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Clinical experience with the use of ferric citrate as a phosphate binder in pediatric dialysis patients
Mark R Hanudel1, Marciana Laster2, Georgina Ramos2
1Department of Pediatrics, David Geffen School of Medicine at UCLA, 10833 Le Conte Avenue, MDCC A2-383, Los Angeles, CA, 90095-1752, USA. mhanudel@mednet.ucla.edu.
Insights
Ferric citrate effectively lowered phosphate and improved iron levels in pediatric dialysis patients. This study suggests its potential for treating both conditions concurrently in this population.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Clinical Trials
Background:
- Ferric citrate, an iron-based phosphate binder, is approved for adults with chronic kidney disease (CKD).
- Its efficacy and safety in pediatric dialysis patients have not been previously described.
- Hyperphosphatemia and iron deficiency are common complications in pediatric CKD.
Purpose of the Study:
- To evaluate the effect of ferric citrate on phosphate levels and iron status in pediatric dialysis patients.
- To assess the feasibility of using ferric citrate as a concurrent treatment for hyperphosphatemia and iron deficiency in this population.
Main Methods:
- Retrospective analysis of 11 pediatric dialysis patients (ages 4-17) treated with ferric citrate from 2015-2017.
- Comparison of time-averaged laboratory values before and after ferric citrate initiation.
- Statistical analysis using the Wilcoxon signed-rank test.
Main Results:
- Ferric citrate treatment significantly decreased serum phosphate levels (6.5 to 5.2 mg/dL, p=0.014).
- Phosphate SDS also decreased significantly (2.3 to 0.9, p=0.019).
- Transferrin saturation increased (26% to 34%, p=0.049), and ferritin levels showed an upward trend (107 to 230 ng/mL, p=0.074).
- Hematocrit levels were maintained during treatment.
Conclusions:
- Ferric citrate may effectively manage both hyperphosphatemia and iron deficiency in pediatric dialysis patients.
- Larger studies are warranted to confirm the safety and efficacy of ferric citrate in pediatric CKD.
- This agent offers a potential dual-action therapeutic option for this vulnerable population.
Background:
Ferric citrate, an iron-based phosphate binder, has been shown to improve both hyperphosphatemia and iron deficiency in adult chronic kidney disease patients, but its use in the pediatric dialysis population has not been described.
Methods:
This is a retrospective analysis of 11 unselected pediatric dialysis patients who received ferric citrate as a phosphate binder between 2015 and 2017. Time-averaged laboratory values were compared pre- and post-ferric citrate initiation using the Wilcoxon signed-rank test.
Results:
The median age of this cohort was 13 years old (range 4-17 years old). Five patients were on hemodialysis, and six patients were on peritoneal dialysis. The median duration of ferric citrate therapy was 214 days (range 39-654 days), with a median time-averaged ferric citrate dose of 3.5 tablets per day (range 1.5-8.4 tablets per day). Compared to the pre-ferric citrate period, ferric citrate treatment was associated with decreased serum phosphate (6.5 to 5.2 mg/dl, p = 0.014), decreased phosphate age-related standard deviation score (SDS) (2.3 to 0.9, p = 0.019), increased transferrin saturation (26 to 34%, p = 0.049), increased ferritin (107 to 230 ng/ml, p = 0.074), and maintenance of hematocrit.
Conclusions:
In pediatric dialysis patients, ferric citrate may be able to concurrently lower phosphate levels and treat iron deficiency. However, larger studies are needed to further evaluate safety and efficacy in the pediatric chronic kidney disease population.
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