Abstract

In the ACUITY trial, the use of bivalirudin (BIV) resulted in superior net clinical outcomes when compared to combination therapy with either unfractionated heparin or enoxaparin plus a glycoprotein inhibitor (H+GPI) in patients with moderate-high risk non-ST-elevation acute coronary syndromes (NSTE ACS). In the early upstream management of patients with high-risk NSTE ACS, the comparison of a consistent antithrombotic regimen from presentation to coronary angiography with H+GPI, BIV+GPI or BIV alone has not been evaluated.

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