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Published on: October 28, 2022
Hepatic Encephalopathy in Children
Johanna Ascher Bartlett1, Rohit Kohli2
1Department of Gastroenterology, Hepatology and Nutrition at Children's Hospital Los Angeles, 4650 Sunset Blvd, MS 78, Los Angeles, CA, 90027, USA. jascherbartlett@chla.usc.edu.
Insights
Hepatic encephalopathy (HE) in children involves mental status changes and requires careful assessment. Early detection and management of HE, including reducing ammonia levels, are crucial for preventing serious complications.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Neuroscience
Background:
- Hepatic encephalopathy (HE) presents with mental status and neuropsychiatric changes in chronic and acute liver disease.
- Clinical manifestations of HE in children can be subtle, making early diagnosis challenging.
- Progression of HE symptoms may signal cerebral edema and systemic deterioration.
Purpose of the Study:
- To highlight the importance of assessing hepatic encephalopathy in pediatric patients.
- To discuss current and emerging diagnostic methods for HE.
- To outline current treatment strategies for HE.
Main Methods:
- Review of clinical manifestations and diagnostic challenges of HE in children.
- Discussion of established and investigational assessment tools (imaging, EEG, neurobiomarkers).
- Analysis of current therapeutic interventions for HE.
Main Results:
- Hyperammonemia can be present in HE, but its level does not correlate with clinical severity.
- Newer diagnostic modalities are under investigation.
- Treatment focuses on the underlying liver disease and ammonia reduction.
Conclusions:
- Prompt recognition and management of HE in children are critical.
- Multifaceted treatment approaches, including medications and liver support, are employed.
- Ongoing research aims to improve HE diagnosis and treatment.
Abstract:
Hepatic encephalopathy, characterized by mental status changes and neuropsychiatric impairment, is associated with chronic liver disease as well as acute liver failure. In children, its clinical manifestations can be challenging to pinpoint. However, careful assessment for the development of hepatic encephalopathy is imperative when caring for these patients as progression of symptoms can indicate impending cerebral edema and systemic deterioration. Hepatic encephalopathy can present with hyperammonemia, but it is important to note that the degree of hyperammonemia is not indicative of severity of clinical manifestations. Newer forms of assessment are undergoing further research, and include imaging, EEG and neurobiomarkers. Mainstay of treatment currently includes management of underlying cause of liver disease, as well as reduction of hyperammonemia with either enteral medications such as lactulose and rifaximin, or even with extracorporeal liver support modalities.
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