PMID- 26681442 OWN - NLM STAT- MEDLINE DCOM- 20160823 LR - 20181202 IS - 1542-6270 (Electronic) IS - 1060-0280 (Linking) VI - 50 IP - 2 DP - 2016 Feb TI - Heparin Versus Bivalirudin Monotherapy in the Setting of Primary Percutaneous Coronary Intervention for Patients With ST-Segment Elevation Myocardial Infarction. PG - 141-51 LID - 10.1177/1060028015618206 [doi] AB - OBJECTIVE: To evaluate direct comparisons of bivalirudin versus unfractionated heparin (UFH) as anticoagulants during ST-segment elevation myocardial infarction (STEMI) in patients undergoing primary percutaneous coronary intervention (PPCI). DATA SOURCES: Relevant information was identified through a search of MEDLINE (1966-September 2015), International Pharmaceutical Abstracts (1960-September 2015), and Cochrane Databases (publications archived until September 2015) using the terms bivalirudin, unfractionated heparin, ST-segment elevation myocardial infarction, and primary percutaneous coronary intervention. STUDY SELECTION AND DATA EXTRACTION: English-language randomized controlled trials and meta-analyses were eligible for inclusion for data review of STEMI where PPCI was performed. DATA SYNTHESIS: Either bivalirudin or UFH is recommended in the setting of STEMI where PPCI is to be performed. Bivalirudin is touted for its predictable pharmacokinetics, effects on thrombin-mediated platelet inhibition, and favorable outcomes with regard to adverse bleeding profiles, whereas UFH, the gold standard anticoagulant during PPCI, remains a viable treatment strategy. Only recently have direct comparisons of UFH and bivalirudin during PPCI become available. The evidence available is complicated by variances in use of glycoprotein IIb/IIIa inhibitors (GPIs), P2Y12 inhibitors, access sites, and anticoagulant dosing strategies. We provide a review of contemporary trials and advancements in this area. CONCLUSIONS: When compared to UFH with limited use of GPI, available evidence demonstrates that bivalirudin reduces bleeding at the expense of increasing risk for acute stent thrombosis. Further randomized studies are needed to determine the potential benefits of a post-PCI infusion of bivalirudin to reduce the risk for acute stent thrombosis, long-term follow-up beyond 30 days, and mortality. CI - (c) The Author(s) 2015. FAU - Faulkenberg, Kathleen D AU - Faulkenberg KD AD - Cleveland Clinic, Cleveland, OH, USA faulkek@ccf.org. FAU - Beavers, Janna C AU - Beavers JC AD - WakeMed Health and Hospitals, Raleigh, NC, USA. FAU - Finks, Shannon W AU - Finks SW AD - University of Tennessee College of Pharmacy, Memphis, TN, USA. LA - eng PT - Comparative Study PT - Journal Article PT - Review DEP - 20151217 PL - United States TA - Ann Pharmacother JT - The Annals of pharmacotherapy JID - 9203131 RN - 0 (Anticoagulants) RN - 0 (Antithrombins) RN - 0 (Hirudins) RN - 0 (Peptide Fragments) RN - 0 (Platelet Aggregation Inhibitors) RN - 0 (Recombinant Proteins) RN - 9005-49-6 (Heparin) RN - TN9BEX005G (bivalirudin) SB - IM MH - Anticoagulants/therapeutic use MH - Antithrombins/therapeutic use MH - Hemorrhage/chemically induced MH - Heparin/adverse effects/*therapeutic use MH - Hirudins MH - Humans MH - Myocardial Infarction/therapy MH - Peptide Fragments/*therapeutic use MH - *Percutaneous Coronary Intervention MH - Platelet Aggregation Inhibitors/therapeutic use MH - Randomized Controlled Trials as Topic MH - Recombinant Proteins/therapeutic use OTO - NOTNLM OT - ST-segment myocardial infarction OT - bivalirudin OT - heparin OT - primary percutaneous coronary intervention EDAT- 2015/12/19 06:00 MHDA- 2016/08/24 06:00 CRDT- 2015/12/19 06:00 PHST- 2015/12/19 06:00 [entrez] PHST- 2015/12/19 06:00 [pubmed] PHST- 2016/08/24 06:00 [medline] AID - 1060028015618206 [pii] AID - 10.1177/1060028015618206 [doi] PST - ppublish SO - Ann Pharmacother. 2016 Feb;50(2):141-51. doi: 10.1177/1060028015618206. Epub 2015 Dec 17.