Literature DB >> 22082947

Biliary atresia in the Netherlands: outcome of patients diagnosed between 1987 and 2008.

Willemien de Vries1, Zacharias J de Langen, Henk Groen, Rene Scheenstra, Paul M J G Peeters, Jan B F Hulscher, Henkjan J Verkade.   

Abstract

OBJECTIVE: To examine the outcome of biliary atresia (BA) and to identify prognostic factors using a national database. STUDY
DESIGN: All children born between January 1987 and December 2008 who underwent the Kasai surgical procedure for BA were retrieved from the Netherlands Study Group on Biliary Atresia Registry database. Outcomes were measured in terms of clearance of jaundice (bilirubin <1.17 g/dL, or 20 μmol/L, within 6 months after surgery) and 4-year transplant-free survival. Two cohorts, one from 1987-1997 and the other from 1998-2008, were compared. Survival rates were determined using Kaplan-Meier analysis, and prognostic factors were tested with univariate and multivariate analyses.
RESULTS: Between January 1987 and December 2008, 214 patients underwent Kasai surgery for BA. In this series, the 4-year transplant-free survival was 46%±4%, and 4-year overall survival was 73%±3%. Clearance of jaundice, surgery within 60 days, and postoperative antibiotic prophylaxis use were independently associated with increased transplant-free survival. The yearly caseload per center (range, 0.5-2.1) was not correlated with transplant-free survival (r=0.024; P=.73).
CONCLUSION: During the past 2 decades, outcome parameters have remained constant and are comparable with those reported from other Western countries, despite a relatively low annual caseload per center. Timely surgical correction and postoperative antibiotic therapy were associated with a higher transplant-free survival rate. Copyright Â
© 2012 Mosby, Inc. All rights reserved.

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Year:  2011        PMID: 22082947     DOI: 10.1016/j.jpeds.2011.09.061

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


  20 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

Review 2.  [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

Review 3.  Adjuvant therapy in biliary atresia: hopelessly optimistic or potential for change?

Authors:  Mark Davenport
Journal:  Pediatr Surg Int       Date:  2017-09-22       Impact factor: 1.827

Review 4.  Biliary atresia: unity in diversity.

Authors:  Claus Petersen
Journal:  Pediatr Surg Int       Date:  2017-10-05       Impact factor: 1.827

5.  Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia.

Authors:  Benjamin L Shneider; John C Magee; Saul J Karpen; Elizabeth B Rand; Michael R Narkewicz; Lee M Bass; Kathleen Schwarz; Peter F Whitington; Jorge A Bezerra; Nanda Kerkar; Barbara Haber; Philip Rosenthal; Yumirle P Turmelle; Jean P Molleston; Karen F Murray; Vicky L Ng; Kasper S Wang; Rene Romero; Robert H Squires; Ronen Arnon; Averell H Sherker; Jeffrey Moore; Wen Ye; Ronald J Sokol
Journal:  J Pediatr       Date:  2015-12-24       Impact factor: 4.406

6.  Home-based color card screening for biliary atresia: the first steps for implementation of a nationwide newborn screening in Germany.

Authors:  Omid Madadi-Sanjani; J Blaser; G Voigt; J F Kuebler; C Petersen
Journal:  Pediatr Surg Int       Date:  2019-07-25       Impact factor: 1.827

7.  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

Review 8.  Biliary atresia: Indications and timing of liver transplantation and optimization of pretransplant care.

Authors:  Shikha S Sundaram; Cara L Mack; Amy G Feldman; Ronald J Sokol
Journal:  Liver Transpl       Date:  2017-01       Impact factor: 5.799

9.  Ductal plate malformation in patients with biliary atresia.

Authors:  Jurica Vuković; Ruža Grizelj; Katarina Bojanić; Marijana Corić; Tomislav Luetić; Stipe Batinica; Mirjana Kujundžić-Tiljak; Darrell R Schroeder; Juraj Sprung
Journal:  Eur J Pediatr       Date:  2012-09-15       Impact factor: 3.183

10.  PELD score and age as a prognostic index of biliary atresia patients undergoing Kasai portoenterostomy.

Authors:  Jinsoo Rhu; Soo-Min Jung; Yon Ho Choe; Jeong-Meen Seo; Suk-Koo Lee
Journal:  Pediatr Surg Int       Date:  2012-02-14       Impact factor: 1.827

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