95% CI 0.17-0.65; P=0.001).
Cohort (n=3,180)
Does β-blocker therapy at discharge reduce all-cause death in patients with acute coronary syndrome undergoing percutaneous coronary intervention?
Beta-blocker therapy at discharge, particularly at doses <50% of target, is associated with significantly reduced all-cause mortality in patients with ACS following successful PCI, with the greatest benefit observed in NSTEMI patients.
Hazard Ratio: 0.33 (95% CI 0.17–0.65)
p-value: p=0.001
BACKGROUND: The evidence supporting the use of β-blockers in patients with acute coronary syndrome after successful percutaneous coronary intervention has been inconsistent and scarce. METHODS AND RESULTS: Between March 1, 2009, and December 30, 2014, a total of 3180 eligible patients with acute coronary syndrome undergoing percutaneous coronary intervention were consecutively enrolled. The primary end point was all-cause death and the secondary end point was a composite of all-cause death, nonfatal myocardial infarction, heart failure readmission, and cardiogenic hospitalization. Patients were compared according to the use of β-blockers at discharge. Compared with the no β-blocker group, the risk of all-cause death was significantly lower in the β-blocker group (hazard ratio HR, 0.33; 95% CI, 0.17-0.65 P=0.001). A consistent result was obtained in multiple adjusted model and propensity score-matched analysis. The use of β-blockers was also associated with decreased risk of composite of adverse cardiovascular events (HR, 0.47; 95% CI, 0.28-0.81 P=0.006), although statistical significance disappeared after multivariable adjustment and propensity score matching. Furthermore, we performed post hoc analysis for the subsets of patients and the results revealed that patients with non-ST-segment elevation myocardial infarction benefited the most from β-blocker therapy at discharge (HR, 0.04; 95% CI, 0.00-0.27 P=0.001), and the use of <50% of target dose was significantly associated with better outcome compared with no β-blocker use, rather than ≥50% of target dose. CONCLUSIONS: The administration of relatively low β-blocker dose is associated with improved clinical outcomes among patients with acute coronary syndrome after successful percutaneous coronary intervention, especially for patients with non-ST-segment elevation myocardial infarction.
Li et al. (Wed,) conducted a cohort in Acute coronary syndrome undergoing percutaneous coronary intervention (n=3,180). β-blocker therapy at discharge vs. No β-blocker therapy was evaluated on All-cause death (HR 0.33, 95% CI 0.17-0.65, p=0.001). β-blocker therapy at discharge was associated with a significantly lower risk of all-cause death in patients with acute coronary syndrome undergoing PCI (HR 0.33; 95% CI 0.17-0.65; P=0.001).
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