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Transmission of COVID-19 in 282 clusters in Catalonia, Spain: a cohort study.

Identifieur interne : 000064 ( Main/Exploration ); précédent : 000063; suivant : 000065

Transmission of COVID-19 in 282 clusters in Catalonia, Spain: a cohort study.

Auteurs : Michael Marks [Royaume-Uni] ; Pere Millat-Martinez [Espagne] ; Dan Ouchi [Espagne] ; Chrissy H. Roberts [Royaume-Uni] ; Andrea Alemany [Espagne] ; Marc Corbacho-Monné [Espagne] ; Maria Ubals [Espagne] ; Aurelio Tobias [Espagne] ; Cristian Tebé [Espagne] ; Ester Ballana [Espagne] ; Quique Bassat [Espagne] ; Bàrbara Baro [Espagne] ; Martí Vall-Mayans [Espagne] ; Camila G-Beiras [Espagne] ; Nuria Prat [Espagne] ; Jordi Ara [Espagne] ; Bonaventura Clotet [Espagne] ; Oriol Mitjà [Papouasie-Nouvelle-Guinée]

Source :

RBID : pubmed:33545090

Descripteurs français

English descriptors

Abstract

BACKGROUND

Scarce data are available on what variables affect the risk of transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the development of symptomatic COVID-19, and, particularly, the relationship with viral load. We aimed to analyse data from linked index cases of COVID-19 and their contacts to explore factors associated with transmission of SARS-CoV-2.

METHODS

In this cohort study, patients were recruited as part of a randomised controlled trial done between March 17 and April 28, 2020, that aimed to assess if hydroxychloroquine reduced transmission of SARS-CoV-2. Patients with COVID-19 and their contacts were identified by use of the electronic registry of the Epidemiological Surveillance Emergency Service of Catalonia (Spain). Patients with COVID-19 included in our analysis were aged 18 years or older, not hospitalised, had quantitative PCR results available at baseline, had mild symptom onset within 5 days before enrolment, and had no reported symptoms of SARS-CoV-2 infections in their accommodation or workplace within the 14 days before enrolment. Contacts included were adults with a recent history of exposure and absence of COVID-19-like symptoms within the 7 days preceding enrolment. Viral load of contacts, measured by quantitative PCR from a nasopharyngeal swab, was assessed at enrolment, at day 14, and whenever the participant reported COVID-19-like symptoms. We assessed risk of transmission and developing symptomatic disease and incubation dynamics using regression analysis. We assessed the relationship of viral load and characteristics of cases (age, sex, number of days from reported symptom onset, and presence or absence of fever, cough, dyspnoea, rhinitis, and anosmia) and associations between risk of transmission and characteristics of the index case and contacts.

FINDINGS

We identified 314 patients with COVID-19, with 282 (90%) having at least one contact (753 contacts in total), resulting in 282 clusters. 90 (32%) of 282 clusters had at least one transmission event. The secondary attack rate was 17% (125 of 753 contacts), with a variation from 12% when the index case had a viral load lower than 1 × 10

INTERPRETATION

In our study, the viral load of index cases was a leading driver of SARS-CoV-2 transmission. The risk of symptomatic COVID-19 was strongly associated with the viral load of contacts at baseline and shortened the incubation time of COVID-19 in a dose-dependent manner.

FUNDING

YoMeCorono, Generalitat de Catalunya.

TRANSLATIONS

For the Catalan translation of the abstract see Supplementary Materials section.


DOI: 10.1016/S1473-3099(20)30985-3
PubMed: 33545090
PubMed Central: PMC7906723


Affiliations:


Links toward previous steps (curation, corpus...)


