Primary prevention
Methods of primary prevention include:
Prevention strategies aimed at reducing excessive alcohol consumption, intravenous drug use, and unprotected intercourse
Vaccination programmes for hepatitis B
Public health strategies to control the rising incidence of obesity and diabetes
Screening patients with risk factors for liver disease with non-invasive markers of liver fibrosis to identify liver disease before cirrhosis develops
Treatment of any underlying chronic liver disease to prevent the progression to cirrhosis
Appropriate screening of family members of patients with cirrhosis secondary to haemochromatosis or Wilson’s disease
Screening of blood donors and products for viral hepatitides.
Secondary prevention
The following secondary preventive strategies are aimed at minimising the level of superimposed hepatic insult in an established cirrhotic liver:
Treatment of any underlying chronic liver disease
Avoidance of alcohol and other hepatotoxins such as non-steroidal anti-inflammatory drugs and high doses of paracetamol (>2-3 g/day)
Immunisation against hepatitis A and B for susceptible patients.
In particular, the US Advisory Committee on Immunization Practices recommends that all patients with cirrhosis should be vaccinated against hepatitis A and B.[209]
There is some evidence to suggest that long-term treatment with beta-blockers (propranolol or carvedilol) increases decompensation-free survival, compared with placebo, in patients with compensated cirrhosis and clinically significant portal hypertension.[210][211] Non-selective beta-blockers such as carvedilol may be considered to prevent decompensation in patients with compensated advanced chronic liver disease with clinically significant portal hypertension, except in those with contraindications such as asthma, advanced heart block, and bradyarrhythmias.[2][212] The American Association for the Study of Liver Diseases recommends against the use of non-selective beta-blockers to prevent decompensation in patients with cirrhosis without clinically significant portal hypertension.[2]
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