PREVENTION OF BILIARY-CIRRHOSIS FOLLOWING HEPATIC ARTERIAL THROMBOSISAFTER LIVER-TRANSPLANTATION IN CHILDREN BY USING URSODEOXYCHOLIC ACID

Citation
R. Bilik et al., PREVENTION OF BILIARY-CIRRHOSIS FOLLOWING HEPATIC ARTERIAL THROMBOSISAFTER LIVER-TRANSPLANTATION IN CHILDREN BY USING URSODEOXYCHOLIC ACID, Journal of pediatric surgery, 30(1), 1995, pp. 49-52
Citations number
8
Categorie Soggetti
Pediatrics,Surgery
ISSN journal
00223468
Volume
30
Issue
1
Year of publication
1995
Pages
49 - 52
Database
ISI
SICI code
0022-3468(1995)30:1<49:POBFHA>2.0.ZU;2-Z
Abstract
Hepatic artery thrombosis (HAT) after liver transplantation is a sever e complication that often requires retransplantation. The authors have adopted a different approach, aimed at treating the perioperative HAT complications aggressively and early, with ursodeoxycholic acid (UDCA ), to try to preserve the original graft. Eighty-six liver transplants were performed in 73 children (age range, 4.5 months to 17.5 years; m edian, 2.6 years). HAT occurred eight times, in seven patients (9.3%). Patients with HAT were significantly younger and smaller (mean age, 0 .8 +/- 0.4 v 4.8 +/- 5.3 years; P < .02; mean weight, 7.4 +/- 0.8 v 18 .7 +/- 16.2 kg; P < .05). The incidence of HAT varied significantly ac cording to the method of arterial reconstruction used: 4 of 16 (25%) w hen a donor iliac artery interposition graft to the aorta was used, 4 of 61 (6.6%) when the native hepatic artery was used, and 0 of 9 when the donor celiac axis was anastomosed directly to the aorta (P < .05). The incidence of HAT was not significantly different when reduced siz e grafts were used. Early retransplantation was performed in three of the eight patients; two survived. All other patients were treated for 4 to 6 weeks with broad-spectrum antibiotics and amphotericin. Five pa tients were treated with UDCA, three immediately after the acute event and two after 4 and 6 months (respectively) post-HAT. The patients wh o had UDCA immediately post-HAT had histologically normal liver biopsy specimens. Results of liver function tests have been normal. One of t hese patients required transhepatic stenting of a common bile duct str icture for several months. For the two patients whose UDCA treatment b egan 4 or 6 months after HAT, sequential biopsy specimens showed progr essive evolution of biliary cirrhosis, which led to the need for retra nsplantation in both patients, 4 and 3.5 years (respectively) after th e original transplants. The authors believe that early initiation of U DCA treatment after liver transplantation and HAT may prevent the hepa totoxic effect of cholestasis and bile salt retention and the accompan ying biliary cirrhosis. Copyright (C) 1995 by W.B. Saunders Company