4.5 Article

Rationale and design of a randomised trial of intravenous iron in patients with heart failure

Journal

HEART
Volume 108, Issue 24, Pages 1979-1985

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/heartjnl-2022-321304

Keywords

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Funding

  1. British Heart Foundation [CS/15/1/31175]

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The INTRONMAN trial evaluated the benefits and safety of intravenous iron treatment in the long-term management of heart failure patients with iron deficiency.
Objectives For patients with a reduced left ventricular ejection fraction (LVEF) heart failure with reduced ejection fraction (HFrEF) and iron deficiency, administration of intravenous iron improves symptoms, exercise capacity and may in the following 12 months, reduce hospitalisations for heart failure. The Effectiveness of Intravenous iron treatment versus standard care in patients with heart failure and iron deficiency (IRONMAN) trial evaluated whether the benefits of intravenous iron persist in the longer term and impact on morbidity and mortality. Methods IRONMAN is a prospective, randomised, open-label, blinded endpoint (PROBE) event-driven trial. Patients aged >= 18 years with HFrEF (LVEF <= 45%) and evidence of iron deficiency (ferritin <100 mu g/L and/or TSAT <20%) were enrolled if they had either a current or recent hospitalisation for heart failure or elevated plasma concentrations of a natriuretic peptide. Participants were randomised to receive, or not to receive, intravenous ferric derisomaltose in addition to guideline-recommended therapy for HFrEF. Every 4 months, intravenous iron was administered if either ferritin was <100 mu g/L or, provided ferritin was <= 400 mu g/L, TSAT was <25%. The primary endpoint is a composite of total hospitalisations for heart failure and cardiovascular death. Hospitalisation and deaths due to infection are safety endpoints. Results Trial recruitment was completed across 70 UK hospital sites in October 2021. Participants were followed until the end of March 2022. We plan to report the results by November 2022. Conclusions IRONMAN will determine whether repeated doses of intravenous ferric derisomaltose are beneficial and safe for the long-term treatment of a broad range of patients with HFrEF and iron deficiency.

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