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The use of technology-based adherence monitoring in the treatment of hepatitis C virus
Direct-acting antivirals (DAAs) achieve high hepatitis C virus (HCV) cure rates and are forgiving to missed doses, but adherence–efficacy relationships have not been well defined. Traditional adherence measures (e.g. pill counts, self-report and pharmacy refills) over-estimate medication adherence....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112320/ https://www.ncbi.nlm.nih.gov/pubmed/35591885 http://dx.doi.org/10.1177/20499361221095664 |
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author | Adje, Yeba H. Brooks, Kristina M. Castillo-Mancilla, Jose R. Wyles, David L. Anderson, Peter L. Kiser, Jennifer J. |
author_facet | Adje, Yeba H. Brooks, Kristina M. Castillo-Mancilla, Jose R. Wyles, David L. Anderson, Peter L. Kiser, Jennifer J. |
author_sort | Adje, Yeba H. |
collection | PubMed |
description | Direct-acting antivirals (DAAs) achieve high hepatitis C virus (HCV) cure rates and are forgiving to missed doses, but adherence–efficacy relationships have not been well defined. Traditional adherence measures (e.g. pill counts, self-report and pharmacy refills) over-estimate medication adherence. Newer technology-based tools have been used to provide more objective adherence data. Herein, electronic medication diaries (e-diaries), medication events monitoring system (MEMS(®)) caps, electronic blister packs, electronic pill boxes, video-based directly observed therapy (vDOT), artificial intelligence platforms (AIPs), and ingestible sensor systems are described, and compared based on existing studies using DAA. Percent adherence, predictors of adherence, and HCV cure rates utilizing these technologies are included. DAA adherence with e-diaries was 95–96%, MEMS(®) caps and ingestible biosensors were between 95% and 97%, blister pack weekly dosing ranged 73–98%, and daily dosing 73–94%, whereas electronic pill boxes ranged between 39% and 89%, vDOT was 98% and AIP 91–96%. Despite a wide range of adherence, high sustained virologic response (SVR) rates (86–100%) were observed across all studies utilizing these different technology-based tools. Current data support the forgiveness of DAA therapies to missed doses using tools that provide more quantitative adherence measures compared with self-report and provide insight on adherence–efficacy relationships for contemporary DAA. |
format | Online Article Text |
id | pubmed-9112320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-91123202022-05-18 The use of technology-based adherence monitoring in the treatment of hepatitis C virus Adje, Yeba H. Brooks, Kristina M. Castillo-Mancilla, Jose R. Wyles, David L. Anderson, Peter L. Kiser, Jennifer J. Ther Adv Infect Dis Infections Associated with Substance Use and Related Behaviors Direct-acting antivirals (DAAs) achieve high hepatitis C virus (HCV) cure rates and are forgiving to missed doses, but adherence–efficacy relationships have not been well defined. Traditional adherence measures (e.g. pill counts, self-report and pharmacy refills) over-estimate medication adherence. Newer technology-based tools have been used to provide more objective adherence data. Herein, electronic medication diaries (e-diaries), medication events monitoring system (MEMS(®)) caps, electronic blister packs, electronic pill boxes, video-based directly observed therapy (vDOT), artificial intelligence platforms (AIPs), and ingestible sensor systems are described, and compared based on existing studies using DAA. Percent adherence, predictors of adherence, and HCV cure rates utilizing these technologies are included. DAA adherence with e-diaries was 95–96%, MEMS(®) caps and ingestible biosensors were between 95% and 97%, blister pack weekly dosing ranged 73–98%, and daily dosing 73–94%, whereas electronic pill boxes ranged between 39% and 89%, vDOT was 98% and AIP 91–96%. Despite a wide range of adherence, high sustained virologic response (SVR) rates (86–100%) were observed across all studies utilizing these different technology-based tools. Current data support the forgiveness of DAA therapies to missed doses using tools that provide more quantitative adherence measures compared with self-report and provide insight on adherence–efficacy relationships for contemporary DAA. SAGE Publications 2022-05-13 /pmc/articles/PMC9112320/ /pubmed/35591885 http://dx.doi.org/10.1177/20499361221095664 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Infections Associated with Substance Use and Related Behaviors Adje, Yeba H. Brooks, Kristina M. Castillo-Mancilla, Jose R. Wyles, David L. Anderson, Peter L. Kiser, Jennifer J. The use of technology-based adherence monitoring in the treatment of hepatitis C virus |
title | The use of technology-based adherence monitoring in the treatment of
hepatitis C virus |
title_full | The use of technology-based adherence monitoring in the treatment of
hepatitis C virus |
title_fullStr | The use of technology-based adherence monitoring in the treatment of
hepatitis C virus |
title_full_unstemmed | The use of technology-based adherence monitoring in the treatment of
hepatitis C virus |
title_short | The use of technology-based adherence monitoring in the treatment of
hepatitis C virus |
title_sort | use of technology-based adherence monitoring in the treatment of
hepatitis c virus |
topic | Infections Associated with Substance Use and Related Behaviors |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112320/ https://www.ncbi.nlm.nih.gov/pubmed/35591885 http://dx.doi.org/10.1177/20499361221095664 |
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