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Am J Trop Med Hyg ; 74(6): 1060-6, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16760520

RESUMEN

Rifaximin was compared with placebo and ciprofloxacin for treatment of travelers' diarrhea in a randomized, double-blind clinical trial. Adult travelers (N = 399) consulting travel clinics in Mexico, Guatemala, and India were randomized to receive rifaximin 200 mg three times a day, ciprofloxacin (500 mg two times a day and placebo once a day), or placebo three times a day for 3 days. Patients recorded in daily diaries the time and consistency of each stool and documented symptoms for 5 days after treatment. Stool samples were collected for microbiologic evaluations before and after treatment. The median time to last unformed stool (TLUS) in the rifaximin group (32.0 hours) was less than one half that in the placebo group (65.5 hours; P = 0.001; risk ratio 1.6; 95% confidence interval 1.2, 2.2; primary efficacy endpoint). The median TLUS in the ciprofloxacin group was 28.8 hours (P = 0.0003 versus placebo; P = 0.35 versus rifaximin). Rifaximin was less effective than ciprofloxacin for invasive intestinal bacterial pathogens. Oral rifaximin is a safe and effective treatment of travelers' diarrhea caused by noninvasive pathogens.


Asunto(s)
Antiinfecciosos/uso terapéutico , Ciprofloxacina/uso terapéutico , Diarrea/tratamiento farmacológico , Fármacos Gastrointestinales/uso terapéutico , Rifamicinas/uso terapéutico , Viaje , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Antiinfecciosos/efectos adversos , Infecciones Bacterianas/complicaciones , Infecciones Bacterianas/tratamiento farmacológico , Ciprofloxacina/administración & dosificación , Ciprofloxacina/efectos adversos , Diarrea/microbiología , Diarrea/parasitología , Método Doble Ciego , Femenino , Fármacos Gastrointestinales/efectos adversos , Humanos , Masculino , Pruebas de Sensibilidad Microbiana , Persona de Mediana Edad , Rifamicinas/administración & dosificación , Rifamicinas/efectos adversos , Rifaximina , Resultado del Tratamiento
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