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European Heart Journal Advance Access published online on August 17, 2005

European Heart Journal, doi:10.1093/eurheartj/ehi459
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European Heart Journal © The European Society of Cardiology 2005; all rights reserved
Received May 12, 2005
Revised June 30, 2005
Accepted July 25, 2005

Clinical research

Mortality at 1 year for the direct comparison of tirofiban and abciximab during percutaneous coronary revascularization: do tirofiban and ReoPro give similar efficacy outcomes at trial 1-year follow-up

Debabrata Mukherjee 1*, Eric J. Topol 2, Michel E. Bertrand 3, Steen D. Kristensen 4, Howard C. Herrmann 5, Franz-Josef Neumann 6, Steven J. Yakubov 7, Jean-Pierre Bassand 8, Rick R. McClure 1, Gregg W. Stone 9, Diego Ardissino 10, David J. Moliterno 1, and for the TARGET Investigators

1 Division of Cardiovascular Medicine, Gill Heart Institute, University of Kentucky, 900 S Limestone, 326 Wethington Building, Lexington, KY 40536-0200, USA
2 Department of Cardiovascular Medicine, Cleveland Clinic Foundation, Cleveland, OH, USA
3 Hôpital Cardiologique, Lille, France
4 Skejby Hospital, Aarhus University Hospital, Brendstrupgaardsvej, Denmark
5 University of Pennsylvania Medical Center, Philadelphia, PA, USA
6 Herz-Zentrum Bad Krozingen, Bad Krozingen, Germany
7 Riverside Methodist Hospital, Columbus, OH, USA
8 Jean-Minjoz Hospital, Besançon, France
9 Columbia University Medical Center, New York, NY, USA
10 Università Degli Studi di Parma, Parma, Italy

* To whom correspondence should be addressed.
Debabrata Mukherjee, E-mail: mukherjee{at}uky.edu


   Abstract

Aims Compared with placebo, abciximab has been associated with mortality reduction at late follow-up. The TARGET trial was performed to test whether tirofiban and abciximab provide similar efficacy outcomes among patients undergoing non-emergent, stent-based percutaneous coronary intervention. We report here the 1-year mortality of the study population.

Methods and results In 18 countries at 149 hospitals, 4809 patients undergoing elective or urgent stent implantation were randomly assigned a bolus and infusion of tirofiban or abciximab. Ischaemic events were assessed at 30 days and 6 months and mortality was assessed at 1 year. We previously reported that abciximab was superior to tirofiban considering the composite rate of death or myocardial infarction at 30 days among all patients and at 6 months among those with an acute coronary syndrome (ACS). At 1-year follow-up death occurred in 46 (1.9%) patients who received tirofiban and 42 (1.7%) patients who received abciximab (hazard ratio 1.10, 95% CI 0.72-1.67; P = 0.660). Mortality rates for patients with ACS were 2.3% with tirofiban vs. 2.2% with abciximab (hazard ratio 1.03, 95% CI 0.64-1.67; P = 0.897) and those without ACS were 1.4 vs. 1.0% (hazard ratio 1.32, 95% CI 0.56-3.13; P = 0.530).

Conclusion At 1 year, tirofiban provided a similar level of survival benefit compared with abciximab.

Keywords: Glycoprotein IIb/IIIa inhibitor; Tirofiban; Abciximab; Mortality; Percutaneous coronary intervention.
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