Evidence map›Paper›PMID 38715187›Full record

ArticleESC heart failure2024

Empagliflozin to prevent progressive adverse remodelling after myocardial infarction (EMPRESS-MI): rationale and design.

Jaclyn Carberry, Mark C Petrie, Matthew M Y Lee, Katriona Brooksbank, Ross T Campbell, Richard Good, Pardeep S Jhund, Peter Kellman, Ninian N Lang, Kenneth Mangion and 11 more

Abstract readClinical Trial Protocol
In one paragraph

Article in ESC heart failure, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Observational
  4. Review
  5. Article
  6. Article
  7. Review
  8. SGLT2 Inhibitors and How They Work Beyond the Glucosuric Effect. State of the Art.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2024
    Review
  9. Review
  10. Article
  11. Article
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

21 authors.

Jaclyn CarberryBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Mark C PetrieBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Matthew M Y LeeBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Katriona BrooksbankWest of Scotland Innovation Hub, National Health Service, Glasgow, UK.
Ross T CampbellBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Richard GoodBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Pardeep S JhundBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Peter KellmanNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Ninian N LangBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Kenneth MangionGolden Jubilee National Hospital, Clydebank, UK.
Patrick B MarkBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Alex McConnachieRobertson Centre for Biostatistics, School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
John J V McMurrayBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Barbara MeyerBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Vanessa OrchardGolden Jubilee National Hospital, Clydebank, UK.
Aadil ShaukatGolden Jubilee National Hospital, Clydebank, UK.
Stuart WatkinsGolden Jubilee National Hospital, Clydebank, UK.
Paul WelshBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Naveed SattarBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Colin BerryBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
Kieran F DochertyBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.ORCID 0000-0002-5446-9969

Funding

Gadgetron Global Network and Intelligence Computing: Clinical Imaging Application Development and Software InfrastructureZIAHL006214 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI KELLMAN, PETER · 2016 to 2025
$7.3M
Boehringer IngelheimBritish Heart Foundation Centre of Research Excellence Grant RE/18/6/34217
6 · The paper itself

Abstract

aimsPatients with a reduced left ventricular ejection fraction (LVEF) following an acute myocardial infarction (MI) are at risk of progressive adverse cardiac remodelling that can lead to the development of heart failure and death. The early addition of a sodium-glucose cotransporter 2 (SGLT2) inhibitor to standard treatment may delay or prevent progressive adverse remodelling in these patients. METHODS AND

resultsEMpagliflozin to PREvent worSening of left ventricular volumes and Systolic function after Myocardial Infarction (EMPRESS-MI) is a randomized, double-blind, placebo-controlled, multi-centre trial designed to assess the effect of empagliflozin on cardiac remodelling evaluated using cardiovascular magnetic resonance (CMR) in 100 patients with left ventricular systolic dysfunction following MI. Eligible patients were those ≥12 h and ≤14 days following acute MI, with an LVEF <45% by CMR. Patients were randomized to empagliflozin 10 mg once a day or matching placebo. The primary outcome will be change in left ventricular end-systolic volume indexed to body surface area over 24 weeks from randomization. Secondary endpoints include measures of left ventricular and atrial volumes, left ventricular mass, LVEF, and circulating cardiac biomarkers.

conclusionsEMPRESS-MI will assess the effect of the SGLT2 inhibitor empagliflozin on cardiac remodelling in patients with left ventricular systolic dysfunction after an acute MI.

Indexed as

Benzhydryl CompoundsGlucosidesMagnetic Resonance Imaging, CineMyocardial InfarctionSodium-Glucose Transporter 2 InhibitorsVentricular Function, LeftVentricular RemodelingAgedDisease ProgressionDouble-Blind MethodFemaleFollow-Up StudiesHumansMaleMiddle AgedMulticenter Studies as TopicBenzhydryl CompoundsempagliflozinGlucosidesSodium-Glucose Transporter 2 InhibitorsHeart failureMyocardial infarctionSGLT2 inhibitor

Identifiers

PMID38715187
PMCPMC11287338

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Registered trials

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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.