Management of Iron Deficiency in Heart Failure: Practical Considerations and Implementation of Evidence-Based Iron Supplementation
- PMID: 39001744
- DOI: 10.1016/j.jchf.2024.05.014
Management of Iron Deficiency in Heart Failure: Practical Considerations and Implementation of Evidence-Based Iron Supplementation
Erratum in
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Correction.JACC Heart Fail. 2024 Nov;12(11):1956-1960. doi: 10.1016/j.jchf.2024.09.002. JACC Heart Fail. 2024. PMID: 39505467 No abstract available.
Abstract
Iron deficiency (ID) is present in approximately 50% of patients with heart failure (HF) and even higher prevalence rate up to 80% in post-acute HF setting. The current guidelines for HF recommend intravenous (IV) iron replacement in HF with reduced or mildly reduced ejection fraction and ID based on clinical trials showing improvements in quality of life and exercise capacity, and an overall treatment benefit for recurrent HF hospitalization. However, several barriers cause challenges in implementing IV iron supplementation in practice due, in part, to clinician knowledge gaps and limited resource availability to protocolize routine utilization in appropriate patients. Thus, the current review will discuss practical considerations in ID treatment, implementation of evidence-based ID treatment to improve regional health disparities with toolkits, inclusion/exclusion criteria of IV iron supplementation, and clinical controversies in ID treatment, as well as gaps in evidence and questions to be answered.
Keywords: anemia; ferric carboxymaltose; heart failure; implementation; intravenous iron; iron; iron sucrose.
Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures Dr Narang has received honoraria from Boehringer Ingelheim, Abbott, and Zoll Medical. Dr Rajagopalan has served as a consultant for Abbott Laboratories. Dr Ramu has received an honorarium from Abbott. Dr Jankowska has received honoraria for lectures and/or participation in advisory boards from Vifor Pharma and Pharmacosmos. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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