Screening immigrants for chronic viral hepatitis in GP surgeries could prevent thousands of deaths from liver disease. Chronic hepatitis B and C infections cause no symptoms for decades but lead to cirrhosis and liver cancer in a large proportion of those infected. In the UK, prevalence among immigrants is over 5%, at least ten times higher than in the indigenous population, and mortality in ethnic minorities is rising rapidly. Despite NICE-approved therapies that are highly cost effective, the UK has one of the lowest treatment rates in Europe, and only a tiny minority of diagnosed patients ever receive treatment. This project will test whether opportunistic screening during routine GP visits or targeted invitations to at-risk patients are feasible, acceptable to communities, and cost effective. It will also run a clinical trial of antiviral therapy delivered in primary care rather than hospitals, to see whether community treatment improves engagement and increases the number of immigrants who access therapy. If successful, the findings could lead to a national screening programme and fundamentally change how the NHS identifies and treats viral hepatitis in immigrant communities.
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Aims & ObjectivesWe will determine whether screening immigrants for chronic viral hepatitis in primary care is feasible, acceptable to the communities at risk, and cost effective. We will determine whether therapy for viral hepatitis in primary care is achievable, and both clinically and cost effective. We will determine whether community treatment improves engagement and increases the number of patients who access the effective therapies that are NICE approved for these potentially lethal infections.BackgroundChronic viral hepatitis (persistent infection with either hepatitis B or hepatitis C) causes an asymptomatic disease that leads to cirrhosis and death in a large proportion of those who are infected. These asymptomatic diseases are often not associated with abormalities of liver function tests precluding identification by simple non-specific testing. The prevalence of viral hepatitis is at least ten fold greater in immigrants than in the indigenous community (prevalence in the UK is ~0.5% but > 5% in immigrants) and there is abundant data (from the Health Protection Agency and liver transplant programs - see later) that the mortality and morbidity in ethnic minorities is growing rapidly. Early identification of people with chronic viral hepatitis allows effective therapy, shown by NICE to be highly cost effective. Given the rising mortality in ethnic minorities from chronic viral hepatitis the Advisory Group on Hepatitis and The National Screening Committee have considered screening in immigrants but there is no data on whether this is feasible and clinically/cost effective.The UK has one of the lowest rates of therapy for viral hepatitis in Europe and this is undoubtedly contributing to the rising mortality from liver disease in the UK (mortality is falling in the rest of Europe). UK studies have shown that access to therapy for patients known to have viral hepatitis is poor with only a tiny minority of diagnosed patients going on to receive treatment. Strategies that improve access to treatment are likely to have a major impact on treatment uptake but alternatives to hospital based treatment have not been studied.Research PlansWe will address the evidence gap in screening immigrants for chronic viral hepatitis. We will examine community attitudes to screening (to ensure that screening is acceptable and determine how best to provide information about it). We will critically evaluate opportunistic screening (testing patients from high risk countries when they attend their GP) and targetted screening (contacting patients at risk and asking them to attend). We will complete a cluster randomised clinical trial of antiviral therapy in primary care to determine whether community treatment is feasible and determine whether it improves engagement and increases the proportion of immigrants who access antiviral therapy. We will complete a full cost effectiveness analysis of our interventions and model the burden of disease to allow a national assessment of the impact of viral hepatitis in immigrants.Research TeamThe research team includes practising research hepatologists,virologists and academic general practitioners who have completed studies of screening in primary care. All have published extensively in this field. Experts in qualitative research, health economics and the chairman of a national patient group are co-applicants. An experienced trials unit will manage the trial.Program managementWe will establish a management and steering committee with independent chairmen, financial expertise and patient representatives OutputsWe will determine the best way to engage immigrant communities at risk of viral hepatitis and determine how best to involve them in health care screeningWe will determine how best to screen immigrants for chronic viral hepatitis and make an evidence based recommendation to The National Screening Committee that may lead to a national program.We will determine the cost effectiveness of screening.Our clin
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