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Sevelamer therapy for pediatric end-stage renal disease
Lara E Storms1, Michael F Chicella, James E Dice
1Department of Pharmacy, Children's Hospital of The King's Daughters, Norfolk, Virginia 23507, USA.
Insights
Sevelamer effectively lowered phosphorus levels in a young child with end-stage renal disease (ESRD). This study suggests sevelamer is a safe and viable phosphate binder for pediatric ESRD patients.
Area of Science:
- Pediatric Nephrology
- Pharmacology
- Renal Disease Management
Background:
- Hyperphosphatemia is a common complication in patients with end-stage renal disease (ESRD).
- Phosphate binders are crucial for managing hyperphosphatemia, but data on sevelamer use in young children is limited.
- Non-calcium, non-aluminum phosphate binders are preferred in certain pediatric populations.
Observation:
- A 19-month-old girl with ESRD presented with severe hyperphosphatemia (serum phosphorus 8.6 mg/dL, calcium-phosphorus product 75 mg²/dL²).
- Aluminum-based binders were contraindicated due to neurotoxicity concerns in renal disease.
- Sevelamer dosing was extrapolated from adult data, starting at 100 mg/kg/day and titrated to 130 mg/kg/day.
Findings:
- Sevelamer therapy resulted in a significant reduction in serum phosphorus levels, reaching as low as 5.2 mg/dL and 5.2 mg/dL at discharge.
- The calcium-phosphorus product decreased to the upper 50s, mitigating calcification risks.
- No adverse effects related to sevelamer administration were observed during the treatment period.
Implications:
- Sevelamer demonstrates efficacy and safety as a phosphate binder in a pediatric patient with ESRD.
- This case report supports the consideration of sevelamer for managing hyperphosphatemia in young children with renal disease.
- Further pediatric studies are warranted to establish optimal dosing and long-term outcomes for sevelamer in this population.
Abstract:
Sevelamer, a non-calcium-containing, non-aluminum-containing phosphate binder, is frequently prescribed for treatment in adults with hyperphosphatemia secondary to end-stage renal disease (ESRD). However, published information regarding sevelamer use in children younger than 11 years is lacking. We report the use of sevelamer as a phosphate binder in a 19-month-old girl with ESRD who was receiving calcium carbonate 1250 mg 3 times/day for hyperphosphatemia. The patient's initial serum phosphorus concentration was 8.6 mg/dl, and the calcium-phosphorus product was 75 mg(2)/dl(2). This was well above the level that places patients at risk for complications such as joint, vessel, and soft-tissue calcification. An aluminum-containing phosphate binder was not an option given the patient's renal disease and the concern for neurotoxicity. Sevelamer was considered, but a MEDLINE search revealed no pediatric dosing information. An initial dosage of 100 mg/kg/day divided every 8 hours was administered, as extrapolated from adult data, and then titrated to 130 mg/kg/day divided every 8 hours based on the patient's response. The child's dietary phosphorus intake remained constant throughout her hospital stay. During sevelamer therapy, her serum phosphorus concentration dropped as low as 5.2 mg/dl; at discharge it was 6.5 mg/dl, with a corresponding calcium-phosphorus product in the upper 50s. No adverse effects associated with sevelamer were observed. In the dosages we used, sevelamer resulted in an acceptable calcium-phosphorus product and returned the patient's serum phosphorus concentration to near normal. Sevelamer appears to be a viable option as a phosphate binder in children with ESRD.
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