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1.
World J Gastroenterol ; 21(18): 5555-9, 2015 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-25987779

RESUMEN

AIM: To evaluate the effectiveness of barium impaction therapy for patients with colonic diverticular bleeding. METHODS: We reviewed the clinical charts of patients in whom therapeutic barium enema was performed for the control of diverticular bleeding between August 2010 and March 2012 at Yokohama Rosai Hospital. Twenty patients were included in the review, consisting of 14 men and 6 women. The median age of the patients was 73.5 years. The duration of the follow-up period ranged from 1 to 19 mo (median: 9.8 mo). Among the 20 patients were 11 patients who required the procedure for re-bleeding during hospitalization, 6 patients who required it for re-bleeding that developed after the patient left the hospital, and 3 patients who required the procedure for the prevention of re-bleeding. Barium (concentration: 150 w%/v%) was administered per the rectum, and the leading edge of the contrast medium was followed up to the cecum by fluoroscopy. After confirmation that the ascending colon and cecum were filled with barium, the enema tube was withdrawn, and the patient's position was changed every 20 min for 3 h. RESULTS: Twelve patients remained free of re-bleeding during the follow-up period (range: 1-19 mo) after the therapeutic barium enema, including 9 men and 3 women with a median age of 72.0 years. Re-bleeding occurred in 8 patients including 5 men and 3 women with a median age of 68.5 years: 4 developed early re-bleeding, defined as re-bleeding that occurs within one week after the procedure, and the remaining 4 developed late re-bleeding. The DFI (disease-free interval) decreased 0.4 for 12 mo. Only one patient developed a complication from therapeutic barium enema (colonic perforation). CONCLUSION: Therapeutic barium enema is effective for the control of diverticular hemorrhage in cases where the active bleeding site cannot be identified by colonoscopy.


Asunto(s)
Sulfato de Bario/administración & dosificación , Medios de Contraste/administración & dosificación , Divertículo del Colon/complicaciones , Hemorragia Gastrointestinal/terapia , Administración Rectal , Adulto , Anciano , Anciano de 80 o más Años , Divertículo del Colon/diagnóstico , Enema , Femenino , Hemorragia Gastrointestinal/diagnóstico por imagen , Hemorragia Gastrointestinal/etiología , Humanos , Japón , Masculino , Persona de Mediana Edad , Posicionamiento del Paciente , Radiografía , Recurrencia , Retratamiento , Estudios Retrospectivos , Factores de Tiempo , Resultado del Tratamiento
2.
Life Sci ; 70(22): 2623-30, 2002 Apr 19.
Artículo en Inglés | MEDLINE | ID: mdl-12269389

RESUMEN

Although dehydroepiandrosterone (DHEA) is recognized as one of the major adrenal androgens, its precise physiological role in the human endocrine system remains to be elucidated. In particular, the effect of DHEA on carcinogenesis has not been fully characterized. We undertook this study to determine whether DHEA has a chemopreventative effect on the precursors of colon cancer in a murine model of azoxymethane (AOM)-induced aberrant crypt foci (ACF). The number of ACF was significantly decreased in mice treated with 0.4% (p < 0.001) and 0.8% DHEA (p < 0.001), but there were no significant differences between DHEA-treated and control mice in terms of the ACF size, 3-catenin expression or level of dysplasia. This is the first study of colon cancer carcinogenesis demonstrating that DHEA treatment can decrease the number of ACF without apparently modifying their malignant potential. These data strongly suggest that DHEA might be a potential chemopreventative agent against human colon cancer.


Asunto(s)
Adyuvantes Inmunológicos/farmacología , Neoplasias del Colon/prevención & control , Deshidroepiandrosterona/farmacología , Lesiones Precancerosas/prevención & control , Animales , Azoximetano/toxicidad , Carcinógenos/toxicidad , Quimioprevención , Neoplasias del Colon/inducido químicamente , Neoplasias del Colon/patología , Proteínas del Citoesqueleto/metabolismo , Dieta , Femenino , Técnicas para Inmunoenzimas , Mucosa Intestinal/efectos de los fármacos , Ratones , Ratones Endogámicos BALB C , Lesiones Precancerosas/inducido químicamente , Lesiones Precancerosas/patología , Transactivadores/metabolismo , beta Catenina
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