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Four-year follow-up of TYPHOON (Trial to assess the use of the CYPHer sirolimus-eluting coronary stent in acute myocardial infarction treated with BallOON angioplasty)

  • Christian Spaulding*
  • , Emmanuel Teiger
  • , Philippe Commeau
  • , Olivier Varenne
  • , Ezio Bramucci
  • , Michel Slama
  • , Keavin Beatt
  • , Ashok Tirouvanziam
  • , Lech Polonski
  • , Pieter R. Stella
  • , Richard Clugston
  • , Jean Fajadet
  • , Xavier De Boisgelin
  • , Christophe Bode
  • , Didier Carri
  • , Andrejs Erglis
  • , Bela Merkely
  • , Stefan Hosten
  • , Ana Cebrian
  • , Patrick Wang
  • Hans Peter Stoll, Patrick Henry
*Corresponding author for this work
  • Université Paris Cité
  • Hôpital Henri Mondor
  • Polyclinique des Fleurs
  • IRCCS Fondazione Policlinico San Matteo - Pavia
  • Hôpital Antoine Béclère
  • Croydon Health Services NHS Trust
  • Nantes Université
  • Medical University of Silesia in Katowice
  • Utrecht University
  • Royal Perth Hospital
  • Clinique Pasteur Toulouse
  • Clinique du Millnaire
  • University of Freiburg
  • CHU de Toulouse
  • Paula Stradina Clinical University Hospital
  • Semmelweis University
  • Johnson & Johnson

Research output: Contribution to journalArticlepeer-review

109 Citations (Scopus)

Abstract

Objectives The aim of this study was to assess the long-term safety and efficacy of the CYPHER (Cordis, Johnson and Johnson, Bridgewater, New Jersey) sirolimus-eluting coronary stent (SES) in percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI). Background Concern over the safety of drug-eluting stents implanted during PCI for STEMI remains, and long-term follow-up from randomized trials are necessary. TYPHOON (Trial to assess the use of the cYPHer sirolimus-eluting stent in acute myocardial infarction treated with ballOON angioplasty) randomized 712 patients with STEMI treated by primary PCI to receive either SES (n = 355) or bare-metal stents (BMS) (n = 357). The primary end point, target vessel failure at 1 year, was significantly lower in the SES group than in the BMS group (7.3% vs. 14.3%, p = 0.004) with no increase in adverse events. Methods A 4-year follow-up was performed. Complete data were available in 501 patients (70%), and the survival status is known in 580 patients (81%). Results Freedom from target lesion revascularization (TLR) at 4 years was significantly better in the SES group (92.4% vs. 85.1%; p = 0.002); there were no significant differences in freedom from cardiac death (97.6% and 95.9%; p = 0.37) or freedom from repeat myocardial infarction (94.8% and 95.6%; p = 0.85) between the SES and BMS groups. No difference in definite/probable stent thrombosis was noted at 4 years (SES: 4.4%, BMS: 4.8%, p = 0.83). In the 580 patients with known survival status at 4 years, the all-cause death rate was 5.8% in the SES and 7.0% in the BMS group (p = 0.61). Conclusions In the 70% of patients with complete follow-up at 4 years, SES demonstrated sustained efficacy to reduce TLR with no difference in death, repeat myocardial infarction or stent thrombosis. (The Study to Assess AMI Treated With Balloon Angioplasty [TYPHOON]; NCT00232830)

Original languageEnglish
Pages (from-to)14-23
Number of pages10
JournalJACC: Cardiovascular Interventions
Volume4
Issue number1
DOIs
Publication statusPublished - Jan 2011
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

  • bare-metal stent
  • percutaneous coronary intervention
  • sirolimus-eluting coronary stent
  • target lesion revascularization

OECD Field of Science

  • 3. Medical and Health Sciences

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