Ranferron (Intravenous Iron) Dosing in Pediatric Patients
For pediatric patients requiring intravenous iron supplementation, Ranferron should be dosed at 50-100 mcg/kg/day up to a maximum of 5 mg/day for routine supplementation in infants and children, with higher doses of 200-250 mcg/kg/day recommended for preterm infants. 1
Age-Based Dosing Recommendations
The ESPGHAN/ESPEN/ESPR/CSPEN guidelines provide specific dosing recommendations for parenteral iron in pediatric patients:
- Preterm infants: 200-250 mcg/kg/day
- Term infants to 3 months: 250 mcg/kg/day
- Infants 3-12 months: 100 mcg/kg/day
- Children >12 months: 50 mcg/kg/day (up to maximum 5 mg/day) 1
Administration Considerations
Route and Method
Parenteral iron can be administered either:
- Added to parenteral nutrition solutions daily, or
- As intermittent, separate infusions 1
If giving as separate infusions, iron sucrose is the most studied iron preparation in children and is recommended for intermittent administration 1
For administration:
Safety Precautions
- Monitor for adverse reactions during administration
- Iron sucrose has shown fewer severe adverse events in children compared to older iron formulations 1
- A test dose is recommended before initiating iron dextran therapy, but newer formulations may not require this precaution 2
Monitoring
Iron status should be regularly monitored in patients on long-term parenteral iron supplementation to prevent both iron deficiency and iron overload:
- Monitor at minimum:
- Hemoglobin
- Serum ferritin 1
- Frequency of monitoring should be increased in patients with high gastrointestinal fluid losses (e.g., ileostomy) 1
Special Considerations
Short-term vs. Long-term Therapy
- Routine provision of iron in parenteral nutrition is not recommended for short-term PN (<3 weeks) 1
- For long-term PN, parenteral iron should be given if enteral iron supplementation is insufficient to maintain adequate iron status 1
Compatibility with PN Solutions
- Iron dextran at 10 mg/L is stable for 48 hours when added to fat-free PN solutions
- Iron dextran cannot be added to lipid emulsions or all-in-one admixtures as it destabilizes the emulsion
- Iron sucrose has been shown to be stable in fat-free PN solutions at concentrations up to 2.5 mg/L 1
Contraindications
- IV iron should not be administered to patients with active infection 2
- Caution should be used during periods of neutropenia due to potential increased infection risk 2
By following these evidence-based dosing recommendations and administration guidelines, clinicians can effectively and safely treat iron deficiency in pediatric patients requiring intravenous iron supplementation.