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Estimating the COVID-19 epidemic trajectory and hospital capacity requirements in South West England: a mathematical modelling framework.

Identifieur interne : 000367 ( Main/Corpus ); précédent : 000366; suivant : 000368

Estimating the COVID-19 epidemic trajectory and hospital capacity requirements in South West England: a mathematical modelling framework.

Auteurs : Ross D. Booton ; Louis Macgregor ; Lucy Vass ; Katharine J. Looker ; Catherine Hyams ; Philip D. Bright ; Irasha Harding ; Rajeka Lazarus ; Fergus Hamilton ; Daniel Lawson ; Leon Danon ; Adrian Pratt ; Richard Wood ; Ellen Brooks-Pollock ; Katherine M E. Turner

Source :

RBID : pubmed:33414147

English descriptors

Abstract

OBJECTIVES

To develop a regional model of COVID-19 dynamics for use in estimating the number of infections, deaths and required acute and intensive care (IC) beds using the South West England (SW) as an example case.

DESIGN

Open-source age-structured variant of a susceptible-exposed-infectious-recovered compartmental mathematical model. Latin hypercube sampling and maximum likelihood estimation were used to calibrate to cumulative cases and cumulative deaths.

SETTING

SW at a time considered early in the pandemic, where National Health Service authorities required evidence to guide localised planning and support decision-making.

PARTICIPANTS

Publicly available data on patients with COVID-19.

PRIMARY AND SECONDARY OUTCOME MEASURES

The expected numbers of infected cases, deaths due to COVID-19 infection, patient occupancy of acute and IC beds and the reproduction ('R') number over time.

RESULTS

SW model projections indicate that, as of 11 May 2020 (when 'lockdown' measures were eased), 5793 (95% credible interval (CrI) 2003 to 12 051) individuals were still infectious (0.10% of the total SW population, 95% CrI 0.04% to 0.22%), and a total of 189 048 (95% CrI 141 580 to 277 955) had been infected with the virus (either asymptomatically or symptomatically), but recovered, which is 3.4% (95% CrI 2.5% to 5.0%) of the SW population. The total number of patients in acute and IC beds in the SW on 11 May 2020 was predicted to be 701 (95% CrI 169 to 1543) and 110 (95% CrI 8 to 464), respectively. The R value in SW was predicted to be 2.6 (95% CrI 2.0 to 3.2) prior to any interventions, with social distancing reducing this to 2.3 (95% CrI 1.8 to 2.9) and lockdown/school closures further reducing the R value to 0.6 (95% CrI 0.5 to 0.7).

CONCLUSIONS

The developed model has proved a valuable asset for regional healthcare services. The model will be used further in the SW as the pandemic evolves, and-as open-source software-is portable to healthcare systems in other geographies.


