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Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study
BACKGROUND: The aim of RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is to assess the diagnostic accuracy of multiple current and emerging point-of-care tests (POCTs) for active and past SARS-CoV2 infection in the community setting. RAPTOR-C19 will provide the community testbed to...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868893/ https://www.ncbi.nlm.nih.gov/pubmed/33557927 http://dx.doi.org/10.1186/s41512-021-00093-8 |
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author | Nicholson, Brian D. Hayward, Gail Turner, Philip J. Lee, Joseph J. Deeks, Alexandra Logan, Mary Moore, Abigail Seeley, Anna Fanshawe, Thomas Oke, Jason Koshiaris, Constantinos Sheppard, James P. Hoang, Uy Parimalanathan, Vaishnavi Edwards, George Liyange, Harshana Sherlock, Julian Byford, Rachel Zambon, Maria Ellis, Joanna Bernal, Jamie Lopez Amirthalingam, Gayatri Linley, Ezra Borrow, Ray Howsam, Gary Baines, Sophie Ferreira, Filipa de Lusignan, Simon Perera, Rafael Hobbs, F. D. Richard |
author_facet | Nicholson, Brian D. Hayward, Gail Turner, Philip J. Lee, Joseph J. Deeks, Alexandra Logan, Mary Moore, Abigail Seeley, Anna Fanshawe, Thomas Oke, Jason Koshiaris, Constantinos Sheppard, James P. Hoang, Uy Parimalanathan, Vaishnavi Edwards, George Liyange, Harshana Sherlock, Julian Byford, Rachel Zambon, Maria Ellis, Joanna Bernal, Jamie Lopez Amirthalingam, Gayatri Linley, Ezra Borrow, Ray Howsam, Gary Baines, Sophie Ferreira, Filipa de Lusignan, Simon Perera, Rafael Hobbs, F. D. Richard |
author_sort | Nicholson, Brian D. |
collection | PubMed |
description | BACKGROUND: The aim of RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is to assess the diagnostic accuracy of multiple current and emerging point-of-care tests (POCTs) for active and past SARS-CoV2 infection in the community setting. RAPTOR-C19 will provide the community testbed to the COVID-19 National DiagnOstic Research and Evaluation Platform (CONDOR). METHODS: RAPTOR-C19 incorporates a series of prospective observational parallel diagnostic accuracy studies of SARS-CoV2 POCTs against laboratory and composite reference standards in patients with suspected current or past SARS-CoV2 infection attending community settings. Adults and children with suspected current SARS-CoV2 infection who are having an oropharyngeal/nasopharyngeal (OP/NP) swab for laboratory SARS-CoV2 reverse transcriptase Digital/Real-Time Polymerase Chain Reaction (d/rRT-PCR) as part of clinical care or community-based testing will be invited to participate. Adults (≥ 16 years) with suspected past symptomatic infection will also be recruited. Asymptomatic individuals will not be eligible. At the baseline visit, all participants will be asked to submit samples for at least one candidate point-of-care test (POCT) being evaluated (index test/s) as well as an OP/NP swab for laboratory SARS-CoV2 RT-PCR performed by Public Health England (PHE) (reference standard for current infection). Adults will also be asked for a blood sample for laboratory SARS-CoV-2 antibody testing by PHE (reference standard for past infection), where feasible adults will be invited to attend a second visit at 28 days for repeat antibody testing. Additional study data (e.g. demographics, symptoms, observations, household contacts) will be captured electronically. Sensitivity, specificity, positive, and negative predictive values for each POCT will be calculated with exact 95% confidence intervals when compared to the reference standard. POCTs will also be compared to composite reference standards constructed using paired antibody test results, patient reported outcomes, linked electronic health records for outcomes related to COVID-19 such as hospitalisation or death, and other test results. DISCUSSION: High-performing POCTs for community use could be transformational. Real-time results could lead to personal and public health impacts such as reducing onward household transmission of SARS-CoV2 infection, improving surveillance of health and social care staff, contributing to accurate prevalence estimates, and understanding of SARS-CoV2 transmission dynamics in the population. In contrast, poorly performing POCTs could have negative effects, so it is necessary to undertake community-based diagnostic accuracy evaluations before rolling these out. TRIAL REGISTRATION: ISRCTN, ISRCTN14226970 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41512-021-00093-8. |
format | Online Article Text |
