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Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19

Quarantine and serial testing strategies for a disease depend principally on its incubation period and infectiousness profile. In the context of COVID-19, these primary public health tools must be modulated with successive SARS CoV-2 variants of concern that dominate transmission. Our analysis shows...

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Autores principales: Wells, Chad R, Pandey, Abhishek, Gokcebel, Senay, Krieger, Gary, Donoghue, A Michael, Singer, Burton H, Moghadas, Seyed M, Galvani, Alison P, Townsend, Jeffrey P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335027/
https://www.ncbi.nlm.nih.gov/pubmed/35909795
http://dx.doi.org/10.1093/pnasnexus/pgac100
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author Wells, Chad R
Pandey, Abhishek
Gokcebel, Senay
Krieger, Gary
Donoghue, A Michael
Singer, Burton H
Moghadas, Seyed M
Galvani, Alison P
Townsend, Jeffrey P
author_facet Wells, Chad R
Pandey, Abhishek
Gokcebel, Senay
Krieger, Gary
Donoghue, A Michael
Singer, Burton H
Moghadas, Seyed M
Galvani, Alison P
Townsend, Jeffrey P
author_sort Wells, Chad R
collection PubMed
description Quarantine and serial testing strategies for a disease depend principally on its incubation period and infectiousness profile. In the context of COVID-19, these primary public health tools must be modulated with successive SARS CoV-2 variants of concern that dominate transmission. Our analysis shows that (1) vaccination status of an individual makes little difference to the determination of the appropriate quarantine duration of an infected case, whereas vaccination coverage of the population can have a substantial effect on this duration, (2) successive variants can challenge disease control efforts by their earlier and increased transmission in the disease time course relative to prior variants, and (3) sufficient vaccine boosting of a population substantially aids the suppression of local transmission through frequent serial testing. For instance, with Omicron, increasing immunity through vaccination and boosters—for instance with 100% of the population is fully immunized and at least 24% having received a third dose—can reduce quarantine durations by up to 2 d, as well as substantially aid in the repression of outbreaks through serial testing. Our analysis highlights the paramount importance of maintaining high population immunity, preferably by booster uptake, and the role of quarantine and testing to control the spread of SARS CoV-2.
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spelling pubmed-93350272022-07-29 Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19 Wells, Chad R Pandey, Abhishek Gokcebel, Senay Krieger, Gary Donoghue, A Michael Singer, Burton H Moghadas, Seyed M Galvani, Alison P Townsend, Jeffrey P PNAS Nexus Brief Report Quarantine and serial testing strategies for a disease depend principally on its incubation period and infectiousness profile. In the context of COVID-19, these primary public health tools must be modulated with successive SARS CoV-2 variants of concern that dominate transmission. Our analysis shows that (1) vaccination status of an individual makes little difference to the determination of the appropriate quarantine duration of an infected case, whereas vaccination coverage of the population can have a substantial effect on this duration, (2) successive variants can challenge disease control efforts by their earlier and increased transmission in the disease time course relative to prior variants, and (3) sufficient vaccine boosting of a population substantially aids the suppression of local transmission through frequent serial testing. For instance, with Omicron, increasing immunity through vaccination and boosters—for instance with 100% of the population is fully immunized and at least 24% having received a third dose—can reduce quarantine durations by up to 2 d, as well as substantially aid in the repression of outbreaks through serial testing. Our analysis highlights the paramount importance of maintaining high population immunity, preferably by booster uptake, and the role of quarantine and testing to control the spread of SARS CoV-2. Oxford University Press 2022-07-27 /pmc/articles/PMC9335027/ /pubmed/35909795 http://dx.doi.org/10.1093/pnasnexus/pgac100 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of National Academy of Sciences. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Wells, Chad R
Pandey, Abhishek
Gokcebel, Senay
Krieger, Gary
Donoghue, A Michael
Singer, Burton H
Moghadas, Seyed M
Galvani, Alison P
Townsend, Jeffrey P
Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19
title Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19
title_full Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19
title_fullStr Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19
title_full_unstemmed Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19
title_short Quarantine and serial testing for variants of SARS-CoV-2 with benefits of vaccination and boosting on consequent control of COVID-19
title_sort quarantine and serial testing for variants of sars-cov-2 with benefits of vaccination and boosting on consequent control of covid-19
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335027/
https://www.ncbi.nlm.nih.gov/pubmed/35909795
http://dx.doi.org/10.1093/pnasnexus/pgac100
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