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Published on: August 1, 2018
Natural history of covert hepatic encephalopathy: An observational study of 366 cirrhotic patients
An-Jiang Wang1, A-Ping Peng1, Bi-Min Li1
1Department of Gastroenterology and Hepatology, The First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi Province, China.
Insights
Covert hepatic encephalopathy (CHE) in cirrhosis patients can worsen, persist, or resolve without treatment. Identifying CHE and its predictors aids in managing complications and mortality.
Area of Science:
- Hepatology
- Gastroenterology
- Internal Medicine
Background:
- Covert hepatic encephalopathy (CHE) is a subtle form of liver dysfunction.
- Its natural history and impact on cirrhosis progression without intervention are not fully understood.
Purpose of the Study:
- To investigate the natural progression of CHE in cirrhotic patients.
- To identify factors influencing CHE outcomes, including overt HE, complications, and mortality.
Main Methods:
- A cohort of 366 cirrhotic outpatients was assessed for CHE.
- Patients were followed for approximately 11 months, recording cirrhosis-related complications, CHE resolution, and mortality.
- Predictors for complications and death were analyzed.
Main Results:
- CHE was diagnosed in 35.8% of patients.
- CHE patients exhibited higher rates of death and hospitalization for complications, including overt HE (OHE).
- Predictors for OHE included low serum albumin; high creatinine predicted mortality; Child-Pugh B/C and OHE history predicted CHE resolution.
Conclusions:
- CHE's course is variable, with exacerbation, persistence, or spontaneous resolution occurring without treatment.
- Predictive factors identified can guide patient triage and management strategies.
- This understanding supports more cost-effective care for cirrhosis patients with CHE.
Aim:
To explore the natural history of covert hepatic encephalopathy (CHE) in absence of medication intervention.
Methods:
Consecutive outpatient cirrhotic patients in a Chinese tertiary care hospital were enrolled and evaluated for CHE diagnosis. They were followed up for a mean of 11.2 ± 1.3 mo. Time to the first cirrhosis-related complications requiring hospitalization, including overt HE (OHE), resolution of CHE and death/transplantation, were compared between CHE and no-CHE patients. Predictors for complication(s) and death/transplantation were also analyzed.
Results:
A total of 366 patients (age: 47.2 ± 8.6 years, male: 73.0%) were enrolled. CHE was identified in 131 patients (35.8%). CHE patients had higher rates of death and incidence of complications requiring hospitalization, including OHE, compared to unimpaired patients. Moreover, 17.6% of CHE patients developed OHE, 42.0% suffered persistent CHE, and 19.8% of CHE spontaneously resolved. In CHE patients, serum albumin < 30 g/L (HR = 5.22, P = 0.03) was the sole predictor for developing OHE, and blood creatinine > 133 μmol/L (HR = 4.75, P = 0.036) predicted mortality. Child-Pugh B/C (HR = 0.084, P < 0.001) and OHE history (HR = 0.15, P = 0.014) were predictors of spontaneous resolution of CHE.
Conclusion:
CHE exacerbates, persists or resolves without medication intervention in clinically stable cirrhosis. Triage of patients based on these predictors will allow for more cost-effect management of CHE.
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