Author:

Keywords:

percutaneous coronary intervention, enoxaparin, STEEPLE, unfractionated heparin, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, ELEVATION MYOCARDIAL-INFARCTION, LOW-MOLECULAR-WEIGHT, CREATINE KINASE-MB, HIGH-RISK PATIENTS, ST-ELEVATION, TASK-FORCE, PREDICTORS, MANAGEMENT, MORTALITY, OUTCOMES, Aged, Angioplasty, Balloon, Coronary, Anticoagulants, Australia, Canada, Enoxaparin, Europe, Female, Fibrinolytic Agents, Hemorrhage, Heparin, Humans, Injections, Intravenous, Kaplan-Meier Estimate, Male, Middle Aged, Myocardial Infarction, New Zealand, Platelet Aggregation Inhibitors, Proportional Hazards Models, Risk Assessment, Risk Factors, Time Factors, Treatment Outcome, United States, STEEPLE Investigators, 1102 Cardiorespiratory Medicine and Haematology, Cardiovascular System & Hematology, 3201 Cardiovascular medicine and haematology

Abstract:

OBJECTIVES: Our purpose was to evaluate long-term mortality and identify factors associated with 1-year mortality in patients who underwent elective percutaneous coronary intervention (PCI). BACKGROUND: While long-term outcomes in PCI patients have been reported previously, limited data are currently available regarding the comparative long-term outcomes in PCI patients who receive enoxaparin versus intravenous unfractionated heparin (UFH). METHODS: We conducted a follow-up analysis of clinical outcomes at 1 year in patients enrolled in the STEEPLE (SafeTy and Efficacy of Enoxaparin in Percutaneous coronary intervention patients, an internationaL randomized Evaluation) trial of 3,528 patients undergoing elective PCI. Patients were randomized to receive either intravenous 0.50-mg/kg or 0.75-mg/kg enoxaparin or intravenous UFH during elective PCI procedures. All-cause mortality at 1 year after index PCI was the main outcome measure. RESULTS: Mortality rates were 1.4%, 2.0%, and 1.5% from 1 month to 1 year, and 2.3%, 2.2%, and 1.9% from randomization to 1 year, after index PCI in patients receiving 0.50 mg/kg enoxaparin, 0.75 mg/kg enoxaparin, and UFH, respectively. Multivariate analysis identified nonfatal myocardial infarction and/or urgent target vessel revascularization up to 30 days after index PCI (hazard ratio: 3.5, 95% confidence interval: 1.7 to 7.3; p < 0.001), and major bleeding within 48 h (hazard ratio: 3.0, 95% confidence interval: 1.1 to 8.5; p = 0.04) as the strongest independent risk factors for 1-year mortality. CONCLUSIONS: The 1-year mortality rates were low and comparable between patients receiving enoxaparin and UFH during elective PCI. Periprocedural ischemic or bleeding events were the strongest independent predictors of 1-year mortality. (The STEEPLE Trial; NCT00077844).