Hepatitis B Virus (HBV) treatment eligibility in the UK: retrospective longitudinal cohort data to explore the impact of changes in clinical guidelines
Hepatitis B Virus (HBV) treatment eligibility in the UK: retrospective longitudinal cohort data to explore the impact of changes in clinical guidelines
Nucleos/tide analogue (NA) drugs are used for long-term treatment of chronic hepatitis B virus (HBV) infection, with treatment eligibility criteria changing rapidly amidst globally evolving clinical guidelines. We aimed to quantify the prescription of NA drugs to date, and to undertake a preliminary assessment of the impact of relaxing treatment eligibility thresholds, leveraging a unique large real-world secondary care dataset. We assimilated longitudinal clinical data, collected between February 1997 and April 2023 from adults with chronic HBV infection from six centres in England through the UK NIHR Health Informatics Collaborative (HIC) Viral Hepatitis and Liver Disease theme. We describe factors currently associated with the receipt of NA treatment and determine the proportion of the population who would become treatment eligible as thresholds change. Across 7558 adults with a mean follow-up of 4.0 years (SD 3.9), NA treatment was prescribed in 2014/7558 (26.6%), and as expected according to guidelines at the time, was associated with HBV e-antigen (HBeAg) positivity and alanine transferase (ALT) above the upper limit of normal (> ULN). Treatment was more likely in males, older adults, in Asian and Other ethnicities (compared to White), and less likely in socioeconomically deprived individuals. The proportion of treatment-eligible individuals was 32.3% based on 2 records of ALT > ULN over 6–12 months, 41.7% based on ALT > ULN and viral load (VL) > 2000 IU/mL, and 95.1% based on detectable VL and either ALT > ULN or age > 30 years. Evolving clinical guidelines will lead to substantial increases in the proportion of individuals living with HBV who are eligible for treatment, underlining the need for services to adapt rapidly to the changing clinical environment.
Adolescent, Adult, Aged, Alanine Transaminase/blood, Antiviral Agents/therapeutic use, Female, Hepatitis B e Antigens/blood, Hepatitis B virus/drug effects, Hepatitis B, Chronic/drug therapy, Humans, Longitudinal Studies, Male, Middle Aged, Practice Guidelines as Topic, Retrospective Studies, United Kingdom/epidemiology, Young Adult, treatment, tenofovir, criteria, eligibility, NA therapy, guidelines, elimination, HBV, hepatitis
Campbell, Cori
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Wang, Tingyan
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Stockdale, Alexander J.
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Todd, Stacy
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Jaworski, Jakub
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Glampson, Ben
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Papadimitriou, Dimitri
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Mayer, Erik
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Roadknight, Gail
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Noble, Theresa
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Várnai, Kinga A.
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Davis, Cai
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Heinson, Ashley I.
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George, Michael
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Borca, Florina
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Roberts, Timothy
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Ribeyre, Baptiste B.
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English, Louise
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Zhu, Leilei
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Woods, Kerrie
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Davies, Jim
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Cooke, Graham S.
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Nastouli, Eleni
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Khakoo, Salim I.
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Gelson, William
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Elsharkawy, Ahmed M.
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Barnes, Eleanor
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Matthews, Philippa C.
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NIHR HIC Viral Hepatitis and Liver Disease Consortium
23 October 2025
Campbell, Cori
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Wang, Tingyan
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Stockdale, Alexander J.
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Todd, Stacy
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Jaworski, Jakub
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Glampson, Ben
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Papadimitriou, Dimitri
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Mayer, Erik
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Salih, Hizni
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Roadknight, Gail
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Little, Stephanie
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Noble, Theresa
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Várnai, Kinga A.
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Davis, Cai
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Heinson, Ashley I.
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George, Michael
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Borca, Florina
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Roberts, Timothy
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Ribeyre, Baptiste B.
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English, Louise
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Zhu, Leilei
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Woods, Kerrie
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Davies, Jim
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Cooke, Graham S.
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Nastouli, Eleni
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Khakoo, Salim I.
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Gelson, William
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Elsharkawy, Ahmed M.
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Barnes, Eleanor
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Matthews, Philippa C.
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