Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years

Gastroenterology

Volumn 99, Issue 6, 1990, Pages 1793-1797

  Laurent, Jocelyne ^a   Gauthier, Frédéric ^a   Bernard, Olivier ^a   Hadchouel, Michelle ^a   Odièvre, Michel ^a   Valayer, Jacques ^a   Alagille, Daniel ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BILE DUCT ATRESIA; HUMAN; INFANT; MAJOR CLINICAL STUDY; PRESCHOOL CHILD; PRIORITY JOURNAL;

ADOLESCENT; BILIARY ATRESIA; CAUSE OF DEATH; CHILD; CHILD, PRESCHOOL; CHOLANGITIS; HUMAN; HYPERTENSION, PORTAL; LIVER; POSTOPERATIVE PERIOD; SURVIVAL ANALYSIS;

EID: 0025223597     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1016/0016-5085(90)90489-N     Document Type: Article

References (18)

1. A new operation for “non correctable” biliary atresia: hepatic portoenterostomy
2. Long-term results of hepatic portoenterostomy for biliary atresia: special reference to postoperative portal hypertension
3. Hepatic portoenterostomy or cholecystostomy in the treatment of extra-hepatic biliary atresia
4. Biliary atresia
5. Long-term prognosis in biliary atresia after hepatic porto-enterostomy: analysis of 35 patients who survived beyond 5 years of age
6. Prognosis of extrahepatic biliary atresia
7. Percutaneous transhepatic cholangiography (PTC) in biliary atresia with special reference to the structure of the intrahepatic bile ducts
8. Bacterial cholangiris after surgery for biliary atresia
9. Portal hypertension in children
10. Percutaneous transhepatic cholangiography in postoperative evaluation of extrahepatic biliary duct atresia in children
11. Lifespan in untreated biliary atresia
12. Surgical limitation for biliary atresia indication for liver transplantation
13. Pulmonary arterial hypertension in portal hypertension
14. A patient with biliary atresia who died 28 years after hepatic portojejunostomy
15. Changes in life-style after liver transplantation
16. Liver transplantation before 1 year of age
17. Late referral for biliary atresia. Missed opportunities for effective surgery
18. Long-term follow-up study of patients with cholangitis after successful Kasaï operation in biliary atresia: selection of recipients for liver transplantation