Back to Search Start Over

Living Donor Liver Transplantation in Children.

Authors :
Gurevich, Michael
Guy-Viterbo, Vanessa
Janssen, Magdalena
Stephenne, Xavier
Smets, Françoise
Sokal, Etienne
Lefebvre, Chantal
Balligand, Jean-Luc
Pirotte, Thierry
Veyckemans, Francis
Clapuyt, Philippe
Menten, Renaud
Dumitriu, Dana
Danse, Etienne
Annet, Laurence
de Clety, Stephan Clement
Detaille, Thierry
Latinne, Dominique
Sempoux, Christine
Laterre, Pierre-François
Source :
Annals of Surgery; Dec2015, Vol. 262 Issue 6, p1141-1149, 9p
Publication Year :
2015

Abstract

Objectives: To evaluate the outcome of pediatric living donor liver transplantation (LDLT) regarding portal vein (PV) reconstruction, ABO compatibility, and impact of maternal donation on graft acceptance. Background: LDLT and ABO-mismatched transplantation constitute feasible options to alleviate organ shortage in children. Vascular complications of portal hypoplasia in biliary atresia (BA) and acute rejection (AR) are still major concerns in this field. Methods: Data from 250 pediatric LDLT recipients, performed at Cliniques Universitaires Saint-Luc between July 1993 and June 2012, were collected retrospectively. Results were analyzed according to ABO matching and PV complications. Uni- and multivariate analyses were performed to study the impact of immunosuppression, sex matching, and maternal donation on AR rate. Results: Overall, the 10-year patient survival rate was 93.2%. Neither patient or graft loss nor vascular rejection, nor hemolysis, was encountered in the ABO nonidentical patients (n=58), provided pretransplant levels of relevant isoagglutinins were below 1/16. In BA recipients, the rate of PV complications was lower after portoplasty (4.6%) than after truncal PV anastomosis (9.8%) and to jump graft interposition (26.9%; P=0.027). In parental donation, maternal grafts were associated with higher 1-year AR-free survival (55.2%) than paternal grafts (39.8%; P=0.041), but only in BA patients. Conclusions: LDLT, including ABO-mismatched transplantation, constitutes a safe and efficient therapy for liver failure in children. In BA patients with PV hypoplasia, portoplasty seems to constitute the best technique for PV reconstruction. Maternal donation might be a protective factor for AR. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00034932
Volume :
262
Issue :
6
Database :
Supplemental Index
Journal :
Annals of Surgery
Publication Type :
Academic Journal
Accession number :
112569594
Full Text :
https://doi.org/10.1097/SLA.0000000000001094