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Intravenous iron for heart failure, iron deficiency definitions, and clinical response: the IRONMAN trial.

Cleland, JGF; Kalra, PA; Pellicori, P; Graham, FJ; Foley, PWX; Squire, IB; Cowburn, PJ; Seed, A; Clark, AL; Szwejkowski, B; et al. Cleland, JGF; Kalra, PA; Pellicori, P; Graham, FJ; Foley, PWX; Squire, IB; Cowburn, PJ; Seed, A; Clark, AL; Szwejkowski, B; Banerjee, P; Cooke, J; Francis, M; Clifford, P; Wong, A; Petrie, C; McMurray, JJV; Thomson, EA; Wetherall, K; Robertson, M; Ford, I; Kalra, PR; IRONMAN Study Group (2024) Intravenous iron for heart failure, iron deficiency definitions, and clinical response: the IRONMAN trial. Eur Heart J, 45 (16). pp. 1410-1426. ISSN 1522-9645 https://doi.org/10.1093/eurheartj/ehae086
SGUL Authors: Ray, Robin

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Abstract

BACKGROUND AND AIMS: What is the relationship between blood tests for iron deficiency, including anaemia, and the response to intravenous iron in patients with heart failure? METHODS: In the IRONMAN trial, 1137 patients with heart failure, ejection fraction ≤ 45%, and either serum ferritin < 100 µg/L or transferrin saturation (TSAT) < 20% were randomized to intravenous ferric derisomaltose (FDI) or usual care. Relationships were investigated between baseline anaemia severity, ferritin and TSAT, to changes in haemoglobin from baseline to 4 months, Minnesota Living with Heart Failure (MLwHF) score and 6-minute walk distance achieved at 4 months, and clinical events, including heart failure hospitalization (recurrent) or cardiovascular death. RESULTS: The rise in haemoglobin after administering FDI, adjusted for usual care, was greater for lower baseline TSAT (Pinteraction < .0001) and ferritin (Pinteraction = .028) and more severe anaemia (Pinteraction = .014). MLwHF scores at 4 months were somewhat lower (better) with FDI for more anaemic patients (overall Pinteraction = .14; physical Pinteraction = .085; emotional Pinteraction = .043) but were not related to baseline TSAT or ferritin. Blood tests did not predict difference in achieved walking distance for those randomized to FDI compared to control. The absence of anaemia or a TSAT ≥ 20% was associated with lower event rates and little evidence of benefit from FDI. More severe anaemia or TSAT < 20%, especially when ferritin was ≥100 µg/L, was associated with higher event rates and greater absolute reductions in events with FDI, albeit not statistically significant. CONCLUSIONS: This hypothesis-generating analysis suggests that anaemia or TSAT < 20% with ferritin > 100 µg/L might identify patients with heart failure who obtain greater benefit from intravenous iron. This interpretation requires confirmation.

Item Type: Article
Additional Information: Correction available at https://doi.org/10.1093/eurheartj/ehae243 © The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: Anaemia, Ferric derisomaltose, Ferritin, Heart failure, Iron deficiency, Morbidity, Mortality, Quality of life, Randomized clinical trial, Transferrin saturation, Humans, Iron, Anemia, Iron-Deficiency, Ferritins, Ferric Compounds, Anemia, Iron Deficiencies, Hemoglobins, Heart Failure, IRONMAN Study Group, Humans, Anemia, Anemia, Iron-Deficiency, Iron, Ferric Compounds, Hemoglobins, Ferritins, Heart Failure, Iron Deficiencies, Heart failure, Anaemia, Iron deficiency, Ferric derisomaltose, Randomized clinical trial, Transferrin saturation, Ferritin, Quality of life, Morbidity, Mortality, 1102 Cardiorespiratory Medicine and Haematology, 1103 Clinical Sciences, Cardiovascular System & Hematology
Journal or Publication Title: Eur Heart J
ISSN: 1522-9645
Language: eng
Dates:
DateEvent
21 April 2024Published
6 March 2024Published Online
30 January 2024Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
CS/15/1/31175British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
RE/18/6/34217British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
PubMed ID: 38446126
Web of Science ID: WOS:001180479200001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116868
Publisher's version: https://doi.org/10.1093/eurheartj/ehae086

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