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Published on: March 14, 2017
Iron therapy in the pediatric hemodialysis population
Bradley A Warady1, Annamaria Kausz, Gary Lerner
1Section of Pediatric Nephrology, Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USA. bwarady@cmh.edu
Insights
Intravenous (IV) iron dextran significantly improved iron stores in pediatric hemodialysis patients compared to oral iron. While both methods maintained iron levels, only IV iron boosted serum ferritin and reduced recombinant human erythropoietin (r-HuEPO) dosage.
Area of Science:
- Nephrology
- Pediatric Hematology
- Pharmacology
Background:
- Iron therapy is crucial for optimizing recombinant human erythropoietin (r-HuEPO) response in end-stage renal failure patients.
- Limited data exists on the optimal iron administration route for pediatric hemodialysis patients.
Purpose of the Study:
- To compare the efficacy of intravenous (IV) versus oral iron in maintaining iron stores and optimizing r-HuEPO response in pediatric hemodialysis patients.
Main Methods:
- Prospective randomized study of 35 iron-replete pediatric patients (>1 to <20 years) on hemodialysis.
- Patients received either IV iron dextran (n=17) or daily oral iron (n=18) for up to 16 weeks.
- Key parameters monitored included hemoglobin, hematocrit, transferrin saturation (TSAT), serum ferritin (SF), reticulocyte hemoglobin content (CHr), and r-HuEPO dose.
Main Results:
- IV iron dextran significantly increased serum ferritin (SF) levels compared to oral iron (P=0.003).
- Only IV iron was associated with a significant decrease in r-HuEPO dose (P=0.046) and an increase in reticulocyte hemoglobin content (CHr) (P=0.049).
- Both routes maintained iron repletion, but only IV iron demonstrated a significant improvement in iron stores.
Conclusions:
- Intravenous iron dextran is superior to oral iron for improving iron stores in pediatric hemodialysis patients.
- IV iron may help optimize r-HuEPO therapy by improving iron status.
- Further research could explore long-term outcomes and optimal dosing strategies.
Abstract:
Iron therapy maintains iron stores and optimizes the response to recombinant human erythropoietin (r-HuEPO) in patients with end-stage renal failure. Information is limited, however, regarding the preferential route of iron administration in pediatric patients receiving hemodialysis. Therefore, we prospectively randomized 35 iron-replete patients (aged >1 to <20 years) to receive up to 16 weeks of maintenance i.v. ( n=17) or daily oral ( n=18) iron. Eligible patients had received hemodialysis for >2 months, had a baseline transferrin saturation [TSAT] >20%, and were receiving maintenance r-HuEPO. Treatment arms were evenly distributed with respect to baseline demographic and clinical characteristics, with no statistically significant differences in baseline hemoglobin (Hb), hematocrit (Hct), reticulocyte Hb content (CHr), serum ferritin (SF), TSAT, or r-HuEPO dose. In the 35 patients, i.v. iron dextran and not oral iron was associated with a significant increase (138.5 to 259.1 ng/ml, P=0.003) in SF. A comparison of the change in SF between the i.v. iron group and the oral iron group was also significant ( P=0.001). Whereas only i.v. iron was associated with a significant decrease in the dose of r-HuEPO (234.0 to 157.6 U/kg per week, P=0.046) and an increase of the CHr (29.2 to 30.1 pg, P=0.049), these changes were not significantly different from those experienced by patients in the oral iron group. In both groups, the Hct remained stable and in neither group was there a significant change in the TSAT. In summary, although both oral and i.v. iron maintained patients in an iron-replete state in this short-term study, only i.v. therapy allowed for a significant improvement in iron stores.
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