Management of biliary atresia in the liver transplantation era: A 15-year, single-center experience
Background/Purpose: The aim of this study was to address the perioperative aspects of hepatoportoenterostomy (HPE) for biliary atresia (BA), through the study of a 15-year, single-center experience of the management of this disease. Methods: One hundred twenty-seven patients were divided into three...
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Veröffentlicht in: | Journal of pediatric surgery 1998, Vol.33 (1), p.115-118 |
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creator | Maksoud, Joäo Gilberto Fauza, Dario O Silva, Marcos M Porta, Gilda Miura, Irene Zerbini, Maria Claudia N |
description | Background/Purpose:
The aim of this study was to address the perioperative aspects of hepatoportoenterostomy (HPE) for biliary atresia (BA), through the study of a 15-year, single-center experience of the management of this disease.
Methods:
One hundred twenty-seven patients were divided into three groups, depending on the variant of HPE performed: group A (n = 53) underwent HPE with external diversion of the Roux-en-Y anastomosis; group B (n = 54) underwent HPE with a long (35 to 40cm) Roux-en-Y anastomosis, without diversion; and group C (n =20) underwent the same kind of HPE as group B, but with a modified, “super extensive” dissection of the porta hepatitis. Eleven children in group B had an intussusception type antireflux valve in the Roux-en-Y loop. The porta hepatitis of 105 children was histologically classified in type I to III and correlated with rate of postoperative bile flow and age at surgery. Liver transplantation was performed after HPE in 20 patients.
Results:
Overall, biliary drainage was achieved in 72.5% of the children after HPE and 26.8% of all patients became jaundice free. Porta hepatitis type III was associated with a significantly higher rate of biliary drainage post-HPE then types I and II. There was no difference in the rate of bile drainage, relative number of jaundice-free patients, and mean number of episodes of cholangitis per year among surgical groups A, B, C. In group A, 43.7% of the patients had complications related to the stoma. The actuarial survival of children who underwent HPE followed by liver transplantation was 85%.
Conclusions:
(1) There is no correlation between type of porta hepatis and age at surgery for BA; (2) type III porta hepatis is associated with higher rates of bile drainage post-HPE; (3) children older than 16 weeks with BA should still be considered for HPE; (4) in these older patients, factors other than the type of porta hepatis, possibly the degree of liver damage, play a role in the lower rate of bile drainage observed; (5) external diversion of the Roux-en-Y in HPE is not beneficial and is detrimental because of stoma-related complications; (6) an antireflux valve in the Roux-en-Y loop does not reduce the incidence of cholangitis post-HPE; (7) Surgical reexploration does not restore biliary drainage; and (8) sequential therapy with HPE followed by liver transplantation remains the treatment of choice for BA. |
doi_str_mv | 10.1016/S0022-3468(98)90375-X |
format | Article |
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The aim of this study was to address the perioperative aspects of hepatoportoenterostomy (HPE) for biliary atresia (BA), through the study of a 15-year, single-center experience of the management of this disease.
Methods:
One hundred twenty-seven patients were divided into three groups, depending on the variant of HPE performed: group A (n = 53) underwent HPE with external diversion of the Roux-en-Y anastomosis; group B (n = 54) underwent HPE with a long (35 to 40cm) Roux-en-Y anastomosis, without diversion; and group C (n =20) underwent the same kind of HPE as group B, but with a modified, “super extensive” dissection of the porta hepatitis. Eleven children in group B had an intussusception type antireflux valve in the Roux-en-Y loop. The porta hepatitis of 105 children was histologically classified in type I to III and correlated with rate of postoperative bile flow and age at surgery. Liver transplantation was performed after HPE in 20 patients.
Results:
Overall, biliary drainage was achieved in 72.5% of the children after HPE and 26.8% of all patients became jaundice free. Porta hepatitis type III was associated with a significantly higher rate of biliary drainage post-HPE then types I and II. There was no difference in the rate of bile drainage, relative number of jaundice-free patients, and mean number of episodes of cholangitis per year among surgical groups A, B, C. In group A, 43.7% of the patients had complications related to the stoma. The actuarial survival of children who underwent HPE followed by liver transplantation was 85%.
