Key result
An abnormal ankle-brachial index independently increased the risk of the primary composite endpoint of all-cause death, myocardial infarction, stroke, and major bleeding (HR 2.21) in patients undergoing PCI.
Why the study?
Data on the influence of an abnormal ankle-brachial index on both ischemic and bleeding events in patients undergoing percutaneous coronary intervention were limited.
Does an abnormal ankle-brachial index predict ischemic and bleeding events in patients undergoing percutaneous coronary intervention?
Cohort (n=4,747)
No
Does an abnormal ankle-brachial index predict ischemic and bleeding events in patients undergoing percutaneous coronary intervention?
An abnormal ankle-brachial index is a significant independent predictor of both long-term ischemic and major bleeding events in patients undergoing PCI, suggesting its utility in secondary risk stratification.
Answers are grounded in this paper and cite their sources.
Abnormal ABI was associated with higher post-PCI death, stroke, and bleeding risk; leaves open whether routine measurement improves outcomes.
BACKGROUND/AIMS: Bleeding events after percutaneous coronary intervention (PCI) have important prognostic implications. Data on the influence of an abnormal ankle-brachial index (ABI) on both ischemic and bleeding events in patients undergoing PCI are limited. METHODS: We included patients who underwent PCI with available ABI data (abnormal ABI, ≤ 0.9 or > 1.4). The primary endpoint was the composite of all-cause death, myocardial infarction (MI), stroke, and major bleeding. RESULTS: Among 4,747 patients, an abnormal ABI was observed in 610 patients (12.9%). During follow-up (median, 31 months), the 5-year cumulative incidence of adverse clinical events was higher in the abnormal ABI group than in the normal ABI group: primary endpoint (36.0% vs. 14.5%, log-rank test, p < 0.001); all-cause death (19.4% vs. 5.1%, log-rank test, p < 0.001); MI (6.3% vs. 4.1%, log-rank test, p = 0.013); stroke (6.2% vs. 2.7%, log-rank test, p = 0.001); and major bleeding (8.9% vs. 3.7%, log-rank test, p < 0.001). An abnormal ABI was an independent risk factor for all-cause death (hazard ratio [HR], 3.05; p < 0.001), stroke (HR, 1.79; p = 0.042), and major bleeding (HR, 1.61; p = 0.034). CONCLUSION: An abnormal ABI is a risk factor for both ischemic and bleeding events after PCI. Our study findings may be helpful in determining the optimal method for secondary prevention after PCI.
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Kim et al. (2023) conducted a cohort in Coronary artery disease requiring percutaneous coronary intervention (n=4,747). Abnormal ankle-brachial index (≤ 0.9 or > 1.4) vs. Normal ankle-brachial index was evaluated on Composite of all-cause death, myocardial infarction, stroke, and major bleeding (HR 2.21, 95% CI 1.74-2.80, p=<0.001). An abnormal ankle-brachial index independently increased the risk of the primary composite endpoint of all-cause death, myocardial infarction, stroke, and major bleeding (HR 2.21) in patients undergoing PCI.
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