Serveur d'exploration sur le Covid à Stanford

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Severe acute respiratory coronavirus virus 2 (SARS-CoV-2) seroprevalence in healthcare personnel in northern California early in the coronavirus disease 2019 (COVID-19) pandemic.

Identifieur interne : 000279 ( Main/Exploration ); précédent : 000278; suivant : 000280

Severe acute respiratory coronavirus virus 2 (SARS-CoV-2) seroprevalence in healthcare personnel in northern California early in the coronavirus disease 2019 (COVID-19) pandemic.

Auteurs : Joelle I. Rosser [États-Unis] ; Katharina Röltgen [États-Unis] ; Melissa Dymock [États-Unis] ; John Shepard [États-Unis] ; Andrew Martin [États-Unis] ; Catherine A. Hogan [États-Unis] ; Andra Blomkalns [États-Unis] ; Roshni Mathew [États-Unis] ; Julie Parsonnet [États-Unis] ; Benjamin A. Pinsky [États-Unis] ; Yvonne A. Maldonado [États-Unis] ; Scott D. Boyd [États-Unis] ; Sang-Ick Chang [États-Unis] ; Marisa Holubar [États-Unis]

Source :

RBID : pubmed:33292895

Abstract

OBJECTIVE

We assessed the magnitude of unidentified coronavirus disease 2019 (COVID-19) in our healthcare personnel (HCP) early in the COVID-19 pandemic, and we evaluated risk factors for infection to identify areas for improvement in infection control practice in a northern California academic medical center.

METHODS

We reviewed anti-severe acute respiratory coronavirus virus 2 (SARS-CoV-2) receptor-binding domain (RBD) IgG serologic test results and self-reported risk factors for seropositivity among 10,449 asymptomatic HCP who underwent voluntary serology testing between April 20 and May 20, 2020.

RESULTS

In total, 136 employees (1.3%) tested positive for SARS-CoV-2 IgG. This included 41 individuals (30.1%) who had previously tested positive for SARS-CoV-2 by nasopharyngeal reverse-transcription polymerase chain reaction (RT-PCR) between March 13 and April 16, 2020. In multivariable analysis, employees of Hispanic ethnicity (odds ratio [OR], 2.01; 95% confidence interval [CI], 1.22-3.46) and those working in environmental services, food services, or patient transport (OR, 4.81; 95% CI, 2.08-10.30) were at increased risk for seropositivity compared to other groups. Employees reporting a household contact with COVID-19 were also at higher risk for seropositivity (OR, 3.25; 95% CI, 1.47-6.44), but those with a work, exposure alone were not (OR, 1.27; 95% CI, 0.58-2.47). Importantly, one-third of seropositive individuals reported no prior symptoms, no suspected exposures, and no prior positive RT-PCR test.

CONCLUSION

In this study, SARS-CoV-2 seropositivity among HCP early in the northern California epidemic appeared to be quite low and was more likely attributable to community rather than occupational exposure.


DOI: 10.1017/ice.2020.1358
PubMed: 33292895
PubMed Central: PMC7783083


Affiliations:


