Impact of recipient age in outcome of ABO-incompatible living-donor liver transplantation

被引:136
作者
Egawa, H
Oike, F
Buhler, L
Shapiro, AMJ
Minamiguchi, S
Haga, H
Uryuhara, K
Kiuchi, T
Kaihara, S
Tanaka, K
机构
[1] Kyoto Univ, Fac Med, Dept Transplantat Immunol, Kyoto, Japan
[2] Univ Hosp Geneva, Dept Surg, Geneva, Switzerland
[3] Univ Alberta, Dept Surg, Fac Med, Edmonton, AB, Canada
[4] Kyoto Univ, Fac Med, Dept Clin Pathol, Kyoto, Japan
关键词
D O I
10.1097/01.TP.0000110295.88926.5C
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Transplantation of hepatic grafts from ABO-incompatible donors is controversial because of the risk of hyperacute rejection mediated by preformed anti-ABO antibodies. The aim of the present study was to evaluate the outcome of liver transplants performed with ABO-incompatible living-donor livers and to detect risk factors for development of complications. Methods. From June 1990 to February 2000, 66 patients, 10 months to 55 years old (median, 2 years old), received 68 ABO-incompatible living-donor liver grafts. The antibody titer and clinical course were followed prospectively during a period ranging from 3 to 11 years. Results. The 5-year patient survival was 59%, 76%, and 80% for ABO-incompatible, ABO-compatible, and ABO-identical grafts, respectively (P<0.01). In patients <1 year old, greater than or equal to1 to <8, greater than or equal to8 to <16, and and greater than or equal to16 years old, 5-year survival was 76%, 68%, 53%, and 22%, respectively. The incidence of intrahepatic biliary complications and hepatic necrosis in ABO-incompatible living-related grafts (18% and 8%, respectively) was significantly (P<0.0001) greater than in ABO-compatible and ABO-identical grafts (both 0.6% and 0%, respectively). Predictive risk factors for increased mortality and morbidity were age greater than 1 year and elevated anti-ABO titers before transplantation. Conclusions. ABO-incompatible liver transplantation was carried out with relative safety in infants <1 year old but was not satisfactory in children >1 year in long-term follow-up. Patients aged >8 years remain at considerable risk of early fatal outcome because of hepatic necrosis, and new strategies to prevent antibody-mediated rejection are required.
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页码:403 / 411
页数:9
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