Cargando…
The Massachusetts Hepatitis C Testing Cascade, 2014-2016
OBJECTIVES: To characterize hepatitis C testing in Massachusetts and guide stakeholders in addressing the needs of people living with hepatitis C. METHODS: All persons with a positive laboratory report for anti-hepatitis C virus (HCV) antibody, between 2014 and 2016, were included in the testing cas...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589943/ https://www.ncbi.nlm.nih.gov/pubmed/31258329 http://dx.doi.org/10.1177/1178636119857961 |
_version_ | 1783429456963043328 |
---|---|
author | Vo, Quynh T Onofrey, Shauna Church, Daniel Cranston, Kevin DeMaria, Alfred Klevens, R Monina |
author_facet | Vo, Quynh T Onofrey, Shauna Church, Daniel Cranston, Kevin DeMaria, Alfred Klevens, R Monina |
author_sort | Vo, Quynh T |
collection | PubMed |
description | OBJECTIVES: To characterize hepatitis C testing in Massachusetts and guide stakeholders in addressing the needs of people living with hepatitis C. METHODS: All persons with a positive laboratory report for anti-hepatitis C virus (HCV) antibody, between 2014 and 2016, were included in the testing cascade. Outcomes were HCV tests received after a positive anti-HCV antibody test: nucleic acid test or genotype test. Logistic regression analyses were performed to determine factors associated with progression through the HCV testing cascade. RESULTS: Among those reported anti-HCV antibody positive, a total of 13 194 (61%) cases had a subsequent RNA-based test, and 79% (10 374/13 194) were confirmed with current, active HCV infection. For confirmed HCV cases, 44% (4557/10 374) had a genotype identified. The median time from an antibody-positive test to a RNA-based test was 29 days (interquartile range [IQR] = 7-151). Differences in moving through the testing cascade were observed by birth cohort and race/ethnicity. CONCLUSIONS: Improved surveillance capture of demographic information is needed to help public health agencies ensure equity in HCV diagnosis and linkage to care. |
format | Online Article Text |
id | pubmed-6589943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-65899432019-06-28 The Massachusetts Hepatitis C Testing Cascade, 2014-2016 Vo, Quynh T Onofrey, Shauna Church, Daniel Cranston, Kevin DeMaria, Alfred Klevens, R Monina Microbiol Insights Original Research OBJECTIVES: To characterize hepatitis C testing in Massachusetts and guide stakeholders in addressing the needs of people living with hepatitis C. METHODS: All persons with a positive laboratory report for anti-hepatitis C virus (HCV) antibody, between 2014 and 2016, were included in the testing cascade. Outcomes were HCV tests received after a positive anti-HCV antibody test: nucleic acid test or genotype test. Logistic regression analyses were performed to determine factors associated with progression through the HCV testing cascade. RESULTS: Among those reported anti-HCV antibody positive, a total of 13 194 (61%) cases had a subsequent RNA-based test, and 79% (10 374/13 194) were confirmed with current, active HCV infection. For confirmed HCV cases, 44% (4557/10 374) had a genotype identified. The median time from an antibody-positive test to a RNA-based test was 29 days (interquartile range [IQR] = 7-151). Differences in moving through the testing cascade were observed by birth cohort and race/ethnicity. CONCLUSIONS: Improved surveillance capture of demographic information is needed to help public health agencies ensure equity in HCV diagnosis and linkage to care. SAGE Publications 2019-06-21 /pmc/articles/PMC6589943/ /pubmed/31258329 http://dx.doi.org/10.1177/1178636119857961 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.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 | Original Research Vo, Quynh T Onofrey, Shauna Church, Daniel Cranston, Kevin DeMaria, Alfred Klevens, R Monina The Massachusetts Hepatitis C Testing Cascade, 2014-2016 |
title | The Massachusetts Hepatitis C Testing Cascade, 2014-2016 |
title_full | The Massachusetts Hepatitis C Testing Cascade, 2014-2016 |
title_fullStr | The Massachusetts Hepatitis C Testing Cascade, 2014-2016 |
title_full_unstemmed | The Massachusetts Hepatitis C Testing Cascade, 2014-2016 |
title_short | The Massachusetts Hepatitis C Testing Cascade, 2014-2016 |
title_sort | massachusetts hepatitis c testing cascade, 2014-2016 |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589943/ https://www.ncbi.nlm.nih.gov/pubmed/31258329 http://dx.doi.org/10.1177/1178636119857961 |
work_keys_str_mv | AT voquynht themassachusettshepatitisctestingcascade20142016 AT onofreyshauna themassachusettshepatitisctestingcascade20142016 AT churchdaniel themassachusettshepatitisctestingcascade20142016 AT cranstonkevin themassachusettshepatitisctestingcascade20142016 AT demariaalfred themassachusettshepatitisctestingcascade20142016 AT klevensrmonina themassachusettshepatitisctestingcascade20142016 AT voquynht massachusettshepatitisctestingcascade20142016 AT onofreyshauna massachusettshepatitisctestingcascade20142016 AT churchdaniel massachusettshepatitisctestingcascade20142016 AT cranstonkevin massachusettshepatitisctestingcascade20142016 AT demariaalfred massachusettshepatitisctestingcascade20142016 AT klevensrmonina massachusettshepatitisctestingcascade20142016 |