The improved outlook for biliary atresia with corticosteroid therapy
Controversy exists regarding the efficacy of corticosteroids on bile flow after Kasai portoenterostomy in biliary atresia (BA). Fourteen patients who had BA and underwent Kasai portojejunostomy between November 1990 and March 1996 were subject of this study. Corticosteroid therapy (“blast” type) was...
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Published in | J Pediatr Surg Vol. 32; no. 7; pp. 1103 - 1107 |
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Main Authors | , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.07.1997
Elsevier BV |
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ISSN | 0022-3468 1531-5037 |
DOI | 10.1016/S0022-3468(97)90408-5 |
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Abstract | Controversy exists regarding the efficacy of corticosteroids on bile flow after Kasai portoenterostomy in biliary atresia (BA). Fourteen patients who had BA and underwent Kasai portojejunostomy between November 1990 and March 1996 were subject of this study. Corticosteroid therapy (“blast” type) was used for inadequate bile drainage. Corticosteroid support was unnecessary in one patient with good bile drainage, and corticosteroids were aggressively used in the remaining 13 patients. Two patients who had no response to an initial blast subsequently responded and now are doing well. The remaining 11 patients responded to corticosteroids with varying degrees. Three had a limited response, and two ultimately underwent liver transplantation. There was one death caused by subdural hematoma. Three had an excellent initial response. However, one subsequently deteriorated because of intractable cholangitis, requiring liver transplantation. Ten survivors with native liver are anicteric with satisfactory growth and quality of life. Aggressive corticosteroid therapy is an important part of the management after Kasai portoenterostomy. The initial response to steroids does not necessarily reflect the final outcome. |
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AbstractList | Controversy exists regarding the efficacy of corticosteroids on bile flow after Kasai portoenterostomy in biliary atresia (BA). Fourteen patients who had BA and underwent Kasai portojejunostomy between November 1990 and March 1996 were subject of this study. Corticosteroid therapy (“blast” type) was used for inadequate bile drainage. Corticosteroid support was unnecessary in one patient with good bile drainage, and corticosteroids were aggressively used in the remaining 13 patients. Two patients who had no response to an initial blast subsequently responded and now are doing well. The remaining 11 patients responded to corticosteroids with varying degrees. Three had a limited response, and two ultimately underwent liver transplantation. There was one death caused by subdural hematoma. Three had an excellent initial response. However, one subsequently deteriorated because of intractable cholangitis, requiring liver transplantation. Ten survivors with native liver are anicteric with satisfactory growth and quality of life. Aggressive corticosteroid therapy is an important part of the management after Kasai portoenterostomy. The initial response to steroids does not necessarily reflect the final outcome. Controversy exists regarding the efficacy of corticosteroids on bile flow after Kasai portoenterostomy in biliary atresia (BA). Fourteen patients who had BA and underwent Kasai portojejunostomy between November 1990 and March 1996 were subject of this study. Corticosteroid therapy ("blast" type) was used for inadequate bile drainage. Corticosteroid support was unnecessary in one patient with good bile drainage, and corticosteroids were aggressively used in the remaining 13 patients. Two patients who had no response to an initial blast subsequently responded and now are doing well. The remaining 11 patients responded to corticosteroids with varying degrees. Three had a limited response, and two ultimately underwent liver transplantation. There was one death caused by subdural hematoma. Three had an excellent initial response. However, one subsequently deteriorated because of intractable cholangitis, requiring liver transplantation. Ten survivors with native liver are anicteric with satisfactory growth and quality of life. Aggressive corticosteroid therapy is an important part of the management after Kasai portoenterostomy. The initial response to steroids does not necessarily reflect the final outcome.Controversy exists regarding the efficacy of corticosteroids on bile flow after Kasai portoenterostomy in biliary atresia (BA). Fourteen patients who had BA and underwent Kasai portojejunostomy between November 1990 and March 1996 were subject of this study. Corticosteroid therapy ("blast" type) was used for inadequate bile drainage. Corticosteroid support was unnecessary in one patient with good bile drainage, and corticosteroids were aggressively used in the remaining 13 patients. Two patients who had no response to an initial blast subsequently responded and now are doing well. The remaining 11 patients responded to corticosteroids with varying degrees. Three had a limited response, and two ultimately underwent liver transplantation. There was one death caused by subdural hematoma. Three had an excellent initial response. However, one subsequently deteriorated because of intractable cholangitis, requiring liver transplantation. Ten survivors with native liver are anicteric with satisfactory growth and quality of life. Aggressive corticosteroid therapy is an important part of the management after Kasai portoenterostomy. The initial response to steroids does not necessarily reflect the final outcome. |
