[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, .

Author: Mektilar Dataur
Country: Ecuador
Language: English (Spanish)
Genre: Marketing
Published (Last): 3 July 2005
Pages: 80
PDF File Size: 11.69 Mb
ePub File Size: 8.52 Mb
ISBN: 285-4-66472-512-1
Downloads: 43471
Price: Free* [*Free Regsitration Required]
Uploader: Daijar

The presentation and evolution of patients was similar to other studies. Biliary atresia splenic malformation syndromes: However, it is not consensual that it is related to worse prognosis [8, 16]. Experiences with MARS liver support therapy in liver failure: J Pediatr Surg, 9pp.

There was a problem providing the content you requested

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

Clin Perinatol, 23pp. Evaluation of liver disease in the pediatric patient. The biliary atresia BA is the end result of a destructive and idiopathic inflammatory process affecting the intrahepatic and extrahepatic bile ducts, leading to fibrosis and biliary cirrhosis.


The global rate to develop portal hypertension is There was only one case in which the exploratory surgery did not confirm the diagnosis of biliary atresia.

Eur J Pediatr Surg, 8pp.

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

Portal hypertension diagnosis was considered when at least two of the following features were present: During follow-up, 11 patients Hepatology, 29pp. J Pediatr Gastroenterol Niliares ; Bilires to cite this article. Extrahepatic biliary atresia; etiopathogenesis; diagnosis; treatment and prognosis.

In order to calculate the postoperative native liver survival rates, Kaplan-Meier method was used, assuming it started at the time of Kasai PE and ended at the time of death or hepatic transplant.

The future role of hepatic portoenterostomy as treatment of biliary atresia. Eur J Pediatr ; Moreover, a portal bilares development rate Preoperative evaluation may include: Future research into the role of interferon-gamma and of other cytokines is necessary in order to assess whether these aspects should be potential targets for therapeutic xtresia. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

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.


Referring to preoperative evaluation, it was analyzed: ERCP in the diagnosis of extrahepatic biliary atresia. J Pediatr Gastroenterol Buliares, 16pp. To improve our services and products, we arresia “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Endoscopic retrograde cholangiography in the diagnosis of biliary malformations in children.

[Prognostic factors related to mortality of children with atresia of bile ducts].

The prognosis of children with BA remains gloomy because they are diagnosed in late stages. When comparing the groups with and without KP, the lower age at the time of delivery, the age of diagnosis, a lower score on the PELD score and the Child-Pugh for the group with Kasai were statistically significant.

Hospital Infantil La Fe.

Lancet,pp. The most important factor associated with mortality in these patients is to perform KP. A plea for surgical intervention within the first two months of life in infants with persistent cholestasis.