High-dose intravenous iron reduces myocardial infarction in patients on haemodialysis

Author:

Petrie Mark C1ORCID,Jhund Pardeep S1ORCID,Connolly Eugene1ORCID,Mark Patrick B1ORCID,MacDonald Michael R2ORCID,Robertson Michele3ORCID,Anker Stefan D4ORCID,Bhandari Sunil5ORCID,Farrington Kenneth6ORCID,Kalra Philip A7ORCID,Wheeler David C89ORCID,Tomson Charles R V10ORCID,Ford Ian3,McMurray John J V1ORCID,Macdougall Iain C11,

Affiliation:

1. BHF Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow G12 8TA, UK

2. Changi General Hospital, Singapore, Singapore

3. Robertson Centre for Biostatistics, University of Glasgow, Glasgow, UK

4. Charite, Universitatsmedizin Berlin, Berlin, Germany

5. Hull and East Yorkshire Hospitals NHS Trust and Hull York, Medical School, Hull, UK

6. Lister Hospital, Stevenage, UK

7. Salford Royal NHS Foundation Trust, Salford, UK

8. University College London, London, UK

9. George Institute for Global Health, Sydney, Australia

10. Freeman Hospital, Newcastle upon Tyne, UKand

11. Department of Renal Medicine, King’s College Hospital, London, UK

Abstract

Abstract Aims To investigate the effect of high-dose iron vs. low-dose intravenous (IV) iron on myocardial infarction (MI) in patients on maintenance haemodialysis. Methods and results This was a pre-specified analysis of secondary endpoints of the Proactive IV Iron Therapy in Hemodialysis Patients trial (PIVOTAL) randomized, controlled clinical trial. Adults who had started haemodialysis within the previous year, who had a ferritin concentration <400 μg per litre and a transferrin saturation <30% were randomized to high-dose or low-dose IV iron. The main outcome measure for this analysis was fatal or non-fatal MI. Over a median of 2.1 years of follow-up, 8.4% experienced a MI. Rates of type 1 MIs (3.2/100 patient-years) were 2.5 times higher than type 2 MIs (1.3/100 patient-years). Non-ST-elevation MIs (3.3/100 patient-years) were 6 times more common than ST-elevation MIs (0.5/100 patient-years). Mortality was high after non-fatal MI (1- and 2-year mortality of 40% and 60%, respectively). In time-to-first event analyses, proactive high-dose IV iron reduced the composite endpoint of non-fatal and fatal MI [hazard ratio (HR) 0.69, 95% confidence interval (CI) 0.52–0.93, P = 0.01] and non-fatal MI (HR 0.69, 95% CI 0.51–0.93; P = 0.01) when compared with reactive low-dose IV iron. There was less effect of high-dose IV iron on recurrent MI events than on the time-to-first event analysis. Conclusion In total, 8.4% of patients on maintenance haemodialysis had an MI over 2 years. High-dose compared to low-dose IV iron reduced MI in patients receiving haemodialysis. EudraCT Registration Number 2013-002267-25.

Funder

Kidney Research UK

British Heart Foundation Centre of Research Excellence

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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