RESUMO
This study reports the results of an evaluation of the effectiveness and tolerability of rifaximin, an intestinal topical antibiotic. It was administered using a nasogastric tube in patients with severe enterocolitis and bacterial superinfections causing intestinal inflammatory diseases and portosystemic encephalopathy. The drug proved highly effective clinically and produced neither local nor systemic side-effects.
Assuntos
Infecções Bacterianas/tratamento farmacológico , Enteropatias/tratamento farmacológico , Rifamicinas/uso terapêutico , Adulto , Idoso , Idoso de 80 Anos ou mais , Amônia/sangue , Feminino , Encefalopatia Hepática/tratamento farmacológico , Humanos , Enteropatias/microbiologia , Intubação Gastrointestinal , Masculino , Pessoa de Meia-Idade , Rifamicinas/efeitos adversos , RifaximinaRESUMO
Intestinal transit patterns were studied in 20 normal volunteers. It was found that small changes in transit time occurred in the passage from the caecum to the sigmoid and rectum, and that most subjects evacuated the capsule 38 hr after its ingestion.
Assuntos
Motilidade Gastrointestinal , Radioisótopos do Iodo , Cápsulas , Humanos , Valva Ileocecal/fisiologia , Fatores de TempoAssuntos
Antibacterianos/uso terapêutico , Colite Ulcerativa/tratamento farmacológico , Doença de Crohn/tratamento farmacológico , Enterite/tratamento farmacológico , Doença Aguda , Adulto , Idoso , Ensaios Clínicos como Assunto , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Infecções Estreptocócicas/tratamento farmacológicoAssuntos
Ácido Desoxicólico/análogos & derivados , Dispepsia/tratamento farmacológico , Dor/tratamento farmacológico , Ácido Ursodesoxicólico/uso terapêutico , Adulto , Idoso , Colelitíase/complicações , Ensaios Clínicos como Assunto , Método Duplo-Cego , Dispepsia/etiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Dor/etiologiaRESUMO
Intestinal transit time was studied in two groups of 8 patients with irritable colon. In the first group, the time was longer than normal, whereas in the second it was accelerated. Three subjects in each group received a placebo, while the other five received 60 mg/day bromopride for 15 days. No change in transit time was noted in the controls. Two subjects in Group I displayed a significant reduction in transit time after bromopride, while deceleration and normalisation were observed in 4/5 patients in Group II.