Evidence map›Paper›PMID 41711194›Full record

Trial reportESC heart failure2026

Effects of empagliflozin on right ventricular free-wall strain in patients with heart failure and reduced ejection fraction: results from the Empire HF Trial.

Massar Omar, Jesper Jensen, Mulham Ali, Peter H Frederiksen, Caroline Kistorp, Lars Videbæk, Mikael Kjær Poulsen, Christian D Tuxen, Barry A Borlaug, Sören Möller and 4 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in ESC heart failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT03198585. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT03198585 phase2completed

Empagliflozin in Heart Failure Patients With Reduced Ejection Fraction: A Randomized Clinical Trial (Empire HF)

Ran2017Enrolled190Registered outcomes16Posted comparisons0ConditionsHeart Failure With Reduced Ejection FractionArmsempagliflozin 10 mg, Placebo
Open the trial in the graph
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Massar OmarDepartment of Cardiology, Odense University Hospital, J. B. Winsløws Vej 4, Odense C 5000, Denmark.ORCID 0000-0002-9634-3889
Jesper JensenDepartment of Cardiology, Herlev and Gentofte University Hospital, Copenhagen, Denmark.
Mulham AliDepartment of Cardiology, Odense University Hospital, J. B. Winsløws Vej 4, Odense C 5000, Denmark.ORCID 0009-0009-2855-1713
Peter H FrederiksenDepartment of Cardiology, Odense University Hospital, J. B. Winsløws Vej 4, Odense C 5000, Denmark.
Caroline KistorpDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-3019-6775
Lars VidebækDepartment of Cardiology, Odense University Hospital, J. B. Winsløws Vej 4, Odense C 5000, Denmark.ORCID 0000-0001-7740-1564
Mikael Kjær PoulsenDepartment of Cardiology, Odense University Hospital, J. B. Winsløws Vej 4, Odense C 5000, Denmark.
Christian D TuxenDepatment of Cardiology, Bispebjerg and Frederiksberg University Hospital, Copenhagen, Denmark.
Barry A BorlaugDivision of Cardiovascular Diseases, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Sören MöllerDepartment of Clinical Research, Odense University Hospital, Odense, Denmark.
Finn GustafssonDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-2144-341X
Lars KøberDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-6635-1466
Morten SchouDepartment of Cardiology, Herlev and Gentofte University Hospital, Copenhagen, Denmark.ORCID 0000-0002-4271-2466
Jacob Eifer MøllerDepartment of Cardiology, Odense University Hospital, J. B. Winsløws Vej 4, Odense C 5000, Denmark.

Funding

A.P. Møller Foundation for the Advancement of Medical Science 17-L-0002A.P. Møller Foundation for the Advancement of Medical Science 17-L-0339Capital Region of Denmark A6058Danish Heart Foundation 17-R116-A7714-22076Danish Heart Foundation 18-R124-A8573-22107Herlev and Gentofte University Hospital, DenmarkResearch and Innovation Foundation of the Department of CardiologyResearch Council at Herlev and Gentofte University Hospital, DenmarkSteno Diabetes Center Odense, Denmark 3363
6 · The paper itself

Abstract

introductionTo investigate the effect of empagliflozin on right ventricular (RV) function in patients with heart failure with reduced ejection fraction (HFrEF). Sodium-glucose cotransporter-2 (SGLT2) inhibitors improve outcomes and reverse left ventricular (LV) remodelling in HFrEF. The impact on RV function remains uncertain.

methodsThe Empire HF trial was an investigator-initiated, double-blind, randomized, placebo-controlled trial of 190 participants with a left ventricular ejection fraction (LVEF) of 40% or lower, with New York Heart Association (NYHA) Class I-III symptoms. Participants were randomized to receive either empagliflozin (at a dose of 10 mg once daily) or placebo, on top of recommended therapy for 12 weeks. The primary endpoint of this exploratory substudy was changes in RV free wall strain (RVFWS) across the whole cohort. RVFWS was also stratified into tertiles based on baseline RVFWS. Secondary endpoints included changes in tricuspid annular plane systolic excursion (TAPSE) and RV S' velocity.

resultsBetween June 2017 and September 2019, a total of 190 patients were enrolled, of whom 160 were included in this substudy. Baseline characteristics were balanced between the groups (mean age of 64 ± 11 years, 86% male, mean LVEF: 29 ± 8%, 79% in NYHA Class II, 83 patients (52%) had an implanted cardiac device, and tricuspid valve regurgitation was absent/trace in 136 (85%) and mild in 24 (15%)). A high proportion of the population were on optimal medical treatment for HFrEF, and device therapy remained unchanged during follow-up. The overall mean RVFWS was -16.7 ± 6.1%, with the empagliflozin group at -16.4 ± 6.2% and the placebo group at -16.9 ± 5.9%. No differences were observed in RVFWS between the groups. When stratified by baseline RVFWS into tertiles, patients in the lowest tertile demonstrated a significant improvement with empagliflozin (treatment effect: -2.9% [95% CI: -5.0 to -0.3]; P = .027). This finding was independent of LVEF, plasma volume, and weight loss, and remained unchanged after additional adjustment for LV remodelling and the presence of resynchronization therapy. No significant treatment effect was observed in the middle or highest tertiles of RVFWS, nor in the overall or lowest tertiles of TAPSE or RV S'.

conclusionThis exploratory substudy of the Empire HF, treatment with empagliflozin exerted no overall effect on RV function in stable HFrEF patients, but significantly improved RVFWS in patients in the lowest tertile of RVFWS after 12 weeks of treatment.

trial registrationClinicalTrials.gov, Unique Identifier: NCT03198585.

Indexed as

Benzhydryl CompoundsGlucosidesHeart FailureHeart VentriclesStroke VolumeVentricular Function, RightVentricular RemodelingAgedDouble-Blind MethodEchocardiographyFemaleFollow-Up StudiesHumansMaleMiddle AgedSodium-Glucose Transporter 2 InhibitorsBenzhydryl CompoundsempagliflozinGlucosidesSodium-Glucose Transporter 2 InhibitorsEmpagliflozinheart failure with reduced ejection fractionright ventricular free wall strainright ventricular functionSGLT2i

Identifiers

PMID41711194
PMCPMC13235861

What Socratic 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 Socratic graph.