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These studies suggest non-selective beta-blockers are effective in treating hypertension, preventing variceal bleeding, reducing mortality in cirrhotic patients, and may reduce the risk of hepatocellular carcinoma, but their safety in end-stage liver disease and effects on lung function in chronic heart failure patients with COPD require careful consideration.
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Non-selective beta blockers (NSBBs) are medications that inhibit the action of endogenous catecholamines on both beta-1 and beta-2 adrenergic receptors. These drugs are widely used in various clinical settings, including the management of hypertension, heart failure, and portal hypertension in cirrhosis. Unlike selective beta blockers, which primarily target beta-1 receptors, NSBBs affect both types of receptors, leading to a broader range of physiological effects.
NSBBs are a cornerstone in the management of portal hypertension in cirrhosis, particularly for preventing variceal bleeding. Studies have shown that NSBBs like propranolol and nadolol are effective in reducing the risk of initial and recurrent variceal bleeding . However, the efficacy of NSBBs in reducing mortality remains debated, with some studies indicating no significant difference in survival rates compared to other interventions like banding ligation.
Carvedilol, a non-selective beta blocker with additional alpha-1 blocking properties, has been compared to traditional NSBBs in patients with cirrhosis and gastroesophageal varices. While carvedilol has shown a greater reduction in hepatic venous pressure gradient, it did not significantly improve clinical outcomes such as mortality or the incidence of upper gastrointestinal bleeding compared to traditional NSBBs.
In patients with ACLF, ongoing treatment with NSBBs has been associated with reduced systemic inflammation and improved short-term survival. A study involving 349 ACLF patients found that those treated with NSBBs had a lower 28-day mortality rate and reduced white cell counts, suggesting a potential anti-inflammatory benefit.
NSBBs have been used for blood pressure control since the mid-20th century. They are particularly effective in managing hypertension and chronic heart failure (CHF). In patients with CHF and coexistent chronic obstructive pulmonary disease (COPD), switching between beta-1 selective beta blockers and NSBBs like carvedilol was well tolerated and resulted in significant hemodynamic changes, although carvedilol was associated with a greater reduction in central augmented pressure and N-terminal pro-hormone brain natriuretic peptide levels.
In patients with rheumatoid arthritis (RA) who have experienced a myocardial infarction (MI), the use of NSBBs has been linked to improved long-term survival. A nationwide cohort study found that NSBBs were more effective than beta-1 selective beta blockers in reducing all-cause mortality in this patient population.
The role of NSBBs in cancer recurrence and survival has been explored, with mixed results. While NSBBs did not significantly affect cancer recurrence rates, they were associated with improved disease-free survival and overall survival in specific cancer types such as ovarian cancer and melanoma. However, the evidence remains variable and tumor-specific.
Non-selective beta blockers are versatile medications with applications ranging from the management of portal hypertension in cirrhosis to improving survival in cardiovascular diseases and potentially influencing cancer outcomes. While they offer significant benefits, their use must be carefully considered, especially in patients with advanced liver disease or coexistent conditions like COPD. Further research is needed to fully understand their long-term effects and optimize their clinical use.
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