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Published on: March 14, 2017
Sodium ferric gluconate complex therapy in anemic children on hemodialysis
Bradley A Warady1, R Howard Zobrist, Jingyang Wu
1The Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USA. bwarady@cmh.edu
Insights
Intravenous iron (sodium ferric gluconate complex) is safe and effective for treating anemia in pediatric hemodialysis patients. A lower dose of 1.5 mg kg(-1) is recommended for iron deficiency management.
Area of Science:
- Nephrology
- Pediatric Hematology
- Clinical Pharmacology
Background:
- Anemia is common in pediatric end-stage renal disease patients on hemodialysis (HD).
- Recombinant human erythropoietin (rHuEPO) therapy for anemia can increase iron demand, leading to deficiency.
- Intravenous (IV) iron is effective in adults but underutilized in pediatrics due to safety concerns.
Purpose of the Study:
- To investigate the safety and efficacy of two sodium ferric gluconate complex (SFGC) dosing regimens in pediatric HD patients.
- To evaluate SFGC in iron-deficient pediatric HD patients receiving rHuEPO therapy.
Main Methods:
- International, multicenter study involving 66 patients for safety and 56 for efficacy.
- Two SFGC dosing regimens: 1.5 mg kg(-1) and 3.0 mg kg(-1) over eight consecutive HD sessions.
- Concomitant rHuEPO therapy was administered.
Main Results:
- Both SFGC doses significantly increased hemoglobin, hematocrit, transferrin saturation, serum ferritin, and reticulocyte hemoglobin content.
- Efficacy and safety profiles were comparable between the 1.5 mg kg(-1) and 3.0 mg kg(-1) groups.
- No unexpected adverse events were observed with either SFGC dose.
Conclusions:
- Sodium ferric gluconate complex (SFGC) administration is safe and efficacious in pediatric HD patients.
- The 1.5 mg kg(-1) and 3.0 mg kg(-1) doses showed equivalent efficacy.
- An initial SFGC dose of 1.5 mg kg(-1) is recommended for this population.
Abstract:
Pediatric patients with end-stage renal disease undergoing hemodialysis (HD) frequently develop anemia. Administration of recombinant human erythropoietin (rHuEPO) is effective in managing this anemia, although the additional demand for iron often results in iron deficiency. In adult patients undergoing HD, intravenous (IV) iron administration is known to replenish iron stores more effectively than oral iron administration. Nevertheless, IV iron supplementation is underutilized in pediatric patients, possibly because of unproved safety in this population. This international, multicenter study investigated the safety and efficacy of two dosing regimens (1.5 mg kg(-1) and 3.0 mg kg(-1)) of sodium ferric gluconate complex (SFGC) therapy, during eight consecutive HD sessions, in iron-deficient pediatric HD patients receiving concomitant rHuEPO therapy. Safety was evaluated in 66 patients and efficacy was evaluated in 56 patients. Significant increases from baseline were observed in both treatment groups 2 and 4 weeks after cessation of SFGC dosing for mean hemoglobin, hematocrit, transferrin saturation, serum ferritin, and reticulocyte hemoglobin content. Efficacy and safety profiles were comparable for 1.5 mg kg(-1) and 3.0 mg kg(-1) SFGC with no unexpected adverse events with either dose. Administration of SFGC was safe and efficacious in the pediatric HD population. Given the equivalent efficacy of the two doses, an initial dosing regimen of 1.5 mg kg(-1) is recommended for pediatric HD patients.
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