Conclusions:
(1) There is no correlation between type of porta hepatis and age at surgery for BA; (2) type III porta hepatis is associated with higher rates of bile drainage post-HPE; (3) children older than 16 weeks with BA should still be considered for HPE; (4) in these older patients, factors other than the type of porta hepatis, possibly the degree of liver damage, play a role in the lower rate of bile drainage observed; (5) external diversion of the Roux-en-Y in HPE is not beneficial and is detrimental because of stoma-related complications; (6) an antireflux valve in the Roux-en-Y loop does not reduce the incidence of cholangitis post-HPE; (7) Surgical reexploration does not restore biliary drainage; and (8) sequential therapy with HPE followed by liver transplantation remains the treatment of choice for BA.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/S0022-3468(98)90375-X</identifier><identifier>PMID: 9473114</identifier><identifier>CODEN: JPDSA3</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Actuarial Analysis ; Anastomosis, Roux-en-Y - methods ; Biliary Atresia - epidemiology ; Biliary Atresia - surgery ; Biological and medical sciences ; Case-Control Studies ; Child ; Child, Preschool ; Drainage ; Humans ; Infant ; Liver Transplantation ; Liver, biliary tract, pancreas, portal circulation, spleen ; Medical sciences ; Portoenterostomy, Hepatic - methods ; Predictive Value of Tests ; Retrospective Studies ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the digestive system ; Time Factors ; Treatment Outcome</subject><ispartof>Journal of pediatric surgery, 1998, Vol.33 (1), p.115-118</ispartof><rights>1998</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-2754c931055e092ac73e57fb6d976b756eec5147462d6f0dfc35f665e5b306193</citedby><cites>FETCH-LOGICAL-c389t-2754c931055e092ac73e57fb6d976b756eec5147462d6f0dfc35f665e5b306193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S002234689890375X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,4010,4036,4037,23909,23910,25118,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2190018$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9473114$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maksoud, Joäo Gilberto</creatorcontrib><creatorcontrib>Fauza, Dario O</creatorcontrib><creatorcontrib>Silva, Marcos M</creatorcontrib><creatorcontrib>Porta, Gilda</creatorcontrib><creatorcontrib>Miura, Irene</creatorcontrib><creatorcontrib>Zerbini, Maria Claudia N</creatorcontrib><title>Management of biliary atresia in the liver transplantation era: A 15-year, single-center experience</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Background/Purpose:
The aim of this study was to address the perioperative aspects of hepatoportoenterostomy (HPE) for biliary atresia (BA), through the study of a 15-year, single-center experience of the management of this disease.
Methods:
One hundred twenty-seven patients were divided into three groups, depending on the variant of HPE performed: group A (n = 53) underwent HPE with external diversion of the Roux-en-Y anastomosis; group B (n = 54) underwent HPE with a long (35 to 40cm) Roux-en-Y anastomosis, without diversion; and group C (n =20) underwent the same kind of HPE as group B, but with a modified, “super extensive” dissection of the porta hepatitis. Eleven children in group B had an intussusception type antireflux valve in the Roux-en-Y loop. The porta hepatitis of 105 children was histologically classified in type I to III and correlated with rate of postoperative bile flow and age at surgery. Liver transplantation was performed after HPE in 20 patients.
Results:
Overall, biliary drainage was achieved in 72.5% of the children after HPE and 26.8% of all patients became jaundice free. Porta hepatitis type III was associated with a significantly higher rate of biliary drainage post-HPE then types I and II. There was no difference in the rate of bile drainage, relative number of jaundice-free patients, and mean number of episodes of cholangitis per year among surgical groups A, B, C. In group A, 43.7% of the patients had complications related to the stoma. The actuarial survival of children who underwent HPE followed by liver transplantation was 85%.
Conclusions:
(1) There is no correlation between type of porta hepatis and age at surgery for BA; (2) type III porta hepatis is associated with higher rates of bile drainage post-HPE; (3) children older than 16 weeks with BA should still be considered for HPE; (4) in these older patients, factors other than the type of porta hepatis, possibly the degree of liver damage, play a role in the lower rate of bile drainage observed; (5) external diversion of the Roux-en-Y in HPE is not beneficial and is detrimental because of stoma-related complications; (6) an antireflux valve in the Roux-en-Y loop does not reduce the incidence of cholangitis post-HPE; (7) Surgical reexploration does not restore biliary drainage; and (8) sequential therapy with HPE followed by liver transplantation remains the treatment of choice for BA.