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A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management
OBJECTIVES: Reverse transcription polymerase chain reaction (RT-PCR) testing is indispensable in management of the coronavirus disease 2019 (COVID-19) pandemic. However, with the emergence of new variants of severe acute respiratory syndrome coronavirus-2, the cause of COVID-19, the screening capaci...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673736/ https://www.ncbi.nlm.nih.gov/pubmed/34922006 http://dx.doi.org/10.1016/j.ijid.2021.12.328 |
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author | Ayaz, Akif Demir, Asli Guner Ozturk Ozturk, Gurkan Kocak, Mehmet |
author_facet | Ayaz, Akif Demir, Asli Guner Ozturk Ozturk, Gurkan Kocak, Mehmet |
author_sort | Ayaz, Akif |
collection | PubMed |
description | OBJECTIVES: Reverse transcription polymerase chain reaction (RT-PCR) testing is indispensable in management of the coronavirus disease 2019 (COVID-19) pandemic. However, with the emergence of new variants of severe acute respiratory syndrome coronavirus-2, the cause of COVID-19, the screening capacity of RT-PCR testing is overburdened, and new strategies and capabilities need to be established. One option is pooled RT-PCR testing. DESIGN: This study used various mixtures of COVID-19 samples known to be negative and positive, and investigated the impact of pool size and mixture level on final cycle threshold (Ct) values. More specifically, 5, 10 and 20 negative samples were combined with one, two or three low Ct or high Ct positive samples. RESULTS: Average baseline Ct and numbers of high and low Ct samples in the pool were found to be the main drivers of the final Ct value, making detectability easier. Pool size was not significantly associated with final Ct, but was suggestive. CONCLUSIONS: A pooled RT-PCR testing strategy does not reduce the sensitivity of RT-PCR, and thus provides a practical way to expand RT-PCR screening capacity in pandemic management. The pool size was not found to be significant, so it is recommended that a pool size of 20 would be a practical number to reduce the time taken to obtain the results and the cost of RT-PCR testing. |
format | Online Article Text |
id | pubmed-8673736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86737362021-12-16 A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management Ayaz, Akif Demir, Asli Guner Ozturk Ozturk, Gurkan Kocak, Mehmet Int J Infect Dis Article OBJECTIVES: Reverse transcription polymerase chain reaction (RT-PCR) testing is indispensable in management of the coronavirus disease 2019 (COVID-19) pandemic. However, with the emergence of new variants of severe acute respiratory syndrome coronavirus-2, the cause of COVID-19, the screening capacity of RT-PCR testing is overburdened, and new strategies and capabilities need to be established. One option is pooled RT-PCR testing. DESIGN: This study used various mixtures of COVID-19 samples known to be negative and positive, and investigated the impact of pool size and mixture level on final cycle threshold (Ct) values. More specifically, 5, 10 and 20 negative samples were combined with one, two or three low Ct or high Ct positive samples. RESULTS: Average baseline Ct and numbers of high and low Ct samples in the pool were found to be the main drivers of the final Ct value, making detectability easier. Pool size was not significantly associated with final Ct, but was suggestive. CONCLUSIONS: A pooled RT-PCR testing strategy does not reduce the sensitivity of RT-PCR, and thus provides a practical way to expand RT-PCR screening capacity in pandemic management. The pool size was not found to be significant, so it is recommended that a pool size of 20 would be a practical number to reduce the time taken to obtain the results and the cost of RT-PCR testing. The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2022-03 2021-12-15 /pmc/articles/PMC8673736/ /pubmed/34922006 http://dx.doi.org/10.1016/j.ijid.2021.12.328 Text en © 2021 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Ayaz, Akif Demir, Asli Guner Ozturk Ozturk, Gurkan Kocak, Mehmet A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management |
title | A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management |
title_full | A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management |
title_fullStr | A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management |
title_full_unstemmed | A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management |
title_short | A pooled RT-PCR testing strategy for more efficient COVID-19 pandemic management |
title_sort | pooled rt-pcr testing strategy for more efficient covid-19 pandemic management |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8673736/ https://www.ncbi.nlm.nih.gov/pubmed/34922006 http://dx.doi.org/10.1016/j.ijid.2021.12.328 |
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