儿童肝移植:澳大利亚试点项目发展的经验。昆士兰肝移植计划。

Australian paediatric journal Pub Date : 1986-08-01
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引用次数: 0

摘要

患有终末期肝病的儿童现在成为适合肝移植(ltp)患者的主要亚群,并且移植后的生存统计数据优于成人。自1984年6月以来,在布里斯班制定了一项儿科长期培训方案,与美国的两个中心(匹兹堡和加州大学洛杉矶分校医疗中心)建立了初步的工作关系和持续的密切联系。14名患有终末期肝病的儿童已被转到昆士兰肝移植方案进行正式评估。在与父母坦诚、知情的讨论之后,其中10个孩子可以选择ltp。在过渡阶段,两名患有胆道闭锁的婴儿应其父母的要求被转到加州大学洛杉矶分校,随后,8名9个月至6岁的儿童被列入布里斯班的移植候选名单。一个捐助者采购小组可以使用昆士兰州政府的一架喷气机,负责除西澳大利亚州以外的所有大陆州。其中6名儿童现在已经接受了原位ltp(两名儿童在加州大学洛杉矶分校医学中心;在布里斯班皇家儿童医院的四个孩子)。一名加州大学洛杉矶分校患者死于无功能移植物,一名布里斯班患者在移植后5周死于排斥反应、肝动脉血栓形成和败血症。在1-20个月的随访中,其他4名儿童存活且健康,其中3名肝功能正常,1名不明原因的肝内胆汁淤积。还有三个孩子死于肝病,没有找到合适的血型和大小的供体,还有一个病人仍在等待合适的供体。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liver transplantation in children: experience with the development of an Australian pilot programme. The Queensland Liver Transplantation Programme.

Children with end-stage liver disease now form a major sub-group of patients considered suitable for liver transplantation (ltp), and enjoy better survival statistics after transplantation than do adults. Since June 1984, a paediatric ltp programme has been developed in Brisbane with an initial working relationship and ongoing close links with two USA centres (Pittsburgh, and the UCLA Medical Center). Fourteen children with end-stage liver disease have been referred to the Queensland Liver Transplantation Programme for formal assessment. Following frank, informed discussion with their parents, 10 of these children were offered the option of ltp. During the transition stage, two infants with biliary atresia were referred to UCLA at their parents' request and, subsequently, eight children aged from 9 months to 6 years have been placed on a transplant candidacy list in Brisbane. A donor procurement team with access to a Queensland Government jet has been available to cover all mainland States except Western Australia. Six of the children have now had orthotopic ltp (two children at the UCLA Medical Center; four children at the Royal Children's Hospital, Brisbane). One UCLA patient died with a non-functioning graft, and one Brisbane patient died 5 weeks post-transplant with rejection, hepatic artery thrombosis and sepsis. The other four children are alive and well, three with normal liver function and one with unexplained intrahepatic cholestasis, during the 1-20 month follow-up to date. Three further children have died of their liver disease without a donor of an appropriate blood group and size being found, and one patient still awaits a suitable donor.(ABSTRACT TRUNCATED AT 250 WORDS)

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