Abstract

Acute liver failure is a clinical syndrome characterized by hepatic encephalopathy and a bleeding tendency due to severe impairment of liver function caused by massive or submassive liver necrosis. Viral hepatitis is the most important and frequent cause of acute liver failure in Japan. The diagnostic criteria for fulminant hepatitis, including that caused by viral infections, autoimmune hepatitis, and drug allergy induced-liver damage, were first established in 1981. Considering the discrepancies between the definition of fulminant hepatitis in Japan and the definitions of acute liver failure in the United States and Europe, the Intractable Hepato-Biliary Disease Study Group established the diagnostic criteria for “acute liver failure” for Japan in 2011, and performed a nationwide survey of patients seen in 2010 to clarify the demographic and clinical features and outcomes of these patients. According to the survey, the survival rates of patients receiving medical treatment alone were low, especially in those with hepatic encephalopathy, despite artificial liver support, consisting of plasma exchange and hemodiafiltration, being provided to almost all patients in Japan. Thus, liver transplantation is inevitable to rescue most patients with hepatic encephalopathy. The indications for liver transplantation had, until recently, been determined according to the guideline published by the Acute Liver Failure Study Group in 1996. Recently, however, the Intractable Hepato-Biliary Disease Study Group established a scoring system to predict the outcomes of acute liver failure patients. Algorithms for outcome prediction have also been developed based on data-mining analyses. These novel guidelines need further evaluation to determine their usefulness.

Highlights

  • Liver failure is a clinical syndrome characterized by jaundice, ascites, hepatic encephalopathy, and a bleeding tendency due to impairment of liver function; the syndrome can be caused by conditions such as viral hepatitis, autoimmune hepatitis, drug-induced liver injuries, metabolic diseases, and circulatory disturbances

  • Acute liver failure is diagnosed in patients in whom severe liver function impairment, as judged from the clinical symptoms, laboratory data, and imaging examinations, develops within 24 or 26 weeks (6 months) following the onset of liver injury in a preexisting normal liver, while chronic liver failure is diagnosed in patients with persistent liver inflammation and injuries who show liver function impairment later than 6 months after the onset of the liver symptoms

  • We describe the clinical features of patients with acute liver failure in Japan, which were analyzed through a nationwide survey conducted using the diagnostic criteria revised in 2011 in reference to those in Europe and the United States

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Summary

Introduction

Liver failure is a clinical syndrome characterized by jaundice, ascites, hepatic encephalopathy, and a bleeding tendency due to impairment of liver function; the syndrome can be caused by conditions such as viral hepatitis, autoimmune hepatitis, drug-induced liver injuries, metabolic diseases, and circulatory disturbances. Note 6: Patients showing prothrombin time values of less than 40 % of the standardized value or INRs of 1.5 or more and grade II or more severe hepatic coma between 8 and 24 weeks of the onset of disease symptoms are diagnosed as having late-onset hepatic failure (LOHF), as a disease related to ‘‘acute liver failure’’. Patients with LOHF are defined as those showing prothrombin time values of B40 % of the standardized value or INRs of 1.5 or more and grade II or more severe hepatic coma between 8 and 24 weeks of the onset of the disease symptoms, and those without histological evidence of hepatitis are included in the disease entity of LOHF, similar to the case of acute liver failure. Reactivation in transiently infected patients by immunosuppressant and/or anticancer drugs (de-novo hepatitis)a (3) Indeterminate infection patterns

Drug toxicity-induced liver injury
Findings
Age C45 years
Full Text
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