Management of biliary atresia in the liver transplantation era: A 15-year, single-center experience

被引:10
作者
Maksoud, JG
Fauza, DO
Silva, MM
Porta, G
Miura, I
Zerbini, MCN
机构
[1] Univ Sao Paulo, Sch Med, Childrens Inst, Div Surg, Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Childrens Inst, Div Hepatol, Sao Paulo, Brazil
[3] Univ Sao Paulo, Sch Med, Childrens Inst, Div Pathol, Sao Paulo, Brazil
关键词
biliary atresia; portoenterostomy; Kasai; cholestasis; liver transplantation; cholangitis;
D O I
10.1016/S0022-3468(98)90375-X
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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 40 cm) 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 types 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. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:115 / 118
页数:4
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