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Updated: Aug 27, 2025

Measurement of the Hepatic Venous Pressure Gradient and Transjugular Liver Biopsy
Published on: June 18, 2020
Nonselective beta-blocker use is associated with increased hepatic encephalopathy-related readmissions in cirrhosis
Mohammad Amin Fallahzadeh1, Sumeet K Asrani2, Elliot B Tapper3
1Department of Internal Medicine, Baylor University Medical Center, Dallas, TX 75246, United States. aminfa91@gmail.com.
Insights
Nonselective beta-blockers (NSBBs) increase hospital readmissions for hepatic encephalopathy (HE) in cirrhosis patients. This finding holds true regardless of liver disease severity, suggesting a need to reconsider NSBB use in this population.
Area of Science:
- Hepatology
- Cardiology
- Pharmacology
Background:
- Hepatic encephalopathy (HE) is a common neurocognitive complication in cirrhosis patients, frequently leading to hospitalizations.
- Nonselective beta-blockers (NSBBs) are standard treatment for portal hypertension in cirrhosis.
- A potential link between NSBBs, reduced liver metabolic filtering, and increased HE hospitalizations was hypothesized.
Purpose of the Study:
- To investigate the association between NSBB administration and HE-related readmissions in patients with cirrhosis.
- To determine if NSBBs impact the incidence of HE-related hospitalizations.
Main Methods:
- Retrospective cohort study of 393 cirrhotic patients admitted for portal hypertension indications.
- Cox proportional hazards analysis and Fine-Gray modeling were used to identify predictors of HE readmissions and account for competing risks (death, liver transplantation).
Main Results:
- Patients on NSBBs had a significantly higher cumulative incidence of first HE-related readmissions (71.8%) compared to those not on NSBBs (41.8%).
- NSBB use was independently associated with an increased risk of HE-related readmissions (Hazard Ratio: 1.74).
- This association persisted after adjusting for disease severity and other medications.
Conclusions:
- Nonselective beta-blocker use is independently linked to a higher rate of hepatic encephalopathy-related readmissions in cirrhosis patients.
- The findings suggest that NSBBs may exacerbate HE, irrespective of the severity of liver disease.
- Clinical practice may need to re-evaluate the role of NSBBs in managing cirrhotic patients prone to HE.
Background:
Hepatic encephalopathy (HE) is a neurocognitive condition in cirrhosis leading to frequent hospitalizations. Nonselective beta-blockers (NSBBs) are the mainstay of pharmacologic treatment in cirrhotic patients. We hypothesized that since NSBBs decrease cardiac output and portal flow, the decreased metabolic filtering process of liver parenchyma may lead to increased HE-related hospitalizations.
Aim:
To evaluate the impact of NSBB administration on HE-related readmissions in cirrhotic patients.
Methods:
In this retrospective cohort study, we included 393 patients admitted to Baylor University Medical Center for liver-related portal hypertension indications between January 2013 and July 2018. Independent predictors of the first HE-related readmissions were identified using Cox proportional hazards analysis. The cumulative incidence of the first HE-related readmissions between patients receiving NSBBs and not receiving NSBBs was examined using Fine-Gray modeling to account for the competing risk of death or liver transplantation.
Results:
The mean age was 58.1 ± 10.2 years and most patients fell into Child class C (49.1%) or B (43.8%). The median Model for End-Stage Liver Disease-Sodium score was 22 (IQR: 11). The cumulative incidence of the first HE-related readmissions was significantly higher in patients taking NSBBs compared to patients not receiving NSBBs (71.8% vs 41.8%, P < 0.0001). In multivariate analysis, after adjusting for demographics, markers of liver disease severity, selective beta-blocker, lactulose and rifaximin use, NSBB use [Hazard ratio: 1.74 (95%CI: 1.29-2.34)] was independently associated with the first HE-related readmissions over a median follow-up of 3.8 years.
Conclusion:
NSBB use is independently associated with increased HE-related readmissions in patients with cirrhosis, regardless of liver disease severity.
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