Literature DB >> 18679691

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

Ho Yu Chung1, Kenneth Kak Yuen Wong, Lawrence Cheun Leung Lan, Paul Kwong Hang Tam.   

Abstract

Although the Kasai operation is still the treatment of choice for infants with biliary atresia, the long-term success rate, as defined by survival without transplantation, is only about 25-40%. It has been proposed that post-operative inflammatory changes affect the bile flow and eventually lead to cholangitis and liver failure. Recent case reports have suggested that the administration of steroids post-operatively can improve outcomes. Since 2004, our unit has adopted a strict protocol for the use of post-operative steroids for patients who undergo Kasai operation. The aim of this study is to access the early outcomes of these patients. A retrospective analysis was carried out for all patients who received Kasai operation between 1996 and 2006. For the treatment group, patients all received prednisolone at 4 mg/kg 1 week after operation as guided by protocol. The demographics and outcomes, including post operative bilirubin level, episodes of cholangitic attack, the need for early liver transplantation (transplant within 1 year of Kasai), and transplantation-free survival, were noted. Statistical analysis was done using Fisher's exact test and unpaired t-test when appropriate. A value of P < 0.05 was considered to be statistically significant. Kasai operation was performed in 30 patients (11 boys and 19 girls) during the study period. Thirteen patients received post-operative prednisolone according to protocol. The average age at operation and the mean preoperative bilirubin levels for the steroid and non-steroid group were not significantly different. A normal post-operative bilirubin (defined as bilirubin level less than 20 mumol/L) was achieved at 6 months in 7 (53.9%) patients who received steroid and 8 (47.0%) patients who did not (P = 0.71). A statistically significant reduction in the post-operative bilirubin level was also seen at 3 and 6 months in the steroid group. Early liver transplantation was required in 5 (38.5%) patients with steroid and 5 (29.4%) patients without it (P = 0.60). No significant difference in terms of cholangitic attack was observed. There was also no steroid-associated complication reported. We conclude that lower post-operative bilirubin level can be achieved with the routine use of prednisolone. However, there is no statistical improvement in terms of early liver transplantation and cholangitis. This may be attributed to the small sample size of our study population. Based on this pilot study, a multi-centre randomized trial is needed.

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Year:  2008        PMID: 18679691     DOI: 10.1007/s00383-008-2200-2

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  14 in total

1.  Postoperative corticosteroid therapy for bile drainage in biliary atresia--a nationwide survey.

Authors:  Toshihiro Muraji; Masaki Nio; Youkatsu Ohhama; Takashi Hashimoto; Tadashi Iwanaka; Hideo Takamatsu; Naomi Ohnuma; Tetsuo Kato; Ryoji Ohi
Journal:  J Pediatr Surg       Date:  2004-12       Impact factor: 2.545

2.  Randomized, double-blind, placebo-controlled trial of corticosteroids after Kasai portoenterostomy for biliary atresia.

Authors:  Mark Davenport; Mark D Stringer; Sarah A Tizzard; Patricia McClean; Giorgina Mieli-Vergani; Nedim Hadzic
Journal:  Hepatology       Date:  2007-12       Impact factor: 17.425

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

Authors:  Mauricio A Escobar; Colleen L Jay; Ronald M Brooks; Karen W West; Frederick J Rescorla; Jean P Molleston; Jay L Grosfeld
Journal:  J Pediatr Surg       Date:  2006-01       Impact factor: 2.545

4.  Immunosuppression as adjuvant therapy for biliary atresia.

Authors:  P W Dillon; E Owings; R Cilley; D Field; A Curnow; K Georgeson
Journal:  J Pediatr Surg       Date:  2001-01       Impact factor: 2.545

5.  Bile flow in response to pharmacologic agents. Hepatic DNA as a reference standard.

Authors:  P B Miner; J M Gaito
Journal:  Biochem Pharmacol       Date:  1979-04-01       Impact factor: 5.858

Review 6.  Biliary atresia.

Authors:  M Nio; R Ohi
Journal:  Semin Pediatr Surg       Date:  2000-11       Impact factor: 2.754

7.  Optimum prednisolone usage in patients with biliary atresia postportoenterostomy.

Authors:  Hiroyuki Kobayashi; Atsuyuki Yamataka; Hiroyuki Koga; Tadaharu Okazaki; Tsuyoshi Tamura; Masahiko Urao; Toshihiro Yanai; Geoffrey J Lane; Takeshi Miyano
Journal:  J Pediatr Surg       Date:  2005-02       Impact factor: 2.545

8.  Contribution of hepatic parenchymal and nonparenchymal cells to hepatic fibrogenesis in biliary atresia.

Authors:  G A Ramm; V G Nair; K R Bridle; R W Shepherd; D H Crawford
Journal:  Am J Pathol       Date:  1998-08       Impact factor: 4.307

9.  Kasai portoenterostomy: 12-year experience with a novel adjuvant therapy regimen.

Authors:  Mark D Stringer; Suzanne M Davison; Sanjay R Rajwal; Patricia McClean
Journal:  J Pediatr Surg       Date:  2007-08       Impact factor: 2.545

Review 10.  High-dose steroids, ursodeoxycholic acid, and chronic intravenous antibiotics improve bile flow after Kasai procedure in infants with biliary atresia.

Authors:  Rebecka L Meyers; Linda S Book; Molly A O'Gorman; W Daniel Jackson; Richard E Black; Dale G Johnson; Michael E Matlak
Journal:  J Pediatr Surg       Date:  2003-03       Impact factor: 2.545

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  8 in total

Review 1.  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 2.  Cholestatic liver disease in children.

Authors:  Jorge L Santos; Monique Choquette; Jorge A Bezerra
Journal:  Curr Gastroenterol Rep       Date:  2010-02

3.  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

Review 4.  Biliary disease in children.

Authors:  Matthew Goldman; Thomas Pranikoff
Journal:  Curr Gastroenterol Rep       Date:  2011-04

Review 5.  Adjuvant steroid treatment following Kasai portoenterostomy and clinical outcomes of biliary atresia patients: an updated meta-analysis.

Authors:  Min-Zhong Zhang; Peng-Cheng Xun; Ka He; Wei Cai
Journal:  World J Pediatr       Date:  2016-10-15       Impact factor: 2.764

6.  Short- and long-term outcomes after Kasai operation for type III biliary atresia: Twenty years of experience in a single tertiary Egyptian center-A retrospective cohort study.

Authors:  Emad Hamdy Gad; Yasmin Kamel; Tahany Abdel-Hameed Salem; Mohammed Abdel-Hafez Ali; Ahmed Nabil Sallam
Journal:  Ann Med Surg (Lond)       Date:  2021-01-23

7.  Effects of postoperative adjuvant steroid therapy on the outcomes of biliary atresia: A systematic review and updated meta-analysis.

Authors:  Chang-Zhen Yang; Yan Zhou; Meng Ke; Ru-Yue Gao; Shi-Ru Ye; Mei Diao; Long Li
Journal:  Front Pharmacol       Date:  2022-09-14       Impact factor: 5.988

Review 8.  Glucocorticosteroids for infants with biliary atresia following Kasai portoenterostomy.

Authors:  Athanasios Tyraskis; Christopher Parsons; Mark Davenport
Journal:  Cochrane Database Syst Rev       Date:  2018-05-14
  8 in total

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