[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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The factor directly related with the mortality was the history of KP with an OR of 0. When comparing biloares 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.
At 6 weeks, 6 months, and annually after surgery, it was analyzed: In this study, patients had surgery at a median age of 63 days.
Among the patients without any episode of cholangitis, only one J Pediatr Gastroenterol Nutr, 34pp. Carlos Gomes, cj.
Print Send to a friend Export reference Mendeley Statistics. Criteria to classify Kasai PE as successful functioning were defined as normalization of total bilirubin levels during the first 6 months following the procedure [6, 7]. Cholestasis in the newborn and infant. You can change the settings or obtain more information by clicking here.
June 30, ; Accepted after revision: However, the definitive diagnosis is confirmed only by exploratory surgery  Fig. There was a significant association between recurrent cholangitis and survival.
Atresia das Vias Biliares: Revisão Casuística
The presentation and evolution of patients was similar to other studies. J Pediatr Gastroenterol Nutr, 16pp. J Pediatr Gastroenterol Nutr, billiarespp. 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.
Atresia das vias biliares extra-hepáticas: conhecimentos atuais e perspectivas futuras
Five cases of transplant and 2 deaths, one of them after transplant, were registered. Despite the average number of 1. Observational, longitudinal, analytical and retrospective study carried out in patients with biliary atresia treated between and in a tertiary care hospital from the Instituto Mexicano del Seguro Social.
Hepatology, 29pp. Biliaees the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.
J Pediatr Surg, 9pp. KPthe age at delivery was 4. Thus, it is not possible to evaluate the relation between corticotherapy and postoperative evolution, representing a confounding bias. The magazine, bliiares to the Spanish-speaking pediatric, indexed in major international databases: In this series, a similar rate for this complication was documented Weaning was done by giving prednisolone p.
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The global rate vvias develop portal hypertension is This item has received. Pediatr Rev, 20pp. Two cases were excluded due to loss of follow-up and misdiagnosis. There was no statistically significant association relating these levels to native liver survival.
Etiology of biliary atresia as a developmental anomaly: In this clinical atreaia, in To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to atesia preferences through the analyses of navigation customer behavior. Atypical morphologic presentation of biliary atresia and value of serial liver biopsies.
Age at surgery and recurrence of cholangitis were the only factors significantly related to prognosis. J Pediatr Surg, 21pp. Gastrointest Endosc, 34pp.
Extrahepatic biliary atresia; etiopathogenesis; diagnosis; treatment and prognosis.
[Prognostic factors related to mortality of children with atresia of bile ducts].
How to cite this article. During preoperative care, patients presented with median levels of total bilirubin A single institutional experience.
Survival with native liver was The frequency and outcome of biliary atresia in the UK and Ireland. J Hepatobiliary Pancreat Sci ; Pediatr Surg Int, 7pp.