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1
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Frontline Gastroenterol. 2019 May 21;11(2):133-139. doi: 10.1136/flgastro-2018-101104. eCollection 2020 Mar.
2
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Granulocyte colony-stimulating factor for alcoholic hepatitis: A systematic review and meta-analysis of randomised controlled trials.粒细胞集落刺激因子治疗酒精性肝炎:随机对照试验的系统评价和荟萃分析
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Outnumbered: Control Prothrombin Time in Maddrey's Discriminant Function Impacts Steroid Use but Not Mortality in Alcoholic Hepatitis.人数劣势:Maddrey判别函数中控制凝血酶原时间对酒精性肝炎中类固醇使用有影响,但对死亡率无影响。
Biology (Basel). 2022 Dec 16;11(12):1833. doi: 10.3390/biology11121833.

本文引用的文献

1
Predicting Low Risk for Sustained Alcohol Use After Early Liver Transplant for Acute Alcoholic Hepatitis: The Sustained Alcohol Use Post-Liver Transplant Score.预测急性酒精性肝炎早期肝移植后持续饮酒的低风险:肝移植后持续饮酒评分。
Hepatology. 2019 Apr;69(4):1477-1487. doi: 10.1002/hep.30478. Epub 2019 Mar 5.
2
A Validated Score Predicts Acute Kidney Injury and Survival in Patients With Alcoholic Hepatitis.验证评分可预测酒精性肝炎患者的急性肾损伤和生存情况。
Liver Transpl. 2018 Dec;24(12):1655-1664. doi: 10.1002/lt.25328.
3
Corticosteroids, nutrition, pentoxifylline, or fecal microbiota transplantation for severe alcoholic hepatitis.用于严重酒精性肝炎的皮质类固醇、营养支持、己酮可可碱或粪便微生物群移植。
Indian J Gastroenterol. 2018 May;37(3):215-225. doi: 10.1007/s12664-018-0859-4. Epub 2018 Jun 21.
4
ACG Clinical Guideline for Alcoholic Liver Disease: The MELD Threshold for Corticosteroid Treatment has Yet to be Established.美国胃肠病学会酒精性肝病临床指南:皮质类固醇治疗的终末期肝病模型(MELD)阈值尚未确定。
Am J Gastroenterol. 2019 Jan;114(1):175-176. doi: 10.1038/s41395-018-0076-x.
5
Corticosteroids Reduce Risk of Death Within 28 Days for Patients With Severe Alcoholic Hepatitis, Compared With Pentoxifylline or Placebo-a Meta-analysis of Individual Data From Controlled Trials.皮质类固醇与己酮可可碱或安慰剂相比可降低重症酒精性肝炎患者 28 天内的死亡率:来自对照试验的个体数据的荟萃分析。
Gastroenterology. 2018 Aug;155(2):458-468.e8. doi: 10.1053/j.gastro.2018.05.011. Epub 2018 May 5.
6
Outcomes of Early Liver Transplantation for Patients With Severe Alcoholic Hepatitis.早期肝移植治疗重症酒精性肝炎患者的结局。
Gastroenterology. 2018 Aug;155(2):422-430.e1. doi: 10.1053/j.gastro.2018.04.009. Epub 2018 Apr 12.
7
EASL Clinical Practice Guidelines: Management of alcohol-related liver disease.欧洲肝脏研究学会临床实践指南:酒精性肝病的管理
J Hepatol. 2018 Jul;69(1):154-181. doi: 10.1016/j.jhep.2018.03.018. Epub 2018 Apr 5.
8
The prognostic value of acute-on-chronic liver failure during the course of severe alcoholic hepatitis.慢性加急性肝衰竭对重症酒精性肝炎病程的预后价值。
J Hepatol. 2018 Aug;69(2):318-324. doi: 10.1016/j.jhep.2018.02.022. Epub 2018 Mar 8.
9
Histological activity score on baseline liver biopsy can predict non-response to steroids in patients with severe alcoholic hepatitis.基线肝活检的组织学活动评分可预测重症酒精性肝炎患者对类固醇治疗的无应答。
Virchows Arch. 2018 Apr;472(4):667-675. doi: 10.1007/s00428-018-2330-4. Epub 2018 Mar 7.
10
Microvesicles in hepatic and peripheral vein can predict nonresponse to corticosteroid therapy in severe alcoholic hepatitis.肝静脉和外周静脉中的微囊泡可预测严重酒精性肝炎患者对皮质类固醇治疗无应答。
Aliment Pharmacol Ther. 2018 Apr;47(8):1151-1161. doi: 10.1111/apt.14564. Epub 2018 Feb 20.

