• Title of article

    The safety and efficacy of subcutaneous enoxaparin versus intravenous unfractionated heparin and tirofiban versus placebo in the treatment of acute ST-segment elevation myocardial infarction patients ineligible for reperfusion (TETAMI): A randomized trial

  • Author/Authors

    Marc Cohen، نويسنده , , Gian Franco Gensini، نويسنده , , Frans Maritz، نويسنده , , Enrique P Gurfinkel، نويسنده , , Kurt Huber، نويسنده , , Ari Timerman، نويسنده , , Maria Krzeminska-Pakula، نويسنده , , Nicolas Danchin، نويسنده , , Harvey D White، نويسنده , , Jose Santopinto، نويسنده , , Frederique Bigonzi، نويسنده , , Carole Hecquet، نويسنده , , Luc Vittori and TETAMI Investigators، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    9
  • From page
    1348
  • To page
    1356
  • Abstract
    Objectives The aims of the Safety and Efficacy of Subcutaneous Enoxaparin Versus Intravenous Unfractionated Heparin and Tirofiban Versus Placebo in the Treatment of Acute ST-Segment Elevation Myocardial Infarction Patients Ineligible for Reperfusion (TETAMI) study were to demonstrate that enoxaparin was superior to unfractionated heparin (UFH) and that tirofiban was better than placebo in patients with acute ST-segment elevation myocardial infarction (STEMI) who do not receive timely reperfusion. Background An optimal treatment strategy has not been identified for the many STEMI patients ineligible for acute reperfusion. Methods A total of 1,224 patients were enrolled in 91 centers in 14 countries between July 1999 and July 2002. Patients with STEMI ineligible for reperfusion were randomized to enoxaparin, enoxaparin plus tirofiban, UFH, or UFH plus tirofiban. All patients received oral aspirin. The primary efficacy end point was the 30-day combined incidence of death, reinfarction, or recurrent angina; the primary analysis was the comparison of the pooled enoxaparin and UFH groups. Results The incidence of the primary efficacy end point was 15.7% enoxaparin versus 17.3% for UFH (odds ratio 0.89 [95% confidence interval {CI} = 0.66 to 1.21]) and 16.6% for tirofiban versus 16.4% for placebo (odds ratio 1.02 [95% CI 0.75 to 1.38]). The Thrombolysis In Myocardial Infarction (TIMI) major hemorrhage rate was 1.5% for enoxaparin versus 1.3% for UFH (odds ratio 1.16 [95% CI 0.44 to 3.02]) and 1.8% versus 1% for tirofiban versus placebo (odds ratio 1.82 [95% CI 0.67 to 4.95]). Conclusions This study did not show that enoxaparin significantly reduced the 30-day incidence of death, reinfarction, and recurrent angina compared with UFH in non-reperfused STEMI patients. However, enoxaparin appears to have a similar safety and efficacy profile to UFH and may be an alternative treatment. Additional therapy with tirofiban did not appear beneficial.
  • Keywords
    PTCA , STEMI , ST-segment elevation myocardial infarction , aPTT , TETAMI , CABG , UFH , activated partial thromboplastin time , Safety and Efficacy of Subcutaneous Enoxaparin Versus Intravenous UFH With and Without Tirofiban in the Treatment of Acute Myocardial Infarction in patients ineligible for reperfusion , coronary artery bypass grafting , unfractionated heparin , CI , Confidence interval , low-molecular-weight heparin , LMWH , MI , myocardial infarction , PCI , percutaneous coronary interventions , percutaneous transluminal coronary angioplasty
  • Journal title
    JACC (Journal of the American College of Cardiology)
  • Serial Year
    2003
  • Journal title
    JACC (Journal of the American College of Cardiology)
  • Record number

    598336