PMID- 10517729 OWN - NLM STAT- MEDLINE DCOM- 19991104 LR - 20231024 IS - 1524-4539 (Electronic) IS - 0009-7322 (Linking) VI - 100 IP - 15 DP - 1999 Oct 12 TI - Enoxaparin prevents death and cardiac ischemic events in unstable angina/non-Q-wave myocardial infarction. Results of the thrombolysis in myocardial infarction (TIMI) 11B trial. PG - 1593-601 AB - BACKGROUND: Low-molecular-weight heparins are attractive alternatives to unfractionated heparin (UFH) for management of unstable angina/non-Q-wave myocardial infarction (UA/NQMI). METHODS AND RESULTS: Patients (n=3910) with UA/NQMI were randomized to intravenous UFH for >/=3 days followed by subcutaneous placebo injections or uninterrupted antithrombin therapy with enoxaparin during both the acute phase (initial 30 mg intravenous bolus followed by injections of 1.0 mg/kg every 12 hours) and outpatient phase (injections every 12 hours of 40 mg for patients weighing <65 kg and 60 mg for those weighing >/=65 kg). The primary end point (death, myocardial infarction, or urgent revascularization) occurred by 8 days in 14.5% of patients in the UFH group and 12.4% of patients in the enoxaparin group (OR 0.83; 95% CI 0.69 to 1.00; P=0. 048) and by 43 days in 19.7% of the UFH group and 17.3% of the enoxaparin group (OR 0.85; 95% CI 0.72 to 1.00; P=0.048). During the first 72 hours and also throughout the entire initial hospitalization, there was no difference in the rate of major hemorrhage in the treatment groups. During the outpatient phase, major hemorrhage occurred in 1.5% of the group treated with placebo and 2.9% of the group treated with enoxaparin (P=0.021). CONCLUSIONS: Enoxaparin is superior to UFH for reducing a composite of death and serious cardiac ischemic events during the acute management of UA/NQMI patients without causing a significant increase in the rate of major hemorrhage. No further relative decrease in events occurred with outpatient enoxaparin treatment, but there was an increase in the rate of major hemorrhage. FAU - Antman, E M AU - Antman EM AD - Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA. eantman@rics.bwh.harvard.edu FAU - McCabe, C H AU - McCabe CH FAU - Gurfinkel, E P AU - Gurfinkel EP FAU - Turpie, A G AU - Turpie AG FAU - Bernink, P J AU - Bernink PJ FAU - Salein, D AU - Salein D FAU - Bayes De Luna, A AU - Bayes De Luna A FAU - Fox, K AU - Fox K FAU - Lablanche, J M AU - Lablanche JM FAU - Radley, D AU - Radley D FAU - Premmereur, J AU - Premmereur J FAU - Braunwald, E AU - Braunwald E LA - eng PT - Clinical Trial PT - Clinical Trial, Phase III PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - United States TA - Circulation JT - Circulation JID - 0147763 RN - 0 (Anticoagulants) RN - 0 (Enoxaparin) RN - 0 (Factor Xa Inhibitors) RN - 0 (Fibrinolytic Agents) RN - 0 (Isoenzymes) RN - 9005-49-6 (Heparin) RN - EC 2.7.3.2 (Creatine Kinase) SB - IM CIN - Circulation. 1999 Oct 12;100(15):1586-9. PMID: 10517727 MH - Acute Disease MH - Aged MH - Angina, Unstable/complications/*drug therapy/surgery MH - Anticoagulants/administration & dosage/adverse effects/therapeutic use MH - Creatine Kinase/blood MH - Double-Blind Method MH - Electrocardiography MH - Emergencies MH - Enoxaparin/administration & dosage/adverse effects/*therapeutic use MH - Europe/epidemiology MH - Factor Xa Inhibitors MH - Female MH - Fibrinolytic Agents/administration & dosage/adverse effects/*therapeutic use MH - Hemorrhage/chemically induced MH - Heparin/administration & dosage/adverse effects/*therapeutic use MH - Humans MH - Isoenzymes MH - Life Tables MH - Male MH - Middle Aged MH - Mortality MH - Myocardial Infarction/*drug therapy/epidemiology/etiology/prevention & control/surgery MH - Myocardial Revascularization/statistics & numerical data MH - North America/epidemiology MH - Partial Thromboplastin Time MH - Recurrence MH - Safety MH - South America/epidemiology MH - *Thrombolytic Therapy/adverse effects MH - Treatment Outcome EDAT- 1999/10/12 00:00 MHDA- 1999/10/12 00:01 CRDT- 1999/10/12 00:00 PHST- 1999/10/12 00:00 [pubmed] PHST- 1999/10/12 00:01 [medline] PHST- 1999/10/12 00:00 [entrez] AID - 10.1161/01.cir.100.15.1593 [doi] PST - ppublish SO - Circulation. 1999 Oct 12;100(15):1593-601. doi: 10.1161/01.cir.100.15.1593.