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Adjudication of Hospitalizations and Deaths in the IRONMAN Trial of Intravenous Iron for Heart Failure

Abstract

Background: Patients with heart failure and iron deficiency have diverse causes for hospitalization and death that might be affected by iron repletion.

Objectives: The purpose of this study was to explore causes of hospitalizations and deaths in a randomized trial (IRONMAN) of heart failure comparing intravenous ferric derisomaltose (FDI) (n = 568) and usual care (n = 569).

Methods: Patients with heart failure, left ventricular ejection fraction ≤45%, and either transferrin saturation <20% or serum ferritin <100 μg/L were enrolled. Median follow-up was 2.7 years (Q1-Q3: 1.8-3.6 years). A committee adjudicated the main and contributory causes of unplanned hospitalizations and deaths. RRs (rate ratios) for selected recurrent events with 95% CIs are also reported.

Results: Compared with usual care, patients randomized to FDI had fewer unplanned hospitalizations (RR: 0.83; 95% CI: 0.71-0.97; P = 0.02), with similar reductions in cardiovascular (RR: 0.83; 95% CI: 0.69-1.01) and noncardiovascular (RR: 0.83; 95% CI: 0.67-1.03) hospitalizations, as well as hospitalizations for heart failure (RR: 0.78; 95% CI: 0.60-1.00), respiratory disease (RR: 0.70; 95% CI: 0.53-0.97), or infection (RR: 0.82; 95% CI: 0.66-1.03). Heart failure was the main cause for 26% of hospitalizations and contributed to or complicated a further 12%. Infection caused or contributed to 38% of all hospitalizations, including 27% of heart failure hospitalizations. Patterns of cardiovascular and all-cause mortality were similar for patients assigned to FDI or usual care.

Conclusions: In IRONMAN, FDI exerted similar reductions in cardiovascular and noncardiovascular hospitalizations, suggesting that correcting iron deficiency might increase resistance or resilience to a broad range of problems that cause hospitalizations in patients with heart failure. (Intravenous Iron Treatment in Patients With Heart Failure and Iron Deficiency; NCT02642562).

References
1.
Cleland J, Massie B, Packer M . Sudden death in heart failure: vascular or electrical?. Eur J Heart Fail. 2000; 1(1):41-5. DOI: 10.1016/S1388-9842(99)00009-4. View

2.
Kalra P, Cleland J, Petrie M, Ahmed F, Foley P, Kalra P . Rationale and design of a randomised trial of intravenous iron in patients with heart failure. Heart. 2022; 108(24):1979-1985. PMC: 9726969. DOI: 10.1136/heartjnl-2022-321304. View

3.
Shoaib A, Van Spall H, Wu J, Cleland J, McDonagh T, Rashid M . Substantial decline in hospital admissions for heart failure accompanied by increased community mortality during COVID-19 pandemic. Eur Heart J Qual Care Clin Outcomes. 2021; 7(4):378-387. PMC: 8244536. DOI: 10.1093/ehjqcco/qcab040. View

4.
Hicks K, Mahaffey K, Mehran R, Nissen S, Wiviott S, Dunn B . 2017 Cardiovascular and Stroke Endpoint Definitions for Clinical Trials. J Am Coll Cardiol. 2018; 71(9):1021-1034. DOI: 10.1016/j.jacc.2017.12.048. View

5.
Elstrott B, Lakshmanan H, Melrose A, Jordan K, Martens K, Yang C . Platelet reactivity and platelet count in women with iron deficiency treated with intravenous iron. Res Pract Thromb Haemost. 2022; 6(2):e12692. PMC: 8941679. DOI: 10.1002/rth2.12692. View