酒精性肝炎的最新进展

Recent advances in alcoholic hepatitis.

作者信息

Veryan Jennifer, Forrest E H

机构信息

Liver Unit, Glasgow Royal Infirmary, Glasgow, Glasgow, UK.

College of Medicine, Veterinary and Life Sciences, University of Glasgow, Glasgow, Glasgow, UK.

出版信息

Frontline Gastroenterol. 2019 May 21;11(2):133-139. doi: 10.1136/flgastro-2018-101104. eCollection 2020 Mar.

DOI:10.1136/flgastro-2018-101104
PMID:32133112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7043083/
Abstract

Alcoholic hepatitis (AH) is an acute deterioration in liver function seen in the context of prolonged excessive alcohol consumption and is characterised by the rapid onset of jaundice. The diagnosis of AH has been controversial for many years: it is now accepted that there are clear clinical criteria which can be used to diagnose AH without the need for a liver biopsy. Corticosteroids remain the only treatment proven to be effective in reducing short-term mortality in severe AH; abstinence from alcohol is the most important factor in determining long-term survival. It is recommended a trial of corticosteroid therapy is considered only in those patients with high baseline 'static' scores (Glasgow Alcoholic Hepatitis score and model for end-stage liver disease). Response to corticosteroid therapy should be assessed using a 'dynamic' score such as the Lille score at day 7, with corticosteroids continuing only in patients with a favourable score. Infection and acute kidney injury are associated with poorer outcomes in AH. Early screening for and treatment of infection is recommended with antibiotic therapy overlapping with any subsequent corticosteroid treatment. A biomarker which predicts benefit from corticosteroids at baseline would avoid a trial of therapy to determine response. More efficacious therapeutic options for AH patients are required with N-acetylcysteine, granulocyte colony stimulating factor, faecal microbiota transplantation and routine antibiotics showing promise, but adequate controlled trials are needed to confirm efficacy. Liver transplant has an emerging role for some patients with severe AH not responding to corticosteroids and is likely to become more acceptable with improved methods of patient selection.

摘要

酒精性肝炎(AH)是在长期过量饮酒情况下出现的肝功能急性恶化,其特征为黄疸迅速出现。多年来,AH的诊断一直存在争议:目前已公认有明确的临床标准可用于诊断AH,无需进行肝活检。皮质类固醇仍然是唯一被证明对降低重度AH短期死亡率有效的治疗方法;戒酒是决定长期生存的最重要因素。建议仅对那些基线“静态”评分较高(格拉斯哥酒精性肝炎评分和终末期肝病模型)的患者考虑进行皮质类固醇治疗试验。应使用“动态”评分(如第7天的里尔评分)评估对皮质类固醇治疗的反应,仅对评分良好的患者继续使用皮质类固醇。感染和急性肾损伤与AH的较差预后相关。建议早期筛查和治疗感染,抗生素治疗与随后的任何皮质类固醇治疗重叠。一种能在基线时预测皮质类固醇治疗获益的生物标志物可避免进行治疗试验来确定反应。AH患者需要更有效的治疗选择,N-乙酰半胱氨酸、粒细胞集落刺激因子、粪便微生物群移植和常规抗生素显示出前景,但需要充分的对照试验来证实疗效。肝移植对一些对皮质类固醇无反应的重度AH患者正发挥着越来越重要的作用,随着患者选择方法的改进,肝移植可能会变得更易接受。