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The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service

BACKGROUND: Hepatitis C treatment uptake in Australia is low. To increase access to hepatitis C virus treatment for people who inject drugs, we developed a community-based, nurse-led service that linked a viral hepatitis service in a tertiary hospital to primary care clinics, and resulted in hepatit...

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Autores principales: Wade, Amanda J., Macdonald, Diana M., Doyle, Joseph S., Gordon, Adam, Roberts, Stuart K., Thompson, Alexander J., Hellard, Margaret E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642931/
https://www.ncbi.nlm.nih.gov/pubmed/26562516
http://dx.doi.org/10.1371/journal.pone.0142770
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author Wade, Amanda J.
Macdonald, Diana M.
Doyle, Joseph S.
Gordon, Adam
Roberts, Stuart K.
Thompson, Alexander J.
Hellard, Margaret E.
author_facet Wade, Amanda J.
Macdonald, Diana M.
Doyle, Joseph S.
Gordon, Adam
Roberts, Stuart K.
Thompson, Alexander J.
Hellard, Margaret E.
author_sort Wade, Amanda J.
collection PubMed
description BACKGROUND: Hepatitis C treatment uptake in Australia is low. To increase access to hepatitis C virus treatment for people who inject drugs, we developed a community-based, nurse-led service that linked a viral hepatitis service in a tertiary hospital to primary care clinics, and resulted in hepatitis C treatment provision in the community. METHODS: A retrospective cohort study of patients referred to the community hepatitis service was undertaken to determine the cascade of care. Logistic regression analyses were used to identify predictors of hepatitis C treatment uptake. RESULTS: Four hundred and sixty-two patients were referred to the community hepatitis service; 344 attended. Among the 279 attendees with confirmed chronic hepatitis C, 257 (99%) reported ever injecting drugs, and 124 (48%) injected in the last month. Of 201 (72%) patients who had their fibrosis staged, 63 (31%) had F3-F4 fibrosis. Fifty-five patients commenced hepatitis C treatment; 26 (47%) were current injectors and 25 (45%) had F3-F4 fibrosis. Nineteen of the 27 (70%) genotype 1 patients and 14 of the 26 (54%) genotype 3 patients eligible for assessment achieved a sustained virologic response. Advanced fibrosis was a significant predictor of treatment uptake in adjusted analysis (AOR 2.56, CI 1.30–5.00, p = 0.006). CONCLUSIONS: Our community hepatitis service produced relatively high rates of fibrosis assessment, hepatitis C treatment uptake and cure, among people who inject drugs. These findings highlight the potential benefits of providing community-based hepatitis C care to people who inject drugs in Australia–benefits that should be realised as direct-acting antiviral agents become available.
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spelling pubmed-46429312015-11-18 The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service Wade, Amanda J. Macdonald, Diana M. Doyle, Joseph S. Gordon, Adam Roberts, Stuart K. Thompson, Alexander J. Hellard, Margaret E. PLoS One Research Article BACKGROUND: Hepatitis C treatment uptake in Australia is low. To increase access to hepatitis C virus treatment for people who inject drugs, we developed a community-based, nurse-led service that linked a viral hepatitis service in a tertiary hospital to primary care clinics, and resulted in hepatitis C treatment provision in the community. METHODS: A retrospective cohort study of patients referred to the community hepatitis service was undertaken to determine the cascade of care. Logistic regression analyses were used to identify predictors of hepatitis C treatment uptake. RESULTS: Four hundred and sixty-two patients were referred to the community hepatitis service; 344 attended. Among the 279 attendees with confirmed chronic hepatitis C, 257 (99%) reported ever injecting drugs, and 124 (48%) injected in the last month. Of 201 (72%) patients who had their fibrosis staged, 63 (31%) had F3-F4 fibrosis. Fifty-five patients commenced hepatitis C treatment; 26 (47%) were current injectors and 25 (45%) had F3-F4 fibrosis. Nineteen of the 27 (70%) genotype 1 patients and 14 of the 26 (54%) genotype 3 patients eligible for assessment achieved a sustained virologic response. Advanced fibrosis was a significant predictor of treatment uptake in adjusted analysis (AOR 2.56, CI 1.30–5.00, p = 0.006). CONCLUSIONS: Our community hepatitis service produced relatively high rates of fibrosis assessment, hepatitis C treatment uptake and cure, among people who inject drugs. These findings highlight the potential benefits of providing community-based hepatitis C care to people who inject drugs in Australia–benefits that should be realised as direct-acting antiviral agents become available. Public Library of Science 2015-11-12 /pmc/articles/PMC4642931/ /pubmed/26562516 http://dx.doi.org/10.1371/journal.pone.0142770 Text en © 2015 Wade 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
Wade, Amanda J.
Macdonald, Diana M.
Doyle, Joseph S.
Gordon, Adam
Roberts, Stuart K.
Thompson, Alexander J.
Hellard, Margaret E.
The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service
title The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service
title_full The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service
title_fullStr The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service
title_full_unstemmed The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service
title_short The Cascade of Care for an Australian Community-Based Hepatitis C Treatment Service
title_sort cascade of care for an australian community-based hepatitis c treatment service
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642931/
https://www.ncbi.nlm.nih.gov/pubmed/26562516
http://dx.doi.org/10.1371/journal.pone.0142770
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