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Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection

OBJECTIVE: The purpose of this study was to compare the costs and cost-effectiveness (C/E) of early hepatitis C virus (HCV) RNA testing (alternative-US recommendations) after occupational exposure to HCV with existing follow-up strategies: (1) French, anti-HCV antibodies and alanine transaminase (AL...

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Autores principales: Deuffic-Burban, S, Abiteboul, D, Lot, F, Branger, M, Bouvet, E, Yazdanpanah, Y
Formato: Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597690/
https://www.ncbi.nlm.nih.gov/pubmed/18824553
http://dx.doi.org/10.1136/gut.2007.145516
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author Deuffic-Burban, S
Abiteboul, D
Lot, F
Branger, M
Bouvet, E
Yazdanpanah, Y
author_facet Deuffic-Burban, S
Abiteboul, D
Lot, F
Branger, M
Bouvet, E
Yazdanpanah, Y
author_sort Deuffic-Burban, S
collection PubMed
description OBJECTIVE: The purpose of this study was to compare the costs and cost-effectiveness (C/E) of early hepatitis C virus (HCV) RNA testing (alternative-US recommendations) after occupational exposure to HCV with existing follow-up strategies: (1) French, anti-HCV antibodies and alanine transaminase (ALT) activity at months 1, 3 and 6; (2) European, monthly ALT activity for 4 months and anti-HCV antibodies at month 6; (3) and baseline-US, anti-HCV antibodies and ALT activity at month 6. METHODS: A decision tree simulated each strategy for 7300 healthcare workers (HCWs) exposed to HCV each year in France, taking into account the impact of early diagnosis on the response to antiviral treatment and the deterioration of HCW quality of life after exposure. RESULTS: For a HCV transmission risk of 0.5% after exposure, the French strategy led to the highest costs/person (€181.40) and the baseline-US strategy to the lowest (€126.60) (€178.50) for alternative-US). The shortest mean time to HCV infection diagnosis (1 month) and the lowest number of chronic hepatitis C (CHC) patients (1.9/7300 HCWs exposed) was obtained with the alternative-US strategy (vs 6 months and 7.9 CHC, respectively with baseline-US). Compared with the alternative-US, the French strategy was associated with higher costs and lower utilities, and the European with a higher incremental C/E ratio. Compared with the baseline-US strategy, the alternative-US strategy C/E ratio was €2020 per quality-adjusted life year saved. CONCLUSION: In HCWs exposed to HCV, a strategy based on early HCV RNA testing shortens the period during which the HCW’s wait for his HCV status, leads to lower risk of progression to CHC and is reasonably cost-effective.
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spelling pubmed-25976902009-11-16 Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection Deuffic-Burban, S Abiteboul, D Lot, F Branger, M Bouvet, E Yazdanpanah, Y Gut Hepatology OBJECTIVE: The purpose of this study was to compare the costs and cost-effectiveness (C/E) of early hepatitis C virus (HCV) RNA testing (alternative-US recommendations) after occupational exposure to HCV with existing follow-up strategies: (1) French, anti-HCV antibodies and alanine transaminase (ALT) activity at months 1, 3 and 6; (2) European, monthly ALT activity for 4 months and anti-HCV antibodies at month 6; (3) and baseline-US, anti-HCV antibodies and ALT activity at month 6. METHODS: A decision tree simulated each strategy for 7300 healthcare workers (HCWs) exposed to HCV each year in France, taking into account the impact of early diagnosis on the response to antiviral treatment and the deterioration of HCW quality of life after exposure. RESULTS: For a HCV transmission risk of 0.5% after exposure, the French strategy led to the highest costs/person (€181.40) and the baseline-US strategy to the lowest (€126.60) (€178.50) for alternative-US). The shortest mean time to HCV infection diagnosis (1 month) and the lowest number of chronic hepatitis C (CHC) patients (1.9/7300 HCWs exposed) was obtained with the alternative-US strategy (vs 6 months and 7.9 CHC, respectively with baseline-US). Compared with the alternative-US, the French strategy was associated with higher costs and lower utilities, and the European with a higher incremental C/E ratio. Compared with the baseline-US strategy, the alternative-US strategy C/E ratio was €2020 per quality-adjusted life year saved. CONCLUSION: In HCWs exposed to HCV, a strategy based on early HCV RNA testing shortens the period during which the HCW’s wait for his HCV status, leads to lower risk of progression to CHC and is reasonably cost-effective. BMJ Publishing Group 2008-01 2008-09-29 /pmc/articles/PMC2597690/ /pubmed/18824553 http://dx.doi.org/10.1136/gut.2007.145516 Text en © Deuffic-Burban et al 2009 http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hepatology
Deuffic-Burban, S
Abiteboul, D
Lot, F
Branger, M
Bouvet, E
Yazdanpanah, Y
Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection
title Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection
title_full Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection
title_fullStr Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection
title_full_unstemmed Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection
title_short Costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis C virus infection
title_sort costs and cost-effectiveness of different follow-up schedules for detection of occupational hepatitis c virus infection
topic Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597690/
https://www.ncbi.nlm.nih.gov/pubmed/18824553
http://dx.doi.org/10.1136/gut.2007.145516
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