# Intravenous Sodium Ferric Gluconate Complex for Hospitalized Pediatric Patients with Iron Deficiency Anemia

**Authors:** Felicia White, Noelle Polakowski, Elena Merlington, Mara Leimanis, Brooke Dudick, Jessica Parker, Ashley Jousma, Alexander Loji, Jeffrey Hanson, Monica Arney, Brian Boville

PMC · DOI: 10.3390/children12020189 · Children · 2025-02-05

## TL;DR

This study examines the use of intravenous iron in children with anemia and finds no additional benefits from higher doses.

## Contribution

The study provides new insights into the safety and efficacy of intravenous iron in hospitalized children.

## Key findings

- Hemoglobin levels increased after SFGC treatment, but no significant dose-response relationship was observed.
- Higher cumulative doses of SFGC did not reduce the need for RBC transfusions.
- Only one adverse event was recorded, suggesting a favorable safety profile.

## Abstract

Background/Objectives: Iron deficiency anemia is common in the pediatric population. Red blood cell transfusions, a common acute treatment, pose well-recognized risks including lung injury, circulatory overload, and immune dysfunction. Intravenous iron, specifically sodium ferric gluconate complex (SFGC), is a potential alternative, however investigation on its use in hospitalized children is lacking. This study aims to describe the physiologic response via change in hematologic values to cumulative dose of SFGC, investigate the effect of cumulative dosing on the amount of RBC transfusions received, and comment on its safety. Methods: This is a retrospective investigation of pediatric patients with iron deficiency who received SFGC during their admission to the Helen DeVos Children’s Hospital between 2016 and 2018 (N = 85). Results: A total of 258 doses of intravenous SFGC were provided to 85 patients. The average pre-treatment serum hemoglobin was 8.73 ± 1.33, and 7 days post-treatment this increased to 10.41 ± 1.43. Mean corpuscular volume, ferritin, serum ion, total iron binding capacity, reticulocyte percentage, and reticulocyte hemoglobin all increased 7 days post-treatment, as would be suspected, but without any statistically significant difference between hematologic outcomes and cumulative dose of SFGC. Our study did not reveal any correlation between the cumulative dose of SFGC administered and the amount of RBC transfusions received. Only one adverse event was recorded. Conclusions: Our results complement the trend of increased use and emerging evidence of favorable safety profiles of IV iron in the pediatric population. This descriptive investigation revealed that administering higher cumulative doses of SFGC provided no further benefits in terms of hematologic response or RBC transfusion administration.

## Linked entities

- **Chemicals:** Iron (PubChem CID 23925)
- **Diseases:** Iron Deficiency Anemia (MONDO:0001356)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** circulatory overload (MESH:D065227), immune dysfunction (MESH:D007154), Iron Deficiency Anemia (MESH:D018798), iron deficiency (MESH:D000090463), lung injury (MESH:D055370)
- **Chemicals:** SFGC (MESH:C035552), iron (MESH:D007501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC11854077/full.md

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Source: https://tomesphere.com/paper/PMC11854077