Literature DB >> 11174620

Is the Kasai operation still indicated in children older than 3 months diagnosed with biliary atresia?

C Chardot1, M Carton, N Spire-Bendelac, C Le Pommelet, J Golmard, R Reding, B Auvert.   

Abstract

OBJECTIVES: The prognosis of hepatoportoenterostomy (the Kasai operation) for biliary atresia worsens when the age at surgery increases. This study examines whether the Kasai operation remains justified after 3 months of life. STUDY
DESIGN: Records for all patients with biliary atresia living in France and born in the years 1986 to 1996 were reviewed, and patients were classified into 3 groups: group 1 (n = 30), no contraindication to the Kasai operation, but orientation to de novo transplantation; group 2 (n = 380), age at Kasai operation <90 days; and group 3 (n = 60), age at Kasai operation > or =90 days. Survival with native liver, survival after liver transplantation, and overall survival (Kaplan-Meier method) were compared by using the log-rank test.
RESULTS: Five-year (10-year) survival with native liver was 35% (30%) in group 2 and 25% (22%) in group 3 (P =.03). Five-year overall survival was 57%, 74%, and 55% in groups 1, 2, and 3, respectively (P =.003). Poor results in groups 1 and 3 were mainly due to increased pre-transplantation mortality, but survival after transplantation was not significantly different in the 3 groups.
CONCLUSIONS: Performance of the Kasai operation after 3 months of age is justified in selected cases, because it may obviate liver transplantation. Preoperative evaluation should exclude patients with advanced liver disease for whom liver transplantation should not be delayed.

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Year:  2001        PMID: 11174620     DOI: 10.1067/mpd.2001.111276

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  18 in total

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2.  Bone marrow mononuclear stem cell infusion improves biochemical parameters and scintigraphy in infants with biliary atresia.

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Review 4.  Biliary atresia: recent progress.

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Journal:  J Clin Gastroenterol       Date:  2008-07       Impact factor: 3.062

5.  Outcomes of late Kasai portoenterostomy in biliary atresia: a single-center experience.

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Review 6.  Biliary atresia: interdisciplinary initiatives focus on a rare disease.

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7.  Early diagnosis of extrahepatic biliary atresia in an open-access medical system.

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8.  Extrahepatic biliary atresia: Correlation of histopathology and liver function tests with surgical outcomes.

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9.  Biliary atresia: 50 years after the first kasai.

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Journal:  ISRN Surg       Date:  2012-12-06

10.  Diagnostic value of anti-smooth muscle antibodies and liver enzymes in differentiation of extrahepatic biliary atresia and idiopathic neonatal hepatitis.

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