Abstract |
A strict control of secondary hyperparathyroidism in patients with chronic kidney disease (CKD) is indicated to avoid serious complications linked to osteitis fibrosa and other parathyroid-hormone (PTH)-related bodily disturbances. However, such a control is often achieved only at the price of unacceptably high plasma calcium and phosphorus levels and the risk of soft tissue calcification, even when using the novel, so-called 'non-hypercalcemic' vitamin D analogs. The advent of a new class of drugs, the calcimimetics, should allow a more adequate control of the disturbed calcium- phosphorus metabolism in CKD patients. In my opinion, the calcimimetics will not replace currently used medications but will be a valuable supplement to presently available treatment options for this major complication in patients with renal failure.
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Authors | Tilman B Drüeke |
Journal | Blood purification
(Blood Purif)
Vol. 22
Issue 1
Pg. 38-43
( 2004)
ISSN: 0253-5068 [Print] Switzerland |
PMID | 14732810
(Publication Type: Comparative Study, Journal Article, Review)
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Copyright | Copyright 2004 S. Karger AG, Basel |
Chemical References |
- Ergocalciferols
- Hydroxycholecalciferols
- Naphthalenes
- Phosphates
- Receptors, Calcitriol
- Receptors, Calcium-Sensing
- Vitamin D
- 1 alpha-hydroxyergocalciferol
- paricalcitol
- Calcitriol
- maxacalcitol
- Cinacalcet
- alfacalcidol
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Topics |
- Calcitriol
(adverse effects, analogs & derivatives, metabolism, pharmacology, therapeutic use)
- Cinacalcet
- Clinical Trials as Topic
- Drug Synergism
- Ergocalciferols
(pharmacology, therapeutic use)
- Humans
- Hydroxycholecalciferols
(adverse effects, therapeutic use)
- Hypercalcemia
(chemically induced)
- Hyperparathyroidism, Secondary
(etiology, prevention & control)
- Intestinal Absorption
(drug effects)
- Kidney Failure, Chronic
(blood, complications)
- Liver
(drug effects, metabolism)
- Naphthalenes
(pharmacokinetics, therapeutic use)
- Phosphates
(blood)
- Receptors, Calcitriol
(drug effects, metabolism)
- Receptors, Calcium-Sensing
(agonists, physiology)
- Vitamin D
(adverse effects, therapeutic use)
- Vitamin D Deficiency
(drug therapy, etiology)
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