Management of Iron Deficiency in Heart Failure: Practical Considerations and Implementation of Evidence-Based Iron Supplementation.

anemia ferric carboxymaltose heart failure implementation intravenous iron iron iron sucrose

Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
28 Jun 2024
Historique:
received: 04 03 2024
revised: 08 05 2024
accepted: 15 05 2024
medline: 14 7 2024
pubmed: 14 7 2024
entrez: 13 7 2024
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 39001744
pii: S2213-1779(24)00433-5
doi: 10.1016/j.jchf.2024.05.014
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

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.

Auteurs

Kazuhiko Kido (K)

West Virginia University School of Pharmacy, Morgantown, West Virginia, USA. Electronic address: kazuhiko.kido0322@gmail.com.

Craig J Beavers (CJ)

University of Kentucky College of Pharmacy, Lexington, Kentucky, USA.

Kenneth Dulnuan (K)

Robert Wood Johnson University Hospital, New Brunswick, New Jersey, USA.

Nadia Fida (N)

Houston Methodist, Houston, Texas, USA.

Maya Guglin (M)

Krannert Cardiovascular Research Center, Indiana University Health School of Medicine, Indianapolis, Indiana, USA.

Onyedika J Ilonze (OJ)

Division of Cardiovascular Medicine, Krannert Cardiovascular Research Center, Indiana University, Indianapolis, Indiana, USA.

Robert J Mentz (RJ)

Duke University School of Medicine, Durham, North Carolina, USA.

Nikhil Narang (N)

Advocate Heart Institute, Oak Lawn, Illinois, USA; Division of Cardiology, Department of Medicine, University of Illinois-Chicago, Chicago, Illinois, USA.

Navin Rajagopalan (N)

Division of Cardiology, University of Kentucky, Lexington, Kentucky, USA.

Bhavadharini Ramu (B)

University of Minnesota, Minneapolis, Minnesota, USA.

Yasar Sattar (Y)

West Virginia University Medicine, Morgantown, West Virginia, USA.

George Sokos (G)

West Virginia University Medicine, Morgantown, West Virginia, USA.

Ewa A Jankowska (EA)

Wroclaw Medical University, Wroclaw, Poland.

Classifications MeSH