PMID- 22591669 OWN - NLM STAT- MEDLINE DCOM- 20121204 LR - 20181201 IS - 1879-1913 (Electronic) IS - 0002-9149 (Linking) VI - 110 IP - 4 DP - 2012 Aug 15 TI - Meta-analysis comparing bivalirudin versus heparin monotherapy on ischemic and bleeding outcomes after percutaneous coronary intervention. PG - 599-606 LID - 10.1016/j.amjcard.2012.03.051 [doi] AB - With femoral access, bivalirudin decreases risks of major bleeding after percutaneous coronary intervention (PCI) and provides better net clinical benefit compared to unfractionated heparin (UFH) plus planned glycoprotein IIb/IIIa inhibitors. Whether this benefit exists compared to UFH monotherapy is less clear. We performed a systematic review and meta-analysis to compare outcomes in patients undergoing transfemoral PCI with UFH or bivalirudin. Randomized trials (n = 3) and observational studies (n = 13) comparing bivalirudin to UFH monotherapy were reviewed. Primary outcomes were 30-day rates of major adverse cardiovascular events (MACEs) including death, myocardial infarction (MI), urgent revascularization, as well as all-cause mortality, MI, major bleeding, and blood transfusion. We collected data from 16 studies involving 32,492 patients undergoing PCI. Most observational studies were performed in the United States, whereas all randomized trials were done in Europe. Compared to UFH monotherapy, bivalirudin was associated with similar risk of MACEs (odds ratios [OR] 0.92, 95% confidence interval [CI] 0.75 to 1.12), a substantial 45% relative decrease in major bleeding (OR 0.55, 95% CI 0.43 to 0.72), and a trend in the decrease of transfusion (OR 0.87, 95% CI 0.70 to 1.08). A decrease in mortality was seen in observational studies (OR 0.62, 95% CI 0.45 to 0.85) but remained inconclusive in randomized trials (OR 0.63, 95% CI 0.20 to 2.01). MI rate was similar with the 2 anticoagulants. In conclusion, in patients undergoing transfemoral PCI, the benefit of bivalirudin over UFH monotherapy is driven by a significant decrease in major bleeding with similar rates of MACE. As PCI practice moves toward other bleeding-avoidance strategies such as the radial approach, future studies should focus on the interaction between anticoagulant strategy and access-site choice. CI - Copyright (c) 2012 Elsevier Inc. All rights reserved. FAU - Bertrand, Olivier F AU - Bertrand OF AD - Quebec Heart-Lung Institute, Quebec City, Quebec, Canada. olivier.bertrand@criucpq.ulaval.ca FAU - Jolly, Sanjit S AU - Jolly SS FAU - Rao, Sunil V AU - Rao SV FAU - Patel, Tejas AU - Patel T FAU - Belle, Loic AU - Belle L FAU - Bernat, Ivo AU - Bernat I FAU - Parodi, Guido AU - Parodi G FAU - Costerousse, Olivier AU - Costerousse O FAU - Mann, Tift AU - Mann T LA - eng PT - Comparative Study PT - Journal Article PT - Meta-Analysis PT - Systematic Review DEP - 20120515 PL - United States TA - Am J Cardiol JT - The American journal of cardiology JID - 0207277 RN - 0 (Antithrombins) RN - 0 (Hirudins) RN - 0 (Peptide Fragments) RN - 0 (Recombinant Proteins) RN - 9005-49-6 (Heparin) RN - TN9BEX005G (bivalirudin) SB - IM MH - *Angioplasty, Balloon, Coronary MH - Antithrombins/*administration & dosage MH - Cardiovascular Diseases/epidemiology/mortality MH - Heparin/*administration & dosage MH - Hirudins/*administration & dosage MH - Humans MH - Myocardial Ischemia/*prevention & control MH - Peptide Fragments/*administration & dosage MH - Postoperative Complications MH - Postoperative Hemorrhage/*prevention & control MH - Recombinant Proteins/administration & dosage MH - Treatment Outcome EDAT- 2012/05/18 06:00 MHDA- 2012/12/10 06:00 CRDT- 2012/05/18 06:00 PHST- 2012/03/03 00:00 [received] PHST- 2012/03/27 00:00 [revised] PHST- 2012/03/27 00:00 [accepted] PHST- 2012/05/18 06:00 [entrez] PHST- 2012/05/18 06:00 [pubmed] PHST- 2012/12/10 06:00 [medline] AID - S0002-9149(12)01195-2 [pii] AID - 10.1016/j.amjcard.2012.03.051 [doi] PST - ppublish SO - Am J Cardiol. 2012 Aug 15;110(4):599-606. doi: 10.1016/j.amjcard.2012.03.051. Epub 2012 May 15.