id | pubmed-7868893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78688932021-02-08 Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study Nicholson, Brian D. Hayward, Gail Turner, Philip J. Lee, Joseph J. Deeks, Alexandra Logan, Mary Moore, Abigail Seeley, Anna Fanshawe, Thomas Oke, Jason Koshiaris, Constantinos Sheppard, James P. Hoang, Uy Parimalanathan, Vaishnavi Edwards, George Liyange, Harshana Sherlock, Julian Byford, Rachel Zambon, Maria Ellis, Joanna Bernal, Jamie Lopez Amirthalingam, Gayatri Linley, Ezra Borrow, Ray Howsam, Gary Baines, Sophie Ferreira, Filipa de Lusignan, Simon Perera, Rafael Hobbs, F. D. Richard Diagn Progn Res Protocol BACKGROUND: The aim of RApid community Point-of-care Testing fOR COVID-19 (RAPTOR-C19) is to assess the diagnostic accuracy of multiple current and emerging point-of-care tests (POCTs) for active and past SARS-CoV2 infection in the community setting. RAPTOR-C19 will provide the community testbed to the COVID-19 National DiagnOstic Research and Evaluation Platform (CONDOR). METHODS: RAPTOR-C19 incorporates a series of prospective observational parallel diagnostic accuracy studies of SARS-CoV2 POCTs against laboratory and composite reference standards in patients with suspected current or past SARS-CoV2 infection attending community settings. Adults and children with suspected current SARS-CoV2 infection who are having an oropharyngeal/nasopharyngeal (OP/NP) swab for laboratory SARS-CoV2 reverse transcriptase Digital/Real-Time Polymerase Chain Reaction (d/rRT-PCR) as part of clinical care or community-based testing will be invited to participate. Adults (≥ 16 years) with suspected past symptomatic infection will also be recruited. Asymptomatic individuals will not be eligible. At the baseline visit, all participants will be asked to submit samples for at least one candidate point-of-care test (POCT) being evaluated (index test/s) as well as an OP/NP swab for laboratory SARS-CoV2 RT-PCR performed by Public Health England (PHE) (reference standard for current infection). Adults will also be asked for a blood sample for laboratory SARS-CoV-2 antibody testing by PHE (reference standard for past infection), where feasible adults will be invited to attend a second visit at 28 days for repeat antibody testing. Additional study data (e.g. demographics, symptoms, observations, household contacts) will be captured electronically. Sensitivity, specificity, positive, and negative predictive values for each POCT will be calculated with exact 95% confidence intervals when compared to the reference standard. POCTs will also be compared to composite reference standards constructed using paired antibody test results, patient reported outcomes, linked electronic health records for outcomes related to COVID-19 such as hospitalisation or death, and other test results. DISCUSSION: High-performing POCTs for community use could be transformational. Real-time results could lead to personal and public health impacts such as reducing onward household transmission of SARS-CoV2 infection, improving surveillance of health and social care staff, contributing to accurate prevalence estimates, and understanding of SARS-CoV2 transmission dynamics in the population. In contrast, poorly performing POCTs could have negative effects, so it is necessary to undertake community-based diagnostic accuracy evaluations before rolling these out. TRIAL REGISTRATION: ISRCTN, ISRCTN14226970 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41512-021-00093-8. BioMed Central 2021-02-08 /pmc/articles/PMC7868893/ /pubmed/33557927 http://dx.doi.org/10.1186/s41512-021-00093-8 Text en © The Author(s) 2021 Open AccessThis 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/. |
spellingShingle | Protocol Nicholson, Brian D. Hayward, Gail Turner, Philip J. Lee, Joseph J. Deeks, Alexandra Logan, Mary Moore, Abigail Seeley, Anna Fanshawe, Thomas Oke, Jason Koshiaris, Constantinos Sheppard, James P. Hoang, Uy Parimalanathan, Vaishnavi Edwards, George Liyange, Harshana Sherlock, Julian Byford, Rachel Zambon, Maria Ellis, Joanna Bernal, Jamie Lopez Amirthalingam, Gayatri Linley, Ezra Borrow, Ray Howsam, Gary Baines, Sophie Ferreira, Filipa de Lusignan, Simon Perera, Rafael Hobbs, F. D. Richard Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study |
title | Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study |
title_full | Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study |
title_fullStr | Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study |
title_full_unstemmed | Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study |
title_short | Rapid community point-of-care testing for COVID-19 (RAPTOR-C19): protocol for a platform diagnostic study |
title_sort | rapid community point-of-care testing for covid-19 (raptor-c19): protocol for a platform diagnostic study |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868893/ https://www.ncbi.nlm.nih.gov/pubmed/33557927 http://dx.doi.org/10.1186/s41512-021-00093-8 |
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