Dual antiplatelet therapy duration and clinical outcomes following treatment with zotarolimus-eluting stents

JACC Cardiovasc Interv. 2011 Oct;4(10):1119-28. doi: 10.1016/j.jcin.2011.06.017.

Abstract

Objectives: We sought to evaluate differences in late safety outcomes relative to dual antiplatelet therapy (DAPT) duration in patients treated with zotarolimus-eluting stents (ZES).

Background: Despite treatment recommendations for at least 12 months of DAPT following drug-eluting stent revascularization, device-specific outcomes relative to DAPT duration are absent.

Methods: Among 2,032 patients undergoing percutaneous coronary revascularization with ZES in 5 trials, late safety events were compared relative to DAPT duration for patients with ≥ 6 months DAPT adherence and survival free of major ischemic and bleeding events.

Results: A total of 1,414 event-free patients on DAPT at 6 months were identified. Patient group comparisons relative to DAPT included: 6 months versus ≥ 12 months, and 6 months versus ≥ 24 months. Through 3 years, risk-adjusted ischemic event rates did not significantly differ between groups: 6 versus ≥ 12 months: death (2.7% vs. 2.2%), myocardial infarction (MI, 0.3% vs. 1.1%), and definite/probable stent thrombosis (ST, 0.3% vs. 0%); 6 versus ≥ 24 months: death (1.6% vs. 1.6%), MI (0.4% vs. 1.2%), and definite/probable ST (0.1% vs. 0.2%). Composite events also did not statistically vary between DAPT durations. In multivariable analysis, 6-month versus longer DAPT duration was not associated with increased likelihood of thrombotic events at 3-year follow-up. Major bleeding was negligible across groups.

Conclusions: Among patients treated with ZES, late-term events of death, MI, stroke, and ST do not significantly differ between patients taking 6 months DAPT compared with continuation beyond 1 year. These findings merit further study to identify the appropriate duration of DAPT according to specific drug-eluting stents.

MeSH terms

  • Antineoplastic Agents, Phytogenic / therapeutic use
  • Aspirin / therapeutic use
  • Belgium
  • Confidence Intervals
  • Coronary Restenosis / drug therapy
  • Coronary Restenosis / prevention & control*
  • Coronary Restenosis / therapy
  • Drug-Eluting Stents / adverse effects*
  • Female
  • France
  • Humans
  • Immunosuppressive Agents / adverse effects*
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Odds Ratio
  • Paclitaxel / therapeutic use
  • Platelet Aggregation Inhibitors / adverse effects
  • Platelet Aggregation Inhibitors / therapeutic use*
  • Risk Assessment
  • Sirolimus / adverse effects
  • Sirolimus / analogs & derivatives*
  • Sirolimus / therapeutic use
  • Thienopyridines / adverse effects
  • Thienopyridines / therapeutic use*
  • Time Factors
  • Treatment Outcome
  • United States

Substances

  • Antineoplastic Agents, Phytogenic
  • Immunosuppressive Agents
  • Platelet Aggregation Inhibitors
  • Thienopyridines
  • zotarolimus
  • Paclitaxel
  • Aspirin
  • Sirolimus