PMID- 26077589 OWN - NLM STAT- MEDLINE DCOM- 20160408 LR - 20181113 IS - 2047-9980 (Electronic) IS - 2047-9980 (Print) IS - 2047-9980 (Linking) VI - 4 IP - 6 DP - 2015 Jun 15 TI - Hospital variability in use of anticoagulant strategies during acute myocardial infarction treated with an early invasive strategy. PG - e002009 LID - 10.1161/JAHA.115.002009 [doi] LID - e002009 AB - BACKGROUND: During a myocardial infarction, no single best approach of systemic anticoagulation is recommended, likely due to a lack of comparative effectiveness studies and trade-offs between treatments. METHODS AND RESULTS: We investigated the patterns of use and site-level variability in anticoagulant strategies (unfractionated heparin [UFH] only, low-molecular-weight heparin [LMWH] only, UFH+LMWH, any bivalirudin) of 63 796 patients with a principal diagnosis of myocardial infarction treated with an early invasive strategy with percutaneous coronary intervention at 257 hospitals. About half (47%) of patients received UFH only, 6% UFH+LMWH, 7% LMWH only, and 40% bivalirudin. Compared with UFH, the median odds ratio was 2.90 for LMWH+UFH, 4.70 for LMWH only, and 3.09 for bivalirudin, indicating that 2 "identical" patients would have a 3- to 4-fold greater likelihood of being treated with anticoagulants other than UFH at one hospital compared with another. We then categorized hospitals as low- or high-users of LMWH and bivalirudin. Using hierarchical, multivariate regression models, we found that low bivalirudin-using hospitals had higher unadjusted bleeding rates, but the risk-adjusted and anticoagulant-adjusted bleeding rates did not differ across the hospital anticoagulation phenotypes. Risk-standardized mortality and risk-standardized length of stay also did not differ across hospital phenotypes. CONCLUSIONS: We found substantial site-level variability in the choice of anticoagulants for invasively managed acute myocardial infarction patients, even after accounting for patient factors. No single hospital-use pattern was found to be clinically superior. More studies are needed to determine which patients would derive the greatest benefit from various anticoagulants and to support consistent treatment of patients with the optimal anticoagulant strategy. CI - (c) 2015 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. FAU - Arnold, Suzanne V AU - Arnold SV AD - Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO (S.V.A., J.A.S., M.K.). FAU - Li, Shu-Xia AU - Li SX AD - Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT (S.X.L., J.P.C., K.D., K.M.S., H.M.K.). FAU - Alexander, Karen P AU - Alexander KP AD - Duke Clinical Research Institute, Durham, NC (K.P.A., T.Y.W.). FAU - Spertus, John A AU - Spertus JA AD - Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO (S.V.A., J.A.S., M.K.). FAU - Nallamothu, Brahmajee K AU - Nallamothu BK AD - University of Michigan and the Ann Arbor VA Medical Center, Ann Arbor, MI (B.K.N.). FAU - Curtis, Jeptha P AU - Curtis JP AD - Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT (S.X.L., J.P.C., K.D., K.M.S., H.M.K.) Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT (J.P.C., K.D., H.M.K.). FAU - Kosiborod, Mikhail AU - Kosiborod M AD - Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO (S.V.A., J.A.S., M.K.). FAU - Gupta, Aakriti AU - Gupta A AD - Department of Internal Medicine, Yale University School of Medicine, New Haven, CT (A.G.). FAU - Wang, Tracy Y AU - Wang TY AD - Duke Clinical Research Institute, Durham, NC (K.P.A., T.Y.W.). FAU - Lin, Haiqun AU - Lin H AD - Department of Biostatistics, Yale School of Public Health, New Haven, CT (H.L.). FAU - Dharmarajan, Kumar AU - Dharmarajan K AD - Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT (S.X.L., J.P.C., K.D., K.M.S., H.M.K.) Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT (J.P.C., K.D., H.M.K.). FAU - Strait, Kelly M AU - Strait KM AD - Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT (S.X.L., J.P.C., K.D., K.M.S., H.M.K.). FAU - Lowe, Timothy J AU - Lowe TJ AD - Premier, Inc, Charlotte, NC (T.J.L., H.M.K.). FAU - Krumholz, Harlan M AU - Krumholz HM AD - Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT (S.X.L., J.P.C., K.D., K.M.S., H.M.K.) Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT (J.P.C., K.D., H.M.K.) Department of Health Policy and Management, Yale School of Public Health, Yale University School of Medicine, New Haven, CT (H.M.K.) Robert Wood Johnson Foundation Clinical Scholars Program, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT (H.M.K.) Premier, Inc, Charlotte, NC (T.J.L., H.M.K.). LA - eng GR - U01 HL105270-05/HL/NHLBI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20150615 PL - England TA - J Am Heart Assoc JT - Journal of the American Heart Association JID - 101580524 RN - 0 (Anticoagulants) RN - 0 (Heparin, Low-Molecular-Weight) RN - 0 (Hirudins) RN - 0 (Peptide Fragments) RN - 0 (Recombinant Proteins) RN - 9005-49-6 (Heparin) RN - TN9BEX005G (bivalirudin) SB - IM MH - Aged MH - Anticoagulants/*therapeutic use MH - Female MH - Heparin/therapeutic use MH - Heparin, Low-Molecular-Weight/therapeutic use MH - Hirudins MH - Hospitals/*statistics & numerical data MH - Humans MH - Length of Stay/statistics & numerical data MH - Male MH - Middle Aged MH - Myocardial Infarction/*drug therapy/mortality/therapy MH - Peptide Fragments/therapeutic use MH - Percutaneous Coronary Intervention/methods/statistics & numerical data MH - Recombinant Proteins/therapeutic use MH - Retrospective Studies MH - Treatment Outcome PMC - PMC4599539 OTO - NOTNLM OT - anticoagulation OT - bleeding OT - myocardial infarction OT - variation EDAT- 2015/06/17 06:00 MHDA- 2016/04/09 06:00 PMCR- 2015/06/01 CRDT- 2015/06/17 06:00 PHST- 2015/06/17 06:00 [entrez] PHST- 2015/06/17 06:00 [pubmed] PHST- 2016/04/09 06:00 [medline] PHST- 2015/06/01 00:00 [pmc-release] AID - JAHA.115.002009 [pii] AID - 10.1161/JAHA.115.002009 [doi] PST - epublish SO - J Am Heart Assoc. 2015 Jun 15;4(6):e002009. doi: 10.1161/JAHA.115.002009.