Hepatic Encephalopathy
Also known as: Liver Brain Disease, Portosystemic Encephalopathy
Hepatic encephalopathy is a decline in brain function occurring when the liver cannot adequately remove toxins, particularly ammonia, from the blood. It is most commonly seen in advanced cirrhosis and ranges from subtle cognitive changes to coma. With appropriate treatment, episodes can be managed and recurrence reduced.
Symptoms
Causes
- Accumulation of ammonia and toxins due to liver failure
- Portal-systemic shunting bypassing liver detoxification
- Precipitating factors: GI bleeding, infection, constipation, dehydration
Risk Factors
- Advanced cirrhosis from any cause
- Previous episodes of hepatic encephalopathy
- TIPS placement
- GI bleeding
- Infection or sepsis
- Kidney dysfunction
Diagnosis
- Clinical assessment of mental status in a patient with liver disease
- Blood ammonia level (elevated)
- Psychometric testing for minimal hepatic encephalopathy
- Exclusion of other causes of altered mental status
- CT or MRI to rule out other conditions
Treatment
- Lactulose to reduce ammonia absorption from the gut
- Rifaximin for secondary prevention of recurrence
- Identification and treatment of precipitating factors
- Adequate nutrition with appropriate protein intake
- Liver transplant evaluation for recurrent or severe episodes
When to See a Doctor
- A person with liver disease becomes confused or disoriented
- Personality changes or excessive drowsiness develop suddenly
- Hand-flapping tremor (asterixis) is noticed
- The person becomes unresponsive
Frequently Asked Questions
Related Conditions
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