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For further information, see CMDT Part 16-05: Acute Liver Failure
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Essentials of Diagnosis
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General Considerations
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Acute liver failure may occur after reactivation of hepatitis B in carriers who receive immunosuppressive therapy
In fulminant liver failure, encephalopathy and coagulopathy develop within 8 weeks after the onset of acute liver injury
Subfulminant liver failure occurs when encephalopathy and coagulopathy appear between 8 weeks and 6 months after the onset of acute liver injury
Acute-on-chronic liver failure
Refers to acute deterioration in liver function and associated failure of other organs in a person with preexisting chronic liver disease
Often precipitated by infection or an alcohol binge and alcoholic hepatitis
Acetaminophen toxicity accounts for 45% of cases; idiosyncratic drug reactions are second most common
Among cases caused by acetaminophen
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Acetaminophen toxicity
Idiosyncratic drug reactions
Mushroom poisoning (Amatoxins)
Viruses (hepatitis A, B, C, D, E, CMV, EBV, HSV, parvovirus B19, influenza virus, yellow fever virus, Middle East respiratory syndrome virus, Ebola virus, SARS coronavirus)
Shock
Heat stroke
Budd-Chiari syndrome
Malignancy (especially lymphomas)
Wilson disease
Reye syndrome
Fatty liver of pregnancy and other disorders of fatty acid oxidation
Autoimmune hepatitis
Grand mal seizures (rarely)
Cause is indeterminate in approximately 5.5% of cases
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Most cases in the United States are caused by
Acetaminophen toxicity
Idiosyncratic drug reactions
Acute viral hepatitis, especially hepatitis B
Some cases are due to hepatitis A or unknown (non-ABCDE) viruses
In endemic areas, hepatitis E is an important cause of acute liver failure particularly in pregnant women
Hepatitis C is a rare cause of acute liver failure; acute hepatitis A or B superimposed on chronic hepatitis C has a high risk of acute liver failure
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Gastrointestinal symptoms (nausea, vomiting, anorexia)
Jaundice may be absent or minimal early
Systemic inflammatory response
Acute kidney injury
Clinically significant bleeding is uncommon and reflects severe systemic inflammation rather than coagulopathy
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Severe hepatocellular damage (Table 16–3)
Coagulopathy
Elevated serum ammonia; correlates with development of encephalopathy and intracranial hypertension
In acetaminophen toxicity, serum aminotransferase elevations are often towering (> 5000 units/L)
Acetaminophen-protein adducts in serum and other biomarkers for early detection are under study
In acute liver failure due to microvesicular steatosis (eg, fatty liver disease of pregnancy), serum aminotransferase elevations may be modest (< 300 units/L)
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