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Previous Volume 359:688-696 August 14, 2008 Number 7 Next

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ABSTRACT

Background Whether bivalirudin is superior to unfractionated heparin in patients with stable or unstable angina who undergo percutaneous coronary intervention (PCI) after pretreatment with clopidogrel is unknown.

Methods We enrolled 4570 patients with stable or unstable angina (with normal levels of troponin T and creatine kinase MB) who were undergoing PCI after pretreatment with a 600-mg dose of clopidogrel at least 2 hours before the procedure; 2289 patients were randomly assigned in a double-blind manner to receive bivalirudin, and 2281 to receive unfractionated heparin. The primary end point was the composite of death, myocardial infarction, urgent target-vessel revascularization due to myocardial ischemia within 30 days after randomization, or major bleeding during the index hospitalization (with a net clinical benefit defined as a reduction in the incidence of the end point). The secondary end point was the composite of death, myocardial infarction, or urgent target-vessel revascularization.

Results The incidence of the primary end point was 8.3% (190 patients) in the bivalirudin group as compared with 8.7% (199 patients) in the unfractionated-heparin group (relative risk, 0.94; 95% confidence interval [CI], 0.77 to 1.15; P=0.57). The secondary end point occurred in 134 patients (5.9%) in the bivalirudin group and 115 patients (5.0%) in the unfractionated-heparin group (relative risk, 1.16; 95% CI, 0.91 to 1.49; P=0.23). The incidence of major bleeding was 3.1% (70 patients) in the bivalirudin group and 4.6% (104 patients) in the unfractionated-heparin group (relative risk, 0.66; 95% CI, 0.49 to 0.90; P=0.008).

Conclusions In patients with stable and unstable angina who underwent PCI after pretreatment with clopidogrel, bivalirudin did not provide a net clinical benefit (i.e., it did not reduce the incidence of the composite end point of death, myocardial infarction, urgent target-vessel revascularization, or major bleeding) as compared with unfractionated heparin, but it did significantly reduce the incidence of major bleeding. (ClinicalTrials.gov number, NCT00262054 [ClinicalTrials.gov] .)

Source Information

From Deutsches Herzzentrum, Technische Universität, Munich (A.K., J. Mehilli, R.A.B., R.I., S.S., J.P., M.S., I.G., A.S.); Herz-Zentrum, Bad Krozingen (F.-J.N., H.J.B., J. Minners); Herzzentrum der Segeberger Kliniken, Bad Segeberg (A.A.K., G.R.); and 1.Medizinische Klinik rechts der Isar, Technische Universität, Munich (J.D., A.S.) — all in Germany; and Geisinger Medical Center, Danville, PA (J.C.B., K.A.S., P.B.B.).

Address reprint requests to Dr. Kastrati at Deutsches Herzzentrum, Lazarettstr. 36, 80636 Munich, Germany, or at kastrati{at}dhm.mhn.de.

Full Text of this Article

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• Giugliano, R. P., Braunwald, E. (2008). The Year in Non-ST-Segment Elevation Acute Coronary Syndrome. J Am Coll Cardiol 52: 1095-1103 [Full Text]  
• (2008). No Net Clinical Benefit for Bivalirudin During Percutaneous Coronary Intervention. Journal Watch Cardiology 2008: 2-2 [Full Text]  
• (2008). Thrombosis Prevention During Percutaneous Coronary Intervention. JWatch Oncology and Hematology 2008: 1-1 [Full Text]