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Development and Validation of a Prognostic Score to Predict Covert Hepatic Encephalopathy in Patients With Cirrhosis
Christian Labenz1,2, Gerrit Toenges3, Yvonne Huber1,2
1Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany.
Insights
A new clinical score helps identify patients with cirrhosis at risk of covert hepatic encephalopathy (CHE). This score correlates with quality of life and predicts the risk of overt hepatic encephalopathy.
Area of Science:
- Hepatology
- Neurology
- Clinical Diagnostics
Background:
- Covert hepatic encephalopathy (CHE) diagnosis is often overlooked in cirrhosis patients.
- CHE significantly impacts patient quality of life and prognosis.
Purpose of the Study:
- To develop and validate an easy-to-perform clinical score for predicting CHE in cirrhosis patients.
- To assess the score's correlation with quality of life and risk of overt hepatic encephalopathy (OHE).
Main Methods:
- Prospective enrollment of 142 (development) and 96 (validation) cirrhosis patients.
- Utilized Psychometric Hepatic Encephalopathy Score, simplified animal naming test, and Chronic Liver Disease Questionnaire.
- Followed TRIPOD guidelines for score development and validation.
Main Results:
- The developed clinical CHE score, incorporating ascites, OHE history, albumin, CLDQ activity, and animal naming test, showed high discrimination (AUC 0.908 development, 0.872 validation).
- Established cutoffs identified low, intermediate, and high-risk groups for CHE with excellent sensitivity (90%) and specificity (91%).
- Higher scores correlated with poorer quality of life and predicted first-time OHE within 180 days.
Conclusions:
- An easy-to-use clinical score effectively identifies cirrhosis patients at risk for CHE.
- The score aids in stratifying CHE risk, informing prognosis, and guiding further testing.
- This tool can improve management of CHE in clinical practice.
Objectives:
Diagnosis of covert hepatic encephalopathy (CHE) is challenging and often neglected in clinical practice. The aim of this study was to develop an easy-to-perform score to predict CHE in patients with cirrhosis.
Methods:
For the development or validation cohort of the proposed clinical CHE score, 142 or 96 consecutive patients with cirrhosis were prospectively enrolled. The Psychometric Hepatic Encephalopathy Score was used to detect minimal hepatic encephalopathy. All patients were examined with the simplified animal naming test and were asked to complete the Chronic Liver Disease Questionnaire. We followed the TRIPOD guideline for development, validation, and reporting of the proposed score.
Results:
The clinical covert hepatic encephalopathy score containing the variables-clinically detectable ascites, history of overt hepatic encephalopathy (OHE), albumin serum level, activity subdomain of the Chronic Liver Disease Questionnaire, and simplified animal naming test-discriminated best between patients with and without CHE. We generated 2 cutoff values for the identification of the high-, intermediate- (with need for additional specialized testing), and low-risk groups for CHE. By applying these cutoffs, the sensitivity, specificity, positive predictive value, and negative predictive value were 90%, 91%, 85%, and 94%, respectively. The AUC was 0.908 or 0.872 for the development or the validation cohort, respectively. Higher scores were further associated with poorer quality of life, and the high-risk group was predictive for first-time OHE within 180 days.
Conclusions:
We developed an easy-to-perform score to identify patients with cirrhosis at risk of CHE, which correlates with quality of life and risk of first-time OHE.
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