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[Experience with sevelamer in peritoneal dialysis].
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|December 9, 2003
Summary
Sevelamer effectively manages hyperphosphatemia in peritoneal dialysis patients, reducing phosphorus levels and the need for aluminum and calcium-based binders. This study demonstrates its clinical utility in improving patient outcomes.
Area of Science:
- Nephrology
- Internal Medicine
- Pharmacology
Background:
- Hyperphosphatemia is a common complication in peritoneal dialysis (PD) patients.
- Traditional phosphate binders like aluminum and calcium salts have potential adverse effects.
- Sevelamer, a non-aluminum, non-calcium-based phosphate binder, offers an alternative treatment option.
Purpose of the Study:
- To evaluate the efficacy of sevelamer in controlling serum phosphorus levels in PD patients.
- To assess changes in phosphorus binder requirements during sevelamer therapy.
- To examine the impact of sevelamer on serum phosphorus, calcium-x-phosphorus product, and lipid profiles.
Main Methods:
- A prospective study involving 14 PD patients with hyperphosphatemia previously treated with aluminum or calcium-based binders.
- Patients were initiated on sevelamer (400 mg) and followed for 12 months.
- Dosage adjustments were made as needed to achieve target phosphorus levels.
Main Results:
- Sevelamer therapy led to a significant reduction in serum phosphorus levels (from 5.9 to 5.0 mg/dL) and the calcium-x-phosphorus product (from 59.8 to 48.6 mg²/dL²).
- The use of aluminum and calcium salts was significantly reduced or eliminated.
- Serum cholesterol levels also decreased significantly, while serum triglycerides, CO2, and PTH remained stable. Alkaline phosphatase initially increased but normalized by 12 months.
Conclusions:
- Sevelamer provides effective control of hyperphosphatemia and the calcium-x-phosphorus product in PD patients.
- It facilitates a reduction in the use of aluminum and calcium-based phosphate binders.
- Sevelamer represents a valuable therapeutic option for managing mineral and bone disorders in PD patients.