Literature DB >> 21335182

Orthotopic liver transplantation in biliary atresia: a single-center experience.

A C A Tannuri1, N E M Gibelli, L R S Ricardi, M M Silva, M M Santos, M L Pinho-Apezzato, J G Maksoud-Filho, M C P Velhote, A A R Ayoub, W C Andrade, A N Backes, H T Miyatani, U Tannuri.   

Abstract

INTRODUCTION: Biliary atresia (BA) is the leading indication for orthotopic liver transplantation (OLT) among children. However, there are technical difficulties, including the limited dimensions of anatomical structures, hypoplasia and/or thrombosis of the portal vein and previous portoenterostomy procedures.
OBJECTIVE: The objective of this study was to present our experience of 239 children with BA who underwent OLT between September 1989 and June 2010 compared with OLT performed for other causes.
METHODS: We performed a retrospective analysis of patient charts and analysis of complications and survival.
RESULTS: BA was the most common indication for OLT (207/409; 50.6%). The median age of subjects was 26 months (range, 7-192). Their median weight was 11 kg (range, 5-63) with 110 children (53.1%) weighing ≤10 kg. We performed 126 transplantations from cadaveric donors (60.8%) and 81 from living-related donors (LRD) (39.2%). Retransplantation was required for 31 recipients (14.9%), primarily due to hepatic artery thrombosis (HAT; 64.5%). Other complications included the following: portal vein thrombosis (PVT; 13.0%), biliary stenosis and/or fistula (22.2%), bowel perforation (7.0%), and posttransplantation lymphoproliferative disorder (PTLD; 5.3%). Among the cases of OLT for other causes, the median age of recipients was 81 months (range, 11-17 years), which was higher than that for children with BA. Retransplantation was required in 3.5% of these patients (P < .05), mostly due to HAT. The incidences of PVT, bowel perforation, and PTLD were significantly lower (P < .05). There was no significant difference between biliary complications in the 2 groups. The overall survival rates at 1 versus 5 years were 79.7% versus 68.1% for BA, and 81.2% versus 75.7% for other causes, respectively.
CONCLUSIONS: Children who undergo OLT for BA are younger than those engrafted for other causes, displaying a higher risk of complications and retransplantations.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21335182     DOI: 10.1016/j.transproceed.2010.11.012

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  4 in total

1.  Living Related Liver Transplantation for Biliary Atresia in the Last 5 years: Experience from the First Liver Transplant Program in India.

Authors:  Smita Malhotra; Anupam Sibal; Vidyut Bhatia; Akshay Kapoor; Sarath Gopalan; Swati Seth; Nameet Jerath; Manav Wadhawan; Subash Gupta
Journal:  Indian J Pediatr       Date:  2015-02-25       Impact factor: 1.967

2.  Changes in NSE and S-100β during the perioperative period and effects on brain injury in infants with biliary atresia undergoing parent donor liver transplantation.

Authors:  Hongli Yu; Wenli Yu; Min Zhu; Guicheng Zhang; Yiwei Shi; Ying Sun
Journal:  Exp Ther Med       Date:  2021-05-04       Impact factor: 2.447

3.  Long-Term Survival of Biliary Atresia without any Surgery: Lessons Learnt from Lamprey.

Authors:  V Raveenthiran
Journal:  J Neonatal Surg       Date:  2014-04-01

4.  Transplantation of Human Amniotic Membrane over the Liver Surface Reduces Hepatic Fibrosis in a Cholestatic Model in Young Rats.

Authors:  M Garrido; C Escobar; C Zamora; C Rejas; J Varas; C Córdova; C Papuzinski; M Párraga; S San Martín; S Montedonico
Journal:  Stem Cells Int       Date:  2018-02-25       Impact factor: 5.443

  4 in total

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