Common clinical problems during treatment of neonatal biliary atresia
10.3969/j.issn.1001-5256.2015.08.011
- VernacularTitle:新生儿胆道闭锁治疗过程中的常见临床问题
- Author:
Gong CHEN
1
;
Shan ZHENG
Author Information
1. Department of General Surgery, Children′s Hospital of Fudan University, Shanghai 201102, China)
- Publication Type:Research Article
- Keywords:
biliary atresia;
therapy;
infant, newborn
- From:
Journal of Clinical Hepatology
2015;31(8):1226-1229
- CountryChina
- Language:Chinese
-
Abstract:
Biliary atresia is an important reason for neonatal jaundice, and it is also the primary cause of liver transplantation in children. Porto-jejunal anastomosis (Kasai procedure) is an effective method for treating biliary atresia. In this article, the complications after Kasai procedure and long-term outcome were introduced. It is emphasized that the Kasai procedure is the first choice for biliary atresia patients. In addition, this article analyzes the possible influencing factors for surgical outcome, describes the possible problems regarding the long-term survival of autologous liver after the operation for biliary atresia, and proposes the need for more attention to the comprehensive treatment after Kasai procedure and before liver transplantation.
