Evidence map›Paper›PMID 26077589›Full record

ArticleJournal of the American Heart Association2015

Hospital variability in use of anticoagulant strategies during acute myocardial infarction treated with an early invasive strategy.

Suzanne V Arnold, Shu-Xia Li, Karen P Alexander, John A Spertus, Brahmajee K Nallamothu, Jeptha P Curtis, Mikhail Kosiborod, Aakriti Gupta, Tracy Y Wang, Haiqun Lin and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 1 country.

Suzanne V ArnoldSaint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO (S.V.A., J.A.S., M.K.).
Shu-Xia LiCenter 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.).
Karen P AlexanderDuke Clinical Research Institute, Durham, NC (K.P.A., T.Y.W.).
John A SpertusSaint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO (S.V.A., J.A.S., M.K.).
Brahmajee K NallamothuUniversity of Michigan and the Ann Arbor VA Medical Center, Ann Arbor, MI (B.K.N.).
Jeptha P CurtisCenter 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.).
Mikhail KosiborodSaint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, MO (S.V.A., J.A.S., M.K.).
Aakriti GuptaDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT (A.G.).
Tracy Y WangDuke Clinical Research Institute, Durham, NC (K.P.A., T.Y.W.).
Haiqun LinDepartment of Biostatistics, Yale School of Public Health, New Haven, CT (H.L.).
Kumar DharmarajanCenter 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.).
Kelly M StraitCenter 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.).
Timothy J LowePremier, Inc, Charlotte, NC (T.J.L., H.M.K.).
Harlan M KrumholzCenter 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.).
Yale University · USYale New Haven Hospital · USClinical Research Institute · USSaint Luke's Hospital · USPremier Research Group · USUniversity of Michigan–Ann Arbor · USUniversity of Missouri–Kansas City · US

Funding

Center for Cardiovascular Outcomes Research at Yale UniversityU01HL105270 · NHLBI · YALE UNIVERSITY · PI CURTIS, JEPTHA PELHAM, KRUMHOLZ, HARLAN MARC · 2010 to 2013
$5.8M
NHLBI NIH HHS U01 HL105270-05
6 · The paper itself

Abstract

backgroundDuring 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

resultsWe 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.

conclusionsWe 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.

Indexed as

AgedAnticoagulantsFemaleHeparinHeparin, Low-Molecular-WeightHirudinsHospitalsHumansLength of StayMaleMiddle AgedMyocardial InfarctionPeptide FragmentsPercutaneous Coronary InterventionRecombinant ProteinsRetrospective StudiesAnticoagulantsbivalirudinHeparinHeparin, Low-Molecular-WeightHirudinsPeptide FragmentsRecombinant Proteinsanticoagulationbleedingmyocardial infarctionvariation

Identifiers

PMID26077589
PMCPMC4599539
OpenAlexW2172353182

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.