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Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation
Outbreaks of infectious diseases, such as influenza, are a major societal burden. Mitigation policies during an outbreak or pandemic are guided by the analysis of data of ongoing or preceding epidemics. The reproduction number, [Formula: see text] , defined as the expected number of secondary infect...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375253/ https://www.ncbi.nlm.nih.gov/pubmed/34419601 http://dx.doi.org/10.1016/j.annepidem.2021.07.008 |
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author | Krishnan, R.G. Cenci, S. Bourouiba, L. |
author_facet | Krishnan, R.G. Cenci, S. Bourouiba, L. |
author_sort | Krishnan, R.G. |
collection | PubMed |
description | Outbreaks of infectious diseases, such as influenza, are a major societal burden. Mitigation policies during an outbreak or pandemic are guided by the analysis of data of ongoing or preceding epidemics. The reproduction number, [Formula: see text] , defined as the expected number of secondary infections arising from a single individual in a population of susceptibles is critical to epidemiology. For typical compartmental models such as the Susceptible-Infected-Recovered (SIR) [Formula: see text] represents the severity of an epidemic. It is an estimate of the early-stage growth rate of an epidemic and is an important threshold parameter used to gain insights into the spread or decay of an outbreak. Models typically use incidence counts as indicators of cases within a single large population; however, epidemic data are the result of a hierarchical aggregation, where incidence counts from spatially separated monitoring sites (or sub-regions) are pooled and used to infer [Formula: see text]. Is this aggregation approach valid when the epidemic has different dynamics across the regions monitored? We characterize bias in the estimation of [Formula: see text] from a merged data set when the epidemics of the sub-regions, used in the merger, exhibit delays in onset. We propose a method to mitigate this bias, and study its efficacy on synthetic data as well as real-world influenza and COVID-19 data. |
format | Online Article Text |
id | pubmed-8375253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83752532021-08-19 Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation Krishnan, R.G. Cenci, S. Bourouiba, L. Ann Epidemiol Original Article Outbreaks of infectious diseases, such as influenza, are a major societal burden. Mitigation policies during an outbreak or pandemic are guided by the analysis of data of ongoing or preceding epidemics. The reproduction number, [Formula: see text] , defined as the expected number of secondary infections arising from a single individual in a population of susceptibles is critical to epidemiology. For typical compartmental models such as the Susceptible-Infected-Recovered (SIR) [Formula: see text] represents the severity of an epidemic. It is an estimate of the early-stage growth rate of an epidemic and is an important threshold parameter used to gain insights into the spread or decay of an outbreak. Models typically use incidence counts as indicators of cases within a single large population; however, epidemic data are the result of a hierarchical aggregation, where incidence counts from spatially separated monitoring sites (or sub-regions) are pooled and used to infer [Formula: see text]. Is this aggregation approach valid when the epidemic has different dynamics across the regions monitored? We characterize bias in the estimation of [Formula: see text] from a merged data set when the epidemics of the sub-regions, used in the merger, exhibit delays in onset. We propose a method to mitigate this bias, and study its efficacy on synthetic data as well as real-world influenza and COVID-19 data. Published by Elsevier Inc. 2022-01 2021-08-19 /pmc/articles/PMC8375253/ /pubmed/34419601 http://dx.doi.org/10.1016/j.annepidem.2021.07.008 Text en © 2021 Published by Elsevier Inc. 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 | Original Article Krishnan, R.G. Cenci, S. Bourouiba, L. Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
title | Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
title_full | Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
title_fullStr | Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
title_full_unstemmed | Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
title_short | Mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
title_sort | mitigating bias in estimating epidemic severity due to heterogeneity of epidemic onset and data aggregation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375253/ https://www.ncbi.nlm.nih.gov/pubmed/34419601 http://dx.doi.org/10.1016/j.annepidem.2021.07.008 |
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