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.

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