PMID- 20102912 OWN - NLM STAT- MEDLINE DCOM- 20100225 LR - 20161125 IS - 1879-1913 (Electronic) IS - 0002-9149 (Linking) VI - 105 IP - 2 DP - 2010 Jan 15 TI - Bleeding after percutaneous coronary intervention with Bivalirudin or unfractionated Heparin and one-year mortality. PG - 163-7 LID - 10.1016/j.amjcard.2009.08.668 [doi] AB - Compared to unfractionated heparin (UFH), bivalirudin decreases bleeding during percutaneous coronary interventions (PCIs). We sought to investigate the association between periprocedural bleeding and 1-year mortality as a function of antithrombotic therapy with bivalirudin or UFH. This analysis of the association between bleeding with bivalirudin or UFH and 1-year mortality included the 4,570 patients with negative biomarkers enrolled in the Intracoronary Stenting and Antithrombotic Regimen: Rapid Early Action for Coronary Treatment (ISAR-REACT 3) trial. Major or minor bleeding occurred in 555 patients (12.1%): 225 patients treated with bivalirudin (9.8%) and 330 patients treated with UFH (14.5%, p <0.001). There were 82 deaths (1.8%) within the first year after PCI: 29 deaths occurred in patients who had bled, and 53 deaths occurred in patients who had not bled (Kaplan-Meier estimates of 1-year mortality 5.2% and 1.3%, odds ratio 4.12, 95% confidence interval 2.59 to 6.54, p <0.001). One year after PCI, there were 15 deaths in patients who bled with bivalirudin versus 14 deaths in patients who bled with UFH (Kaplan-Meier estimates of 1-year mortality 6.7% vs 4.2%, odds ratio 1.61, 95% confidence interval 0.76 to 3.40, p = 0.20). Major bleeding occurred in 70 patients (3.0%) treated with bivalirudin and 104 patients treated with UFH (4.5%, p = 0.008). One-year mortality was 11.4% (n = 8) in patients with major bleeding with bivalirudin versus 4.8% (n = 5) in patients with major bleeding with UFH (p = 0.10). In conclusion, these data suggest that in patients with negative biomarkers undergoing PCI, bivalirudin decreases bleeding after PCI compared to UFH, without affecting 1-year mortality in those who had bled. CI - Copyright 2010 Elsevier Inc. All rights reserved. FAU - Ndrepepa, Gjin AU - Ndrepepa G AD - Deutsches Herzzentrum, Technische Universitat, Munich, Germany. ndrepepa@dhm.mhn.de FAU - Schulz, Stefanie AU - Schulz S FAU - Keta, Dritan AU - Keta D FAU - Mehilli, Julinda AU - Mehilli J FAU - Birkmeier, Anette AU - Birkmeier A FAU - Massberg, Steffen AU - Massberg S FAU - Laugwitz, Karl-Ludwig AU - Laugwitz KL FAU - Neumann, Franz-Josef AU - Neumann FJ FAU - Seyfarth, Melchior AU - Seyfarth M FAU - Berger, Peter B AU - Berger PB FAU - Schomig, Albert AU - Schomig A FAU - Kastrati, Adnan AU - Kastrati A LA - eng PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20091114 PL - United States TA - Am J Cardiol JT - The American journal of cardiology JID - 0207277 RN - 0 (Anticoagulants) RN - 0 (Hirudins) RN - 0 (Peptide Fragments) RN - 0 (Recombinant Proteins) RN - 9005-49-6 (Heparin) RN - TN9BEX005G (bivalirudin) SB - IM MH - Aged MH - *Angioplasty, Balloon, Coronary MH - Anticoagulants/*therapeutic use MH - Cohort Studies MH - Coronary Artery Disease/mortality/*therapy MH - Female MH - Heparin/*therapeutic use MH - Hirudins MH - Humans MH - Kaplan-Meier Estimate MH - Male MH - Middle Aged MH - Peptide Fragments/*therapeutic use MH - Postoperative Hemorrhage/*etiology/mortality MH - Recombinant Proteins/therapeutic use MH - Risk Factors MH - Stents MH - Treatment Outcome EDAT- 2010/01/28 06:00 MHDA- 2010/02/26 06:00 CRDT- 2010/01/28 06:00 PHST- 2009/08/03 00:00 [received] PHST- 2009/08/25 00:00 [revised] PHST- 2009/08/25 00:00 [accepted] PHST- 2010/01/28 06:00 [entrez] PHST- 2010/01/28 06:00 [pubmed] PHST- 2010/02/26 06:00 [medline] AID - S0002-9149(09)02312-1 [pii] AID - 10.1016/j.amjcard.2009.08.668 [doi] PST - ppublish SO - Am J Cardiol. 2010 Jan 15;105(2):163-7. doi: 10.1016/j.amjcard.2009.08.668. Epub 2009 Nov 14.