• Title of article

    Effect of timing of clopidogrel administration on 30-day clinical outcomes: 300-mg loading dose immediately after coronary stenting versus pretreatment 6 to 24 hours before stenting in a large unselected patient cohort

  • Author/Authors

    Tibor Szük، نويسنده , , Mariann Gyongyosi، نويسنده , , N?ra Homorodi، نويسنده , , Eva Krist?f، نويسنده , , Csaba Kir?ly، نويسنده , , Istv?n F. Edes، نويسنده , , Andrea Facsk?، نويسنده , , Noemi Pavo، نويسنده , , Gottfried Sodeck، نويسنده , , Christoph Strehblow، نويسنده , , Serdar Farhan، نويسنده , , Gerald Maurer، نويسنده , , Dietmar Glogar، نويسنده , , Hans Domanovits، نويسنده , , Kurt Huber، نويسنده , , Istvan Edes، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    7
  • From page
    289
  • To page
    295
  • Abstract
    Background The aim of our prospective multicenter Clopidogrel Registry was to evaluate the efficacy and safety of a 300-mg loading dose of clopidogrel at the time of ad hoc stenting in patients with suspected coronary artery disease who were not pretreated with clopidogrel for any reason, and to compare the 30-day clinical event rates with the outcome of patients pretreated with a loading dose of clopidogrel 6 to 24 hours before stenting. Methods Between March 2002 and February 2004, 4160 consecutively included patients received a 300-mg loading dose of clopidogrel immediately after (group 1, n = 2679) or 6 to 24 hours before stenting (group 2, n = 1481). Results The primary end point (triple composite end point of acute myocardial infarction, all-cause death, and urgent repeat target vessel revascularization) at 30 days occurred in 4.74% versus 2.77% in groups 1 and 2, respectively (P = .002). The secondary end point events, the stent thrombosis, occurred significantly more frequently in group 1, with a trend toward increase in incidence of death, target vessel revascularization, or need for glycoprotein IIb/IIIa antagonists during percutaneous coronary intervention. Pretreatment with clopidogrel was associated with more major bleeding (secondary safety end point) (0.41% vs 1.35% in groups 1 and 2, respectively; P = .001). Conclusions The results of our multicenter prospective Clopidogrel Registry demonstrate lower efficacy of a 300-mg loading dose of clopidogrel at the time of stenting compared with pretreatment 6 to 24 hours before percutaneous coronary intervention on the 30-day composite clinical end point in the large unselected patient cohort, which suggests the benefit of clopidogrel pretreatment in all incoming patients with suspected significant coronary artery disease scheduled for coronary angiography.
  • Journal title
    American Heart Journal
  • Serial Year
    2007
  • Journal title
    American Heart Journal
  • Record number

    534765