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Updated: Aug 19, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Anemia in chronic kidney disease
Meredith A Atkinson1, Bradley A Warady2
1Division of Pediatric Nephrology, Johns Hopkins University School of Medicine, 200 N. Wolfe St, Baltimore, MD, 21287, USA. matkins3@jhmi.edu.
Insights
Anemia is common in children with chronic kidney disease (CKD). Current treatments like erythropoiesis-stimulating agents (ESA) and iron are often insufficient, and new therapies need safety and efficacy assessment in pediatric CKD patients.
Area of Science:
- Pediatric Nephrology
- Hematology
- Chronic Kidney Disease (CKD) Management
Background:
- Anemia is a frequent complication in pediatric chronic kidney disease (CKD), linked to poor health outcomes.
- Key contributors include reduced erythropoietin production and hepcidin-mediated iron restriction, impacting iron availability for red blood cell production.
Purpose of the Study:
- To review the current landscape of anemia management in children with CKD.
- To highlight the limitations of existing therapies and explore emerging treatment options.
Main Methods:
- Literature review of anemia in pediatric CKD.
- Analysis of current treatment strategies, including erythropoiesis-stimulating agents (ESA) and iron supplementation.
- Examination of novel therapeutic agents and their potential application in this population.
Main Results:
- Despite standard treatments (ESA, iron), many children with CKD remain anemic.
- Optimal dosing of ESA and appropriate iron supplementation present challenges, with limited data on adverse effects in children.
- Novel therapies like HIF stabilizers and prolyl hydroxylase inhibitors show promise but lack pediatric data.
Conclusions:
- Current anemia management in pediatric CKD is often suboptimal.
- Further research is needed to establish the safety and efficacy of novel anemia therapies in children with CKD.
Abstract:
Anemia is common and associated with adverse outcomes in children with chronic kidney disease (CKD). Many factors contribute to declining hemoglobin as CKD progresses, but impaired production of erythropoietin by failing kidneys is a central cause. Hepcidin-mediated iron restriction also contributes to anemia by downregulating both intestinal iron absorption and release of stored iron for erythropoiesis. The core components of anemia management remain erythropoiesis-stimulating agents (ESA) and iron supplementation, but despite these therapies, a substantial number of children remain anemic. Although escalating ESA dose to target higher hemoglobin has been associated with adverse outcomes in adults, no trials have investigated this association in children, and maintaining hemoglobin levels in a narrow range with conservative ESA dosing is challenging. Judicious use of iron supplementation can enhance the response to ESAs, but the iron storage markers most commonly used in clinical practice have limitations in distinguishing which patients will benefit most from additional iron. Several novel anemia therapies, including hypoxia-inducible factor stabilizers, prolyl hydroxylase inhibitors, and dialysate-delivered iron supplements, have been developed and may offer options for alternative anemia management. However, the safety and efficacy of these agents in children with CKD has yet to be assessed.
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