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Pediatric Nephrology

, Volume 22, Issue 11, pp 1931–1938 | Cite as

Intermittent or daily administration of 1-alpha calcidol for nephrectomised infants on peritoneal dialysis?

  • Tuure T. SaarinenEmail author
  • Pekka Arikoski
  • Christer Holmberg
  • Kai Rönnholm
Original Article

Abstract

Secondary hyperparathyroidism and renal osteodystrophy are major problems in patients with end-stage renal failure and may result in poor growth in children on dialysis. Whether vitamin D sterols should be given intermittently or daily remains a controversial issue. We studied 16 bilaterally nephrectomised infants with congenital nephrosis of the Finnish type (median age 0.54 years), all on peritoneal dialysis. Nine of them were receiving intermittent 1-α calcidol therapy and seven daily 1-α calcidol therapy. The target serum parathyroid hormone (PTH) level was 2–3 times the upper limit of normal (ULN). There were no statistically significant differences in PTH values between the groups (1.7-times vs 0.5-times the ULN at 3 months and 3.1-times vs 3.4-times the ULN at 6 months, respectively). The required weekly doses of 1-α calcidol were low, and there were no significant differences between the intermittent and daily groups (0.06 μg/kg vs 0.04 μg/kg at 3 months and 0.09 μg/kg vs 0.05 μg/kg at 6 months, respectively). The infants on intermittent 1-α calcidol showed significant catch-up growth during dialysis after nephrectomy relative to the infants on daily 1-α calcidol (−1.6 SD to −0.7 SD vs −1.4 SD to −1.0 SD, respectively; P < 0.05). Our results indicate that either intermittent or daily vitamin D analogue therapy, if started early, will prevent secondary hyperparathyroidism equally well in children on peritoneal dialysis (PD), but intermittent therapy might be more favourable for growth.

Keywords

Growth Children Vitamin D analogue treatment Parathyroid hormone (PTH) Congenital nephrosis End-stage renal failure 

Notes

Acknowledgements

The authors wish to thank Hannu Jalanko, MD, Hanne Laakkonen, MD, and Tuula Hölttä, MD, for their valuable contributions to this study. We also wish to thank the staff on the paediatric wards caring for these children for their valuable contribution to the practical administration of the therapy. This research was supported by the Sigrid Juselius Foundation, Helsinki, Finland.

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Copyright information

© IPNA 2007

Authors and Affiliations

  • Tuure T. Saarinen
    • 1
    Email author
  • Pekka Arikoski
    • 2
  • Christer Holmberg
    • 1
  • Kai Rönnholm
    • 1
  1. 1.Department of Paediatric Nephrology and Transplantation, Hospital for Children and AdolescentsUniversity of HelsinkiHelsinkiFinland
  2. 2.Department of Paediatrics, Kuopio University HospitalUniversity of KuopioKuopioFinland

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