医学
阿拉吉尔综合征
酪氨酸血症
肝移植
胆道闭锁
尿素循环
胆汁淤积
背景(考古学)
进行性家族性肝内胆汁淤积症
移植
胆汁酸
儿科
肝病
重症监护医学
内科学
古生物学
生物化学
化学
物理
氨基酸
核磁共振
精氨酸
酪氨酸
生物
作者
Irena Jankowska,Piotr Socha,Dorota Gliwicz,Patryk Lipiński,Dariusz Rokicki,Piotr Kaliciński,Ewa Danielewska,Ryszard Grenda
摘要
ABSTRACT Background Liver transplantation (LTx) constitutes a major life‐saving routine treatment for children with end‐stage liver disease. However, the analysis of LTx registries in children provides much information about changes in the indication profiles in the recent years. Methods The article provides a comprehensive review about the successes, hopes, and challenges related to changing indications for LTx in children based on the literature review and our own experience. Retrospective review of the indications for LTx at a tertiary referral pediatric hospital was also presented. Results and Conclusions In the context of the new therapies that have emerged, the need for LTx has decreased in patients with chronic hepatitis B and C infection and tyrosinemia type 1. In primary hyperoxaluria type 1, new RNAi‐based therapy has eliminated the requirement for LTx (both isolated or combined). There is a hope that introduction of ileal bile acid transporter (IBAT) blockers reduces the need for LTx in patients with Alagille syndrome or progressive familial intrahepatic cholestasis. The number of children qualified for LTx with urea cycle disorders (UCDs) as a prophylaxis of neurodevelopmental impairment is increasing.
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