Alsunaid A, Spencer S, Bhandari S. Intravenous iron in chronic kidney disease without anaemia but iron deficiency: A scoping review. World J Nephrol 2025; 14(1): 101576 [DOI: 10.5527/wjn.v14.i1.101576]
Corresponding Author of This Article
Sebastian Spencer, MBBS, Academic Fellow, Doctor, Department of Medical Science, University of Hull, Allam Medical Building, Bain, Hull, Kingston Upon Hull HU6 7RU, United Kingdom. sebastian.spencer2@nhs.net
Research Domain of This Article
Urology & Nephrology
Article-Type of This Article
Evidence Review
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Nephrol. Mar 25, 2025; 14(1): 101576 Published online Mar 25, 2025. doi: 10.5527/wjn.v14.i1.101576
Intravenous iron in chronic kidney disease without anaemia but iron deficiency: A scoping review
Abdulrahman Alsunaid, Sebastian Spencer, Sunil Bhandari
Abdulrahman Alsunaid, Sebastian Spencer, Sunil Bhandari, Department of Medical Science, Hull York Medical School, Kingston Upon Hull HU6 7RU, United Kingdom
Sebastian Spencer, Department of Medical Science, University of Hull, Kingston Upon Hull HU6 7RU, United Kingdom
Sebastian Spencer, Sunil Bhandari, Department of Academic Renal, Hull University Teaching Hospitals NHS Trust, Kingston Upon Hull HU3 2JZ, United Kingdom
Author contributions: Alsunaid A performed database searches and majority of writing; Spencer S provided concept, guidance, writing and submission; Bhandari S provided oversight and final editing.
Conflict-of-interest statement: Bhandari S was a previous trustee for KRUK, and has received honorarium from Vifor CSL, Pharmacosmos, GSK and Astellas for lectures. Alsunaid A, and Spencer S have no conflicts to declare.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Sebastian Spencer, MBBS, Academic Fellow, Doctor, Department of Medical Science, University of Hull, Allam Medical Building, Bain, Hull, Kingston Upon Hull HU6 7RU, United Kingdom. sebastian.spencer2@nhs.net
Received: September 19, 2024 Revised: December 30, 2024 Accepted: January 9, 2025 Published online: March 25, 2025 Processing time: 122 Days and 22.5 Hours
Abstract
Iron deficiency (ID) is a prevalent complication of chronic kidney disease (CKD), often managed reactively when associated with anaemia. This scoping review evaluates the evidence supporting intravenous (IV) iron therapy in non-anaemic individuals with CKD and ID, focusing on safety, efficacy, and emerging therapeutic implications. Current diagnostic markers, including serum ferritin, transferrin saturation, and reticulocyte haemoglobin content, are reviewed alongside their limitations in the context of inflammation and variability. The pathophysiology of ID in CKD is explored, highlighting the roles of hepcidin, hypoxia-inducible factor pathways, and uraemic toxins. Comparative studies reveal that IV iron offers a more rapid correction of iron stores, improved compliance, and fewer gastrointestinal side effects compared to oral iron. Evidence from trials such as “iron and heart” and “iron and muscle” suggests potential benefits of IV iron on functional capacity and fatigue, though findings were statistically non-significant. Insights from heart failure trials support the safety and efficacy of IV iron in improving quality of life and reducing hospitalizations, with newer formulations like ferric derisomaltose demonstrating favourable safety profiles. This review underscores the need for standardized screening protocols for ID in CKD, even in the absence of anaemia, to facilitate earlier intervention. Future research should prioritise robust outcome measures, larger sample sizes, and person-specific treatment strategies to optimise dosing and administration frequency. Tailored approaches to IV iron therapy have the potential to significantly improve functional outcomes, quality of life, and long-term health in people with CKD.
Core Tip: Intravenous iron therapy can effectively address iron deficiency in individuals with chronic kidney disease who are non-dialysis-dependent and not anaemic, particularly when oral iron is insufficient. This review highlights the pathophysiology of iron deficiency in chronic kidney disease, the advantages of newer intravenous iron formulations, and the potential benefit of treatment in managing symptoms like restless legs syndrome. However, evidence on improvements in physical function remain uncertain, and more research is needed to refine treatment protocols.