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Bayesian modelling of an epidemic of severe acute respiratory syndrome

This paper analyses data arising from a SARS epidemic in Shanxi province of China involving a total of 354 people infected with SARS-CoV between late February and late May 2003. Using Bayesian inference, we have estimated critical epidemiological determinants. The estimated mean incubation period wa...

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Autores principales: McBryde, E. S., Gibson, G., Pettitt, A. N., Zhang, Y., Zhao, B., McElwain, D. L. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089340/
https://www.ncbi.nlm.nih.gov/pubmed/16802088
http://dx.doi.org/10.1007/s11538-005-9005-4
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author McBryde, E. S.
Gibson, G.
Pettitt, A. N.
Zhang, Y.
Zhao, B.
McElwain, D. L. S.
author_facet McBryde, E. S.
Gibson, G.
Pettitt, A. N.
Zhang, Y.
Zhao, B.
McElwain, D. L. S.
author_sort McBryde, E. S.
collection PubMed
description This paper analyses data arising from a SARS epidemic in Shanxi province of China involving a total of 354 people infected with SARS-CoV between late February and late May 2003. Using Bayesian inference, we have estimated critical epidemiological determinants. The estimated mean incubation period was 5.3 days (95% CI 4.2–6.8 days), mean time to hospitalisation was 3.5 days (95% CI 2.8–3.6 days), mean time from symptom onset to recovery was 26 days (95% CI 25–27 days) and mean time from symptom onset to death was 21 days (95% CI 16–26 days). The reproduction ratio was estimated to be 4.8 (95% CI 2.2–8.8) in the early part of the epidemic (February and March 2003) reducing to 0.75 (95% CI 0.65–0.85) in the later part of the epidemic (April and May 2003). The infectivity of symptomatic SARS cases in hospital and in the community was estimated. Community SARS cases caused transmission to others at an estimated rate of 0.4 per infective per day during the early part of the epidemic, reducing to 0.2 in the later part of the epidemic. For hospitalised patients, the daily infectivity was approximately 0.15 early in the epidemic, but fell to 0.0006 in the later part of the epidemic. Despite the lower daily infectivity level for hospitalised patients, the long duration of the hospitalisation led to a greater number of transmissions within hospitals compared with the community in the early part of the epidemic, as estimated by this study. This study investigated the individual infectivity profile during the symptomatic period, with an estimated peak infectivity on the ninth symptomatic day.
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spelling pubmed-70893402020-03-23 Bayesian modelling of an epidemic of severe acute respiratory syndrome McBryde, E. S. Gibson, G. Pettitt, A. N. Zhang, Y. Zhao, B. McElwain, D. L. S. Bull Math Biol Original Article This paper analyses data arising from a SARS epidemic in Shanxi province of China involving a total of 354 people infected with SARS-CoV between late February and late May 2003. Using Bayesian inference, we have estimated critical epidemiological determinants. The estimated mean incubation period was 5.3 days (95% CI 4.2–6.8 days), mean time to hospitalisation was 3.5 days (95% CI 2.8–3.6 days), mean time from symptom onset to recovery was 26 days (95% CI 25–27 days) and mean time from symptom onset to death was 21 days (95% CI 16–26 days). The reproduction ratio was estimated to be 4.8 (95% CI 2.2–8.8) in the early part of the epidemic (February and March 2003) reducing to 0.75 (95% CI 0.65–0.85) in the later part of the epidemic (April and May 2003). The infectivity of symptomatic SARS cases in hospital and in the community was estimated. Community SARS cases caused transmission to others at an estimated rate of 0.4 per infective per day during the early part of the epidemic, reducing to 0.2 in the later part of the epidemic. For hospitalised patients, the daily infectivity was approximately 0.15 early in the epidemic, but fell to 0.0006 in the later part of the epidemic. Despite the lower daily infectivity level for hospitalised patients, the long duration of the hospitalisation led to a greater number of transmissions within hospitals compared with the community in the early part of the epidemic, as estimated by this study. This study investigated the individual infectivity profile during the symptomatic period, with an estimated peak infectivity on the ninth symptomatic day. Springer-Verlag 2006-04-08 2006 /pmc/articles/PMC7089340/ /pubmed/16802088 http://dx.doi.org/10.1007/s11538-005-9005-4 Text en © Society for Mathematical Biology 2006 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
McBryde, E. S.
Gibson, G.
Pettitt, A. N.
Zhang, Y.
Zhao, B.
McElwain, D. L. S.
Bayesian modelling of an epidemic of severe acute respiratory syndrome
title Bayesian modelling of an epidemic of severe acute respiratory syndrome
title_full Bayesian modelling of an epidemic of severe acute respiratory syndrome
title_fullStr Bayesian modelling of an epidemic of severe acute respiratory syndrome
title_full_unstemmed Bayesian modelling of an epidemic of severe acute respiratory syndrome
title_short Bayesian modelling of an epidemic of severe acute respiratory syndrome
title_sort bayesian modelling of an epidemic of severe acute respiratory syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089340/
https://www.ncbi.nlm.nih.gov/pubmed/16802088
http://dx.doi.org/10.1007/s11538-005-9005-4
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