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Published on: November 4, 2011
Intravenous Ferumoxytol in Pediatric Patients With Iron Deficiency Anemia
Nabil Hassan1, Brian Boville2, Diann Reischmann3
11 Children's Hospital of Illinois at OSF St Frances, Peoria, IL, USA.
Insights
Ferumoxytol effectively treats iron deficiency anemia in children, showing significant improvements in hemoglobin and ferritin levels. Adverse drug reactions were infrequent and manageable with slow infusion and monitoring.
Area of Science:
- Pediatric Hematology
- Pharmacology
- Anemia Management
Background:
- Iron deficiency anemia (IDA) is a prevalent condition in pediatric populations.
- Limited data exist regarding the efficacy and safety of ferumoxytol in children.
Purpose of the Study:
- To evaluate the effectiveness of a 10 mg/kg ferumoxytol dose administered over 15-60 minutes for correcting IDA in children.
- To document any adverse drug reactions (ADRs) associated with ferumoxytol treatment.
Main Methods:
- A retrospective review of pediatric patients treated with ferumoxytol for IDA between October 2010 and March 2015.
- Analysis of pre- and post-infusion hemoglobin and serum ferritin levels.
- Documentation of all reported adverse drug reactions.
Main Results:
- Ferumoxytol treatment led to a significant increase in hemoglobin and serum ferritin levels at 1 and 4 weeks post-infusion.
- Concomitant erythropoietin use was associated with a greater hemoglobin rise at 4 weeks.
- Infrequent ADRs included pruritus, urticaria, and multisymptom episodes, all responsive to treatment.
Conclusions:
- Ferumoxytol demonstrates efficacy in treating pediatric iron deficiency anemia.
- Slow infusion rates and close patient monitoring facilitate early detection of rare adverse events.
Background:
Iron deficiency anemia (IDA) is common in children. Limited data exist on the efficacy and safety of ferumoxytol in children.
Objective:
To assess the efficacy of 10 mg/kg dose given over 15-60 minutes in correcting IDA and report any adverse drug reactions (ADRs).
Methods:
We conducted a retrospective review of all patients who received ferumoxytol infusions for the management of IDA by the Pediatric Blood Management Program between October 2010 and March 2015.
Results:
A total of 110 infusions were given to 54 patients. Compared with baseline preinfusion hemoglobin (Hb; 9.2 ± 1.9 g/dL), a significant rise was seen at 1 week and 4 weeks postinfusion (11.5 ± 1.5 and 11.8 ± 1.7 g/dL, respectively, P < 0.001). Also, a significant rise in serum ferritin at 1 week and 4 weeks postinfusion was seen (51 ± 71 vs 192 ± 148 and 89 ± 135 ng/mL, P < 0.001 and <0.035, respectively). Patients who concomitantly received erythropoietin had a significantly larger Hb rise from baseline than those who did not at 4 weeks (2.7 ± 2.2 vs 1.6 ± 1.1 g/dL, P < 0.017). ADRs included pruritus (n = 1), urticaria (n = 1), and multisymptom episodes (n = 3) that included shortness of breath, chest tightness, back pain, and epigastric cramping that responded to therapy with IV diphenhydramine and methylprednisolone.
Conclusion:
Ferumoxytol was effective in treating IDA in our small study. Slow infusion rate and close monitoring allowed early detection of the infrequent ADRs.
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