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Antithrombotic regimens for percutaneous coronary intervention of the left main coronary artery: The EXCEL trial

  • Sorin J. Brener
  • , Nicholas J. Lembo
  • , David E. Kandzari
  • , Manel Sabaté
  • , Anthony H. Gershlick
  • , Adrian P. Banning
  • , Paweł E. Buszman
  • , Ioanna Kosmidou
  • , Charles A. Simonton
  • , Marie Claude Morice
  • , Ori Ben-Yehuda
  • , Ovidiu Dressler
  • , Zixuan Zhang
  • , Joseph F. Sabik
  • , Arie Pieter Kappetein
  • , Patrick W. Serruys
  • , Gregg W. Stone
  • NY Methodist Hospital
  • Columbia University Medical Center
  • Cardiovascular Research Foundation
  • Piedmont Heart Institute
  • Hospital Clínic
  • University Hospitals of Leicester NHS Trust
  • John Radcliffe Hospital
  • Medical University of Silesia
  • American Heart of Poland
  • Abbott Vascular
  • Générale de Santé Massy
  • UH Cleveland Medical Center
  • Erasmus MC
  • Imperial College London
  • Icahn School of Medicine at Mount Sinai

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

3 Citations (Scopus)

Abstract

Objectives: We compared the effect of bivalirudin or heparin and use or nonuse of glycoprotein IIb/IIIa inhibitors (GPI) on the outcome of left main coronary artery (LMCA) percutaneous coronary intervention (PCI) in the randomized EXCEL trial. Background: The optimal antithrombotic regimen to support PCI of the LMCA remains controversial because of low representation of this subset in clinical trials. Methods: The PCI cohort (n = 928) in EXCEL was divided according to bivalirudin versus heparin antithrombin treatment and compared for the primary composite endpoint of death, myocardial infarction (MI), or stroke at 30 days and 5 years. RESULTS: Bivalirudin was used in 319 patients (34.4%). The composite endpoint at 30 days occurred in 7.2% versus 3.8% bivalirudin and heparin patients, respectively, p =.02; at 5 years, the composite endpoint occurred in 26.3% versus 19.9% bivalirudin and heparin patients, respectively, p =.02. Major bleeding was more frequent in bivalirudin patients (4.1% versus 1.3%, p =.008). There were no differences in stent thrombosis between the groups. Bivalirudin use was an independent predictor of the 30-day composite endpoint (OR 2.88, 95% CI 1.28–6.48, p =.01) but not of the 5-year composite endpoint (OR 1.30, 95% CI 0.84–2.02, p =.23). GPI use was infrequent (n = 67, 7.2%) and was not associated with adverse outcomes. Conclusion: Among patients undergoing LMCA PCI in the EXCEL trial, procedural use of bivalirudin was associated with greater rates of periprocedural MI and the 30-day composite endpoint without reducing bleeding complications. Five-year outcomes were similar. GPIs were used infrequently and were not associated with clinical outcomes.

Original languageEnglish
Pages (from-to)766-773
Number of pages8
JournalCatheterization and Cardiovascular Interventions
Volume97
Issue number5
DOIs
Publication statusPublished - 1 Apr 2021
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • bivalirudin
  • glycoprotein IIb/IIIa inhibitors
  • heparin
  • left main coronary artery
  • percutaneous coronary intervention

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