Literature DB >> 20543720

Biliary atresia in Canada: the effect of centre caseload experience on outcome.

Richard A Schreiber1, Collin C Barker, Eve A Roberts, Steven R Martin.   

Abstract

OBJECTIVES: : Biliary atresia (BA) is a leading cause of end-stage paediatric liver disease. Standard BA treatment is sequential surgery with an initial Kasai procedure (KP) followed by liver transplant (LT) for patients who progress to liver failure. A key determinant for the post-KP patient survival with their native liver is patient age at KP (older age, poorer outcome). Recently, European studies have reported that caseload experience influences prognosis with centres managing <5 cases per year (UK) or <2 cases per year (France) having worse survival. Our study investigates the effect of caseload experience on outcomes of Canadian patients with BA. PATIENTS AND METHODS: : A national database of cases with BA, born from 1992 to 2002, was examined. Patients were grouped according to treatment centre size (A: on average <1 case per year; B: 1 to 3 cases per year; and C: >3 cases per year). Overall patient, post-KP native liver, and LT survivals were compared between centres. Outcome parameters were reevaluated for patients grouped by the largest Canadian centre (>5 cases per year) and all other centres (<5 cases per year).
RESULTS: : Two-hundred thirty patients were identified among 6 group A, 4 group B, and 2 group C centres. The overall median age at KP was 64 days. There were no significant differences in patient, post-KP native liver, or LT survivals between the sized centres and even the largest centre, with the overall 4-year post-KP native liver survival being 39%.
CONCLUSIONS: : Caseload experience does not importantly affect the outcomes for Canadian children with BA. Although outcomes in Canada are comparable to those elsewhere, national policies directed towards timely referral and earlier age at KP rather than centralisation of care are needed.

Entities:  

Mesh:

Year:  2010        PMID: 20543720     DOI: 10.1097/MPG.0b013e3181d67e5e

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  13 in total

1.  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

2.  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

3.  Biliary Atresia - Too Few, Too Many Centers.

Authors:  Jorge Amil Dias
Journal:  GE Port J Gastroenterol       Date:  2017-11-16

Review 4.  Does adjuvant steroid therapy post-Kasai portoenterostomy improve outcome of biliary atresia? Systematic review and meta-analysis.

Authors:  Ahmed Sarkhy; Richard A Schreiber; Ruth A Milner; Collin C Barker
Journal:  Can J Gastroenterol       Date:  2011-08       Impact factor: 3.522

Review 5.  Recent advances in the pathogenesis and management of biliary atresia.

Authors:  Jessica A Zagory; Marie V Nguyen; Kasper S Wang
Journal:  Curr Opin Pediatr       Date:  2015-06       Impact factor: 2.856

6.  Use of corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia: the START randomized clinical trial.

Authors:  Jorge A Bezerra; Cathie Spino; John C Magee; Benjamin L Shneider; Philip Rosenthal; Kasper S Wang; Jessi Erlichman; Barbara Haber; Paula M Hertel; Saul J Karpen; Nanda Kerkar; Kathleen M Loomes; Jean P Molleston; Karen F Murray; Rene Romero; Kathleen B Schwarz; Ross Shepherd; Frederick J Suchy; Yumirle P Turmelle; Peter F Whitington; Jeffrey Moore; Averell H Sherker; Patricia R Robuck; Ronald J Sokol
Journal:  JAMA       Date:  2014-05-07       Impact factor: 56.272

7.  The need for early Kasai portoenterostomy: a Western Pediatric Surgery Research Consortium study.

Authors:  Lorraine I Kelley-Quon; Eveline Shue; Rita V Burke; Caitlin Smith; Karen Kling; Elaa Mahdi; Shadassa Ourshalimian; Michael Fenlon; Matthew Dellinger; Stephen B Shew; Justin Lee; Benjamin Padilla; Thomas Inge; Jonathan Roach; Ahmed I Marwan; Katie W Russell; Romeo Ignacio; Elizabeth Fialkowski; Amar Nijagal; Cecilia Im; Kenneth S Azarow; Daniel J Ostlie; Kasper Wang
Journal:  Pediatr Surg Int       Date:  2021-12-02       Impact factor: 1.827

8.  Primary Liver Transplantation vs. Transplant after Kasai Portoenterostomy for Infants with Biliary Atresia.

Authors:  Caroline P Lemoine; John P LeShock; Katherine A Brandt; Riccardo Superina
Journal:  J Clin Med       Date:  2022-05-26       Impact factor: 4.964

9.  Laparoscopic versus open Kasai portoenterostomy in infant with biliary atresia: a retrospective review on the 5-year native liver survival.

Authors:  Kin Wai E Chan; Kim Hung Lee; Siu Yan B Tsui; Yuen Shan Wong; Kit Yi K Pang; Jennifer Wai Cheung Mou; Yuk Him Tam
Journal:  Pediatr Surg Int       Date:  2012-09-18       Impact factor: 1.827

10.  The Impact of Hospital/Surgeon Volume on Acute Renal Failure and Mortality in Liver Transplantation: A Nationwide Cohort Study.

Authors:  Chih-Wen Cheng; Fu-Chao Liu; Jr-Rung Lin; Yung-Fong Tsai; Hsiu-Pin Chen; Huang-Ping Yu
Journal:  PLoS One       Date:  2016-10-05       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.