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Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?

BACKGROUND: Widely access to interferon-free direct-acting antiviral regimens (IFN-free DAA) is poised to dramatically change the impact of the HCV epidemic among people who inject drugs (PWID). We evaluated the long-term effect of increasing HCV testing, treatment and engagement into harm-reduction...

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Autores principales: Lima, Viviane D., Rozada, Ignacio, Grebely, Jason, Hull, Mark, Lourenco, Lillian, Nosyk, Bohdan, Krajden, Mel, Yoshida, Eric, Wood, Evan, Montaner, Julio S. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669174/
https://www.ncbi.nlm.nih.gov/pubmed/26633652
http://dx.doi.org/10.1371/journal.pone.0143836
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author Lima, Viviane D.
Rozada, Ignacio
Grebely, Jason
Hull, Mark
Lourenco, Lillian
Nosyk, Bohdan
Krajden, Mel
Yoshida, Eric
Wood, Evan
Montaner, Julio S. G.
author_facet Lima, Viviane D.
Rozada, Ignacio
Grebely, Jason
Hull, Mark
Lourenco, Lillian
Nosyk, Bohdan
Krajden, Mel
Yoshida, Eric
Wood, Evan
Montaner, Julio S. G.
author_sort Lima, Viviane D.
collection PubMed
description BACKGROUND: Widely access to interferon-free direct-acting antiviral regimens (IFN-free DAA) is poised to dramatically change the impact of the HCV epidemic among people who inject drugs (PWID). We evaluated the long-term effect of increasing HCV testing, treatment and engagement into harm-reduction activities, focused on active PWID, on the HCV epidemic in British Columbia (BC), Canada. METHODS: We built a compartmental model of HCV disease transmission stratified by disease progression, transmission risk, and fibrosis level. We explored the effect of: (1) Increasing treatment rates from 8 to 20, 40 and 80 per 1000 infected PWID/year; (2) Increasing treatment eligibility based on fibrosis level; (3) Maximizing the effect of testing by performing it immediately upon ending the acute phase; (4) Increasing access to harm-reduction activities to reduce the risk of re-infection; (5) Different HCV antiviral regimens on the Control Reproduction Number R (c). We assessed the impact of these interventions on incidence, prevalence and mortality from 2016 to 2030. RESULTS: Of all HCV antiviral regimens, only IFN-free DAAs offered a high chance of disease elimination (i.e. R (c) < 1), but it would be necessary to substantially increase the current low testing and treatment rates. Assuming a treatment rate of 80 per 1000 infected PWID per year, coupled with a high testing rate, the incidence rate, at the end of 2030, could decrease from 92.9 per 1000 susceptible PWID per year (Status Quo) to 82.8 (by treating only PWID with fibrosis level F (2) and higher) or to 65.5 (by treating PWID regardless of fibrosis level). If PWID also had access to increased harm-reduction activities, the incidence rate further decreased to 53.1 per 1000 susceptible PWID per year. We also obtained significant decreases in prevalence and mortality at the end of 2030. CONCLUSIONS: The combination of increased access to HCV testing, highly efficacious antiviral treatment and harm-reduction programs can substantially decrease the burden of the HCV epidemic among PWID. However, unless we increase the current levels of treatment and testing, the HCV epidemic among PWID in BC, and in other parts of the world with similar epidemiological background, will remain a substantial public health concern for many years.
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spelling pubmed-46691742015-12-10 Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs? Lima, Viviane D. Rozada, Ignacio Grebely, Jason Hull, Mark Lourenco, Lillian Nosyk, Bohdan Krajden, Mel Yoshida, Eric Wood, Evan Montaner, Julio S. G. PLoS One Research Article BACKGROUND: Widely access to interferon-free direct-acting antiviral regimens (IFN-free DAA) is poised to dramatically change the impact of the HCV epidemic among people who inject drugs (PWID). We evaluated the long-term effect of increasing HCV testing, treatment and engagement into harm-reduction activities, focused on active PWID, on the HCV epidemic in British Columbia (BC), Canada. METHODS: We built a compartmental model of HCV disease transmission stratified by disease progression, transmission risk, and fibrosis level. We explored the effect of: (1) Increasing treatment rates from 8 to 20, 40 and 80 per 1000 infected PWID/year; (2) Increasing treatment eligibility based on fibrosis level; (3) Maximizing the effect of testing by performing it immediately upon ending the acute phase; (4) Increasing access to harm-reduction activities to reduce the risk of re-infection; (5) Different HCV antiviral regimens on the Control Reproduction Number R (c). We assessed the impact of these interventions on incidence, prevalence and mortality from 2016 to 2030. RESULTS: Of all HCV antiviral regimens, only IFN-free DAAs offered a high chance of disease elimination (i.e. R (c) < 1), but it would be necessary to substantially increase the current low testing and treatment rates. Assuming a treatment rate of 80 per 1000 infected PWID per year, coupled with a high testing rate, the incidence rate, at the end of 2030, could decrease from 92.9 per 1000 susceptible PWID per year (Status Quo) to 82.8 (by treating only PWID with fibrosis level F (2) and higher) or to 65.5 (by treating PWID regardless of fibrosis level). If PWID also had access to increased harm-reduction activities, the incidence rate further decreased to 53.1 per 1000 susceptible PWID per year. We also obtained significant decreases in prevalence and mortality at the end of 2030. CONCLUSIONS: The combination of increased access to HCV testing, highly efficacious antiviral treatment and harm-reduction programs can substantially decrease the burden of the HCV epidemic among PWID. However, unless we increase the current levels of treatment and testing, the HCV epidemic among PWID in BC, and in other parts of the world with similar epidemiological background, will remain a substantial public health concern for many years. Public Library of Science 2015-12-03 /pmc/articles/PMC4669174/ /pubmed/26633652 http://dx.doi.org/10.1371/journal.pone.0143836 Text en © 2015 Lima et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Lima, Viviane D.
Rozada, Ignacio
Grebely, Jason
Hull, Mark
Lourenco, Lillian
Nosyk, Bohdan
Krajden, Mel
Yoshida, Eric
Wood, Evan
Montaner, Julio S. G.
Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?
title Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?
title_full Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?
title_fullStr Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?
title_full_unstemmed Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?
title_short Are Interferon-Free Direct-Acting Antivirals for the Treatment of HCV Enough to Control the Epidemic among People Who Inject Drugs?
title_sort are interferon-free direct-acting antivirals for the treatment of hcv enough to control the epidemic among people who inject drugs?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669174/
https://www.ncbi.nlm.nih.gov/pubmed/26633652
http://dx.doi.org/10.1371/journal.pone.0143836
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