DOI: 10.1136/bmjopen-2020-041536
PubMed: 33414147
PubMed Central: PMC7797241

Links to Exploration step

pubmed:33414147

Le document en format XML

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<name sortKey="Pratt, Adrian" sort="Pratt, Adrian" uniqKey="Pratt A" first="Adrian" last="Pratt">Adrian Pratt</name>
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<name sortKey="Wood, Richard" sort="Wood, Richard" uniqKey="Wood R" first="Richard" last="Wood">Richard Wood</name>
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<nlm:affiliation>Modelling and Analytics Team, NHS Bristol, North Somerset and South Gloucestershire CCG, Bristol, UK.</nlm:affiliation>
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<name sortKey="Brooks Pollock, Ellen" sort="Brooks Pollock, Ellen" uniqKey="Brooks Pollock E" first="Ellen" last="Brooks-Pollock">Ellen Brooks-Pollock</name>
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<nlm:affiliation>Population Health Science Institute, University of Bristol Medical School, Bristol, UK.</nlm:affiliation>
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<nlm:affiliation>NIHR Health Protection Research Unit in Behavioural Science and Evaluation, Bristol, UK.</nlm:affiliation>
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<nlm:affiliation>Population Health Science Institute, University of Bristol Medical School, Bristol, UK.</nlm:affiliation>
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<nlm:affiliation>Consultant in Microbiology and Infectious Diseases, University Hospitals Bristol, Bristol, UK.</nlm:affiliation>
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<name sortKey="Hamilton, Fergus" sort="Hamilton, Fergus" uniqKey="Hamilton F" first="Fergus" last="Hamilton">Fergus Hamilton</name>
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<nlm:affiliation>Infection Science, Southmead Hospital, North Bristol NHS Trust, Bristol, UK.</nlm:affiliation>
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<name sortKey="Lawson, Daniel" sort="Lawson, Daniel" uniqKey="Lawson D" first="Daniel" last="Lawson">Daniel Lawson</name>
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<name sortKey="Danon, Leon" sort="Danon, Leon" uniqKey="Danon L" first="Leon" last="Danon">Leon Danon</name>
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<nlm:affiliation>Department of Engineering Mathematics, University of Bristol, Bristol, UK.</nlm:affiliation>
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<nlm:affiliation>Alan Turing Institute, London, UK.</nlm:affiliation>
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<nlm:affiliation>Health Data Research UK South-West of England Partnership, Bristol, UK.</nlm:affiliation>
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<name sortKey="Pratt, Adrian" sort="Pratt, Adrian" uniqKey="Pratt A" first="Adrian" last="Pratt">Adrian Pratt</name>
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<nlm:affiliation>Modelling and Analytics Team, NHS Bristol, North Somerset and South Gloucestershire CCG, Bristol, UK.</nlm:affiliation>
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<name sortKey="Wood, Richard" sort="Wood, Richard" uniqKey="Wood R" first="Richard" last="Wood">Richard Wood</name>
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<nlm:affiliation>Modelling and Analytics Team, NHS Bristol, North Somerset and South Gloucestershire CCG, Bristol, UK.</nlm:affiliation>
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<name sortKey="Brooks Pollock, Ellen" sort="Brooks Pollock, Ellen" uniqKey="Brooks Pollock E" first="Ellen" last="Brooks-Pollock">Ellen Brooks-Pollock</name>
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<term>Adolescent (MeSH)</term>
<term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>COVID-19 (epidemiology)</term>
<term>Child (MeSH)</term>
<term>Child, Preschool (MeSH)</term>
<term>Critical Care (statistics & numerical data)</term>
<term>Decision Making (MeSH)</term>
<term>England (epidemiology)</term>
<term>Female (MeSH)</term>
<term>Hospital Bed Capacity (statistics & numerical data)</term>
<term>Hospitalization (statistics & numerical data)</term>
<term>Humans (MeSH)</term>
<term>Infant (MeSH)</term>
<term>Infant, Newborn (MeSH)</term>
<term>Intensive Care Units (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Models, Theoretical (MeSH)</term>
<term>Regional Health Planning (MeSH)</term>
<term>SARS-CoV-2 (MeSH)</term>
<term>State Medicine (MeSH)</term>
<term>Surge Capacity (MeSH)</term>
<term>Young Adult (MeSH)</term>
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<term>England</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>COVID-19</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en">
<term>Critical Care</term>
<term>Hospital Bed Capacity</term>
<term>Hospitalization</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Decision Making</term>
<term>Female</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Intensive Care Units</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Models, Theoretical</term>
<term>Regional Health Planning</term>
<term>SARS-CoV-2</term>
<term>State Medicine</term>
<term>Surge Capacity</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVES</b>
</p>
<p>To develop a regional model of COVID-19 dynamics for use in estimating the number of infections, deaths and required acute and intensive care (IC) beds using the South West England (SW) as an example case.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>DESIGN</b>
</p>
<p>Open-source age-structured variant of a susceptible-exposed-infectious-recovered compartmental mathematical model. Latin hypercube sampling and maximum likelihood estimation were used to calibrate to cumulative cases and cumulative deaths.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>SETTING</b>
