• Title of article

    Clinical and Angiographic Outcomes After Treatment of De Novo Coronary Stenoses With a Novel Platinum Chromium Thin-Strut Stent: Primary Results of the PERSEUS (Prospective Evaluation in a Randomized Trial of the Safety and Efficacy of the Use of the TAXU

  • Author/Authors

    Kereiakes، نويسنده , , Dean J. and Cannon، نويسنده , , Louis A. and Feldman، نويسنده , , Robert L. and Popma، نويسنده , , Jeffrey J. and Magorien، نويسنده , , Raymond and Whitbourn، نويسنده , , Robert and Dauber، نويسنده , , Ira M. and Rabinowitz، نويسنده , , Abram C. and Ball، نويسنده , , Michael W. and Bertolet، نويسنده , , Barry and Kabour، نويسنده , , Ameer and Foster، نويسنده , , Michael C. and Wang، نويسنده , , John C. and Underwood، نويسنده , , Paul and Dawkins، نويسنده , , Keith D.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2010
  • Pages
    8
  • From page
    264
  • To page
    271
  • Abstract
    Objectives m of this study was to evaluate the safety and efficacy of the novel platinum chromium TAXUS Element paclitaxel-eluting stent (PES) compared with the TAXUS Express PES (Boston Scientific, Natick, Massachusetts) in treating coronary artery stenoses. ound XUS Element is a novel thin-strut (81 μm), platinum chromium alloy PES designed to improve radial strength, radiopacity, and deliverability, while safely providing comparable restenosis benefit compared with a previous-generation PES. s RSEUS (Prospective Evaluation in a Randomized Trial of the Safety and Efficacy of the Use of the TAXUS Element Paclitaxel-Eluting Coronary Stent System) Workhorse (WH) trial is a prospective, randomized (3:1), controlled, multicenter study of the TAXUS Element (vs. TAXUS Express) PES for the treatment of de novo coronary atherosclerotic lesions ≤28 mm in length in reference vessels ≥2.75 to ≤4.0 mm in diameter. The primary end point was the 12-month rate of target lesion failure, and the secondary end point was 9-month angiographic in-segment percentage diameter stenosis. The study was powered to demonstrate noninferiority to TAXUS Express for both end points. s tent-to-treat analysis included 1,262 patients (320 TAXUS Express, 942 TAXUS Element). The TAXUS Element was noninferior to TAXUS Express with respect to both the incidence of target lesion failure (5.57% vs. 6.14%, respectively; difference: 0.57%; 95% credible interval: 1.85%; Bayesian posterior probability of noninferiority = 0.9996) and percentage diameter stenosis (ln[%DS] 3.09 vs. 3.12, respectively; difference: 0.03; 95% credible interval: 0.11; Bayesian posterior probability of noninferiority = 0.9970). No differences in clinical outcomes to 12 months were observed between stent treatments, and stent thrombosis was infrequent (0.3% Express, 0.4% Element). sions ear, the TAXUS Element is comparable in efficacy to the TAXUS Express PES. Furthermore, no safety concerns related to the novel platinum chromium alloy or stent design were observed. (A Prospective Evaluation in a Randomized Trial of the Safety and Efficacy of the Use of the TAXUS Element Paclitaxel-Eluting Coronary Stent System for the Treatment of De Novo Coronary Artery Lesions; NCT00484315)
  • Keywords
    Chromium , drug-eluting stent , Paclitaxel , restenosis , Platinum
  • Journal title
    JACC (Journal of the American College of Cardiology)
  • Serial Year
    2010
  • Journal title
    JACC (Journal of the American College of Cardiology)
  • Record number

    1747911