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Assistant Professor, Department of Pharmacy Clinical and Administrative Sciences, College of Pharmacy, The University of Oklahoma Health Sciences Center, Oklahoma City, OK; Clinical Pharmacy Specialist, University of Oklahoma Family Medicine Center, Oklahoma City
Clinical Assistant Professor, Department of Pharmacy Clinical and Administrative Sciences, College of Pharmacy, The University of Oklahoma Health Sciences Center, Oklahoma City
Reprints: Dr. Dennis, The University of Oklahoma Health Sciences Center, College of Pharmacy, 1110 N. Stonewall, Oklahoma City, OK 73190-5040, fax 405/271-6430, vincent-dennis{at}ouhsc.edu
OBJECTIVE: To review the pharmacology, pharmacokinetics, effectiveness, safety, and therapeutic considerations related to the use of doxercalciferol in the treatment of secondary hyperparathyroidism.
DATA SOURCES: A MEDLINE search (1966-June 2006) was conducted using
the key words vitamin D, ergocalciferols, and secondary hyperparathyroidism.
Text word searches were also performed for the terms 1-
-hydroxy-vitamin
D2, 1-
-hydroxyergocalciferol, Hectorol, and
doxercalciferol. Searches were limited to studies published in English and
conducted in human subjects.
STUDY SELECTION AND DATA EXTRACTION: All published clinical studies evaluating the safety and effectiveness of doxercalciferol in secondary hyperparathyroidism were reviewed, and anecdotal patient reports were also evaluated. Selected clinical studies involving the use of calcitriol and/or paricalcitol in the treatment of secondary hyperparathyroidism were also included.
DATA SYNTHESIS: Doxercalciferol effectively reduces parathyroid hormone levels in patients with chronic kidney disease (CKD). Both oral and intravenous administration can significantly increase serum calcium and/or phosphorus levels as evidenced by placebo-controlled clinical trials. This agent has not been studied comparatively with calcitriol or paricalcitol to assess relative safety.
CONCLUSIONS: Doxercalciferol is approved for and effective in the treatment of secondary hyperparathyroidism related to CKD, both before and during dialysis, but has not demonstrated a lower incidence of hypercalcemia and/or hyperphosphatemia in relation to other vitamin D therapies. The drug is available in both oral and intravenous dosage forms. Doxercalciferol should be maintained as a formulary alternative for patients unresponsive to or intolerant of other vitamin D therapies, but comparative randomized studies are needed to differentiate its place in therapy.
Key Words: doxercalciferol, chronic kidney disease, secondary hyperparathyroidism
Published Online, October 24, 2006. www.theannals.com, DOI 10.1345/aph.1G523
THIS ARTICLE IS APPROVED FOR CONTINUING EDUCATION CREDIT
ACPE
UNIVERSAL PROGRAM NUMBER: 407-000-06-026-H01
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