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慢加急性肝衰竭的发病机制和治疗进展

尚大宝 项晓刚

引用本文:
Citation:

慢加急性肝衰竭的发病机制和治疗进展

DOI: 10.3969/j.issn.1001-5256.2021.04.005
基金项目: 

国家自然科学基金面上项目 (81970544);

上海市青年优秀学术带头人计划 (20XD1422600);

上海市教委高峰高原学科建设计划 (20172008)

利益冲突声明:所有作者均声明不存在利益冲突。
作者贡献声明:尚大宝参与文献检索和论文撰写;项晓刚参与课题思路的确定和论文修改。
详细信息
    作者简介:

    尚大宝(1995—),男,主要从事慢加急性肝衰竭临床与发病机制方面的研究

    通信作者:

    项晓刚,shine-xxg@163.com

  • 中图分类号: R575.3

Advances in the pathogenesis and treatment of acute-on-chronic liver failure

  • 摘要: 慢加急性肝衰竭(ACLF)是一类在慢性肝病基础上发生的以急性肝功能失代偿、肝外器官损伤和高短期死亡率为主要临床特征的严重临床综合征。欧美国家慢性肝病基础疾病以酒精性肝炎和慢性丙型肝炎为主,而我国及亚太地区以慢性乙型肝炎为主。尽管东西方肝脏基础疾病存在差异,但大多数ACLF患者发病的共同病理基础通常以长期慢性肝损伤导致的肝纤维化或肝硬化为主。目前,关于ACLF的研究正在世界各地广泛开展,但由于地域、患病人群及疾病诱因等多方面的差异,在ACLF定义、诊断标准及疾病管理等方面始终没有达成东西方共识。旨在从ACLF的定义、发病机制和疾病管理等方面展开阐述,以期为临床工作者提供能改善患者预后的新治疗策略。

     

  • 表  1  评价ACLF中使用ECLS的研究

    研究
    (第一作者及年份)
    试验设计 样本数
    (例)
    ECLS类型 生化功能
    改善
    血流动力学
    改善
    肝性脑病
    改善
    生存率改善
    ECLS vs SMT
    Hassanein 2007[17] RCT(8个中心) 70 MARS 未测 未测
    Kribben 2012[18] RCT(10个中心) 143 Prometheus 未测 未测 否(66% vs 63% 28 d)
    Bañares 2013[19] RCT(19个中心) 189 MARS 未测 未测 否(60.7% vs 58.9% 28 d)
    Yao 2019[20] 非RCT(1个中心) 54 PE+DPMAS 未测 未测 是(57.4% vs 41.7% 28 d)
    下载: 导出CSV
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  • 收稿日期:  2021-01-07
  • 录用日期:  2021-03-02
  • 出版日期:  2021-04-20
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