</description><subject>Actuarial Analysis</subject><subject>Anastomosis, Roux-en-Y - methods</subject><subject>Biliary Atresia - epidemiology</subject><subject>Biliary Atresia - surgery</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Drainage</subject><subject>Humans</subject><subject>Infant</subject><subject>Liver Transplantation</subject><subject>Liver, biliary tract, pancreas, portal circulation, spleen</subject><subject>Medical sciences</subject><subject>Portoenterostomy, Hepatic - methods</subject><subject>Predictive Value of Tests</subject><subject>Retrospective Studies</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the digestive system</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1rGzEQQEVpSJ20P8GgQygJZNPRaiWtcgnB5AtSemgLuQmtdtZVWO86kmySf185Nr4GBIM0b0Yzj5ApgwsGTP74DVCWBa9kfarrMw1cieLpE5kwwVkh8vUzmeyRL-QoxmeA_AzskBzqSnHGqglxP-1g57jAIdGxo43vvQ1v1KaA0VvqB5r-Ie39GgNNwQ5x2dsh2eTHgWKwl_SaMlG8oQ3nNPph3mPhcq9M4-sSg8fB4Vdy0Nk-4rddPCZ_b2_-zO6Lx193D7Prx8LxWqeiVKJymjMQAkGX1imOQnWNbLWSjRIS0QlWqUqWreyg7RwXnZQCRcNBMs2Pyfdt32UYX1YYk1n46LDPE-O4ikZpWddQQgbFFnRhjDFgZ5bBL_LehoHZyDXvcs3GnNH5bOSap1w33X2wahbY7qt2NnP-ZJe30dm-y76cj3usZBqA1Rm72mKYZaw9BhPdu6jWB3TJtKP_YJD_P_eVpQ</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Maksoud, Joäo Gilberto</creator><creator>Fauza, Dario O</creator><creator>Silva, Marcos M</creator><creator>Porta, Gilda</creator><creator>Miura, Irene</creator><creator>Zerbini, Maria Claudia N</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1998</creationdate><title>Management of biliary atresia in the liver transplantation era: A 15-year, single-center experience</title><author>Maksoud, Joäo Gilberto ; Fauza, Dario O ; Silva, Marcos M ; Porta, Gilda ; Miura, Irene ; Zerbini, Maria Claudia N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-2754c931055e092ac73e57fb6d976b756eec5147462d6f0dfc35f665e5b306193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Actuarial Analysis</topic><topic>Anastomosis, Roux-en-Y - methods</topic><topic>Biliary Atresia - epidemiology</topic><topic>Biliary Atresia - surgery</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Drainage</topic><topic>Humans</topic><topic>Infant</topic><topic>Liver Transplantation</topic><topic>Liver, biliary tract, pancreas, portal circulation, spleen</topic><topic>Medical sciences</topic><topic>Portoenterostomy, Hepatic - methods</topic><topic>Predictive Value of Tests</topic><topic>Retrospective Studies</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the digestive system</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maksoud, Joäo Gilberto</creatorcontrib><creatorcontrib>Fauza, Dario O</creatorcontrib><creatorcontrib>Silva, Marcos M</creatorcontrib><creatorcontrib>Porta, Gilda</creatorcontrib><creatorcontrib>Miura, Irene</creatorcontrib><creatorcontrib>Zerbini, Maria Claudia N</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maksoud, Joäo Gilberto</au><au>Fauza, Dario O</au><au>Silva, Marcos M</au><au>Porta, Gilda</au><au>Miura, Irene</au><au>Zerbini, Maria Claudia N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of biliary atresia in the liver transplantation era: A 15-year, single-center experience</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>1998</date><risdate>1998</risdate><volume>33</volume><issue>1</issue><spage>115</spage><epage>118</epage><pages>115-118</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><coden>JPDSA3</coden><abstract>Background/Purpose:
The aim of this study was to address the perioperative aspects of hepatoportoenterostomy (HPE) for biliary atresia (BA), through the study of a 15-year, single-center experience of the management of this disease.
Methods:
One hundred twenty-seven patients were divided into three groups, depending on the variant of HPE performed: group A (n = 53) underwent HPE with external diversion of the Roux-en-Y anastomosis; group B (n = 54) underwent HPE with a long (35 to 40cm) Roux-en-Y anastomosis, without diversion; and group C (n =20) underwent the same kind of HPE as group B, but with a modified, “super extensive” dissection of the porta hepatitis. Eleven children in group B had an intussusception type antireflux valve in the Roux-en-Y loop. The porta hepatitis of 105 children was histologically classified in type I to III and correlated with rate of postoperative bile flow and age at surgery. Liver transplantation was performed after HPE in 20 patients.
Results:
Overall, biliary drainage was achieved in 72.5% of the children after HPE and 26.8% of all patients became jaundice free. Porta hepatitis type III was associated with a significantly higher rate of biliary drainage post-HPE then types I and II. There was no difference in the rate of bile drainage, relative number of jaundice-free patients, and mean number of episodes of cholangitis per year among surgical groups A, B, C. In group A, 43.7% of the patients had complications related to the stoma. The actuarial survival of children who underwent HPE followed by liver transplantation was 85%.
Conclusions:
(1) There is no correlation between type of porta hepatis and age at surgery for BA; (2) type III porta hepatis is associated with higher rates of bile drainage post-HPE; (3) children older than 16 weeks with BA should still be considered for HPE; (4) in these older patients, factors other than the type of porta hepatis, possibly the degree of liver damage, play a role in the lower rate of bile drainage observed; (5) external diversion of the Roux-en-Y in HPE is not beneficial and is detrimental because of stoma-related complications; (6) an antireflux valve in the Roux-en-Y loop does not reduce the incidence of cholangitis post-HPE; (7) Surgical reexploration does not restore biliary drainage; and (8) sequential therapy with HPE followed by liver transplantation remains the treatment of choice for BA.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>9473114</pmid><doi>10.1016/S0022-3468(98)90375-X</doi><tpages>4</tpages></addata></record> |
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subjects | Actuarial Analysis Anastomosis, Roux-en-Y - methods Biliary Atresia - epidemiology Biliary Atresia - surgery Biological and medical sciences Case-Control Studies Child Child, Preschool Drainage Humans Infant Liver Transplantation Liver, biliary tract, pancreas, portal circulation, spleen Medical sciences Portoenterostomy, Hepatic - methods Predictive Value of Tests Retrospective Studies Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system Time Factors Treatment Outcome |
title | Management of biliary atresia in the liver transplantation era: A 15-year, single-center experience |
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