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Intravenous iron sucrose for children with iron deficiency anemia: a single institution study
Elpis Mantadakis1, Emmanouela Tsouvala2, Varvara Xanthopoulou2
1Department of Pediatrics, Democritus University of Thrace Faculty of Medicine, University General Hospital of Evros, Alexandroupolis, Thrace, Greece. emantada@med.duth.gr.
Insights
Intravenous iron sucrose is safe and effective for children with iron deficiency anemia (IDA) who don't respond to oral iron. This treatment successfully raised hemoglobin levels in pediatric patients.
Area of Science:
- Pediatric Hematology
- Pharmacology
Background:
- Intravenous iron sucrose is not typically recommended for pediatric use by manufacturers.
- Extensive safety and efficacy data exist for adult use.
Purpose of the Study:
- To evaluate the safety and efficacy of intravenous iron sucrose in children.
- To assess its utility in cases of iron deficiency anemia (IDA) unresponsive to oral iron therapy.
Main Methods:
- Retrospective review of pediatric patients (≤14 years) treated with intravenous iron sucrose.
- Data collected from January 2011 to February 2014.
- Analysis of treatment outcomes for IDA, transfusion avoidance, and iron refractory IDA (IRIDA).
Main Results:
- Twelve children received intravenous iron sucrose for IDA, transfusion avoidance, or IRIDA.
- All patients with IDA showed normalization of hemoglobin levels (7.6±2.38 to 12.4±0.64 g/dL) within 31-42 days.
- Minor side effects included injection site disorders (3 cases) and transient taste perversion (1 case).
Conclusions:
- Intravenous iron sucrose is a safe and highly effective treatment option for pediatric patients with IDA.
- It is particularly beneficial for children who fail to respond to or tolerate oral iron therapy.
Background:
Intravenous iron sucrose is not recommended by its manufacturers for use in children despite extensive safety and efficacy data in adults.
Methods:
We reviewed the experience of our department between January, 2011 and February, 2014 with the use of intravenous iron sucrose in children ≤14 years of age who failed in oral iron therapy for iron deficiency anemia (IDA).
Results:
Twelve children (6 females) aged 1.2-14 years (median age 8.9 years) received at least one dose of intravenous iron sucrose. Ten patients had IDA inadequately treated or non-responsive to oral iron therapy. One patient received therapy for blood transfusion avoidance and one for presumed iron refractory iron deficiency anemia (IRIDA). Iron sucrose infusions were given on alternate days up to three times per week. The number of infusions per patient ranged from 2 to 6 (median, 3), the individual doses from 100 mg to 200 mg (median, 200 mg), and the total doses from 200 mg to 1200 mg (median, 400 mg). Iron sucrose was effective in raising the hemoglobin concentration to normal in all patients with IDA, i.e., from 7.6±2.38 g/dL to 12.4±0.64 g/dL, within 31-42 days after the first infusion. The single patient with IRIDA demonstrated a 1.8 g/dL rise. Injection site disorders in three cases and transient taste perversion in one case were the only side effects.
Conclusion:
Intravenous iron sucrose appears to be safe and very effective in children with IDA who do not respond or cannot tolerate oral iron therapy.
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