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1.
Respir Med ; 84(3): 211-5, 1990 May.
Artigo em Inglês | MEDLINE | ID: mdl-2218006

RESUMO

Enprofylline, a recently developed xanthine derivative, is a more potent bronchodilator than theophylline. This study compares the efficacy and safety of enprofylline with theophylline for chronic obstructive airways disease (COAD) in elderly subjects. The study was of a randomized double-blind parallel design and commenced with a 1-week reference period when oral bronchodilators were withdrawn. Patients were then treated with either enprofylline or theophylline 150 mg bd for 2 weeks (period 1) followed by 300 mg bd for a further 3 weeks (period 2). Patients recorded peak expiratory flow rate (PEFR) and adverse experiences, if any, in a diary, daily. Of 111 patients recruited for the study, 85 entered active treatment (theophylline, n = 44; enprofylline, n = 41). Mean age was 72 years and mean bronchodilator reversibility was 22%. Enprofylline increased mean morning PEFR by 11% (period 1) and 19% (period 2) whereas theophylline increased PEFR by 13% and 19%, respectively. From the enprofylline group 29% were withdrawn from the study due mainly to headache and nausea/vomiting and from the theophylline group 7% were withdrawn due mainly to nausea/vomiting. Mean plasma concentrations of enprofylline were 2.0 mg l-1 and 3.4 mg l-1, and with theophylline 5.4 mg l-1 and 10.0 mg l-1 at the end of periods 1 and 2, respectively. Enprofylline and theophylline produced similar improvements in lung functions and symptoms of chronic obstructive airways disease, but enprofylline was less well tolerated than theophylline.


Assuntos
Broncodilatadores/uso terapêutico , Pneumopatias Obstrutivas/tratamento farmacológico , Teofilina/uso terapêutico , Xantinas/uso terapêutico , Idoso , Método Duplo-Cego , Feminino , Cefaleia/induzido quimicamente , Humanos , Pneumopatias Obstrutivas/fisiopatologia , Masculino , Pico do Fluxo Expiratório/efeitos dos fármacos , Teofilina/efeitos adversos , Xantinas/efeitos adversos
3.
Lancet ; 2(7880): 548-51, 1974 Sep 07.
Artigo em Inglês | MEDLINE | ID: mdl-4140269

RESUMO

A patient with Addison's disease required increased corticosteroid dosage whilst receiving rifampicin. The pharmacological half-life of cortisol was reduced, but returned to normal when rifampicin was stopped. Cortisolproduction rates in four patients with pulmonary tuberculosis rose during treatment with rifampicin, as did urinary D-glucaric-acid excretion, an index of liver microsomal-enzyme activity. The alteration of the corticosteroid requirement in the patient with Addison's disease and the elevation of the cortisol-production rates were attributed to increased cortisol catabolism following hepatic macrosomal-enzyme induction by rifampicin.


Assuntos
Doença de Addison/tratamento farmacológico , Hidrocortisona/metabolismo , Rifampina/uso terapêutico , Tuberculose Pulmonar/tratamento farmacológico , Doença de Addison/complicações , Doença de Addison/metabolismo , Doença de Addison/urina , Adipatos/urina , Glândulas Suprarrenais/efeitos dos fármacos , Adulto , Cortisona/uso terapêutico , Relação Dose-Resposta a Droga , Antagonismo de Drogas , Quimioterapia Combinada , Fludrocortisona/uso terapêutico , Meia-Vida , Humanos , Isoniazida/uso terapêutico , Masculino , Rifampina/farmacologia , Estreptomicina/uso terapêutico , Açúcares Ácidos/urina , Tuberculose Pulmonar/complicações , Tuberculose Pulmonar/urina
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