</p>
<p>SW at a time considered early in the pandemic, where National Health Service authorities required evidence to guide localised planning and support decision-making.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>PARTICIPANTS</b>
</p>
<p>Publicly available data on patients with COVID-19.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>PRIMARY AND SECONDARY OUTCOME MEASURES</b>
</p>
<p>The expected numbers of infected cases, deaths due to COVID-19 infection, patient occupancy of acute and IC beds and the reproduction ('R') number over time.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>SW model projections indicate that, as of 11 May 2020 (when 'lockdown' measures were eased), 5793 (95% credible interval (CrI) 2003 to 12 051) individuals were still infectious (0.10% of the total SW population, 95% CrI 0.04% to 0.22%), and a total of 189 048 (95% CrI 141 580 to 277 955) had been infected with the virus (either asymptomatically or symptomatically), but recovered, which is 3.4% (95% CrI 2.5% to 5.0%) of the SW population. The total number of patients in acute and IC beds in the SW on 11 May 2020 was predicted to be 701 (95% CrI 169 to 1543) and 110 (95% CrI 8 to 464), respectively. The R value in SW was predicted to be 2.6 (95% CrI 2.0 to 3.2) prior to any interventions, with social distancing reducing this to 2.3 (95% CrI 1.8 to 2.9) and lockdown/school closures further reducing the R value to 0.6 (95% CrI 0.5 to 0.7).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The developed model has proved a valuable asset for regional healthcare services. The model will be used further in the SW as the pandemic evolves, and-as open-source software-is portable to healthcare systems in other geographies.</p>
</div>
</front>
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<Year>2021</Year>
<Month>01</Month>
<Day>18</Day>
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<ISSN IssnType="Electronic">2044-6055</ISSN>
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<ArticleTitle>Estimating the COVID-19 epidemic trajectory and hospital capacity requirements in South West England: a mathematical modelling framework.</ArticleTitle>
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<Abstract>
<AbstractText Label="OBJECTIVES">To develop a regional model of COVID-19 dynamics for use in estimating the number of infections, deaths and required acute and intensive care (IC) beds using the South West England (SW) as an example case.</AbstractText>
<AbstractText Label="DESIGN">Open-source age-structured variant of a susceptible-exposed-infectious-recovered compartmental mathematical model. Latin hypercube sampling and maximum likelihood estimation were used to calibrate to cumulative cases and cumulative deaths.</AbstractText>
<AbstractText Label="SETTING">SW at a time considered early in the pandemic, where National Health Service authorities required evidence to guide localised planning and support decision-making.</AbstractText>
<AbstractText Label="PARTICIPANTS">Publicly available data on patients with COVID-19.</AbstractText>
<AbstractText Label="PRIMARY AND SECONDARY OUTCOME MEASURES">The expected numbers of infected cases, deaths due to COVID-19 infection, patient occupancy of acute and IC beds and the reproduction ('R') number over time.</AbstractText>
<AbstractText Label="RESULTS">SW model projections indicate that, as of 11 May 2020 (when 'lockdown' measures were eased), 5793 (95% credible interval (CrI) 2003 to 12 051) individuals were still infectious (0.10% of the total SW population, 95% CrI 0.04% to 0.22%), and a total of 189 048 (95% CrI 141 580 to 277 955) had been infected with the virus (either asymptomatically or symptomatically), but recovered, which is 3.4% (95% CrI 2.5% to 5.0%) of the SW population. The total number of patients in acute and IC beds in the SW on 11 May 2020 was predicted to be 701 (95% CrI 169 to 1543) and 110 (95% CrI 8 to 464), respectively. The R value in SW was predicted to be 2.6 (95% CrI 2.0 to 3.2) prior to any interventions, with social distancing reducing this to 2.3 (95% CrI 1.8 to 2.9) and lockdown/school closures further reducing the R value to 0.6 (95% CrI 0.5 to 0.7).</AbstractText>
<AbstractText Label="CONCLUSIONS">The developed model has proved a valuable asset for regional healthcare services. The model will be used further in the SW as the pandemic evolves, and-as open-source software-is portable to healthcare systems in other geographies.</AbstractText>
<CopyrightInformation>© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.</CopyrightInformation>
</Abstract>
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<LastName>Booton</LastName>
<ForeName>Ross D</ForeName>
<Initials>RD</Initials>
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<Affiliation>School of Veterinary Sciences, University of Bristol, Bristol, UK.</Affiliation>
</AffiliationInfo>
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<Affiliation>Population Health Science Institute, University of Bristol Medical School, Bristol, UK.</Affiliation>
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<AffiliationInfo>
<Affiliation>NIHR Health Protection Research Unit in Behavioural Science and Evaluation, Bristol, UK.</Affiliation>
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<Affiliation>School of Veterinary Sciences, University of Bristol, Bristol, UK.</Affiliation>
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<Affiliation>Population Health Science Institute, University of Bristol Medical School, Bristol, UK.</Affiliation>
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<LastName>Looker</LastName>
<ForeName>Katharine J</ForeName>
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