Effect of Repeat Kasai Hepatic Portoenterostomy on Pediatric Live-Donor Liver Graft for Biliary Atresia
Authors:
- Taizen UrahashiTUTaizen Urahashi
- Yoshiyuki IharaYIYoshiyuki Ihara
- Yukihiro SanadaYSYukihiro Sanada
- Taiichi WakiyaTWTaiichi Wakiya
- Naoya YamadaNYNaoya Yamada
- Noriki OkadaNONoriki Okada
- Koichi MizutaKMKoichi Mizuta
- 17 June 2013
- journal article
- Published by Baskent University in Experimental and Clinical Transplantation
- Vol. 11 (3) , 259-263
Abstract
Treatment for patients with biliary atresia is a Kasai hepatic portoenterostomy; however, the efficacy of repeat Kasai hepatic portoenterostomy is unclear. This study sought to examine the effect of a prior Kasai hepatic portoenterostomy, especially a repeat Kasai hepatic portoenterostomy, on the outcomes of living-donor liver transplant. One hundred twenty-six of 170 children that underwent a living-donor liver transplant between May 2001, and March 2010, received a living-donor liver transplant for biliary atresia. These patients were divided into 2 groups according to the number of previous portoenterostomies: 1 (group A, n=100) or 2 or more Kasai hepatic portoenterostomies (group B, n=26). Portoenterostomy was performed twice in 24 patients in group B, 3 times in 1, and 4 times in 1. Preoperative, operative factors, mortality, morbidity, and survival rates were examined and compared between groups. The surgical factors such as operative time, blood loss per weight, cold ischemia time, and weight of the native liver were significantly greater in group B than they were in group A. The patient survival rates were comparable in the 2 groups (94.5% in group A and 93.3% in group B), and the difference was not statistically significant. No statistically significant difference was observed between the groups with regard to vascular complications, biliary complications, and other factors including postoperative variables. Bowel perforation requiring surgical repair was more frequent in group B than it was in group A. Repeat Kasai hepatic portoenterostomy might have a negative effect on patients who undergo living-donor liver transplant for biliary atresia patients with potential lethal complications such as bowel perforation. More biliary atresia patients could have a liver transplant, with improved survival and better life expectancy, if they have inadequate biliary drainage after the initial Kasai hepatic portoenterostomy.Keywords
This publication has 27 references indexed in Scilit:
- The influence of portoenterostomy on transplantation for biliary atresiaLiver Transplantation, 2004
- Past and future of biliary atresiaJournal of Pediatric Surgery, 2000
- The frequency and outcome of biliary atresia in the UK and IrelandThe Lancet, 2000
- The impact of a previous Kasai procedure on liver transplantation for biliary atresiaJournal of Pediatric Surgery, 1997
- Improved survival in biliary atresia patients in the present era of liver transplantationJournal of Pediatric Surgery, 1993
- The influence of portoenterostomy with stoma on morbidity in pediatric patients with biliary atresia undergoing orthotopic liver transplantationJournal of Pediatric Surgery, 1993
- Long-term outcome after surgery for biliary atresiaGastroenterology, 1990
- Optimal therapy for patients with biliary atresia: Portoenterostomy (“Kasai” procedures) versus primary transplantationJournal of Pediatric Surgery, 1990
- Biliary appendico-duodenostomy: A nonrefluxing conduit for biliary reconstructionJournal of Pediatric Surgery, 1989
- Technique and results of operative management of biliary atresiaWorld Journal of Surgery, 1978