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. 2018 May 18;23:334–344. doi: 10.12659/AOT.909050

Table 2.

Patient characteristics.

Variables Patients (n=75)
Age (y)a 2.3 (0.4–11.2)
Male gender (%) 39 (52.0)
Height (cm)a 87 (60–145)
Weight (kg)a 12.0 (5.5–35.0)
CTP scorea 8 (5–14)
PELD scorea 6 (−11–45)
Indication for LT (%)
 Biliary atresia 38 (50.7)
 Irreversible graft failureb 11 (14.7)
 UCDsc 7 (9.3)
 Hepatoblastoma 3 (4.0)
 MMA 3 (4.0)
 PFIC 3 (4.0)
 Othersd 10 (13.3)
a

Data are mean (range).

b

Irreversible graft failure may result from primary nonfunction or vascular or biliary complications after liver transplantation.

c

Ornithine transcarbamylase deficiency (OTCD) 3 cases, hyperornithinemia-hyperammonemia-homocitrullinuria (3H) syndrome 2 cases, argininosuccinic aciduria (ASA) 1 case, and argininemia 1 case.

d

Caroli disease 2cases, Wilson’s disease 1 case, maple syrup urine disease (MSUD) 1 case, familial hypercholesterolemia 1 case, Alagille syndrome 1 case, congenital hepatic fibrosis 1 case, cryptogenic cirrhosis 1 case, choledochal cyst 1 case, and fulminant hepatic failure 1 case.

CTP – Child-Turcotte-Pugh; MMA – methylmalonic academia; PELD – Pediatric End-stage Liver Disease; PFIC – progressive familial intrahepatic cholestasis; UCD – urea cycle disorder.