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Published on: January 19, 2024
Treatment targeting pediatric inflammatory bowel disease-associated anemia: experience from a single tertiary center
Ana Sc Fernandes1,2, Sara Azevedo1,2, Ana Rita Martins1
1Pediatric Department, University Hospital Santa Maria, Lisbon Medical Centre, Lisbon, Portugal.
Insights
Iron deficiency (ID) and iron deficiency anemia (IDA) are common in pediatric inflammatory bowel disease (IBD). Intravenous iron sucrose (IS) and ferric carboxymaltose (FCM) are safe and effective treatments, but ID often recurs, necessitating proactive management.
Area of Science:
- Pediatric Gastroenterology
- Hematology
- Internal Medicine
Background:
- Iron deficiency (ID) and iron deficiency anemia (IDA) are frequent complications in pediatric inflammatory bowel disease (IBD).
- These conditions are often overlooked and undertreated due to uncertainties in optimal iron formulation, dosage, administration route, and safety.
- Undertreatment negatively impacts pediatric patient development and quality of life.
Purpose of the Study:
- To evaluate the safety and efficacy of iron sucrose (IS) and ferric carboxymaltose (FCM) for treating ID and IDA in pediatric IBD patients.
- To compare the outcomes of IS and FCM in this specific patient population.
Main Methods:
- Retrospective review of medical records for pediatric IBD patients treated with IS (age < 14) or FCM (age ≥ 14) over 10 years.
- Iron doses calculated using the Ganzoni formula; adverse reactions monitored during and after treatment.
- Efficacy defined by hemoglobin increase (≥2 g/dL) or anemia resolution within 12 weeks for IDA, and transferrin saturation or ferritin normalization for ID.
Main Results:
- Sixty-three patients received IV iron (104 treatment courses: 63 FCM, 41 IS).
- Treatment efficacy was 66.7% for FCM and 67.6% for IS in IDA patients; 77.8% for ID without anemia.
- Recurrent ID required retreatment in 41.3% of patients; only one adverse reaction (hypotension and rash) noted with IS.
Conclusions:
- Ferric carboxymaltose (FCM) and iron sucrose (IS) are safe and effective for correcting iron deficiency in pediatric IBD patients.
- Iron deficiency frequently recurs in this population, highlighting the importance of proactive screening and management.
- This study provides valuable data from a large, long-term follow-up cohort on IV iron use in pediatric IBD.
Background:
Iron deficiency (ID) and iron deficiency anemia (IDA) are common complications of pediatric inflammatory bowel disease (IBD). Owing to questions regarding optimal iron formulation, dosage, route of administration, and safety, these complications are frequently overlooked and undertreated, negatively impacting patient development and quality of life.
Purpose:
To assess the safety and efficacy of iron sucrose (IS) and ferric carboxymaltose (FCM) in the treatment of ID and IDA in pediatric IBD.
Methods:
We retrospectively reviewed the medical records of pediatric patients with IBD treated for 10 years with IS (age <14 years) or FCM (age ≥14 years) in a single regional referral center. The Ganzoni formula was used to calculate the iron dose administered. Adverse reactions were monitored during treatment and after discharge. Efficacy was defined as a ≥2 g/dL rise in Hb or anemia resolution within 12 weeks after treatment in cases of IDA and transferrin saturation or ferritin normalization in cases of ID.
Results:
Sixty-three patients were treated with IV iron (41 with Crohn disease, 15 with ulcerative colitis, 7 with IBD-unclassified; median age, 14.6 years; 104 treatment courses [63 FCM, 41 IS during the 10-year study period]). Retreatment was necessary after a median 1.4 years in 26 patients (41.3%). The median activity scores of patients with recurrent ID indicated inactive disease. The treatment efficacy was 66.7% (FCM) and 67.6% (IS) in patients with IDA and 77.8% in patients with ID but without anemia. One adverse reaction (hypotension and rash) was associated with IS treatment.
Conclusion:
In one of the largest and longest follow-up cohorts, FCM and IS were safe and effective for correcting ID in pediatric patients with IBD. As ID recurs frequently, proactive screening and treatment are important.
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