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Kidney Int Suppl ; (85): S79-82, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12753272

RESUMO

BACKGROUND: To assess the usefulness of starting calcitriol therapy with a dose proportional to the degree of hyperparathyroidism, 141 patients from 28 centers were treated with intravenous calcitriol for 6 months. The aim was to achieve a final PTH between 125 and 250 pg/mL. Patients with serum PTH>250 pg/mL were included in the study and divided into 4 groups according to baseline PTH levels. METHODS: The study was completed by 100 patients, a third of which were treated strictly according to the protocol, labeled "compliants"; thus, calcitriol was started according to baseline PTH levels. Two thirds of patients, labeled "noncompliants," showed one or more violation in the dosage regimen. RESULTS: After 2 months of treatment with calcitriol, 59% of the "compliants" and 35% of the "noncompliants" decreased their PTH levels>40% (P = 0.022), 70%, and 49%, respectively after 3 months of treatment. After 3 months of treatment, 67% of the "compliants" reached the target (PTH 125 to 250 pg/mL) in contrast with 23% of the "noncompliants" (P < 0.001). The number of hypercalcemic and hyperphosphatemic episodes was significantly lower in the "compliants" group (P < 0.006). CONCLUSION: These results demonstrate several advantages when calcitriol therapy is started with a dose proportional to the severity of hyperparathyroidism.


Assuntos
Calcitriol/administração & dosagem , Calcitriol/uso terapêutico , Agonistas dos Canais de Cálcio/administração & dosagem , Agonistas dos Canais de Cálcio/uso terapêutico , Hormônio Paratireóideo/sangue , Idoso , Calcitriol/efeitos adversos , Agonistas dos Canais de Cálcio/efeitos adversos , Relação Dose-Resposta a Droga , Feminino , Humanos , Hiperparatireoidismo Secundário/tratamento farmacológico , Injeções Intravenosas , Falência Renal Crônica/sangue , Falência Renal Crônica/complicações , Masculino , Pessoa de Meia-Idade , Cooperação do Paciente , Diálise Renal/efeitos adversos
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