Long-term outcome in type I biliary atresia

被引:34
作者
Nio, Masaki
Sano, Nobuyuki
Ishii, Tomohiro
Sasaki, Hideyuki
Hayashi, Yutaka
Ohi, Ryoji
机构
[1] Miyagi Childrens Hosp, Dept Surg, Aoba Ku, Sendai, Miyagi 9893126, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Pediat Surg, Sendai, Miyagi 9808574, Japan
关键词
biliary atresia; type I; long-term follow-up;
D O I
10.1016/j.jpedsurg.2006.08.019
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: This retrospective study reviews the long-term outcome of type I biliary atresia (BA). -three patients with BA, including 50 with type 1, underwent corrective Methods: Three hundred twenty surgery. The surgical results, role of cholangiograms during the corrective surgery, late complications, and current statuses were evaluated. Results: The overall survival rate of the nontransplant type I patients was better than that of the type II/ III patients (52% vs 33%, P = .0009). Cholangiograms of 32 patients were classified into 3 types: cloudy (48%), treelike (13%), and mixed (39%). Of 26 patients who underwent corrective surgery in 1972 or later, 7 (50%), 7 (78%), and 3 (100%) patients of the cloudy type, mixed type, and treelike type, respectively, have survived without liver transplantation (LTx). Of 18 type I patients who survived more than 20 years without LTx, 7 developed severe late complications. Two of them eventually required LTx after 20 years old. Conclusions: Use of cholangiograms during corrective surgery might have a long-term prognostic value. The overall survival rate of type I BA was better than that of type II/III. The incidence of late complications was, however, considerably high in the type I survivors. All patients required careful long-term follow-up. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1973 / 1975
页数:3
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