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慢加急性肝衰竭

Acute-on-chronic Liver Failure.

作者信息

Sarin Shiv Kumar, Choudhury Ashok

机构信息

Department of Hepatology and Liver Transplant, Institute of Liver and Biliary Sciences, D-1, VasantKunj, New Delhi, 110070, India.

出版信息

Curr Gastroenterol Rep. 2016 Dec;18(12):61. doi: 10.1007/s11894-016-0535-8.

Abstract

Acute-on-chronic liver failure (ACLF) is a distinct entity that differs from acute liver failure and decompensated cirrhosis in timing, presence of treatable acute precipitant, and course of disease, with a potential for self-recovery. The core concept is acute deterioration of existing liver function in a patient of chronic liver disease with or without cirrhosis in response to an acute insult. The insult should be a hepatic one and presentation in the form of liver failure (jaundice, encephalopathy, coagulopathy, ascites) with or without extrahepatic organ failure in a defined time frame. ACLF is characterized by a state of deregulated inflammation. Initial cytokine burst presenting as SIRS, progression to CARS and associated immunoparalysis leads to sepsis and multi-organ failure. Early identification of the acute insult and mitigation of the same, use of nucleoside analogue in HBV-ACLF, steroid in severe alcoholic hepatitis, steroid in severe autoimmune hepatitis and/or bridging therapy lead to recovery, with a 90-day transplant-free survival rate of up to 50 %. First-week presentation is crucial concerning SIRS/sepsis, development, multiorgan failure and consideration of transplant. A protocol-based multi-disciplinary approach including critical care hepatology, early liver transplant before multi-organ involvement, or priority for organ allocation may improve the outcome. Presentation with extrahepatic organ involvement or inclusion of sepsis as an acute insult in definition restricts the therapy, i.e., liver transplant or bridging therapy, and needs serious consideration. Augmentation of regeneration, cell-based therapy, immunotherapy, and gut microbiota modulation are the emerging areas and need further research.

摘要

慢加急性肝衰竭(ACLF)是一种独特的疾病实体,在发病时间、是否存在可治疗的急性诱发因素以及疾病进程方面与急性肝衰竭和失代偿期肝硬化不同,具有自我恢复的可能性。其核心概念是慢性肝病患者(无论有无肝硬化)的现有肝功能因急性损伤而急性恶化。该损伤应为肝脏相关损伤,并在规定时间内以肝衰竭(黄疸、肝性脑病、凝血功能障碍、腹水)的形式出现,可伴有或不伴有肝外器官衰竭。ACLF的特征是炎症调节失控状态。最初表现为全身炎症反应综合征(SIRS)的细胞因子爆发,进展为代偿性抗炎反应综合征(CARS)及相关的免疫麻痹,会导致脓毒症和多器官衰竭。早期识别并减轻急性损伤、在乙肝相关慢加急性肝衰竭中使用核苷类似物、在严重酒精性肝炎中使用类固醇、在严重自身免疫性肝炎中使用类固醇和/或进行桥接治疗可实现恢复,90天无移植生存率可达50%。第一周的表现对于SIRS/脓毒症、病情发展、多器官衰竭以及移植考虑至关重要。基于方案的多学科方法,包括重症肝病学、在多器官受累之前尽早进行肝移植或优先进行器官分配,可能会改善治疗结果。伴有肝外器官受累或在定义中将脓毒症列为急性损伤会限制治疗,即肝移植或桥接治疗,需要认真考虑。促进再生、细胞治疗、免疫治疗和肠道微生物群调节是新兴领域,需要进一步研究。

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