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Inference of COVID-19 epidemiological distributions from Brazilian hospital data
Knowing COVID-19 epidemiological distributions, such as the time from patient admission to death, is directly relevant to effective primary and secondary care planning, and moreover, the mathematical modelling of the pandemic generally. We determine epidemiological distributions for patients hospita...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729050/ https://www.ncbi.nlm.nih.gov/pubmed/33234065 http://dx.doi.org/10.1098/rsif.2020.0596 |
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author | Hawryluk, Iwona Mellan, Thomas A. Hoeltgebaum, Henrique Mishra, Swapnil Schnekenberg, Ricardo P. Whittaker, Charles Zhu, Harrison Gandy, Axel Donnelly, Christl A. Flaxman, Seth Bhatt, Samir |
author_facet | Hawryluk, Iwona Mellan, Thomas A. Hoeltgebaum, Henrique Mishra, Swapnil Schnekenberg, Ricardo P. Whittaker, Charles Zhu, Harrison Gandy, Axel Donnelly, Christl A. Flaxman, Seth Bhatt, Samir |
author_sort | Hawryluk, Iwona |
collection | PubMed |
description | Knowing COVID-19 epidemiological distributions, such as the time from patient admission to death, is directly relevant to effective primary and secondary care planning, and moreover, the mathematical modelling of the pandemic generally. We determine epidemiological distributions for patients hospitalized with COVID-19 using a large dataset (N = 21 000 − 157 000) from the Brazilian Sistema de Informação de Vigilância Epidemiológica da Gripe database. A joint Bayesian subnational model with partial pooling is used to simultaneously describe the 26 states and one federal district of Brazil, and shows significant variation in the mean of the symptom-onset-to-death time, with ranges between 11.2 and 17.8 days across the different states, and a mean of 15.2 days for Brazil. We find strong evidence in favour of specific probability density function choices: for example, the gamma distribution gives the best fit for onset-to-death and the generalized lognormal for onset-to-hospital-admission. Our results show that epidemiological distributions have considerable geographical variation, and provide the first estimates of these distributions in a low and middle-income setting. At the subnational level, variation in COVID-19 outcome timings are found to be correlated with poverty, deprivation and segregation levels, and weaker correlation is observed for mean age, wealth and urbanicity. |
format | Online Article Text |
id | pubmed-7729050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77290502020-12-22 Inference of COVID-19 epidemiological distributions from Brazilian hospital data Hawryluk, Iwona Mellan, Thomas A. Hoeltgebaum, Henrique Mishra, Swapnil Schnekenberg, Ricardo P. Whittaker, Charles Zhu, Harrison Gandy, Axel Donnelly, Christl A. Flaxman, Seth Bhatt, Samir J R Soc Interface Life Sciences–Mathematics interface Knowing COVID-19 epidemiological distributions, such as the time from patient admission to death, is directly relevant to effective primary and secondary care planning, and moreover, the mathematical modelling of the pandemic generally. We determine epidemiological distributions for patients hospitalized with COVID-19 using a large dataset (N = 21 000 − 157 000) from the Brazilian Sistema de Informação de Vigilância Epidemiológica da Gripe database. A joint Bayesian subnational model with partial pooling is used to simultaneously describe the 26 states and one federal district of Brazil, and shows significant variation in the mean of the symptom-onset-to-death time, with ranges between 11.2 and 17.8 days across the different states, and a mean of 15.2 days for Brazil. We find strong evidence in favour of specific probability density function choices: for example, the gamma distribution gives the best fit for onset-to-death and the generalized lognormal for onset-to-hospital-admission. Our results show that epidemiological distributions have considerable geographical variation, and provide the first estimates of these distributions in a low and middle-income setting. At the subnational level, variation in COVID-19 outcome timings are found to be correlated with poverty, deprivation and segregation levels, and weaker correlation is observed for mean age, wealth and urbanicity. The Royal Society 2020-11 2020-11-25 /pmc/articles/PMC7729050/ /pubmed/33234065 http://dx.doi.org/10.1098/rsif.2020.0596 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://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/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Mathematics interface Hawryluk, Iwona Mellan, Thomas A. Hoeltgebaum, Henrique Mishra, Swapnil Schnekenberg, Ricardo P. Whittaker, Charles Zhu, Harrison Gandy, Axel Donnelly, Christl A. Flaxman, Seth Bhatt, Samir Inference of COVID-19 epidemiological distributions from Brazilian hospital data |
title | Inference of COVID-19 epidemiological distributions from Brazilian hospital data |
title_full | Inference of COVID-19 epidemiological distributions from Brazilian hospital data |
title_fullStr | Inference of COVID-19 epidemiological distributions from Brazilian hospital data |
title_full_unstemmed | Inference of COVID-19 epidemiological distributions from Brazilian hospital data |
title_short | Inference of COVID-19 epidemiological distributions from Brazilian hospital data |
title_sort | inference of covid-19 epidemiological distributions from brazilian hospital data |
topic | Life Sciences–Mathematics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729050/ https://www.ncbi.nlm.nih.gov/pubmed/33234065 http://dx.doi.org/10.1098/rsif.2020.0596 |
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