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Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain
OBJECTIVES: To evaluate the cost-effectiveness of direct-acting antiviral (DAAs) treatment versus non-treatment in prisoners awaiting treatment for chronic hepatitis C (CHC) and to analyse the clinical and economic impact of the treatment on liver complications and mortality. MATERIAL AND METHOD: A...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedad Española de Sanidad Penitenciaria
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537362/ https://www.ncbi.nlm.nih.gov/pubmed/32697276 http://dx.doi.org/10.18176/resp.00012 |
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author | Marco, A Domínguez-Hernández, R Casado, MA |
author_facet | Marco, A Domínguez-Hernández, R Casado, MA |
author_sort | Marco, A |
collection | PubMed |
description | OBJECTIVES: To evaluate the cost-effectiveness of direct-acting antiviral (DAAs) treatment versus non-treatment in prisoners awaiting treatment for chronic hepatitis C (CHC) and to analyse the clinical and economic impact of the treatment on liver complications and mortality. MATERIAL AND METHOD: A lifetime Markov model was developed to simulate treatment and disease progression from an estimated cohort of 4,408 CHC prisoners treated with DAAs over 2 years (50% of patient each year) versus no treatment. In the treated cohort, a sustained viral response of 95% was associated. Patient characteristics, transition probabilities, utilities and costs (pharmacological and healthcare states) were obtained from published literature. The model estimated healthcare costs and benefits, incremental cost-utility ratio (ICUR) based on total costs and the quality-adjusted life year (QALY) and avoided clinical events. A National Healthcare System perspective was adopted with a 3% annual discount rate for both costs and health outcomes. Sensitivity analyses were performed to assess uncertainty. RESULTS: In the DDA treated cohort, the model estimated a decrease of 92% of decompensated cirrhosis and 83% of hepatocellular carcinoma, 88% liver-related mortality cases were reduced, 132 liver transplants were avoided. The treatment achieved an additional 5.0/QALYs (21.2 vs. 16.2) with an incremental cost of €3,473 (€24,088 vs. €20,615) per patient with an ICUR of €690 per QALY gained. DISCUSSION: Considering the willingness-to-pay threshold used in Spain (€22,000-30,000/QALY), DAAs treatment for prisoners with CHC is a highly cost-effective strategy, reduces infection transmission, increases survival and reduces complications due to liver disease, as well as the cost associated with its management. |
format | Online Article Text |
id | pubmed-7537362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sociedad Española de Sanidad Penitenciaria |
record_format | MEDLINE/PubMed |
spelling | pubmed-75373622020-10-06 Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain Marco, A Domínguez-Hernández, R Casado, MA Rev Esp Sanid Penit Original Articles OBJECTIVES: To evaluate the cost-effectiveness of direct-acting antiviral (DAAs) treatment versus non-treatment in prisoners awaiting treatment for chronic hepatitis C (CHC) and to analyse the clinical and economic impact of the treatment on liver complications and mortality. MATERIAL AND METHOD: A lifetime Markov model was developed to simulate treatment and disease progression from an estimated cohort of 4,408 CHC prisoners treated with DAAs over 2 years (50% of patient each year) versus no treatment. In the treated cohort, a sustained viral response of 95% was associated. Patient characteristics, transition probabilities, utilities and costs (pharmacological and healthcare states) were obtained from published literature. The model estimated healthcare costs and benefits, incremental cost-utility ratio (ICUR) based on total costs and the quality-adjusted life year (QALY) and avoided clinical events. A National Healthcare System perspective was adopted with a 3% annual discount rate for both costs and health outcomes. Sensitivity analyses were performed to assess uncertainty. RESULTS: In the DDA treated cohort, the model estimated a decrease of 92% of decompensated cirrhosis and 83% of hepatocellular carcinoma, 88% liver-related mortality cases were reduced, 132 liver transplants were avoided. The treatment achieved an additional 5.0/QALYs (21.2 vs. 16.2) with an incremental cost of €3,473 (€24,088 vs. €20,615) per patient with an ICUR of €690 per QALY gained. DISCUSSION: Considering the willingness-to-pay threshold used in Spain (€22,000-30,000/QALY), DAAs treatment for prisoners with CHC is a highly cost-effective strategy, reduces infection transmission, increases survival and reduces complications due to liver disease, as well as the cost associated with its management. Sociedad Española de Sanidad Penitenciaria 2020-07-10 /pmc/articles/PMC7537362/ /pubmed/32697276 http://dx.doi.org/10.18176/resp.00012 Text en https://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License |
spellingShingle | Original Articles Marco, A Domínguez-Hernández, R Casado, MA Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain |
title | Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain |
title_full | Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain |
title_fullStr | Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain |
title_full_unstemmed | Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain |
title_short | Cost-effectiveness analysis of chronic hepatitis C treatment in the prison population in Spain |
title_sort | cost-effectiveness analysis of chronic hepatitis c treatment in the prison population in spain |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537362/ https://www.ncbi.nlm.nih.gov/pubmed/32697276 http://dx.doi.org/10.18176/resp.00012 |
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