High-Risk Patients With Acute Coronary Syndromes Treated With Low-Molecular-Weight or Unfractionated Heparin

Abstract
Patients with non–ST-segment elevation (NSTE) acute coronary syndromes (ACS) comprise a spectrum of risk for adverse cardiac events. In the Superior Yield of the New Strategy of Enoxaparin, Revascularization, and Glycoprotein IIb/IIIa Inhibitors (SYNERGY) trial, patients at high risk for recurrent ischemic cardiac events were randomly assigned to receive low-molecular-weight heparin (enoxaparin) or unfractionated heparin. These patients were treated with an early invasive management strategy. The primary results of the trial end point at 30 days showed that enoxaparin was at least as effective as unfractionated heparin.1

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