[Prognostic factors related to mortality of children with atresia of bile ducts]. Publisher: Introducción: la atresia de vías biliares (AVB) es el resultado final de un. Atresia de vías biliares vs. Hepatitis neonatal por citomegalovirus y toxoplasmosis, ¿patologías coexistentes o relación causa efecto?. Biliary Atresia – Clinical Series. Atresia das Vias Biliares – Revisão Casuística. Bárbara Netoa, Mariana Borges-Diasa, Eunice Trindadeb, José Estevão-Costaa, .

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Full text is only aviable in PDF. The objective was to identify factors associated with mortality in children with BA. Pediatr Infect Dis J, 13pp. Surgery,pp.

Experiences with MARS liver support therapy in liver failure: Pediatr Surg Int, 7pp. There was no statistically significant association relating these levels to native liver survival. Among those patients who had other associated malformations 5only biliarees needed liver transplant. CiteScore measures average citations received per document published.

Atresia das vias biliares extra-hepáticas: conhecimentos atuais e perspectivas futuras

Global survival rate is Prognosis of biliary atresia in the era of liver transplantation: Clin Res Hepatol Gastroenterol ; The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas buliares pediatrics. J Pediatr Gastroenterol Nutr, 4pp.


The kasai procedure in the treatment of biliary atresia. Out of the possible complications, the most common are cholangitis, portal hypertension, and cirrhosis [1]. J Pediatr Rio J ; J Hepatobiliary Pancreat Ztresia ; The presentation and evolution of patients was similar to other studies.

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Pediatr Clin North Am, 35pp. J Pediatr Gastroenterol Nutr, 34pp. Association between HLA and extrahepatic biliary atresia. International incidence and outcomes of biliary atresia. Nonetheless, there was a statistically significant association between the development of multiple cholangitis episodes and the survival prognosis, which is in accordance to the literature [6, 7], where it is thought that the recurrence of this viqs is an important prognostic factor bilaires it comes to the evolution of this disease.

Portal hypertension diagnosis was considered when at least two of the following features were present: As to its etiology, cytomegalovirus, reovirus and rotavirus have been widely investigated as possible triggers of the immunomediated obstruction of the biliary tree.

It was noticed that, during the period of this study, vas hepatobiliary scintigraphy lost relevance, MRCP gained some importance bilaires a diagnostic method. Continuing navigation will be considered as acceptance of this use. Extrahepatic biliary atresia is still the major indication for pediatric liver transplantation, and to change this scenario some more light should be shed upon the etiopathogenesis of biliary atresia in different disease phenotypes.


Biliary biliarew and survival into adulthood without transplantation: The prognosis of children with BA remains gloomy because they are diagnosed in late stages. Descriptive, observational, and retrospective study, including the patients with biliary atresia, diagnosed and treated between January 1, and December 31, A year UNOS review of mortality and risk factors in young children awaiting liver transplantation.

Atresia de vías biliares | Anales de Pediatría (English Edition)

J Paediatr Gastroenterol Nutr, 34pp. A descriptive statistical analysis was made, with measures of both central and dispersion tendency.

Pediatric gastrointestinal disease, 3rd ed, pp. J Clin Gastroenterol ; Description and study of risk factors for the diagnostic Pediatric Bilires, 7 ed: An Esp Pediatr, 26pp.

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Arch Dis Child ; French national study from to Thus, atreia is not possible to evaluate the relation between corticotherapy and postoperative evolution, representing a confounding bias. The global rate to develop portal hypertension is During follow-up, 11 patients