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Cited by 1,459

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Bivalirudin for Patients with Acute Coronary Syndromes

Open access
Stone, Gregg W., McLaurin, Brent T., Cox, David A., Bertrand, Michel E., Lincoff, A. Michael, Moses, Jeffrey W., White, Harvey D., Pocock, Stuart J., Ware, James H., Feit, Frederick, Colombo, Antonio, Aylward, Philip E., Cequier, Angel R., Darius, Harald, Desmet, Walter, Ebrahimi, Ramin, Hamon, Martial, Rasmussen, Lars H., Rupprecht, Hans-Jürgen, Hoekstra, James, Mehran, Roxana, Ohman, E. Magnus·2006·New England Journal of Medicine

Abstract

BACKGROUND: Current guidelines for patients with moderate- or high-risk acute coronary syndromes recommend an early invasive approach with concomitant antithrombotic therapy, including aspirin, clopidogrel, unfractionated or low-molecular-weight heparin, and glycoprotein IIb/IIIa inhibitors. We evaluated the role of thrombin-specific anticoagulation with bivalirudin in such patients. METHODS: We assigned 13,819 patients with acute coronary syndromes to one of three antithrombotic regimens: unfractionated heparin or enoxaparin plus a glycoprotein IIb/IIIa inhibitor, bivalirudin plus a glycoprotein IIb/IIIa inhibitor, or bivalirudin alone. The primary end points were a composite ischemia end point (death, myocardial infarction, or unplanned revascularization for ischemia), major bleeding, and the net clinical outcome, defined as the combination of composite ischemia or major bleeding. RESULTS: Bivalirudin plus a glycoprotein IIb/IIIa inhibitor, as compared with heparin plus a glycoprotein IIb/IIIa inhibitor, was associated with noninferior 30-day rates of the composite ischemia end point (7.7% and 7.3%, respectively), major bleeding (5.3% and 5.7%), and the net clinical outcome end point (11.8% and 11.7%). Bivalirudin alone, as compared with heparin plus a glycoprotein IIb/IIIa inhibitor, was associated with a noninferior rate of the composite ischemia end point (7.8% and 7.3%, respectively; P=0.32; relative risk, 1.08; 95% confidence interval [CI], 0.93 to 1.24) and significantly reduced rates of major bleeding (3.0% vs. 5.7%; P<0.001; relative risk, 0.53; 95% CI, 0.43 to 0.65) and the net clinical outcome end point (10.1% vs. 11.7%; P=0.02; relative risk, 0.86; 95% CI, 0.77 to 0.97). CONCLUSIONS: In patients with moderate- or high-risk acute coronary syndromes who were undergoing invasive treatment with glycoprotein IIb/IIIa inhibitors, bivalirudin was associated with rates of ischemia and bleeding that were similar to those with heparin. Bivalirudin alone was associated with similar rates of ischemia and significantly lower rates of bleeding. (ClinicalTrials.gov number, NCT00093158 [ClinicalTrials.gov].).

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Crossref · 10.1056/nejmoa062437

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Metadata

Authors
Stone, G. W., McLaurin, B. T., Cox, D. A., Bertrand, M. E., Lincoff, A. M., Moses, J. W., White, H. D., Pocock, S. J., Ware, J. H., Feit, F., Colombo, A., Aylward, P. E., Cequier, A. R., Darius, H., Desmet, W., Ebrahimi, R., Hamon, M., Rasmussen, L. H., Rupprecht, H.-J., Hoekstra, J., Mehran, R., & Ohman, E. M.
Venue
New England Journal of Medicine
Published
2006-11-23
Volume
355
Issue
21
Pages
2203-2216
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2121251309
Cited by
1,459
References
2
FWCI
76.11
Type
journal article
Language
en
Open access
bronze

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