Literature DB >> 16410116

Effect of corticosteroid therapy on outcomes in biliary atresia after Kasai portoenterostomy.

Mauricio A Escobar1, Colleen L Jay, Ronald M Brooks, Karen W West, Frederick J Rescorla, Jean P Molleston, Jay L Grosfeld.   

Abstract

PURPOSE: This study tests the hypothesis that steroid administration improves the outcome of biliary atresia (BA) by evaluating the efficacy of postoperative steroid use on surgical outcomes in infants with BA.
METHODS: Steroid use and outcomes in patients with BA were retrospectively analyzed at a tertiary pediatric hospital. Institutional review board approval was obtained.
RESULTS: Kasai portoenterostomy (PE) was performed in 43 patients with BA treated from 1992 to 2004 (16 boys and 27 girls). Twenty-one PE patients received steroids and 22 did not. Portoenterostomy was successful in 24 patients (55.8%) with consistent serum bilirubin less than 2 mg/dL. Sixteen (66%) received postoperative steroids. A normal postoperative bilirubin was achieved at 6 months in 16 (76%) of 21 patients with steroids compared with 8 (37%) of 22 in untreated controls (Fisher's Exact test, P = .01). Of the 43 patients, 19 (44%) required liver transplantation, including 7 (37%) of 19 with steroids vs 12 (63%) of 19 without (P = .2). Twenty-eight infants developed cholangitis (fever with and without changes in hepatic function): 25 after PE and 3 after transplant. Of the 25, 12 (48%) received steroids. Seven died (16%) (range, 7 months to 4 years): 2 while awaiting transplantation (received steroids) and 5 after transplantation (1 received steroids and 4 were untreated). Survival was 86% (18/21) in patients with steroids and 82% (18/22) in those without. Transplant survival (74%) was comparable to previously reported historical controls (82%).
CONCLUSIONS: The Kasai PE continues to be the procedure of choice in infants with BA younger than 3 months. A significantly improved clearance of postoperative jaundice and lower serum bilirubin levels were observed in patients receiving steroids. However, steroids had no effect on the incidence of cholangitis, need for liver transplantation, and overall survival. A prospective study with standardized dose and length of steroid administration and longer period of follow-up is necessary to more accurately assess the effectiveness of steroids after PE.

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Year:  2006        PMID: 16410116     DOI: 10.1016/j.jpedsurg.2005.10.072

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  22 in total

1.  Corticosteroid treatment in biliary atresia: Tonic or toast?

Authors:  Ronald J Sokol
Journal:  Hepatology       Date:  2007-12       Impact factor: 17.425

Review 2.  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 3.  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

4.  Evaluating patients' outcome post-Kasai operation: a 19-year experience with modification of the hepatic portoenterostomy and applying a novel steroid therapy regimen.

Authors:  Tatsuya Suzuki; Takashi Hashimoto; Satoshi Kondo; Yoko Sato; Mohamed Hamed Hussein
Journal:  Pediatr Surg Int       Date:  2010-06-30       Impact factor: 1.827

5.  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

Review 6.  Current management of biliary atresia.

Authors:  Deirdre A Kelly; Mark Davenport
Journal:  Arch Dis Child       Date:  2007-09-18       Impact factor: 3.791

7.  Evaluation of a standardized protocol in the use of steroids after Kasai operation.

Authors:  Ho Yu Chung; Kenneth Kak Yuen Wong; Lawrence Cheun Leung Lan; Paul Kwong Hang Tam
Journal:  Pediatr Surg Int       Date:  2008-08-05       Impact factor: 1.827

Review 8.  Biliary atresia.

Authors:  Giorgina Mieli-Vergani; Diego Vergani
Journal:  Semin Immunopathol       Date:  2009-06-17       Impact factor: 9.623

Review 9.  Current concept about postoperative cholangitis in biliary atresia.

Authors:  Yi Luo; Shan Zheng
Journal:  World J Pediatr       Date:  2008-02       Impact factor: 2.764

10.  Multicenter randomized trial of postoperative corticosteroid therapy for biliary atresia.

Authors:  Masaki Nio; Toshihiro Muraji
Journal:  Pediatr Surg Int       Date:  2013-11       Impact factor: 1.827

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