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Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study

Despite promising steps towards the elimination of hepatitis C virus (HCV) in the UK, several indicators provide a cause for concern for future disease burden. We aimed to improve understanding of geographical variation in HCV-related severe liver disease and historic risk factor prevalence among cl...

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Autores principales: Nickbakhsh, Sema, McWilliam Leitch, E. Carol, Smith, Shanley, Davis, Chris, Hutchinson, Sharon, Irving, William L., McLauchlan, John, Thomson, Emma C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126891/
https://www.ncbi.nlm.nih.gov/pubmed/36915219
http://dx.doi.org/10.1017/S0950268823000377
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author Nickbakhsh, Sema
McWilliam Leitch, E. Carol
Smith, Shanley
Davis, Chris
Hutchinson, Sharon
Irving, William L.
McLauchlan, John
Thomson, Emma C.
author_facet Nickbakhsh, Sema
McWilliam Leitch, E. Carol
Smith, Shanley
Davis, Chris
Hutchinson, Sharon
Irving, William L.
McLauchlan, John
Thomson, Emma C.
author_sort Nickbakhsh, Sema
collection PubMed
description Despite promising steps towards the elimination of hepatitis C virus (HCV) in the UK, several indicators provide a cause for concern for future disease burden. We aimed to improve understanding of geographical variation in HCV-related severe liver disease and historic risk factor prevalence among clinic attendees in England and Scotland. We used metadata from 3829 HCV-positive patients consecutively enrolled into HCV Research UK from 48 hospital centres in England and Scotland during 2012–2014. Employing mixed-effects statistical modelling, several independent risk factors were identified: age 46–59 y (OR(adj) 3.06) and ≥60 y (OR(adj) 5.64) relative to <46 y, male relative to female sex (OR(adj) 1.58), high BMI (OR(adj) 1.73) and obesity (OR(adj) 2.81) relative to normal BMI, diabetes relative to no diabetes (OR(adj) 2.75), infection with HCV genotype (GT)-3 relative to GT-1 (OR(adj) 1.75), route of infection through blood products relative to injecting drug use (OR(adj) 1.40), and lower odds were associated with black ethnicity (OR(adj) 0.31) relative to white ethnicity. A small proportion of unexplained variation was attributed to differences between hospital centres and local health authorities. Our study provides a baseline measure of historic risk factor prevalence and potential geographical variation in healthcare provision, to support ongoing monitoring of HCV-related disease burden and the design of risk prevention measures.
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spelling pubmed-101268912023-04-26 Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study Nickbakhsh, Sema McWilliam Leitch, E. Carol Smith, Shanley Davis, Chris Hutchinson, Sharon Irving, William L. McLauchlan, John Thomson, Emma C. Epidemiol Infect Original Paper Despite promising steps towards the elimination of hepatitis C virus (HCV) in the UK, several indicators provide a cause for concern for future disease burden. We aimed to improve understanding of geographical variation in HCV-related severe liver disease and historic risk factor prevalence among clinic attendees in England and Scotland. We used metadata from 3829 HCV-positive patients consecutively enrolled into HCV Research UK from 48 hospital centres in England and Scotland during 2012–2014. Employing mixed-effects statistical modelling, several independent risk factors were identified: age 46–59 y (OR(adj) 3.06) and ≥60 y (OR(adj) 5.64) relative to <46 y, male relative to female sex (OR(adj) 1.58), high BMI (OR(adj) 1.73) and obesity (OR(adj) 2.81) relative to normal BMI, diabetes relative to no diabetes (OR(adj) 2.75), infection with HCV genotype (GT)-3 relative to GT-1 (OR(adj) 1.75), route of infection through blood products relative to injecting drug use (OR(adj) 1.40), and lower odds were associated with black ethnicity (OR(adj) 0.31) relative to white ethnicity. A small proportion of unexplained variation was attributed to differences between hospital centres and local health authorities. Our study provides a baseline measure of historic risk factor prevalence and potential geographical variation in healthcare provision, to support ongoing monitoring of HCV-related disease burden and the design of risk prevention measures. Cambridge University Press 2023-03-14 /pmc/articles/PMC10126891/ /pubmed/36915219 http://dx.doi.org/10.1017/S0950268823000377 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Paper
Nickbakhsh, Sema
McWilliam Leitch, E. Carol
Smith, Shanley
Davis, Chris
Hutchinson, Sharon
Irving, William L.
McLauchlan, John
Thomson, Emma C.
Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study
title Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study
title_full Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study
title_fullStr Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study
title_full_unstemmed Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study
title_short Geographical variation in hepatitis C-related severe liver disease and patient risk factors: a multicentre cross-sectional study
title_sort geographical variation in hepatitis c-related severe liver disease and patient risk factors: a multicentre cross-sectional study
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126891/
https://www.ncbi.nlm.nih.gov/pubmed/36915219
http://dx.doi.org/10.1017/S0950268823000377
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