Literature DB >> 23402746

Improving outcomes of biliary atresia: French national series 1986-2009.

Christophe Chardot1, Chantal Buet, Marie-Odile Serinet, Jean-Louis Golmard, Alain Lachaux, Bertrand Roquelaure, Frédéric Gottrand, Pierre Broué, Alain Dabadie, Frédéric Gauthier, Emmanuel Jacquemin.   

Abstract

BACKGROUND & AIMS: This study analyses the prognosis of biliary atresia (BA) in France since liver transplantation (LT) became widely available.
METHODS: The charts of all BA patients living in France and born between 1986 and 2009 were reviewed. Patients were divided into 3 cohorts according to their years of birth: 1986-1996, 1997-2002, and 2003-2009.
RESULTS: 1107 BA children were identified, 990 born in metropolitan France (incidence 1/18,400 live births). Kasai operation was performed in 1044 (94%), leading to complete clearance of jaundice (total serum bilirubin ≤ 20 μmol/L) in 38% of patients. Survival with native liver (SNL) after Kasai operation was 40%, 36%, and 30% at 5, 10, and 20 years, stable in the 3 cohorts. Median age at Kasai operation was 59 days, unchanged over time. Twenty-year SNL was 39%, 32%, 28%, and 19% after Kasai operation performed in the first, second, third months of life or thereafter (p=0.0002). 588 children underwent 692 LTs. Mortality without transplantation decreased over time: 16%, 7%, and 4% in the 3 cohorts (p<0.0001). Survival after transplantation was 83%, 82%, and 77% at 5, 10, and 20 years in the whole series. Five-year post-transplant survival was 75%, 90%, and 89% in the 3 cohorts (p<0.0001). In the whole series, overall BA patient survival was 81%, 80%, and 77% at 5, 10, and 20 years. Five-year BA patient overall survival increased over time: 72%, 88%, and 89% in the 3 cohorts (p<0.0001).
CONCLUSIONS: BA patients currently have an 89% live expectancy, and a 30% chance to reach adulthood without transplantation. Early Kasai operation, without age threshold, reduces the need for liver transplantation until adulthood.
Copyright © 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23402746     DOI: 10.1016/j.jhep.2013.01.040

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  53 in total

1.  Reduction of the ages at diagnosis and operation of biliary atresia in Taiwan: A 15-year population-based cohort study.

Authors:  Jen-Shyang Lin; Solomon Chih-Cheng Chen; Chin-Li Lu; Hung-Chang Lee; Chun-Yan Yeung; Wai-Tao Chan
Journal:  World J Gastroenterol       Date:  2015-12-14       Impact factor: 5.742

2.  The Canadian Biliary Atresia Registry: Improving the care of Canadian infants with biliary atresia.

Authors:  Alison E Butler; Richard A Schreiber; Natalie Yanchar; Sherif Emil; Jean-Martin Laberge
Journal:  Paediatr Child Health       Date:  2016-04       Impact factor: 2.253

3.  Long-term results of biliary atresia in the era of liver transplantation.

Authors:  Sanghoon Lee; Hyojun Park; Suk-Bae Moon; Soo-Min Jung; Jong Man Kim; Choon Hyuck David Kwon; Sung Joo Kim; Jae-Won Joh; Jeong-Meen Seo; Suk-Koo Lee
Journal:  Pediatr Surg Int       Date:  2013-08-15       Impact factor: 1.827

4.  [Value of serum gamma-glutamyl transpeptidase combined with direct bilirubin in the diagnosis of biliary atresia in infants].

Authors:  Hai-Yan Fu; Rui-Qin Zhao; Ge-Lan Bai; Chun-Lan Yin; Run-Kai Yin; Hai-Hua Li; Wei-Na Shi; Ya-Li Liu; Li-Juan Cheng; Xiao-Yun Jia; Gui-Gui Li; Shi-Guang Zhao
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2019-12

Review 5.  Pathogenesis of biliary atresia: defining biology to understand clinical phenotypes.

Authors:  Akihiro Asai; Alexander Miethke; Jorge A Bezerra
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2015-05-26       Impact factor: 46.802

Review 6.  [Biliary atresia and congenital cholestatic syndromes : Characteristics before, after and during transition].

Authors:  N Junge; J Dingemann; C Petersen; M P Manns; N Richter; J Klempnauer; U Baumann; A Schneider
Journal:  Internist (Berl)       Date:  2018-11       Impact factor: 0.743

7.  Comparison of laparoscopic portoenterostomy and open portoenterostomy for the treatment of biliary atresia.

Authors:  Yanan Li; Jinran Gan; Chuan Wang; Zhicheng Xu; Yiyang Zhao; Yi Ji
Journal:  Surg Endosc       Date:  2019-06-12       Impact factor: 4.584

Review 8.  Recent developments in diagnostics and treatment of neonatal cholestasis.

Authors:  Amy G Feldman; Ronald J Sokol
Journal:  Semin Pediatr Surg       Date:  2020-07-23       Impact factor: 2.754

9.  The effect of APTR, Fn14 and CD133 expressions on liver fibrosis in biliary atresia patients.

Authors:  Akhmad Makhmudi; Reinaldo Supanji; Bayu Pratama Putra
Journal:  Pediatr Surg Int       Date:  2019-09-23       Impact factor: 1.827

10.  Liver transplantation for biliary atresia: A single-center study from mainland China.

Authors:  Qi-Gen Li; Ping Wan; Jian-Jun Zhang; Qi-Min Chen; Xiao-Song Chen; Long-Zhi Han; Qiang Xia
Journal:  World J Gastroenterol       Date:  2015-08-28       Impact factor: 5.742

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