胆道闭锁诊断及治疗指南(2018版)

中华医学会小儿外科学分会肝胆外科学组; 中国医师协会器官移植医师分会儿童器官移植学组

doi:10.3969/j.issn.1001-5256.2019.11.009

胆道闭锁诊断及治疗指南(2018版)

DOI: 10.3969/j.issn.1001-5256.2019.11.009

详细信息

中图分类号: R725.7
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出版历程
- 出版日期: 2019-11-20

Guidelines for diagnosing & treating biliary atresia (2018 Edition)

Section of Hepatobiliary Surgery, Branch of Pediatric Surgery, Chinese Medical Association,
Section of Pediatric Hepatic Transplantation, Branch of Organ Transplantation, Chinese Medical Doctor Association

摘要

摘要:
<正>胆道闭锁(biliary atresia,BA)是婴儿期常见的严重肝胆系统疾病之一,以肝内、外胆管进行性炎症和纤维化为特征;如不及时治疗,晚期会出现胆汁性肝硬化、门静脉高压、肝衰竭。目前早期诊断困难,手术治疗效果欠佳,可能与诊断方法、Kasai手术标准化程度及该病知识普及程度有关。制订一个明确、可靠并在临床上切实可行的指南是当下亟需解决的问题。本指南涵盖近年来相关研究,将所有证据基于GRADE系
- 胆道闭锁 /
- 儿童 /
- 诊疗准则(主题)
- biliary atresia /
- child /
- practice guidelines as topic

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参考文献(48)

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