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Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK
Innovative testing approaches and care pathways are required to meet HIV, hepatitis B (HBV) and hepatitis C (HCV) elimination goals. Routine testing for blood-borne viruses (BBVs) within emergency departments (EDs) is suggested by the European Centre for Disease Prevention and Control but there is a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648896/ https://www.ncbi.nlm.nih.gov/pubmed/36357472 http://dx.doi.org/10.1038/s41598-022-23602-1 |
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author | Smout, Elizabeth Phyu, Khine Hughes, Gareth J. Parker, Lee Rezai, Roozbeh Evans, Amy McLaren, Joscelyne Bush, Stephen Davey, Sarah Aldersley, Mark A. Ruf, Murad Page, Emma E. |
author_facet | Smout, Elizabeth Phyu, Khine Hughes, Gareth J. Parker, Lee Rezai, Roozbeh Evans, Amy McLaren, Joscelyne Bush, Stephen Davey, Sarah Aldersley, Mark A. Ruf, Murad Page, Emma E. |
author_sort | Smout, Elizabeth |
collection | PubMed |
description | Innovative testing approaches and care pathways are required to meet HIV, hepatitis B (HBV) and hepatitis C (HCV) elimination goals. Routine testing for blood-borne viruses (BBVs) within emergency departments (EDs) is suggested by the European Centre for Disease Prevention and Control but there is a paucity of supporting evidence. We evaluated the introduction of routine BBV testing in EDs at a large teaching hospital in northern England. In October 2018, we modified the electronic laboratory ordering system to reflex opt-out HIV, HBV and HCV testing for all ED attendees aged 16–65 years who had a routine blood test for urea and electrolytes (U&Es). Linkage to care (LTC) was attempted for newly diagnosed patients, those never referred and those who had previously disengaged from care. The project operated for 18 months, here we present evaluation of the initial nine months (2 October 2018–1 July 2019). We analysed testing uptake, BBV seropositivity, LTC and treatment initiation within six months post-diagnosis. Over 9 months, 17,026/28,178 (60.4%) ED attendees who had U&Es performed were tested for ≥ 1 BBV. 299 active BBV infections were identified: 70 HIV Ab/Ag-positive (0.4% seroprevalence), 73 HBsAg-positive (0.4%) and 156 HCV RNA-positive (1.0%). Only 24.3% (17/70) HIV Ab/Ag-positive individuals required LTC, compared to 94.9% (148/156) HCV RNA-positive and 53.4% (39/73) HBsAg-positive individuals. LTC was successful in 94.1% (16/17) HIV Ab/Ag-positive and 69.3% (27/39) HBsAg-positive individuals. However, at 6 months LTC was just 39.2% (58/148) for HCV RNA-positive individuals, with 64% (37/58) of these commencing treatment. Universal opt-out ED BBV testing proved feasible and effective in identifying active BBV infections, especially among marginalised populations with reduced healthcare access. Our integrated approach achieved good LTC rates although further service development is necessary, particularly for HCV RNA-positive people who inject drugs. |
format | Online Article Text |
id | pubmed-9648896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96488962022-11-14 Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK Smout, Elizabeth Phyu, Khine Hughes, Gareth J. Parker, Lee Rezai, Roozbeh Evans, Amy McLaren, Joscelyne Bush, Stephen Davey, Sarah Aldersley, Mark A. Ruf, Murad Page, Emma E. Sci Rep Article Innovative testing approaches and care pathways are required to meet HIV, hepatitis B (HBV) and hepatitis C (HCV) elimination goals. Routine testing for blood-borne viruses (BBVs) within emergency departments (EDs) is suggested by the European Centre for Disease Prevention and Control but there is a paucity of supporting evidence. We evaluated the introduction of routine BBV testing in EDs at a large teaching hospital in northern England. In October 2018, we modified the electronic laboratory ordering system to reflex opt-out HIV, HBV and HCV testing for all ED attendees aged 16–65 years who had a routine blood test for urea and electrolytes (U&Es). Linkage to care (LTC) was attempted for newly diagnosed patients, those never referred and those who had previously disengaged from care. The project operated for 18 months, here we present evaluation of the initial nine months (2 October 2018–1 July 2019). We analysed testing uptake, BBV seropositivity, LTC and treatment initiation within six months post-diagnosis. Over 9 months, 17,026/28,178 (60.4%) ED attendees who had U&Es performed were tested for ≥ 1 BBV. 299 active BBV infections were identified: 70 HIV Ab/Ag-positive (0.4% seroprevalence), 73 HBsAg-positive (0.4%) and 156 HCV RNA-positive (1.0%). Only 24.3% (17/70) HIV Ab/Ag-positive individuals required LTC, compared to 94.9% (148/156) HCV RNA-positive and 53.4% (39/73) HBsAg-positive individuals. LTC was successful in 94.1% (16/17) HIV Ab/Ag-positive and 69.3% (27/39) HBsAg-positive individuals. However, at 6 months LTC was just 39.2% (58/148) for HCV RNA-positive individuals, with 64% (37/58) of these commencing treatment. Universal opt-out ED BBV testing proved feasible and effective in identifying active BBV infections, especially among marginalised populations with reduced healthcare access. Our integrated approach achieved good LTC rates although further service development is necessary, particularly for HCV RNA-positive people who inject drugs. Nature Publishing Group UK 2022-11-10 /pmc/articles/PMC9648896/ /pubmed/36357472 http://dx.doi.org/10.1038/s41598-022-23602-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Smout, Elizabeth Phyu, Khine Hughes, Gareth J. Parker, Lee Rezai, Roozbeh Evans, Amy McLaren, Joscelyne Bush, Stephen Davey, Sarah Aldersley, Mark A. Ruf, Murad Page, Emma E. Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK |
title | Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK |
title_full | Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK |
title_fullStr | Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK |
title_full_unstemmed | Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK |
title_short | Real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the UK |
title_sort | real-world clinical effectiveness and sustainability of universal bloodborne virus testing in an urban emergency department in the uk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648896/ https://www.ncbi.nlm.nih.gov/pubmed/36357472 http://dx.doi.org/10.1038/s41598-022-23602-1 |
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