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Early Aspirin Discontinuation Versus 12-Month Dual Antiplatelet Therapy after Percutaneous Coronary Intervention for
Abhigna Kolupoti1, Eduardo Itaya2, Bryan O Perez Martinez3
1Department of Cardiovascular Disease, University of Connecticut Health, Farmington, CT, USA.
Insights
Early aspirin discontinuation after percutaneous coronary intervention for acute coronary syndrome significantly reduces net adverse clinical events, primarily by lowering bleeding risk. This strategy maintains ischemic protection compared to standard 12-month dual antiplatelet therapy.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- 12-month dual antiplatelet therapy (DAPT) is standard for acute coronary syndrome (ACS) patients post-percutaneous coronary intervention (PCI).
- Emerging evidence suggests early aspirin cessation with P2Y12 inhibitor monotherapy may reduce bleeding without impacting ischemic events.
Purpose of the Study:
- To evaluate the clinical outcomes of early aspirin discontinuation versus standard 12-month DAPT in ACS patients after PCI.
- To assess the impact on net adverse clinical events (NACE), major adverse cardiovascular events (MACE), and bleeding.
Main Methods:
- Systematic review and meta-analysis of randomized clinical trials and post-hoc analyses.
- Included studies compared early aspirin discontinuation (1-3 months) to 12-month DAPT in ACS populations.
- Random-effects model used to calculate pooled odds ratios (ORs) with 95% confidence intervals (CIs).
Main Results:
- Nine studies with 31,505 patients were analyzed.
- Early aspirin discontinuation significantly reduced NACE (OR 0.77, P=0.002) due to decreased bleeding (BARC ≥2, OR 0.41, P<0.00001).
- Risks of MACE, mortality, MI, stroke, stent thrombosis, and TVR were similar between groups.
Conclusions:
- Early aspirin discontinuation in ACS patients post-PCI offers a net clinical benefit.
- This strategy reduces adverse events by lowering bleeding risk without compromising ischemic outcomes.
- Supports a shift from standard 12-month DAPT towards P2Y12 inhibitor monotherapy after initial treatment period.
Abstract:
In patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS), 12-month dual antiplatelet therapy (DAPT) has long been the standard of care. However, emerging evidence suggests that discontinuing aspirin early while maintaining P2Y12 inhibitor monotherapy may reduce bleeding without compromising ischemic protection. We performed a systematic review and meta-analysis to evaluate the impact of early aspirin discontinuation compared with standard 12-month DAPT on clinical outcomes after PCI for ACS. A meta-analysis was performed including randomized clinical trials and post-hoc analyses of randomized trials comparing early aspirin discontinuation (within 1 to 3 months post-PCI) to standard 12-month DAPT in ACS populations. The major endpoints were a composite of net adverse clinical events (NACE), major adverse cardiovascular events (MACE), all cause and cardiovascular mortality, MI, stroke, stent thrombosis (ST), target vessel revascularization (TVR), and bleeding. A random-effects model was used to calculate pooled odds ratios (ORs) with 95% confidence intervals (CIs). Heterogeneity was assessed using I² statistics. Nine studies were included, encompassing 31,505 patients (15,700 early discontinuation; 15,805 standard DAPT). Across the 9 included studies, early aspirin discontinuation was associated with a significant reduction in NACE compared with standard DAPT (OR 0.77, 95% CI 0.65 to 0.91; p = 0.002) due to reduction in BARC ≥2 bleeding [0.41; 0.32 to 0.52; p <0.00001]. Early aspirin discontinuation, compared to 12-month DAPT resulted in similar risk of MACE [0.88; 0.73 to 1.07; p = .19], all-cause mortality [0.84; 0.69 to 1.03; p = 0.09], cardiovascular mortality [1.02; 0.74 to 1.41; p = 0.92], MI [0.98; 0.77 to 1.25; p = 0.87], stroke [0.97; 0.73 to 1.29; p = 0.82], ST [1.29; 0.83 to 2.0; p = 0.26] and TVR [1.00; 0.79 to 1.27; p = 1.00]. In ACS patients treated with PCI, early discontinuation of aspirin while maintaining P2Y12 inhibitor monotherapy appears to reduce adverse clinical events compared with standard 12-month DAPT. These findings show net benefit of following early aspirin discontinuation strategy due to reduction in major bleeding events without jeopardizing ischemic outcomes.
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