A Multivariable Risk Factor Analysis of the Portoenterostomy (Kasai) Procedure for Biliary Atresia
- 1 September 1997
- journal article
- clinical trial
- Published by Wolters Kluwer Health in Annals of Surgery
- Vol. 226 (3) , 348-355
- https://doi.org/10.1097/00000658-199709000-00014
Abstract
The authors investigated risk factors for failure after portoenterostomy for biliary atresia using univariate and multivariable methods. Kasai's portoenterostomy has gained worldwide acceptance as the initial surgical therapy for infants with biliary atresia. Although extended survival has been achieved for many patients, factors influencing outcome have not been defined clearly. The authors analyzed risks for failure in 266 patients treated from 1972 to 1996 by the Kaplan-Meier product limit estimate and Cox proportional hazards model. Failure was defined as death or transplant. Age at surgery, surgical decade, and anatomy of atretic bile ducts were identified as independent risk factors. Five-year survival was 49% and median survival was 15 years when bile drainage was achieved. Sixty-five patients had liver transplants. Mean age at transplant was 5.4 years. The outcome after portoenterostomy for biliary atresia is determined by age at surgery and anatomy of the atretic extrahepatic bile ducts. Liver transplant will salvage patients with failed Kasai with 10-year posttransplant survival of 71%.Keywords
This publication has 14 references indexed in Scilit:
- The impact of a previous Kasai procedure on liver transplantation for biliary atresiaJournal of Pediatric Surgery, 1997
- Biliary atresia: The King's College Hospital Experience (1974–1995)Journal of Pediatric Surgery, 1997
- Biliary atresia: Should all patients undergo a portoenterostomy?Journal of Pediatric Surgery, 1997
- Low vitamin E content in plasma of patients with alcoholic liver disease, hemochromatosis and wilson's diseaseJournal of Hepatology, 1994
- Optimal therapy for patients with biliary atresia: Portoenterostomy (“Kasai” procedures) versus primary transplantationJournal of Pediatric Surgery, 1990
- Surgical limitation for biliary atresia: Indication for liver transplantationJournal of Pediatric Surgery, 1989
- The Portoenterostomy Procedure for Biliary AtresiaAnnals of Surgery, 1978
- Lymphocyte responsiveness to Pseudomonas aeruginosa in cystic fibrosis: Relationship to status of pulmonary disease in sibling pairsThe Journal of Pediatrics, 1978
- Surgical treatment of biliary atresiaJournal of Pediatric Surgery, 1968
- Nonparametric Estimation from Incomplete ObservationsJournal of the American Statistical Association, 1958