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Hepatic Encephalopathy
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Hepatic encephalopathy (HE) is a complex neurological syndrome, characteristic of patients with liver disease, that causes a wide and complex spectrum of nonspecific neurological and psychiatric manifestations, ranging from a subclinical entity such as minimal or covert hepatic encephalopathy to a deep form in which a complete alteration of consciousness can be observed: overt hepatic encephalopathy. Both minimal and overt hepatic encephalopathy have a high impact on patients, caregivers, and national health services, driving substantial consumption of economic resources. In this Special Issue, we discussed the current state-of-the-art research, address ongoing knowledge gaps, and ongoing controversies related to the pathogenesis, diagnosis, and therapeutic management of hepatic encephalopathy.
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Keywords
- antibiotic resistance
- autonomic testing
- bile acids
- brain energy crisis
- capsules
- cirrhosis
- Cognitive function
- Coma
- Delirium
- dietary intervention
- encephalopathy
- Enema
- Epidemiology
- gluconeogenesis
- hepatic encephalopathy
- Hospitalizations
- hyperammonemia
- idiopathic non-cirrhotic portal hypertension
- ketogenesis
- Liver
- Liver cirrhosis
- Liver disease
- liver failure
- medicine
- minimal hepatic encephalopathy
- Mitochondria
- Mortality
- myosteatosis
- n/a
- nerve conduction
- non-absorbable disaccharides
- portal vein thrombosis
- porto-sinusoidal vascular liver disease
- porto-systemic shunt
- protein caloric-malnutrition
- Quality of life
- rifaximin
- Sarcopenia
- Sleep Disorders
- Therapy
- thermal sensitivity
- transjugular portosystemic intrahepatic shunt
Links
DOI: 10.3390/books978-3-0365-6339-8Editions