• Title of article

    Efficacy and safety of enoxaparin compared with unfractionated heparin in high-risk patients with non–ST-segment elevation acute coronary syndrome undergoing percutaneous coronary intervention in the Superior Yield of the New Strategy of Enoxaparin, Revas

  • Author/Authors

    Harvey D. White، نويسنده , , Neal S. Kleiman، نويسنده , , Kenneth W. Mahaffey، نويسنده , , Yuliya Lokhnygina، نويسنده , , Karen S. Pieper، نويسنده , , Karen Chiswell، نويسنده , , Marc Cohen، نويسنده , , Robert A. Harrington، نويسنده , , Derek P. Chew، نويسنده , , John L. Petersen، نويسنده , , Lisa G. Berdan، نويسنده , , Philip E.G. Aylward، نويسنده , , Christopher C. Nessel، نويسنده , , James J. Ferguson III، نويسنده , , Robert M. Califf، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2006
  • Pages
    9
  • From page
    1042
  • To page
    1050
  • Abstract
    Background Enoxaparin reduces ischemic events more effectively than unfractionated heparin (UFH) in patients treated conservatively for non–ST-segment elevation acute coronary syndrome. The SYNERGY trial compared these agents in high-risk patients undergoing early invasive treatment. Enoxaparin was noninferior to UFH for the 30-day primary end point of death/myocardial infarction (MI), but modestly increased bleeding. Methods and Results This article compares the outcomes of the 4687 SYNERGY patients (47%) undergoing percutaneous coronary intervention, who were randomized to receive enoxaparin or UFH. Antithrombotic therapy was administered prerandomization in 78%. Crossover (usually in the catheterization laboratory) to the alternative antithrombotic occurred in 14.6% of enoxaparin patients and 2.9% of UFH-treated patients (P < .0001). Stenting was performed in 86.3%. Abrupt vessel closure occurred in 1.3% of enoxaparin patients and 1.7% of UFH-treated patients (P = .318). The rates of death/MI were similar at 30 days (13.1% with enoxaparin vs 14.2% with UFH, P = .289). GUSTO severe bleeding occurred with similar frequency in both groups (1.5% vs 1.6%, P = .688). TIMI major bleeding was more common with enoxaparin (3.7% vs 2.5% with UFH, P = .028). Transfusions were more frequent with enoxaparin than with UFH (6.8% vs 5.4%, P = .047). TIMI major bleeding increased with crossover from enoxaparin to UFH (from 3.7% to 7.8%) and from UFH to enoxaparin (from 2.5% to 8.6%). Statistical adjustment to model reasons for crossover did not affect the overall safety and efficacy outcomes. Conclusions In high-risk patients undergoing early percutaneous coronary intervention for acute coronary syndrome, enoxaparin avoids the need for monitoring and achieves similar effectiveness to UFH but is associated with more bleeding.
  • Journal title
    American Heart Journal
  • Serial Year
    2006
  • Journal title
    American Heart Journal
  • Record number

    534682