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<name sortKey="Vall Mayans, Marti" sort="Vall Mayans, Marti" uniqKey="Vall Mayans M" first="Martí" last="Vall-Mayans">Martí Vall-Mayans</name>
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<name sortKey="G Beiras, Camila" sort="G Beiras, Camila" uniqKey="G Beiras C" first="Camila" last="G-Beiras">Camila G-Beiras</name>
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<name sortKey="Clotet, Bonaventura" sort="Clotet, Bonaventura" uniqKey="Clotet B" first="Bonaventura" last="Clotet">Bonaventura Clotet</name>
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<nlm:affiliation>IrsiCaixa AIDS Research Institute, Badalona, Spain; Fight AIDS and Infectious Diseases Foundation, Badalona, Spain; Infectious Disease Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain; Càtedra de Malalties Infeccioses i Immunitat, Universitat de Vic, Universtiat Central de Catalunya, Vic, Spain.</nlm:affiliation>
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<name sortKey="Mitja, Oriol" sort="Mitja, Oriol" uniqKey="Mitja O" first="Oriol" last="Mitjà">Oriol Mitjà</name>
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<nlm:affiliation>Fight AIDS and Infectious Diseases Foundation, Badalona, Spain; Infectious Disease Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain; Department of Clinical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain; Càtedra de Malalties Infeccioses i Immunitat, Universitat de Vic, Universtiat Central de Catalunya, Vic, Spain; Lihir Medical Centre, International SOS, Lihir Island, Papua New Guinea.</nlm:affiliation>
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<title level="j">The Lancet. Infectious diseases</title>
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<term>Adult (MeSH)</term>
<term>COVID-19 (epidemiology)</term>
<term>COVID-19 (transmission)</term>
<term>Cohort Studies (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Incidence (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>SARS-CoV-2 (MeSH)</term>
<term>Spain (epidemiology)</term>
<term>Viral Load (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Charge virale (MeSH)</term>
<term>Espagne (épidémiologie)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Incidence (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Études de cohortes (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en">
<term>Spain</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>COVID-19</term>
</keywords>
<keywords scheme="MESH" qualifier="transmission" xml:lang="en">
<term>COVID-19</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Espagne</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Incidence</term>
<term>Male</term>
<term>Middle Aged</term>
<term>SARS-CoV-2</term>
<term>Viral Load</term>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Charge virale</term>
<term>Femelle</term>
<term>Humains</term>
<term>Incidence</term>
<term>Mâle</term>
<term>Études de cohortes</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Scarce data are available on what variables affect the risk of transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the development of symptomatic COVID-19, and, particularly, the relationship with viral load. We aimed to analyse data from linked index cases of COVID-19 and their contacts to explore factors associated with transmission of SARS-CoV-2.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>In this cohort study, patients were recruited as part of a randomised controlled trial done between March 17 and April 28, 2020, that aimed to assess if hydroxychloroquine reduced transmission of SARS-CoV-2. Patients with COVID-19 and their contacts were identified by use of the electronic registry of the Epidemiological Surveillance Emergency Service of Catalonia (Spain). Patients with COVID-19 included in our analysis were aged 18 years or older, not hospitalised, had quantitative PCR results available at baseline, had mild symptom onset within 5 days before enrolment, and had no reported symptoms of SARS-CoV-2 infections in their accommodation or workplace within the 14 days before enrolment. Contacts included were adults with a recent history of exposure and absence of COVID-19-like symptoms within the 7 days preceding enrolment. Viral load of contacts, measured by quantitative PCR from a nasopharyngeal swab, was assessed at enrolment, at day 14, and whenever the participant reported COVID-19-like symptoms. We assessed risk of transmission and developing symptomatic disease and incubation dynamics using regression analysis. We assessed the relationship of viral load and characteristics of cases (age, sex, number of days from reported symptom onset, and presence or absence of fever, cough, dyspnoea, rhinitis, and anosmia) and associations between risk of transmission and characteristics of the index case and contacts.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>FINDINGS</b>
</p>
<p>We identified 314 patients with COVID-19, with 282 (90%) having at least one contact (753 contacts in total), resulting in 282 clusters. 90 (32%) of 282 clusters had at least one transmission event. The secondary attack rate was 17% (125 of 753 contacts), with a variation from 12% when the index case had a viral load lower than 1 × 10</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>INTERPRETATION</b>
</p>
<p>In our study, the viral load of index cases was a leading driver of SARS-CoV-2 transmission. The risk of symptomatic COVID-19 was strongly associated with the viral load of contacts at baseline and shortened the incubation time of COVID-19 in a dose-dependent manner.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>FUNDING</b>
</p>
<p>YoMeCorono, Generalitat de Catalunya.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>TRANSLATIONS</b>
</p>
<p>For the Catalan translation of the abstract see Supplementary Materials section.</p>
</div>
</front>
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<Day>03</Day>
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<Day>08</Day>
</DateRevised>
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<Volume>21</Volume>
<Issue>5</Issue>
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</PubDate>
</JournalIssue>
<Title>The Lancet. Infectious diseases</Title>
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<ArticleTitle>Transmission of COVID-19 in 282 clusters in Catalonia, Spain: a cohort study.</ArticleTitle>
