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2.
Calcif Tissue Int ; 51(2): 105-10, 1992 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-1422948

RESUMO

In order to investigate the effect of a supplementation of vitamin D in the prophylaxis of fractures of the bones of aged people, an annual intramuscular injection of ergocalciferol (150,000-300,000 IU) was given to two series of aged subjects: first to 199 (45 male) of 479 subjects (110 male) aged more than 85 years who were living in their own home, and second to 142 (29 male) of 320 (58 male) subjects aged 75-84 and living in a home for aged people. This prospective series was divided into treatment groups according to month of birth. These injections were given annually from September to December in the years 1985-1989, two to five times to each participant. The fracture rates, laboratory values, vitamin D levels, possible side effects, and mortality were followed until October 1990. A total of 56 fractures occurred in the 341 vitamin D recipients (16.4%) and 100 in 458 controls (21.8%) (P = 0.034). The fracture rate was about the same in both outpatient and municipal home series. Fractures of the upper limb were fewer in the vitamin D recipients, 10/341 = 2.9% (P = 0.025), than in the controls, 28/458 = 6.1%, during the follow-up. A similar result was obtained in fractures of ribs, 3/341 = 0.9% and 12/458 = 2.6%, respectively. Fractures of the lower limbs occurred almost as frequently, 31/341 = 9.1%, among the vitamin D recipients as among the controls, 49/458 = 10.7%. The fracture rate was higher in females (22.2%) than in males (9.5%). The fractures were fewer in the vitamin D recipients only in females.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Envelhecimento , Ergocalciferóis/administração & dosagem , Fraturas Ósseas/prevenção & controle , Idoso , Ergocalciferóis/uso terapêutico , Feminino , Fraturas Ósseas/epidemiologia , Fraturas Ósseas/etiologia , Humanos , Incidência , Masculino , Osteoporose Pós-Menopausa/complicações , Osteoporose Pós-Menopausa/epidemiologia , Estudos Prospectivos , Fatores Sexuais
3.
Calcif Tissue Int ; 49 Suppl: S68-9, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1933603

RESUMO

Fluoride has been used for the treatment of osteoporosis since 1961, because it increases trabecular bone mass in the spine and may be effective in the treatment of spinal osteoporosis. Fluoride treatment is still controversial because of its side effects, the high rate of non-responders, possible osteomalacic effect on bone, deleterious effects on cortical bone, and especially because of its uncertain effect on fracture rate. At present, fluoride therapy is highly questionable in the prophylaxis and treatment of osteoporosis.


Assuntos
Fluoretos/uso terapêutico , Osteoporose/tratamento farmacológico , Feminino , Fluoretos/efeitos adversos , Fraturas Ósseas/prevenção & controle , Humanos , Osteoporose Pós-Menopausa/tratamento farmacológico
4.
Calcif Tissue Int ; 49 Suppl: S87, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1933611

RESUMO

An annual intramuscular injection of ergocalciferol (150,000 IU) normalized low serum (25(OH)D concentrations in elderly people for 1 year. The treatment had a slight effect on serum 24,25(OH)2D levels but no effect on 1,25(OH)2D levels.


Assuntos
Ergocalciferóis/administração & dosagem , Deficiência de Vitamina D/tratamento farmacológico , Vitamina D/sangue , Idoso , Idoso de 80 Anos ou mais , Humanos , Injeções Intramusculares , Fatores de Tempo , Deficiência de Vitamina D/sangue
5.
Am J Cardiol ; 63(17): 1227-30, 1989 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-2711992

RESUMO

The antihypertensive efficacy and frequency of adverse reactions following administration of diltiazem in a new slow-release formulation were compared with placebo in 34 patients with mild to moderate essential hypertension in a randomized, double-blind, crossover study. After 6 weeks of treatment with diltiazem (240 or 360 mg/day), average supine blood pressure (BP) decreased from 165 +/- 21/101 +/- 5 mm Hg at baseline to 152 +/- 16/93 +/- 4 mm Hg compared with 160 +/- 19/100 +/- 7 mm Hg with placebo (p less than 0.01/p less than 0.001). Standing BP decreased from 162 +/- 20/107 +/- 6 mm Hg at baseline to 150 +/- 14/101 +/- 5 mm Hg compared to 159 +/- 18/107 +/- 8 mm Hg with placebo (p less than 0.01/p less than 0.001). The supine heart rate after diltiazem was 65 +/- 7 beats/min and after placebo 69 +/- 9 beats/min (p less than 0.01). There were no hematologic side effects. Only minor differences between diltiazem and placebo were observed in some of the biochemical laboratory values. Four patients were withdrawn due to side effects during treatment with diltiazem and 2 with placebo. Diltiazem in a slow-release formulation given twice a day lowered blood pressure significantly as monotherapy in patients with mild to moderate hypertension and was well tolerated.


Assuntos
Diltiazem/administração & dosagem , Hipertensão/tratamento farmacológico , Adulto , Idoso , Preparações de Ação Retardada , Diltiazem/efeitos adversos , Método Duplo-Cego , Eletrocardiografia , Feminino , Frequência Cardíaca/efeitos dos fármacos , Humanos , Hipertensão/enzimologia , Masculino , Pessoa de Meia-Idade , Distribuição Aleatória , Supinação
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