Hepatic artery thrombosis after orthotopic liver transplantation is a
serious complication, especially in children, We report our experience
with intensive anticoagulant therapy during and after living-related
liver transplantation in pediatric recipients, Twenty-four patients be
tween 5 months and 15 years of age were studied. The mean diameter of
the anastomosed hepatic arteries was 2.7 mm, The anticoagulant therapy
consisted of low-molecular-weight heparin, antithrombin III concentra
tes, prostaglandin E(1), fresh frozen plasma, and a protease inhibitor
, The profiles of the coagulation and fibrinolytic systems were monito
red by measuring several parameters, including plasma levels of thromb
in-antithrombin III complex, antithrombin III, plasmin-alpha 2 plasmin
inhibitor complex, fibrin degradation product D-dimer, tissue type-pl
asminogen activator, and plasminogen activator inhibitor-1. Accelerati
on of the coagulation system and delayed recovery of the fibrinolytic
system were observed during the early postoperative days, The plasma l
evel of antithrombin III activity was maintained within the normal ran
ge by the administration of antithrombin III concentrates, None of the
recipients developed hepatic artery thrombosis, Children have been re
ported to be at a greater risk of developing hepatic artery thrombosis
than adults due to the small diameters of their hepatic arteries and
the postoperative hypercoagulable state. We believe that the intensive
anticoagulation therapy described in this study, the main concept of
which is the early correction of imbalance between the coagulant and a
nticoagulant systems, could become a model for the prevention of hepat
ic artery thrombosis in pediatric Liver transplantation patients.