Biliary atresia: 20-40-year follow-up with native liver in an Italian centre
Biliary atresia: 20-40-year follow-up with native liver in an Italian centre
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DOI：
10.1016/j.jpedsurg.2018.10.060
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发表时间：
2019-07-01
影响因子：
2.4
通讯作者：
Alberti, Daniele
中科院分区：
文献类型：
--
作者：
Parolini, Filippo;Boroni, Giovanni;Alberti, Daniele
Introduction: Biliary atresia (BA) represents the leading indication for liver transplantation in childhood. Only few studies reported the outcome of patients who survived more than 20 years on their native liver, and up to date there are no Italian data available. We reported our 40-year single centre experience with long-term follow-up of BA patients.Materials and methods: All consecutive patients who underwent Kasai portoenterostomy (KPE) for BA managed at our Institution between 1975 and 1996 were retrospectively reviewed. Native liver (NIS) and overall survival (OS) were analyzed with Kaplan-Meyer curves and LogRank test. A p value of
