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Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays
OBJECTIVE: There is a lack of evidence addressing several important human factors questions pertaining to the quality of supportive information provided by commercial manufacturers that can affect the adoption and use of lateral flow serology assays in practice. We aimed to: (1) identify and assess...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985936/ https://www.ncbi.nlm.nih.gov/pubmed/33741675 http://dx.doi.org/10.1136/bmjopen-2020-047163 |
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author | Kierkegaard, Patrick McLister, Anna Buckle, Peter |
author_facet | Kierkegaard, Patrick McLister, Anna Buckle, Peter |
author_sort | Kierkegaard, Patrick |
collection | PubMed |
description | OBJECTIVE: There is a lack of evidence addressing several important human factors questions pertaining to the quality of supportive information provided by commercial manufacturers that can affect the adoption and use of lateral flow serology assays in practice. We aimed to: (1) identify and assess the quality of information that commercial manufacturers provided for their point-of-care tests (POCTs) and (2) examine the implications of these findings on real-world settings. DESIGN: We used a content analysis methodology in two stages to systematically, code and analyse textual data from documents of commercial manufacturers. A deductive approach was applied using a coding guide based on the validated Point-of-Care Key Evidence Tool (POCKET) multidimensional checklist. An inductive approach was used to identify new patterns or themes generated from our textual analysis. SETTING: Publicly available supportive information documents by commercial manufacturers for lateral flow serology, were identified and gathered from online searches. PARTICIPANTS: Supportive information documents retrieved from online searches over 3 months (March 2020 to June 2020). RESULTS: A total of 79 POCTs were identified that met the study inclusion criteria. Using the POCKET coding guide, we found that the quality of information varied significantly between the manufacturers and was often lacking in detail. Our inductive approach further examined these topics and found that several statements were vague and that significant variations in the level of details existed between manufacturers. CONCLUSIONS: This study revealed significant concerns surrounding the supportive information reported by manufacturers for lateral flow serology assays. Information transparency was poor and human factor issues were not properly addressed to mitigate the risk of improper device use, although it should be noted that the results of our study are limited by the data that manufactures were prepared to disclose. Overall, commercial manufacturers should improve the quality and value of information presented in their supporting documentation. |
format | Online Article Text |
id | pubmed-7985936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-79859362021-03-23 Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays Kierkegaard, Patrick McLister, Anna Buckle, Peter BMJ Open Diagnostics OBJECTIVE: There is a lack of evidence addressing several important human factors questions pertaining to the quality of supportive information provided by commercial manufacturers that can affect the adoption and use of lateral flow serology assays in practice. We aimed to: (1) identify and assess the quality of information that commercial manufacturers provided for their point-of-care tests (POCTs) and (2) examine the implications of these findings on real-world settings. DESIGN: We used a content analysis methodology in two stages to systematically, code and analyse textual data from documents of commercial manufacturers. A deductive approach was applied using a coding guide based on the validated Point-of-Care Key Evidence Tool (POCKET) multidimensional checklist. An inductive approach was used to identify new patterns or themes generated from our textual analysis. SETTING: Publicly available supportive information documents by commercial manufacturers for lateral flow serology, were identified and gathered from online searches. PARTICIPANTS: Supportive information documents retrieved from online searches over 3 months (March 2020 to June 2020). RESULTS: A total of 79 POCTs were identified that met the study inclusion criteria. Using the POCKET coding guide, we found that the quality of information varied significantly between the manufacturers and was often lacking in detail. Our inductive approach further examined these topics and found that several statements were vague and that significant variations in the level of details existed between manufacturers. CONCLUSIONS: This study revealed significant concerns surrounding the supportive information reported by manufacturers for lateral flow serology assays. Information transparency was poor and human factor issues were not properly addressed to mitigate the risk of improper device use, although it should be noted that the results of our study are limited by the data that manufactures were prepared to disclose. Overall, commercial manufacturers should improve the quality and value of information presented in their supporting documentation. BMJ Publishing Group 2021-03-19 /pmc/articles/PMC7985936/ /pubmed/33741675 http://dx.doi.org/10.1136/bmjopen-2020-047163 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Diagnostics Kierkegaard, Patrick McLister, Anna Buckle, Peter Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays |
title | Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays |
title_full | Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays |
title_fullStr | Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays |
title_full_unstemmed | Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays |
title_short | Rapid point-of-care testing for COVID-19: quality of supportive information for lateral flow serology assays |
title_sort | rapid point-of-care testing for covid-19: quality of supportive information for lateral flow serology assays |
topic | Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985936/ https://www.ncbi.nlm.nih.gov/pubmed/33741675 http://dx.doi.org/10.1136/bmjopen-2020-047163 |
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