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<Abstract>
<AbstractText Label="BACKGROUND">Scarce data are available on what variables affect the risk of transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the development of symptomatic COVID-19, and, particularly, the relationship with viral load. We aimed to analyse data from linked index cases of COVID-19 and their contacts to explore factors associated with transmission of SARS-CoV-2.</AbstractText>
<AbstractText Label="METHODS">In this cohort study, patients were recruited as part of a randomised controlled trial done between March 17 and April 28, 2020, that aimed to assess if hydroxychloroquine reduced transmission of SARS-CoV-2. Patients with COVID-19 and their contacts were identified by use of the electronic registry of the Epidemiological Surveillance Emergency Service of Catalonia (Spain). Patients with COVID-19 included in our analysis were aged 18 years or older, not hospitalised, had quantitative PCR results available at baseline, had mild symptom onset within 5 days before enrolment, and had no reported symptoms of SARS-CoV-2 infections in their accommodation or workplace within the 14 days before enrolment. Contacts included were adults with a recent history of exposure and absence of COVID-19-like symptoms within the 7 days preceding enrolment. Viral load of contacts, measured by quantitative PCR from a nasopharyngeal swab, was assessed at enrolment, at day 14, and whenever the participant reported COVID-19-like symptoms. We assessed risk of transmission and developing symptomatic disease and incubation dynamics using regression analysis. We assessed the relationship of viral load and characteristics of cases (age, sex, number of days from reported symptom onset, and presence or absence of fever, cough, dyspnoea, rhinitis, and anosmia) and associations between risk of transmission and characteristics of the index case and contacts.</AbstractText>
<AbstractText Label="FINDINGS">We identified 314 patients with COVID-19, with 282 (90%) having at least one contact (753 contacts in total), resulting in 282 clusters. 90 (32%) of 282 clusters had at least one transmission event. The secondary attack rate was 17% (125 of 753 contacts), with a variation from 12% when the index case had a viral load lower than 1 × 10
<sup>6</sup>
copies per mL to 24% when the index case had a viral load of 1 × 10
<sup>10</sup>
copies per mL or higher (adjusted odds ratio per log
<sub>10</sub>
increase in viral load 1·3, 95% CI 1·1-1·5). Increased risk of transmission was also associated with household contact (3·0, 1·59-5·65) and age of the contact (per year: 1·02, 1·01-1·04). 449 contacts had a positive PCR result at baseline. 28 (6%) of 449 contacts had symptoms at the first visit. Of 421 contacts who were asymptomatic at the first visit, 181 (43%) developed symptomatic COVID-19, with a variation from approximately 38% in contacts with an initial viral load lower than 1 × 10
<sup>7</sup>
copies per mL to greater than 66% for those with an initial viral load of 1 × 10
<sup>10</sup>
copies per mL or higher (hazard ratio per log
<sub>10</sub>
increase in viral load 1·12, 95% CI 1·05-1·20; p=0·0006). Time to onset of symptomatic disease decreased from a median of 7 days (IQR 5-10) for individuals with an initial viral load lower than 1 × 10
<sup>7</sup>
copies per mL to 6 days (4-8) for those with an initial viral load between 1 × 10
<sup>7</sup>
and 1 × 10
<sup>9</sup>
copies per mL, and 5 days (3-8) for those with an initial viral load higher than 1 × 10
<sup>9</sup>
copies per mL.</AbstractText>
<AbstractText Label="INTERPRETATION">In our study, the viral load of index cases was a leading driver of SARS-CoV-2 transmission. The risk of symptomatic COVID-19 was strongly associated with the viral load of contacts at baseline and shortened the incubation time of COVID-19 in a dose-dependent manner.</AbstractText>
<AbstractText Label="FUNDING">YoMeCorono, Generalitat de Catalunya.</AbstractText>
<AbstractText Label="TRANSLATIONS">For the Catalan translation of the abstract see Supplementary Materials section.</AbstractText>
<CopyrightInformation>Copyright © 2021 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
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<ForeName>Dan</ForeName>
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</AffiliationInfo>
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<LastName>Tobias</LastName>
<ForeName>Aurelio</ForeName>
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</AffiliationInfo>
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<LastName>Tebé</LastName>
<ForeName>Cristian</ForeName>
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<Affiliation>Biostatistics Unit, Institut d'Investigació Biomèdica de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain; Department of Clinical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.</Affiliation>
</AffiliationInfo>
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<LastName>Ballana</LastName>
<ForeName>Ester</ForeName>
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<AffiliationInfo>
<Affiliation>Barcelona Institute for Global Health, Hospital Clínic, University of Barcelona, Barcelona, Spain; Catalan Institution for Research and Advanced Studies, Barcelona, Spain.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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<Affiliation>Fight AIDS and Infectious Diseases Foundation, Badalona, Spain; Infectious Disease Department, Hospital Universitari Germans Trias i Pujol, Badalona, Spain; Department of Clinical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain; Càtedra de Malalties Infeccioses i Immunitat, Universitat de Vic, Universtiat Central de Catalunya, Vic, Spain; Lihir Medical Centre, International SOS, Lihir Island, Papua New Guinea.</Affiliation>
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<li>Espagne</li>
<li>Papouasie-Nouvelle-Guinée</li>
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<li>Angleterre</li>
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<name sortKey="Vall Mayans, Marti" sort="Vall Mayans, Marti" uniqKey="Vall Mayans M" first="Martí" last="Vall-Mayans">Martí Vall-Mayans</name>
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