Evidence map›Paper›PMID 36029465›Full record

Trial reportCirculation2022

Efficacy and Safety of Dapagliflozin According to Frailty in Patients With Heart Failure: A Prespecified Analysis of the DELIVER Trial.

Jawad H Butt, Pardeep S Jhund, Jan Belohlávek, Rudolf A de Boer, Chern-En Chiang, Akshai S Desai, Jarosław Drożdż, Adrian F Hernandez, Silvio E Inzucchi, Tzvetana Katova and 17 more

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Circulation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT03619213. Cited by 101 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 7 pooled it
17.2field-weighted citation impact, top 1% 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.

NCT03619213 phase3completed

An International, Double-blind, Randomised, Placebo-Controlled Phase III Study to Evaluate the Effect of Dapagliflozin on Reducing CV Death or Worsening Heart Failure in Patients With Heart Failure With Preserved Ejection Fraction (HFpEF)

Ran2018Enrolled6,263Registered outcomes7Posted comparisons7ConditionsHeart Failure With Preserved Ejection FractionArmsdapagliflozin, Placebo
Open the trial in the graph
3 · Its place in the literature

Who cites it

101 citing papers in PubMed, 7 syntheses or guidelines pooled it, 146 citations in OpenAlex.

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  15. Efficacy and Safety of Dapagliflozin in Patients With Chronic Kidney Disease Across the Spectrum of Frailty.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
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41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 19 institutions in 13 countries.

Jawad H ButtBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (J.H.B., P.S.J., J.J.V.M.).
Pardeep S JhundBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (J.H.B., P.S.J., J.J.V.M.).ORCID 0000-0003-4306-5317
Jan BelohlávekSecond Department of Internal Medicine, Cardiovascular Medicine, General Teaching Hospital, First Faculty of Medicine, Charles University, Prague, Czech Republic (J.B.).
Rudolf A de BoerErasmus Medical Center, Rotterdam, the Netherlands (R.A.d.B.).ORCID 0000-0002-4775-9140
Chern-En ChiangGeneral Clinical Research Center and Division of Cardiology, Taipei Veterans General Hospital and National Yang Ming Chiao Tung University, Taiwan (C.-E.C.).
Akshai S DesaiDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (A.S.D.).ORCID 0000-0002-1443-0701
Jarosław DrożdżDepartment of Cardiology, Medical University of Lodz, Poland (J.D.).
Adrian F HernandezDuke University Medical Center, Durham, NC (A.F.H.).ORCID 0000-0003-3387-9616
Silvio E InzucchiYale School of Medicine, New Haven, CT (S.E.I.).ORCID 0000-0003-1254-6636
Tzvetana KatovaDepartment of Noninvasive Cardiology, National Cardiology Hospital, Sofia, Bulgaria (T.K.).
Masafumi KitakazeCardiovascular Division of Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (M.K.).
Mikhail N KosiborodSaint Luke's Mid America Heart Institute, Kansas City, MO (M.N.K.).ORCID 0000-0002-3750-9789
Carolyn S P LamNational Heart Centre Singapore and Duke National University of Singapore (C.S.P.L.).ORCID 0000-0003-1903-0018
Anna Maria LangkildeLate-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., D.L., E.B., M.P., U.W.).
Daniel LindholmLate-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., D.L., E.B., M.P., U.W.).ORCID 0000-0003-3526-0614
Erasmus BachusLate-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., D.L., E.B., M.P., U.W.).
Felipe MartinezUniversity of Cordoba, Argentina (F.M.).ORCID 0000-0002-5836-972X
Béla MerkelyHeart and Vascular Centre, Semmelweis University, Budapest, Hungary (B.M.).ORCID 0000-0001-6514-0723
Magnus PeterssonLate-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., D.L., E.B., M.P., U.W.).ORCID 0000-0002-4099-0710
Jose F Kerr SaraivaCardiovascular Division, Instituto de Pesquisa Clínica de Campinas, Brazil (J.F.K.S.).
Sanjiv J ShahNorthwestern University Feinberg School of Medicine, Chicago, IL (S.J.S.).ORCID 0000-0002-5655-8201
Muthiah VaduganathanCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.V., B.C.C., S.D.S.).
Orly VardenyMinneapolis VA Center for Care Delivery and Outcomes Research, University of Minnesota (O.V.).
Ulrica WilderängLate-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden (A.M.L., D.L., E.B., M.P., U.W.).ORCID 0000-0002-0939-4128
Brian L ClaggettCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (M.V., B.C.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.C.C., S.D.S.).ORCID 0000-0003-3698-9597
John J V McMurrayBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, UK (J.H.B., P.S.J., J.J.V.M.).ORCID 0000-0002-6317-3975
AstraZeneca (Finland) · FIBrigham and Women's Hospital · USBritish Heart Foundation · GBCharles University · CZCopenhagen University Hospital · DKCordoba University · USDuke Medical Center · USErasmus MC · NLInstituto Paulista de Ensino e Pesquisa · BRMedical University of Lodz · PLMinneapolis VA Health Care System · USNational Cerebral and Cardiovascular Center · JPNational Heart Hospital · BGNational University Heart Centre Singapore · SGNorthwestern University · USSaint Luke's Health System · USSemmelweis University · HUTaipei Veterans General Hospital · TWYale University · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI GERALD I SHULMAN · 1993 to 2026
$44.0M
British Heart Foundation RE/18/6/34217NIDDK NIH HHS P30 DK045735
6 · The paper itself

Abstract

backgroundFrailty is increasing in prevalence. Because patients with frailty are often perceived to have a less favorable risk/benefit profile, they may be less likely to receive new pharmacologic treatments. We investigated the efficacy and tolerability of dapagliflozin according to frailty status in patients with heart failure with mildly reduced or preserved ejection fraction randomized in DELIVER (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure).

methodsFrailty was measured using the Rockwood cumulative deficit approach. The primary end point was time to a first worsening heart failure event or cardiovascular death.

resultsOf the 6263 patients randomized, a frailty index (FI) was calculable in 6258. In total, 2354 (37.6%) patients had class 1 frailty (FI ≤0.210; ie, not frail), 2413 (38.6%) had class 2 frailty (FI 0.211-0.310; ie, more frail), and 1491 (23.8%) had class 3 frailty (FI ≥0.311; ie, most frail). Greater frailty was associated with a higher rate of the primary end point (per 100 person-years): FI class 1, 6.3 (95% CI 5.7-7.1); class 2, 8.3 (7.5-9.1); and class 3, 13.4 (12.1-14.7;

conclusionsIn DELIVER, frailty was common and associated with worse outcomes. The benefit of dapagliflozin was consistent across the range of frailty studied. The improvement in health-related quality of life with dapagliflozin occurred early and was greater in patients with a higher level of frailty. REGISTRATION: URL: https://www. CLINICALTRIALS: gov; Unique identifier: NCT03619213.

Indexed as

Benzhydryl CompoundsFrailtyGlucosidesHeart FailureHumansQuality of LifeStroke VolumeBenzhydryl CompoundsdapagliflozinGlucosidesclinical trialdapagliflozinfrailtyheart failure

Identifiers

PMID36029465
PMCPMC9815819
OpenAlexW4293332312

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.