Late complications and current status of long-term survivals over 10 years after Kasai portoenterostomy.
10.4174/jkss.2011.81.4.271
- Author:
Eunyoung JUNG
1
;
Woo Hyun PARK
;
Soon Ok CHOI
Author Information
1. Department of Pediatric Surgery, Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea. choi1635@dsmc.or.kr
- Publication Type:Original Article
- Keywords:
Biliary atresia;
Hepatic portoenterostomy;
Survivors;
Portal hypertension;
Cholangitis
- MeSH:
Bile;
Biliary Atresia;
Cholangitis;
Drainage;
Humans;
Hypertension, Portal;
Infant;
Intestinal Obstruction;
Medical Records;
Portoenterostomy, Hepatic;
Retrospective Studies;
Survival Rate;
Survivors;
Transplants
- From:Journal of the Korean Surgical Society
2011;81(4):271-275
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Whereas the Kasai portoenterostomy (KPE) is an accepted first line of surgery for bile drainage in infants with biliary atresia, its long-term effectiveness is not clear because its etiology and pathogenesis remains unknown. This study was aimed to investigate the late complications occurring in long-term survivors and the current status of living patients who survived over 10 years after KPE. METHODS: A retrospective analysis of the medical records of 32 patients who underwent KPE from 1990 to 2000 was done. We analyzed 10-year survival rates with the Kaplan-Meier method and the current status of the long-term survivors. RESULTS: The overall 10-year survival rate by Kaplan-Meier method after KPE was 76.2%. Eight (25%) patients had died, including 4 who were transplanted. Nineteen (59.4%) patients survived over 10 years. Among them, 6 (31.6%) patients had portal hypertension, and 5 (26.3%) had episodes of cholangitis. Two had intrahepatic cyst and 2 had intestinal obstruction. Six (31.6%) patients have been well without any complications. CONCLUSION: The long-term survival rate of biliary atresia is slightly improving. However, two thirds of patients suffer from various complications. One-third of survivors go on without any complication. As biliary atresia is known as a progressive inflammatory disease, careful life-long follow- up is needed in long-term survivals after KPE.