Author | Muraji, Toshihiro Higashimoto, Yasuyuki |
Author_xml | – sequence: 1 givenname: Toshihiro surname: Muraji fullname: Muraji, Toshihiro organization: Department of Surgery, Kobe Children's Hospital, Kobe, Japan – sequence: 2 givenname: Yasuyuki surname: Higashimoto fullname: Higashimoto, Yasuyuki organization: Department of Surgery, Kobe Children's Hospital, Kobe, Japan |
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References_xml | – volume: 9 start-page: 285 year: 1995 end-page: 293 ident: BIB2 article-title: Progress of the treatment of biliary aresia publication-title: World J Surg – volume: 17 start-page: 894 year: 1982 end-page: 900 ident: BIB10 article-title: Surgical management of intractable cholangitis following successful Kasai procedure publication-title: J Pediatr Surg – volume: 25 start-page: 149 year: 1990 end-page: 152 ident: BIB1 article-title: The therapy of biliary atresia combining the Kasai portoenterostomy with liver transplantation: A single-center experience publication-title: J Pediatr Surg – volume: 29 start-page: 896 year: 1994 end-page: 899 ident: BIB5 article-title: Extensive dissection at the porta hepatis for biliary atresia publication-title: J Pediatr Surg – volume: 28 start-page: 1063 year: 1979 end-page: 1066 ident: BIB11 article-title: Bile flow in response to pharmacologic agents: Hepatic DNA as a reference standard publication-title: Biochem Pharmacol – volume: 14 start-page: 27 year: 1979 end-page: 32 ident: BIB3 article-title: Technical aspects of hepatic portal dissection in biliary atresia publication-title: J Pediatr Surg – volume: 20 start-page: 693 year: 1985 end-page: 695 ident: BIB8 article-title: Corticosteroid therapy in biliary atresia publication-title: J Pediatr Surg – volume: 18 start-page: 784 year: 1983 end-page: 793 ident: BIB4 article-title: Extended dissection of the porta hepatis and creation of an intussuscepted ileocolic conduit for biliary atresia publication-title: J Pediatr Surg – volume: 15 start-page: 811 year: 1980 end-page: 816 ident: BIB6 article-title: Percutaneous transhepatic cholangiodrainage after hepatic portoenterostomy for biliary atresia publication-title: J Pediatr Surg – volume: 210 start-page: 289 year: 1989 end-page: 296 ident: BIB7 article-title: The surgery of biliary atresia publication-title: Ann Surg – volume: 2 start-page: 571 year: 1978 end-page: 580 ident: BIB9 article-title: Technique and results of operative management of biliary atresia publication-title: World J Surg – volume: 17 start-page: 894 year: 1982 ident: 10.1016/S0022-3468(97)90408-5_BIB10 article-title: Surgical management of intractable cholangitis following successful Kasai procedure publication-title: J Pediatr Surg doi: 10.1016/S0022-3468(82)80463-6 – volume: 18 start-page: 784 year: 1983 ident: 10.1016/S0022-3468(97)90408-5_BIB4 article-title: Extended dissection of the porta hepatis and creation of an intussuscepted ileocolic conduit for biliary atresia publication-title: J Pediatr Surg doi: 10.1016/S0022-3468(83)80024-4 – volume: 15 start-page: 811 year: 1980 ident: 10.1016/S0022-3468(97)90408-5_BIB6 article-title: Percutaneous transhepatic cholangiodrainage after hepatic portoenterostomy for biliary atresia publication-title: J Pediatr Surg doi: 10.1016/S0022-3468(80)80285-5 – volume: 210 start-page: 289 year: 1989 ident: 10.1016/S0022-3468(97)90408-5_BIB7 article-title: The surgery of biliary atresia publication-title: Ann Surg doi: 10.1097/00000658-198909000-00004 – volume: 9 start-page: 285 year: 1995 ident: 10.1016/S0022-3468(97)90408-5_BIB2 article-title: Progress of the treatment of biliary aresia publication-title: World J Surg doi: 10.1007/BF01656322 – volume: 20 start-page: 693 year: 1985 ident: 10.1016/S0022-3468(97)90408-5_BIB8 article-title: Corticosteroid therapy in biliary atresia publication-title: J Pediatr Surg doi: 10.1016/S0022-3468(85)80026-9 – volume: 28 start-page: 1063 year: 1979 ident: 10.1016/S0022-3468(97)90408-5_BIB11 article-title: Bile flow in response to pharmacologic agents: Hepatic DNA as a reference standard publication-title: Biochem Pharmacol doi: 10.1016/0006-2952(79)90304-6 – volume: 14 start-page: 27 year: 1979 ident: 10.1016/S0022-3468(97)90408-5_BIB3 article-title: Technical aspects of hepatic portal dissection in biliary atresia publication-title: J Pediatr Surg doi: 10.1016/S0022-3468(79)80571-0 – volume: 29 start-page: 896 year: 1994 ident: 10.1016/S0022-3468(97)90408-5_BIB5 article-title: Extensive dissection at the porta hepatis for biliary atresia publication-title: J Pediatr Surg doi: 10.1016/0022-3468(94)90011-6 – volume: 2 start-page: 571 year: 1978 ident: 10.1016/S0022-3468(97)90408-5_BIB9 article-title: Technique and results of operative management of biliary atresia publication-title: World J Surg doi: 10.1007/BF01556048 – volume: 25 start-page: 149 year: 1990 ident: 10.1016/S0022-3468(97)90408-5_BIB1 article-title: The therapy of biliary atresia combining the Kasai portoenterostomy with liver transplantation: A single-center experience publication-title: J Pediatr Surg doi: 10.1016/S0022-3468(05)80182-4 |
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SubjectTerms | Biliary Atresia Biliary Atresia - surgery Bilirubin Bilirubin - blood Cholangitis Cholangitis - prevention & control Cholestasis Cholestasis - prevention & control Dose-Response Relationship, Drug Female Glucocorticoids Glucocorticoids - therapeutic use Humans Infant Male Portoenterostomy, Hepatic Portoenterostomy, Hepatic - methods Postoperative Care Prednisolone Prednisolone - therapeutic use |
Title | The improved outlook for biliary atresia with corticosteroid therapy |
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