Current options for management of biliary atresia

被引：30
|
作者：
Gallo, Amy [1 ]
Esquivel, Carlos O. [1 ]
机构：
[1] Stanford Univ, Div Abdominal Transplantat, Sch Med, Lucile Packard Childrens Hosp Stanford, Stanford, CA 94305 USA
来源：
PEDIATRIC TRANSPLANTATION | 2013年 / 17卷 / 02期
关键词：
pediatric liver transplantation; quality-of-life; surgery; outcome; biliary atresia; PEDIATRIC LIVER-TRANSPLANTATION; HEPATIC PORTOENTEROSTOMY; KASAI OPERATION; EXPERIENCE; CHILDREN; INJURY; TISSUE;
D O I：
10.1111/petr.12040
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
It is encouraging that we are improving the technical aspects of treatment modalities for biliary atresia. However, it is clear that more needs to be done to best develop new treatment plans while applying the modalities we have (porto-enterostomy or liver transplantation or both) in a way that will afford the best survival and quality-of-life. This review article will discuss a number of points that are vital to improving care and illustrates the need to further scrutinize treatment decisions.
引用
收藏
页码：95 / 98
页数：4
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