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本文引用的文献

1
Occult liver disease burden: Analysis from a large general practitioners' database.隐匿性肝病负担:来自大型全科医生数据库的分析。
United European Gastroenterol J. 2017 Nov;5(7):982-986. doi: 10.1177/2050640617696402. Epub 2017 Feb 26.
2
Use of Liver Imaging and Biopsy in Clinical Practice.肝脏成像与活检在临床实践中的应用。
N Engl J Med. 2017 Aug 24;377(8):756-768. doi: 10.1056/NEJMra1610570.
3
EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection.EASL 2017 临床实践指南:乙型肝炎病毒感染管理。
J Hepatol. 2017 Aug;67(2):370-398. doi: 10.1016/j.jhep.2017.03.021. Epub 2017 Apr 18.
4
Increased risk of mortality by fibrosis stage in nonalcoholic fatty liver disease: Systematic review and meta-analysis.非酒精性脂肪性肝病中纤维化阶段导致的死亡风险增加:系统评价与荟萃分析
Hepatology. 2017 May;65(5):1557-1565. doi: 10.1002/hep.29085. Epub 2017 Mar 31.
5
Cost-Effectiveness Analysis: Risk Stratification of Nonalcoholic Fatty Liver Disease (NAFLD) by the Primary Care Physician Using the NAFLD Fibrosis Score.成本效益分析:初级保健医生使用非酒精性脂肪性肝病(NAFLD)纤维化评分对非酒精性脂肪性肝病进行风险分层
PLoS One. 2016 Feb 23;11(2):e0147237. doi: 10.1371/journal.pone.0147237. eCollection 2016.
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AASLD guidelines for treatment of chronic hepatitis B.美国肝病研究学会慢性乙型肝炎治疗指南。
Hepatology. 2016 Jan;63(1):261-83. doi: 10.1002/hep.28156. Epub 2015 Nov 13.
7
Cost-Effective Evaluation of Nonalcoholic Fatty Liver Disease With NAFLD Fibrosis Score and Vibration Controlled Transient Elastography.使用非酒精性脂肪性肝病纤维化评分和振动控制瞬时弹性成像对非酒精性脂肪性肝病进行成本效益评估。
Am J Gastroenterol. 2015 Sep;110(9):1298-304. doi: 10.1038/ajg.2015.241. Epub 2015 Aug 25.
8
Liver Fibrosis, but No Other Histologic Features, Is Associated With Long-term Outcomes of Patients With Nonalcoholic Fatty Liver Disease.肝纤维化而非其他组织学特征与非酒精性脂肪性肝病患者的长期预后相关。
Gastroenterology. 2015 Aug;149(2):389-97.e10. doi: 10.1053/j.gastro.2015.04.043. Epub 2015 Apr 29.
9
Fibrosis stage is the strongest predictor for disease-specific mortality in NAFLD after up to 33 years of follow-up.纤维化分期是经过长达 33 年随访后,NAFLD 患者疾病特异性死亡率的最强预测因子。
Hepatology. 2015 May;61(5):1547-54. doi: 10.1002/hep.27368. Epub 2015 Mar 23.
10
Noninvasive methods to assess liver disease in patients with hepatitis B or C.用于评估乙型肝炎或丙型肝炎患者肝脏疾病的非侵入性方法。
Gastroenterology. 2012 May;142(6):1293-1302.e4. doi: 10.1053/j.gastro.2012.02.017.

肝纤维化的实用临床方法。

A practical clinical approach to liver fibrosis.

作者信息

Kumar Rahul, Teo Eng Kiong, How Choon How, Wong Teck Yee, Ang Tiing Leong

机构信息

Department of Gastroenterology and Hepatology, Changi General Hospital, Singapore.

Care and Health Integration, Changi General Hospital, Singapore.

出版信息

Singapore Med J. 2018 Dec;59(12):628-633. doi: 10.11622/smedj.2018145.

DOI:10.11622/smedj.2018145
PMID:30631885
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6301869/
Abstract

Liver fibrosis is a slow, insidious process involving accumulation of extracellular matrix protein in the liver. The stage of liver fibrosis in chronic liver disease (CLD) determines overall morbidity and mortality; the higher the stage, the worse the prognosis. Noninvasive composite scores can be used to determine whether patients with CLD have significant or advanced fibrosis. Patients with low composite scores can be safely followed up in primary care with periodic reassessment. Those with higher scores should be referred to a specialist. As the epidemic of diabetes mellitus, obesity and non-alcoholic fatty liver diseases is rising, CLD is becoming more prevalent. Easy-to-use fibrosis assessment composite scores can identify patients with minimal or advanced fibrosis, and should be an integral part of decision-making. Patients with cirrhosis, high composite scores, chronic hepatitis B with elevated alanine aminotransferase and aspartate aminotransferase, or deranged liver panel of uncertain aetiology should be referred to a specialist.

摘要

肝纤维化是一个缓慢、隐匿的过程,涉及肝脏细胞外基质蛋白的积累。慢性肝病(CLD)中的肝纤维化阶段决定了总体发病率和死亡率;阶段越高,预后越差。非侵入性综合评分可用于确定CLD患者是否存在显著或晚期纤维化。综合评分低的患者可在初级保健中进行安全随访,并定期重新评估。评分较高的患者应转诊至专科医生处。随着糖尿病、肥胖症和非酒精性脂肪性肝病的流行率上升,CLD正变得越来越普遍。易于使用的纤维化评估综合评分可以识别轻度或晚期纤维化患者,应成为决策的一个组成部分。患有肝硬化、综合评分高、丙氨酸氨基转移酶和天冬氨酸氨基转移酶升高的慢性乙型肝炎或病因不明的肝功能检查异常的患者应转诊至专科医生处。