Evidence map›Paper›PMID 33368858›Full record

Trial reportEuropean journal of heart failure2021

Effects of dapagliflozin in heart failure with reduced ejection fraction and chronic obstructive pulmonary disease: an analysis of DAPA-HF.

Pooja Dewan, Kieran F Docherty, Olof Bengtsson, Rudolf A de Boer, Akshay S Desai, Jaroslaw Drozdz, Nathaniel M Hawkins, Silvio E Inzucchi, Masafumi Kitakaze, Lars Køber and 14 more

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

Trial report in European journal of heart failure, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT03036124. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% 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.

NCT03036124 phase3completed

Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure With Reduced Ejection Fraction

Ran2017Enrolled4,744Registered outcomes6Posted comparisons6ConditionsChronic Heart Failure With Reduced Ejection Fraction (HFrEF)Armsdapagliflozin, Placebo
Open the trial in the graph
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  11. Biomarkers in COPD-Associated PH/CCP: Circulating Molecules and Cell-Intrinsic Marker.International journal of chronic obstructive pulmonary disease · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 16 institutions in 12 countries.

Pooja DewanBHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Kieran F DochertyBHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Olof BengtssonLate Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Rudolf A de BoerDepartment of Cardiology, University Medical Centre and University of Groningen, Groningen, The Netherlands.
Akshay S DesaiDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Jaroslaw DrozdzDepartment of Cardiology, Medical University of Lodz, Lodz, Poland.
Nathaniel M HawkinsDivision of Cardiology, University of British Columbia, Vancouver, Canada.
Silvio E InzucchiSection of Endocrinology, Yale University School of Medicine, New Haven, CT, USA.
Masafumi KitakazeCardiovascular Division of Medicine, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Lars KøberRigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
Mikail N KosiborodSaint Luke's Mid America Heart Institute, University of Missouri, Kansas City, MO, USA.
Anna Maria LangkildeLate Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Daniel LindholmLate Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Felipe A MartinezNational University of Cordoba, Cordoba, Argentina.
Béla MerkelyHeart and Vascular Centre, Semmelweis University, Budapest, Hungary.
Mark C PetrieBHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Piotr PonikowskiWroclaw Medical University, Wroclaw, Poland.
Marc S SabatineTIMI Study Group, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Morten SchouDepartment of Cardiology, Gentofte University Hospital, Copenhagen, Denmark.
Mikaela SjöstrandLate Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Scott D SolomonDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Subodh VermaSt Michael's Hospital, University of Toronto, Toronto, Canada.
Pardeep S JhundBHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
John J V McMurrayBHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
University of Glasgow · GBAstraZeneca (Sweden) · SEBrigham and Women's Hospital · USAstraZeneca (Spain) · ESGentofte Hospital · DKMedical University of Lodz · PLNational Cerebral and Cardiovascular Center · JPRigshospitalet · DKSemmelweis University · HUSt. Michael's Hospital · CAUniversidad Nacional de Córdoba · ARUniversity of British Columbia · CAUniversity of Groningen · NLUniversity of Missouri–Kansas City · USWroclaw Medical University · PLYale University · US

Funding

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

Abstract

aimsChronic obstructive pulmonary disease (COPD) is an important comorbidity in heart failure (HF) with reduced ejection fraction (HFrEF), associated with worse outcomes and often suboptimal treatment because of under-prescription of beta-blockers. Consequently, additional effective therapies are especially relevant in patients with COPD. The aim of this study was to examine outcomes related to COPD in a post hoc analysis of the Dapagliflozin And Prevention of Adverse-outcomes in Heart Failure (DAPA-HF) trial. METHODS AND

resultsWe examined whether the effects of dapagliflozin in DAPA-HF were modified by COPD status. The primary outcome was the composite of an episode of worsening HF or cardiovascular death. Overall, 585 (12.3%) of the 4744 patients randomized had a history of COPD. Patients with COPD were more likely to be older men with a history of smoking, worse renal function, and higher baseline N-terminal pro B-type natriuretic peptide, and less likely to be treated with a beta-blocker or mineralocorticoid receptor antagonist. The incidence of the primary outcome was higher in patients with COPD than in those without [18.9 (95% confidence interval 16.0-22.2) vs. 13.0 (12.1-14.0) per 100 person-years; hazard ratio (HR) for COPD vs. no COPD 1.44 (1.21-1.72); P < 0.001]. The effect of dapagliflozin, compared with placebo, on the primary outcome, was consistent in patients with [HR 0.67 (95% confidence interval 0.48-0.93)] and without COPD [0.76 (0.65-0.87); interaction P-value 0.47].

conclusionsIn DAPA-HF, one in eight patients with HFrEF had concomitant COPD. Participants with COPD had a higher risk of the primary outcome. The benefit of dapagliflozin on all pre-specified outcomes was consistent in patients with and without COPD. CLINICAL

trial registrationClinicalTrials.gov ID NCT03036124.

Indexed as

Heart FailurePulmonary Disease, Chronic ObstructiveAgedBenzhydryl CompoundsGlucosidesHumansMaleStroke VolumeBenzhydryl CompoundsdapagliflozinGlucosidesChronic obstructive pulmonary diseaseDapagliflozinHeart failure

Identifiers

PMID33368858
PMCPMC8247863
OpenAlexW3113765054

What OpenQuestion holds

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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.