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Updated: Jul 13, 2026

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Prolonged dual antiplatelet therapy after percutaneous coronary intervention reduces ischemic events without
Sorin J Brener1, Steven R Steinhubl, Peter B Berger
1Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, OH 44122, USA. breners@ccf.org
Insights
Dual antiplatelet therapy with aspirin and clopidogrel significantly reduces ischemic events after percutaneous coronary intervention (PCI). This benefit is linked to the patient's overall atherothrombotic risk, not the specific treated artery.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Dual antiplatelet therapy (DAPT) is standard after percutaneous coronary intervention (PCI) and for acute coronary syndromes.
- The impact of DAPT on target vessel revascularization (TVR) versus other ischemic events from 1 month to 1 year post-PCI remains understudied.
Purpose of the Study:
- To investigate the relationship between TVR and ischemic events in patients treated with aspirin plus clopidogrel versus aspirin alone.
- To assess the long-term efficacy of DAPT in reducing ischemic events after PCI.
Main Methods:
- Analysis of patients from the CREDO trial treated with aspirin and clopidogrel or aspirin and placebo for up to 1 year.
- Comparison of TVR rates and ischemic events (cardiac death, myocardial infarction, stroke) between treatment groups.
- Statistical modeling to determine the effect of clopidogrel on ischemic events, adjusting for covariates.
Main Results:
- Ischemic events occurred in 3.1% of clopidogrel-treated patients versus 5.3% in the placebo group by 1 year (p=0.02).
- Target vessel revascularization (TVR) rates were similar between groups (11.9% vs. 12.2%, p=0.82).
- Adjusted analysis showed DAPT associated with a 48% reduction in ischemic events (p=0.01). Patients with TVR had higher ischemic event rates (12.3% vs. 3.1%, p<0.001).
Conclusions:
- Prolonged DAPT effectively reduces ischemic events post-PCI without increasing TVR.
- The benefit of DAPT appears related to the patient's systemic atherothrombotic risk rather than the specific intervention site.
- Ischemic events in patients with TVR were often unrelated to the stented vessel, highlighting the importance of managing underlying disease.
Background:
Dual antiplatelet therapy reduces ischemic events after percutaneous coronary intervention (PCI) and in patients with acute coronary syndromes. The relationship between target vessel revascularization (TVR) and ischemic events in patients treated with aspirin and clopidogrel or aspirin alone from 1 month to 1 year after PCI has not been studied.
Methods:
Patients enrolled in the CREDO trial were treated with aspirin and clopidogrel or aspirin and placebo for up to 1 year. We compared the rates of TVR and ischemic events (cardiac death, myocardial infarction or stroke) in the two groups, and modeled the effect of clopidogrel treatment on ischemic events after adjusting for relevant parameters. RESULTS One month after PCI, 1,955 patients have remained asymptomatic. By 1 year, ischemic events occurred in 5.3% of placebo- and 3.1% of clopidogrel-treated patients; p = 0.02. The rate of TVR was 11.9% and 12.2%, respectively; p = 0.82. Only 7 patients (clopidogrel: 3 and placebo: 4) experienced TVR within 7 days of an ischemic event. After adjustment, long-term dual antiplatelet therapy was associated with a 48% reduction in events; p = 0.01. Patients who experienced TVR had a significantly higher rate of ischemic events than those without TVR, regardless of treatment assignment: 12.3% vs. 3.1%, respectively; p < 0.001.
Conclusion:
Thus, after successful PCI, prolonged dual antiplatelet therapy reduces ischemic events without affecting TVR. Overall, patients with TVR experienced an ischemic event much more often that was not related to the PCI vessel. This suggests that the benefit of antiplatelet therapy after coronary revascularization is indexed to the patient's underlying atherothrombotic process, rather than the artery that underwent intervention.
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