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.
Abstract

Related Concept Videos

Heart Failure Drugs: β-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
418
Antihypertensive Drugs: Types of β-Blockers01:28

Antihypertensive Drugs: Types of β-Blockers

β receptors are classified into three subclasses: β1, β2, and β3. β1 receptors are primarily located in the heart and kidneys. When they get activated, they increase heart rate, contractility, and renin release. This process enhances blood pressure and aids in stress management. In contrast, β2 receptors are situated mainly in the lungs, blood vessels, and skeletal muscles. Upon activation, they trigger smooth muscle relaxation, causing bronchodilation and...
825
Esophageal Varices-II: Clinical Features and Management01:28

Esophageal Varices-II: Clinical Features and Management

Esophageal varices often manifest as gastrointestinal bleeding episodes, presenting symptoms like hematemesis (vomiting of blood), hematochezia (passing fresh blood via the rectum), and melena (black, tarry stools). Other signs can include weight loss, anorexia, abdominal discomfort, jaundice, pruritus, altered mental status, and muscle cramps.
In the initial assessment, a thorough review of the patient's medical history is vital to identify risk factors such as liver disease, alcohol...
122
Hepatic Drug Excretion: Enterohepatic Cycling01:17

Hepatic Drug Excretion: Enterohepatic Cycling

Enterohepatic cycling involves the active secretion of drugs and their metabolites into the bile via transporters in the canalicular membrane of hepatocytes. This secretion is an integral part of the digestive process, releasing these substances into the gastrointestinal (GI) tract.
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...
1.7K
Hepatic Drug Clearance: Effect of Protein Binding01:09

Hepatic Drug Clearance: Effect of Protein Binding

Hepatic clearance is influenced by protein binding based on the drug's extraction ratio. Drugs with high extraction ratios are considered flow-limited and remain unaffected by protein binding during hepatic clearance. On the other hand, drugs with low extraction ratios may be impacted by plasma protein binding, although the extent of this influence depends on the fraction of the drug bound.
For low-extraction-ratio drugs that are less than 80% protein-bound, minor changes in protein binding...
277
Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers01:27

Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers

β-receptor blockers significantly impact the cardiovascular system by counteracting catecholamine-induced sympathetic responses. These medications decrease heart rate, contractility, and cardiac output, potentially leading to cardiac depression, life-threatening bradycardia, and death. Therapeutically, β-blockers function as mild antihypertensives and are utilized in treating angina pectoris and cardiac arrhythmias. However, nonselective β-blockers inhibit β2-receptors in...
934