Abstract | BACKGROUND: METHODS: RESULTS: The mean dose of alfacalcidol per week was 3.63 +/- 1.71 microg. Patients previously treated with vitamin D(3) metabolites needed higher doses of alfacalcidol (4.0 +/- 1.7 vs. 3.2 +/- 1.6; p = 0.01). Only 50.8% of the patients had received vitamin D(3) metabolites prior to the start of the study and at baseline they had higher i-PTH levels (600.3 +/- 360.5 vs. 489.9 +/- 292.6, p = 0.02). i-PTH levels decreased from 546 +/- 332.6 to 332.4 +/- 274.5 pg/ml (p < 0.001). 60.5% of the patients had i-PTH < 300 pg/ml at the last observation. Serum calcium increased (9.4 +/- 0.8 to 9.97 +/- 1.0 mg/l, p < 0.001). CONCLUSION:
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Authors | M T González, J V Torregrosa, E Colomé, A Mendia, M Pavesi |
Journal | Nephron. Clinical practice
(Nephron Clin Pract)
Vol. 108
Issue 2
Pg. c141-7
( 2008)
ISSN: 1660-2110 [Electronic] Switzerland |
PMID | 18259100
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial)
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Copyright | (c) 2008 S. Karger AG, Basel |
Chemical References |
- Hydroxycholecalciferols
- Parathyroid Hormone
- alfacalcidol
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Topics |
- Aged
- Analysis of Variance
- Dose-Response Relationship, Drug
- Drug Administration Schedule
- Female
- Follow-Up Studies
- Humans
- Hydroxycholecalciferols
(therapeutic use)
- Hyperparathyroidism, Secondary
(drug therapy, etiology)
- Infusions, Intravenous
- Kidney Failure, Chronic
(complications, diagnosis, therapy)
- Male
- Middle Aged
- Parathyroid Hormone
(blood)
- Prospective Studies
- Reference Values
- Renal Dialysis
(adverse effects, methods)
- Risk Assessment
- Treatment Outcome
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