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Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework

BACKGROUND: The COVID-19 pandemic has led to many countries implementing lockdown procedures, resulting in the suspension of laboratory research. With lockdown measures now easing in some areas, many laboratories are preparing to reopen. This is particularly challenging for clinical research laborat...

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Autores principales: Walker, Eloise M, Jasper, Alice E, Davis, Lauren, Yip, Kay Por, Faniyi, Aduragbemi A, Hughes, Michael J, Crisford, Helena A, Spittle, Daniella A, Sapey, Elizabeth, Belchamber, Kylie B R, Scott, Aaron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721628/
https://www.ncbi.nlm.nih.gov/pubmed/33146625
http://dx.doi.org/10.2196/22570
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author Walker, Eloise M
Jasper, Alice E
Davis, Lauren
Yip, Kay Por
Faniyi, Aduragbemi A
Hughes, Michael J
Crisford, Helena A
Spittle, Daniella A
Sapey, Elizabeth
Belchamber, Kylie B R
Scott, Aaron
author_facet Walker, Eloise M
Jasper, Alice E
Davis, Lauren
Yip, Kay Por
Faniyi, Aduragbemi A
Hughes, Michael J
Crisford, Helena A
Spittle, Daniella A
Sapey, Elizabeth
Belchamber, Kylie B R
Scott, Aaron
author_sort Walker, Eloise M
collection PubMed
description BACKGROUND: The COVID-19 pandemic has led to many countries implementing lockdown procedures, resulting in the suspension of laboratory research. With lockdown measures now easing in some areas, many laboratories are preparing to reopen. This is particularly challenging for clinical research laboratories due to the dual risk of patient samples carrying the virus that causes COVID-19, SARS-CoV-2, and the risk to patients being exposed to research staff during clinical sampling. To date, no confirmed transmission of the virus has been confirmed within a laboratory setting; however, operating processes and procedures should be adapted to ensure safe working of samples of positive, negative, or unknown COVID-19 status. OBJECTIVE: In this paper, we propose a framework for reopening a clinical research laboratory and resuming operations with the aim to maximize research capacity while minimizing the risk to research participants and staff. METHODS: This framework was developed by consensus among experienced laboratory staff who have prepared to reopen a clinical research laboratory. RESULTS: Multiple aspects need to be considered to reopen a clinical laboratory. We describe our process to stratify projects by risk, including assessment of donor risk and COVID-19 clinical status, the COVID-19 status of the specific sample type, and how to safely process each sample type. We describe methods to prepare the laboratory for safe working including maintaining social distancing through signage, one-way systems and access arrangements for staff and patients, limiting staff numbers on site and encouraging home working for all nonlaboratory tasks including data analysis and writing. Shared equipment usage was made safe by adapting booking systems to allow for the deployment of cleaning protocols. All risk assessments and standard operating procedures were rewritten and approved by local committees, and staff training was initiated to ensure compliance. CONCLUSIONS: Laboratories can adopt and adapt this framework to expedite reopening a clinical laboratory during the current COVID-19 pandemic while mitigating the risk to research participants and staff.
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spelling pubmed-77216282020-12-11 Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework Walker, Eloise M Jasper, Alice E Davis, Lauren Yip, Kay Por Faniyi, Aduragbemi A Hughes, Michael J Crisford, Helena A Spittle, Daniella A Sapey, Elizabeth Belchamber, Kylie B R Scott, Aaron JMIR Res Protoc Proposal BACKGROUND: The COVID-19 pandemic has led to many countries implementing lockdown procedures, resulting in the suspension of laboratory research. With lockdown measures now easing in some areas, many laboratories are preparing to reopen. This is particularly challenging for clinical research laboratories due to the dual risk of patient samples carrying the virus that causes COVID-19, SARS-CoV-2, and the risk to patients being exposed to research staff during clinical sampling. To date, no confirmed transmission of the virus has been confirmed within a laboratory setting; however, operating processes and procedures should be adapted to ensure safe working of samples of positive, negative, or unknown COVID-19 status. OBJECTIVE: In this paper, we propose a framework for reopening a clinical research laboratory and resuming operations with the aim to maximize research capacity while minimizing the risk to research participants and staff. METHODS: This framework was developed by consensus among experienced laboratory staff who have prepared to reopen a clinical research laboratory. RESULTS: Multiple aspects need to be considered to reopen a clinical laboratory. We describe our process to stratify projects by risk, including assessment of donor risk and COVID-19 clinical status, the COVID-19 status of the specific sample type, and how to safely process each sample type. We describe methods to prepare the laboratory for safe working including maintaining social distancing through signage, one-way systems and access arrangements for staff and patients, limiting staff numbers on site and encouraging home working for all nonlaboratory tasks including data analysis and writing. Shared equipment usage was made safe by adapting booking systems to allow for the deployment of cleaning protocols. All risk assessments and standard operating procedures were rewritten and approved by local committees, and staff training was initiated to ensure compliance. CONCLUSIONS: Laboratories can adopt and adapt this framework to expedite reopening a clinical laboratory during the current COVID-19 pandemic while mitigating the risk to research participants and staff. JMIR Publications 2020-12-04 /pmc/articles/PMC7721628/ /pubmed/33146625 http://dx.doi.org/10.2196/22570 Text en ©Eloise M Walker, Alice E Jasper, Lauren Davis, Kay Por Yip, Aduragbemi A Faniyi, Michael J Hughes, Helena A Crisford, Daniella A Spittle, Elizabeth Sapey, Kylie B R Belchamber, Aaron Scott. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 04.12.2020. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on http://www.researchprotocols.org, as well as this copyright and license information must be included.
spellingShingle Proposal
Walker, Eloise M
Jasper, Alice E
Davis, Lauren
Yip, Kay Por
Faniyi, Aduragbemi A
Hughes, Michael J
Crisford, Helena A
Spittle, Daniella A
Sapey, Elizabeth
Belchamber, Kylie B R
Scott, Aaron
Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework
title Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework
title_full Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework
title_fullStr Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework
title_full_unstemmed Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework
title_short Mitigating Health Risks to Reopen a Clinical Research Laboratory During the COVID-19 Pandemic: A Framework
title_sort mitigating health risks to reopen a clinical research laboratory during the covid-19 pandemic: a framework
topic Proposal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721628/
https://www.ncbi.nlm.nih.gov/pubmed/33146625
http://dx.doi.org/10.2196/22570
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