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Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England
The time-varying reproduction number (R(t): the average number of secondary infections caused by each infected person) may be used to assess changes in transmission potential during an epidemic. While new infections are not usually observed directly, they can be estimated from data. However, data ma...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165604/ https://www.ncbi.nlm.nih.gov/pubmed/34053260 http://dx.doi.org/10.1098/rstb.2020.0283 |
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author | Sherratt, Katharine Abbott, Sam Meakin, Sophie R. Hellewell, Joel Munday, James D. Bosse, Nikos Jit, Mark Funk, Sebastian |
author_facet | Sherratt, Katharine Abbott, Sam Meakin, Sophie R. Hellewell, Joel Munday, James D. Bosse, Nikos Jit, Mark Funk, Sebastian |
author_sort | Sherratt, Katharine |
collection | PubMed |
description | The time-varying reproduction number (R(t): the average number of secondary infections caused by each infected person) may be used to assess changes in transmission potential during an epidemic. While new infections are not usually observed directly, they can be estimated from data. However, data may be delayed and potentially biased. We investigated the sensitivity of R(t) estimates to different data sources representing COVID-19 in England, and we explored how this sensitivity could track epidemic dynamics in population sub-groups. We sourced public data on test-positive cases, hospital admissions and deaths with confirmed COVID-19 in seven regions of England over March through August 2020. We estimated R(t) using a model that mapped unobserved infections to each data source. We then compared differences in R(t) with the demographic and social context of surveillance data over time. Our estimates of transmission potential varied for each data source, with the relative inconsistency of estimates varying across regions and over time. R(t) estimates based on hospital admissions and deaths were more spatio-temporally synchronous than when compared to estimates from all test positives. We found these differences may be linked to biased representations of subpopulations in each data source. These included spatially clustered testing, and where outbreaks in hospitals, care homes, and young age groups reflected the link between age and severity of the disease. We highlight that policy makers could better target interventions by considering the source populations of R(t) estimates. Further work should clarify the best way to combine and interpret R(t) estimates from different data sources based on the desired use. This article is part of the theme issue ‘Modelling that shaped the early COVID-19 pandemic response in the UK’. |
format | Online Article Text |
id | pubmed-8165604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81656042021-06-03 Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England Sherratt, Katharine Abbott, Sam Meakin, Sophie R. Hellewell, Joel Munday, James D. Bosse, Nikos Jit, Mark Funk, Sebastian Philos Trans R Soc Lond B Biol Sci Articles The time-varying reproduction number (R(t): the average number of secondary infections caused by each infected person) may be used to assess changes in transmission potential during an epidemic. While new infections are not usually observed directly, they can be estimated from data. However, data may be delayed and potentially biased. We investigated the sensitivity of R(t) estimates to different data sources representing COVID-19 in England, and we explored how this sensitivity could track epidemic dynamics in population sub-groups. We sourced public data on test-positive cases, hospital admissions and deaths with confirmed COVID-19 in seven regions of England over March through August 2020. We estimated R(t) using a model that mapped unobserved infections to each data source. We then compared differences in R(t) with the demographic and social context of surveillance data over time. Our estimates of transmission potential varied for each data source, with the relative inconsistency of estimates varying across regions and over time. R(t) estimates based on hospital admissions and deaths were more spatio-temporally synchronous than when compared to estimates from all test positives. We found these differences may be linked to biased representations of subpopulations in each data source. These included spatially clustered testing, and where outbreaks in hospitals, care homes, and young age groups reflected the link between age and severity of the disease. We highlight that policy makers could better target interventions by considering the source populations of R(t) estimates. Further work should clarify the best way to combine and interpret R(t) estimates from different data sources based on the desired use. This article is part of the theme issue ‘Modelling that shaped the early COVID-19 pandemic response in the UK’. The Royal Society 2021-07-19 2021-05-31 /pmc/articles/PMC8165604/ /pubmed/34053260 http://dx.doi.org/10.1098/rstb.2020.0283 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Sherratt, Katharine Abbott, Sam Meakin, Sophie R. Hellewell, Joel Munday, James D. Bosse, Nikos Jit, Mark Funk, Sebastian Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England |
title | Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England |
title_full | Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England |
title_fullStr | Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England |
title_full_unstemmed | Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England |
title_short | Exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of COVID-19 in England |
title_sort | exploring surveillance data biases when estimating the reproduction number: with insights into subpopulation transmission of covid-19 in england |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165604/ https://www.ncbi.nlm.nih.gov/pubmed/34053260 http://dx.doi.org/10.1098/rstb.2020.0283 |
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