American Heart Journal
Volume 145, Issue 6 , Pages 971-978, June 2003

What is the role for improved long-term antiplatelet therapy after percutaneous coronary intervention?

  • Steven Steinhubl, MD

      Affiliations

    • University of North Carolina, Chapel Hill, NC, USA
    • Corresponding Author InformationReprint requests: Steven Steinhubl, MD, Division of Cardiology, University of North Carolina, CB#7075, 338 Burnett-Womack Building, Chapel Hill, NC 27599-7075, USA.
  • ,
  • Peter Berger, MD

      Affiliations

    • Mayo Clinic, Rochester, Minn, USA

Received 13 May 2002; accepted 14 October 2002.

Abstract 

Background

Coronary stent placement has replaced balloon angioplasty as the percutaneous coronary intervention (PCI) method of choice, primarily because of its lower restenosis rate. Compared with aspirin (ASA) monotherapy or ASA plus warfarin, the ticlopidine and ASA combination is superior in reducing thrombotic events after stenting. Clopidogrel plus ASA appears to be at least as effective as ticlopidine and ASA. Intravenous glycoprotein IIb/IIIa inhibitors effectively prevent periprocedural thrombotic complications, but their short duration of action and parenteral dosing don’t allow for long-term protection. This review aimed to answer how long after PCI with a stent patients are at risk for recurrent thrombotic events and what the optimal way to prevent them is.

Results

Classically, ASA has been prescribed indefinitely, whereas adenosine diphosphate receptor antagonists have been discontinued after 2 to 4 weeks. However, the Clopidogrel in Unstable Angina to Prevent Recurrent Events (CURE) trial found that long-term dual antiplatelet therapy with clopidogrel and ASA was more effective than ASA alone in preventing major cardiovascular events in patients with acute coronary syndrome, including those treated with PCI.

Conclusion

Results from additional ongoing studies are needed to clarify the role of long-term dual oral antiplatelet therapy in preventing ischemic events in patients who have undergone PCI.

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 Supported by an unrestricted educational grant from Sanofi-Synthelabo and Bristol-Myers Squibb Company.

PII: S0002-8703(03)00104-2

doi:10.1016/S0002-8703(03)00104-2

American Heart Journal
Volume 145, Issue 6 , Pages 971-978, June 2003