Evidence map›Paper›PMID 37926238›Full record

Trial reportJournal of cardiac failure2024

The Impact of Ferric Derisomaltose on Cardiovascular and Noncardiovascular Events in Patients With Anemia, Iron Deficiency, and Heart Failure With Reduced Ejection Fraction.

Robin Ray, Ian Ford, John G F Cleland, Fraser Graham, Fozia Z Ahmed, Abdallah Al-Mohammad, Peter J Cowburn, Chris Critoph, Philip A Kalra, Rebecca E Lane and 11 more

Open access · hybridAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Journal of cardiac failure, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 16% 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.

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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
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 at 14 institutions in 1 country.

Robin RayDepartment of Cardiology, St George's University Hospitals NHS Foundation Trust, London, UK; Molecular and Clinical Sciences Institute, St. George's University of London, United.
Ian FordRobertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.
John G F ClelandSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Fraser GrahamRobertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.
Fozia Z AhmedDepartment of Cardiology, Manchester University NHS Foundation Trust, Manchester, UK.
Abdallah Al-MohammadDepartment of Cardiology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK; Department of Infection, Immunity and Cardiovascular Disease, The University of Sheffield, Sheffield, UK.
Peter J CowburnDepartment of Cardiology, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
Chris CritophDepartment of Cardiology, University Hospitals Dorset NHS Foundation Trust, Bournemouth, UK.
Philip A KalraDepartment of Renal Medicine, Northern Care Alliance NHS Foundation Trust Salford Care Organisation, Salford, UK.
Rebecca E LaneDepartment of Cardiology, Royal Brompton and Harefield Hospitals, London, UK.
Andrew LudmanDepartment of Cardiology, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.
Pierpaolo PellicoriSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Mark C PetrieSchool of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Michelle RobertsonRobertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.
Alison SeedDepartment of Cardiology, Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, UK.
Iain SquireDepartment of Cardiovascular Sciences, University of Leicester, Leicester, UK.
Paul R KalraDepartment of Cardiology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK; College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK; Faculty of Science and Health, University of Portsmouth, Portsmouth, UK. Electronic address: paulkalra@doctors.org.uk.
INVESTIGATORS
CLINICAL TRIALS UNIT AND DATA AND STATISTICAL CENTRE
NURSING AND ADMINISTRATIVE SUPPORT
SPONSOR SUPPORT
University of Glasgow · GBRoyal Devon & Exeter NHS Foundation Trust · GBManchester University NHS Foundation Trust · GBUniversity of Leicester · GBBlackpool Teaching Hospitals NHS Foundation Trust · GBHarefield Hospital · GBSalford Royal Hospital · GBSt George’s University Hospitals NHS Foundation Trust · GBUniversity Hospitals Dorset NHS Foundation TrustUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Sheffield · GBBradford District Care NHS Foundation Trust · GBPortsmouth Hospitals NHS Trust · GBUniversity of Portsmouth · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn some countries, intravenous ferric derisomaltose (FDI) is only licensed for treating iron deficiency with anemia. Accordingly, we investigated the effects of intravenous FDI in a subgroup of patients with anemia in the IRONMAN (Effectiveness of Intravenous (IV) Iron Treatment Versus Standard Care in Patients With Heart Failure and Iron Deficiency) trial. METHOD AND

resultsIRONMAN enrolled patients with heart failure, a left ventricular ejection fraction of ≤45%, and iron deficiency (ferritin <100 µg/L or transferrin saturation of <20%), 771 (68%) of whom had anemia (hemoglobin <12 g/dL for women and <13 g/dL for men). Patients were randomized, open label, to FDI (n = 397) or usual care (n = 374) and followed for a median of 2.6 years. The primary end point, recurrent hospitalization for heart failure and cardiovascular death, occurred less frequently for those assigned to FDI (rate ratio 0.78, 95% confidence interval 0.61-1.01; P = .063). First event analysis for cardiovascular death or hospitalization for heart failure, less affected by the coronavirus disease 2019 pandemic, gave similar results (hazard ratio 0.77, 95% confidence interval 0.62-0.96; P = .022). Patients randomized to FDI reported a better Minnesota Living with Heart Failure quality of life, for overall (P = .013) and physical domain (P = .00093) scores at 4 months.

conclusionsIn patients with iron deficiency anemia and heart failure with reduced left ventricular ejection fraction, intravenous FDI improves quality of life and may decrease cardiovascular events.

Indexed as

Anemia, Iron-DeficiencyFerric CompoundsHeart FailureStroke VolumeAgedCOVID-19FemaleHumansMaleMaltoseMiddle AgedQuality of LifeTreatment OutcomeFerric CompoundsMaltose

Identifiers

PMID37926238
PMCPMC11096866
OpenAlexW4388348097

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.