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A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations
Indoor event locations are particularly affected by the SARS-CoV-2 pandemic. At large venues, only incomplete risk assessments exist, whereby no suitable measures can be derived. In this study, a physical and data-driven statistical model for a comprehensive infection risk assessment has been develo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357618/ https://www.ncbi.nlm.nih.gov/pubmed/37474924 http://dx.doi.org/10.1186/s12889-023-16154-0 |
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author | Siebler, Lukas Rathje, Torben Calandri, Maurizio Stergiaropoulos, Konstantinos Donker, Tjibbe Richter, Bernhard Spahn, Claudia Nusseck, Manfred |
author_facet | Siebler, Lukas Rathje, Torben Calandri, Maurizio Stergiaropoulos, Konstantinos Donker, Tjibbe Richter, Bernhard Spahn, Claudia Nusseck, Manfred |
author_sort | Siebler, Lukas |
collection | PubMed |
description | Indoor event locations are particularly affected by the SARS-CoV-2 pandemic. At large venues, only incomplete risk assessments exist, whereby no suitable measures can be derived. In this study, a physical and data-driven statistical model for a comprehensive infection risk assessment has been developed. At venues displacement ventilation concepts are often implemented. Here simplified theoretical assumptions fail for the prediction of relevant airflows for airborne transmission processes. Thus, with locally resolving trace gas measurements infection risks are computed more detailed. Coupled with epidemiological data such as incidences, vaccination rates, test sensitivities, and audience characteristics such as masks and age distribution, predictions of new infections (mean), situational R-values (mean), and individual risks on- and off-seat can be achieved for the first time. Using the Stuttgart State Opera as an example, the functioning of the model and its plausibility are tested and a sensitivity analysis is performed with regard to masks and tests. Besides a reference scenario on 2022-11-29, a maximum safety scenario with an obligation of FFP2 masks and rapid antigen tests as well as a minimum safety scenario without masks and tests are investigated. For these scenarios the new infections (mean) are 10.6, 0.25 and 13.0, respectively. The situational R-values (mean) – number of new infections caused by a single infectious person in a certain situation – are 2.75, 0.32 and 3.39, respectively. Besides these results a clustered consideration divided by age, masks and whether infections occur on-seat or off-seat are presented. In conclusion this provides an instrument that can enable policymakers and operators to take appropriate measures to control pandemics despite ongoing mass gathering events. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-023-16154-0. |
format | Online Article Text |
id | pubmed-10357618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103576182023-07-21 A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations Siebler, Lukas Rathje, Torben Calandri, Maurizio Stergiaropoulos, Konstantinos Donker, Tjibbe Richter, Bernhard Spahn, Claudia Nusseck, Manfred BMC Public Health Research Indoor event locations are particularly affected by the SARS-CoV-2 pandemic. At large venues, only incomplete risk assessments exist, whereby no suitable measures can be derived. In this study, a physical and data-driven statistical model for a comprehensive infection risk assessment has been developed. At venues displacement ventilation concepts are often implemented. Here simplified theoretical assumptions fail for the prediction of relevant airflows for airborne transmission processes. Thus, with locally resolving trace gas measurements infection risks are computed more detailed. Coupled with epidemiological data such as incidences, vaccination rates, test sensitivities, and audience characteristics such as masks and age distribution, predictions of new infections (mean), situational R-values (mean), and individual risks on- and off-seat can be achieved for the first time. Using the Stuttgart State Opera as an example, the functioning of the model and its plausibility are tested and a sensitivity analysis is performed with regard to masks and tests. Besides a reference scenario on 2022-11-29, a maximum safety scenario with an obligation of FFP2 masks and rapid antigen tests as well as a minimum safety scenario without masks and tests are investigated. For these scenarios the new infections (mean) are 10.6, 0.25 and 13.0, respectively. The situational R-values (mean) – number of new infections caused by a single infectious person in a certain situation – are 2.75, 0.32 and 3.39, respectively. Besides these results a clustered consideration divided by age, masks and whether infections occur on-seat or off-seat are presented. In conclusion this provides an instrument that can enable policymakers and operators to take appropriate measures to control pandemics despite ongoing mass gathering events. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12889-023-16154-0. BioMed Central 2023-07-20 /pmc/articles/PMC10357618/ /pubmed/37474924 http://dx.doi.org/10.1186/s12889-023-16154-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Siebler, Lukas Rathje, Torben Calandri, Maurizio Stergiaropoulos, Konstantinos Donker, Tjibbe Richter, Bernhard Spahn, Claudia Nusseck, Manfred A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations |
title | A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations |
title_full | A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations |
title_fullStr | A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations |
title_full_unstemmed | A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations |
title_short | A coupled experimental and statistical approach for an assessment of SARS-CoV-2 infection risk at indoor event locations |
title_sort | coupled experimental and statistical approach for an assessment of sars-cov-2 infection risk at indoor event locations |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357618/ https://www.ncbi.nlm.nih.gov/pubmed/37474924 http://dx.doi.org/10.1186/s12889-023-16154-0 |
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