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Paricalcitol versus calcitriol treatment for hyperparathyroidism in pediatric hemodialysis patients
Wacharee Seeherunvong1, Obioma Nwobi, Carolyn L Abitbol
1Division of Pediatric Nephrology, Department of Pediatrics, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Insights
Paricalcitol and calcitriol show similar efficacy in treating secondary hyperparathyroidism in pediatric dialysis patients. Paricalcitol may reduce elevated calcium x phosphorus product, suggesting its safety and effectiveness.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Pharmacology
Background:
- Secondary hyperparathyroidism (SHPT) presents a treatment challenge in pediatric dialysis.
- Paricalcitol, a vitamin D analogue, has shown promise in adults with SHPT.
Purpose of the Study:
- To compare the efficacy and safety of paricalcitol versus calcitriol for SHPT in pediatric dialysis patients.
- To evaluate treatment outcomes including intact parathyroid hormone (iPTH) levels and calcium x phosphorus product (CaxP).
Main Methods:
- A study involving 21 pediatric dialysis patients with SHPT.
- Patients were treated with either calcitriol followed by paricalcitol, or calcitriol/paricalcitol alone.
- Intact parathyroid hormone (iPTH) levels and calcium x phosphorus product (CaxP) were monitored.
Main Results:
- Both calcitriol and paricalcitol demonstrated similar reductions in iPTH levels (approximately -60% to -65%).
- Episodes of hypercalcemia were comparable between groups.
- Elevated CaxP (> or =70 mg(2)/dl(2)) occurred more frequently with calcitriol treatment (odds ratio=1.5; p=0.01).
Conclusions:
- Paricalcitol is a safe and effective treatment option for SHPT in pediatric dialysis patients.
- Dosing of paricalcitol should be individualized based on SHPT severity.
- Further pharmacokinetic studies in pediatric populations are warranted.
Abstract:
Secondary hyperparathyroidism (SHPT) remains a treatment dilemma in pediatric dialysis patients. Recent experience with paricalcitol (P), a vitamin D analogue, in adults with SHPT has shown equal efficacy and improved survival compared to traditional treatment with calcitriol (C). We present our experience with (C) compared to (P) treatment in our pediatric dialysis patients with SHPT. Twenty-one patients (mean age 11.5+/-5 years) with SHPT (intact parathyroid hormone (iPTH) averaging 1,228+/-496 pg/ml) were studied. Seventeen received (C) followed by (P); while an additional four were treated with either (C=1) or (P=3) alone. After 26+/-8 weeks, average percent (%) decrease in iPTH was similar with (C) and (P) (-60.4+/-34% versus -65.4+/-28%, respectively; p=0.6). In the (P) group, the effective dose in children was greater than in adult trials based on kilogram weight. Episodes of hypercalcemia between the treatment groups were not different. However, episodes of elevated calcium x phosphorus product (CaxP)> or =70 mg(2)/dl(2) occurred more frequently in the (C) group (odds ratio=1.5; p=0.01). Paricalcitol appears to be safe and effective in pediatric patients. Data suggest that dosing should be gauged according to degree of SHPT. This should serve as impetus for future pharmacokinetic studies in pediatric dialysis patients.
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