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Published on: March 14, 2017
Sodium ferric gluconate complex maintenance therapy in children on hemodialysis
Bradley A Warady1, R Howard Zobrist, Eileen Finan
1The Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USA. bwarady@cmh.edu
Insights
This study shows that intravenous sodium ferric gluconate complex (SFGC) is safe and effective for pediatric hemodialysis patients. The recommended starting dose is 1.0 mg/kg weekly, adjusted by iron levels.
Area of Science:
- Nephrology
- Pediatric Hematology
- Pharmacology
Background:
- Intravenous iron is recommended for hemodialysis (HD) patients on recombinant human erythropoietin (rHuEPO).
- Limited data exists on maintenance IV iron regimens in pediatric HD patients.
Purpose of the Study:
- To evaluate the safety and efficacy of a maintenance therapy with sodium ferric gluconate complex (SFGC) in pediatric HD patients.
- To establish an appropriate starting dose for SFGC in this population.
Main Methods:
- Prospective, multicenter, open-label trial.
- 23 iron-replete pediatric HD patients receiving rHuEPO were enrolled.
- SFGC was administered weekly at 1.0 mg/kg, not exceeding 125 mg, with dose adjustments based on iron indices.
Main Results:
- After 12 weeks, the mean SFGC dose was 1.0 mg/kg.
- Transferrin saturation (TSAT) and serum ferritin remained within target ranges.
- Hemoglobin (Hgb) levels were unchanged from baseline; no safety risks were observed.
Conclusions:
- Maintenance therapy with SFGC is safe and effective in pediatric HD patients.
- A starting dose of 1.0 mg/kg weekly (max 125 mg) is recommended, adjusted by TSAT and/or ferritin levels.
Abstract:
Intravenous iron therapy is recommended for children and adults who receive hemodialysis (HD) and recombinant human erythropoietin (rHuEPO). However, limited information exists on the use of any maintenance IV iron regimen in children. Therefore, we conducted a prospective, multicenter, open-label trial of maintenance therapy with sodium ferric gluconate complex (SFGC) in iron-replete pediatric HD patients receiving rHuEPO. Patients received SFGC weekly at an initial dose of 1.0 mg kg(-1) week(-1), not to exceed 125 mg. Doses could be adjusted based on iron indices. Twenty-three patients (mean age: 13.2+/-2.39 years) were enrolled and received at least one dose of SFGC, while twelve patients completed the study. After 12 weeks of treatment, the mean SFGC dose delivered was 1.0 mg/kg. Mean TSAT and serum ferritin levels remained within NKF-K/DOQI target ranges and the mean Hgb level remained unchanged from baseline. No unexpected or unusual safety risks were associated with SFGC use. In summary, this experience provides evidence for the safety and efficacy of intravenous SFGC and supports the recommendation that the maintenance SFGC starting dose should be 1.0 mg/kg, not to exceed 125 mg, with subsequent adjustments made according to TSAT and/or serum ferritin levels.
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