Evidence map›Paper›PMID 36809039›Full record

ArticleCirculation. Heart failure2023

A Composite Score Summarizing Use and Dosing of Evidence-Based Medical Therapies in Heart Failure: A Nationwide Cohort Study.

Niklas Dyrby Johansen, Muthiah Vaduganathan, Deewa Zahir, Mona Fiuzat, Ersilia M DeFilippis, James L Januzzi, Javed Butler, Christopher M O'Connor, William T Abraham, Mitchell A Psotka and 12 more

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Article in Circulation. Heart failure, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
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  5. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Niklas Dyrby JohansenDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Denmark (N.D.J., D.Z., D.M., M.S., G.H.G., T.B.-S.).ORCID 0000-0001-6959-3236
Muthiah VaduganathanCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.V., B.L.C., S.D.S.).ORCID 0000-0003-0885-1953
Deewa ZahirDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Denmark (N.D.J., D.Z., D.M., M.S., G.H.G., T.B.-S.).
Mona FiuzatDivision of Cardiology, Department of Medicine, Duke University Medical Center, Durham, NC (M.F.).
Ersilia M DeFilippisDivision of Cardiology, Columbia University Irving Medical Center, New York, NY (E.M.D.).ORCID 0000-0002-0493-1326
James L JanuzziDivision of Cardiology, Massachusetts General Hospital, Boston (J.L.J.).ORCID 0000-0002-8338-1798
Javed ButlerDepartment of Medicine, University of Mississippi, Jackson (J.B.).ORCID 0000-0001-7683-4720
Christopher M O'ConnorInova Heart and Vascular Institute, Falls Church, VA (C.M.O., M.A.P.).
William T AbrahamDivision of Cardiovascular Medicine, Davis Heart and Lung Research Institute, Ohio State University, Columbus (W.T.A.).ORCID 0000-0003-4805-1037
Mitchell A PsotkaInova Heart and Vascular Institute, Falls Church, VA (C.M.O., M.A.P.).
John J V McMurrayBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (J.J.V.M., P.D.).ORCID 0000-0002-6317-3975
Pooja DewanBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (J.J.V.M., P.D.).
Brian L ClaggettCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.V., B.L.C., S.D.S.).ORCID 0000-0002-4215-9218
Scott D SolomonCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.V., B.L.C., S.D.S.).ORCID 0000-0003-3698-9597
Daniel ModinDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Denmark (N.D.J., D.Z., D.M., M.S., G.H.G., T.B.-S.).ORCID 0000-0002-7566-0519
Jawad H ButtDepartment of Cardiology, Copenhagen University Hospital-Rigshospitalet, Denmark (J.H.B., L.K.).ORCID 0000-0002-7380-4144
Jens Ulrik Stæhr JensenRespiratory Medicine Section, Department of Medicine, Copenhagen University Hospital-Herlev and Gentofte, Denmark (J.U.S.J.).ORCID 0000-0003-4036-0521
Morten SchouDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Denmark (N.D.J., D.Z., D.M., M.S., G.H.G., T.B.-S.).ORCID 0000-0002-4271-2466
Christian Torp-PedersenDepartment of Cardiology, Copenhagen University Hospital-North Zealand, Denmark (C.T.-P.).ORCID 0000-0003-2892-6131
Lars KøberDepartment of Cardiology, Copenhagen University Hospital-Rigshospitalet, Denmark (J.H.B., L.K.).ORCID 0000-0002-6635-1466
Gunnar H GislasonDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Denmark (N.D.J., D.Z., D.M., M.S., G.H.G., T.B.-S.).ORCID 0000-0002-0548-402X
Tor Biering-SørensenDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Denmark (N.D.J., D.Z., D.M., M.S., G.H.G., T.B.-S.).ORCID 0000-0003-4209-2778

Funding

The Heart Failure Collaboratory Public-Private Partnership Between the United States Food and Drug Administration, the Inova Heart and Vascular Institute, and the Heart Failure CommunityR18FD006920 · FDA · INOVA HEALTH CARE SERVICES · PI O'CONNOR, CHRISTOPHER M · 2020 to 2024
$698k
FDA HHS R18 FD006920
6 · The paper itself

Abstract

backgroundAs heart failure therapeutic care becomes increasingly complex, a composite medical therapy score could be useful to conveniently summarize background medical therapy. We applied the composite medical therapy score developed by the Heart Failure Collaboratory (HFC) to the Danish heart failure with reduced ejection fraction population to evaluate its external validation including assessing the distribution of the score and its association with survival.

methodsIn a retrospective nationwide cohort study, we identified all Danish heart failure with reduced ejection fraction patients alive on July 1, 2018, and assessed their treatment doses. Patients were excluded if they did not have at least 365 days for up-titration of medical therapy prior to identification. The HFC score (range 0-8) accounts for use and dosing of multiple therapies prescribed to each patient. Risk-adjusted association between the composite score and all-cause mortality was examined.

resultsIn total, 26 779 patients (mean age 71.9 years; 32% women) were identified. At baseline, angiotensin-converting enzyme inhibitor/angiotensin receptor blocker was used in 77%, β-blocker in 81%, mineralocorticoid receptor antagonist in 30%, angiotensin receptor-neprilysin inhibitor in 2%, and ivabradine in 2%. The median HFC score was 4. After multivariable adjustment, higher HFC scores were independently associated with lower mortality (≥median versus <median: hazard ratio, 0.72 [0.67-0.78];

conclusionsNationwide assessment of therapeutic optimization in heart failure with reduced ejection fraction using the HFC score was feasible and the score was strongly and independently associated with survival.

Indexed as

Heart FailureVentricular Dysfunction, LeftAdrenergic beta-AntagonistsAgedAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsCohort StudiesFemaleHumansMaleMineralocorticoid Receptor AntagonistsRetrospective StudiesStroke VolumeAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsMineralocorticoid Receptor Antagonistsdrug therapyepidemiologyheart failuremortalitysurvival analysis

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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.