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<name sortKey="Martin, Andrew" sort="Martin, Andrew" uniqKey="Martin A" first="Andrew" last="Martin">Andrew Martin</name>
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<region type="state">Californie</region>
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<wicri:cityArea>Stanford Health Care, Stanford</wicri:cityArea>
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<name sortKey="Hogan, Catherine A" sort="Hogan, Catherine A" uniqKey="Hogan C" first="Catherine A" last="Hogan">Catherine A. Hogan</name>
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<nlm:affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
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<region type="state">Californie</region>
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<wicri:cityArea>Department of Pathology, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Blomkalns, Andra" sort="Blomkalns, Andra" uniqKey="Blomkalns A" first="Andra" last="Blomkalns">Andra Blomkalns</name>
<affiliation wicri:level="2">
<nlm:affiliation>Department of Emergency Medicine, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Department of Emergency Medicine, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Mathew, Roshni" sort="Mathew, Roshni" uniqKey="Mathew R" first="Roshni" last="Mathew">Roshni Mathew</name>
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<nlm:affiliation>Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Parsonnet, Julie" sort="Parsonnet, Julie" uniqKey="Parsonnet J" first="Julie" last="Parsonnet">Julie Parsonnet</name>
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<region type="state">Californie</region>
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<wicri:cityArea>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<affiliation wicri:level="2">
<nlm:affiliation>Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
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<region type="state">Californie</region>
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<wicri:cityArea>Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Pinsky, Benjamin A" sort="Pinsky, Benjamin A" uniqKey="Pinsky B" first="Benjamin A" last="Pinsky">Benjamin A. Pinsky</name>
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<region type="state">Californie</region>
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<nlm:affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Department of Pathology, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Maldonado, Yvonne A" sort="Maldonado, Yvonne A" uniqKey="Maldonado Y" first="Yvonne A" last="Maldonado">Yvonne A. Maldonado</name>
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<nlm:affiliation>Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Boyd, Scott D" sort="Boyd, Scott D" uniqKey="Boyd S" first="Scott D" last="Boyd">Scott D. Boyd</name>
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<nlm:affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
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<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Department of Pathology, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<name sortKey="Chang, Sang Ick" sort="Chang, Sang Ick" uniqKey="Chang S" first="Sang-Ick" last="Chang">Sang-Ick Chang</name>
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<nlm:affiliation>Stanford Health Care, Stanford, California.</nlm:affiliation>
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<region type="state">Californie</region>
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<wicri:cityArea>Stanford Health Care, Stanford</wicri:cityArea>
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<name sortKey="Holubar, Marisa" sort="Holubar, Marisa" uniqKey="Holubar M" first="Marisa" last="Holubar">Marisa Holubar</name>
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<nlm:affiliation>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.</nlm:affiliation>
<country>États-Unis</country>
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<region type="state">Californie</region>
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<wicri:cityArea>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford</wicri:cityArea>
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<nlm:affiliation>Stanford Health Care, Stanford, California.</nlm:affiliation>
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<title level="j">Infection control and hospital epidemiology</title>
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<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVE</b>
</p>
<p>We assessed the magnitude of unidentified coronavirus disease 2019 (COVID-19) in our healthcare personnel (HCP) early in the COVID-19 pandemic, and we evaluated risk factors for infection to identify areas for improvement in infection control practice in a northern California academic medical center.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>We reviewed anti-severe acute respiratory coronavirus virus 2 (SARS-CoV-2) receptor-binding domain (RBD) IgG serologic test results and self-reported risk factors for seropositivity among 10,449 asymptomatic HCP who underwent voluntary serology testing between April 20 and May 20, 2020.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>In total, 136 employees (1.3%) tested positive for SARS-CoV-2 IgG. This included 41 individuals (30.1%) who had previously tested positive for SARS-CoV-2 by nasopharyngeal reverse-transcription polymerase chain reaction (RT-PCR) between March 13 and April 16, 2020. In multivariable analysis, employees of Hispanic ethnicity (odds ratio [OR], 2.01; 95% confidence interval [CI], 1.22-3.46) and those working in environmental services, food services, or patient transport (OR, 4.81; 95% CI, 2.08-10.30) were at increased risk for seropositivity compared to other groups. Employees reporting a household contact with COVID-19 were also at higher risk for seropositivity (OR, 3.25; 95% CI, 1.47-6.44), but those with a work, exposure alone were not (OR, 1.27; 95% CI, 0.58-2.47). Importantly, one-third of seropositive individuals reported no prior symptoms, no suspected exposures, and no prior positive RT-PCR test.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>In this study, SARS-CoV-2 seropositivity among HCP early in the northern California epidemic appeared to be quite low and was more likely attributable to community rather than occupational exposure.</p>
</div>
</front>
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</JournalIssue>
<Title>Infection control and hospital epidemiology</Title>
<ISOAbbreviation>Infect Control Hosp Epidemiol</ISOAbbreviation>
</Journal>
<ArticleTitle>Severe acute respiratory coronavirus virus 2 (SARS-CoV-2) seroprevalence in healthcare personnel in northern California early in the coronavirus disease 2019 (COVID-19) pandemic.</ArticleTitle>
<Pagination>
<MedlinePgn>1-7</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1017/ice.2020.1358</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">We assessed the magnitude of unidentified coronavirus disease 2019 (COVID-19) in our healthcare personnel (HCP) early in the COVID-19 pandemic, and we evaluated risk factors for infection to identify areas for improvement in infection control practice in a northern California academic medical center.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We reviewed anti-severe acute respiratory coronavirus virus 2 (SARS-CoV-2) receptor-binding domain (RBD) IgG serologic test results and self-reported risk factors for seropositivity among 10,449 asymptomatic HCP who underwent voluntary serology testing between April 20 and May 20, 2020.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">In total, 136 employees (1.3%) tested positive for SARS-CoV-2 IgG. This included 41 individuals (30.1%) who had previously tested positive for SARS-CoV-2 by nasopharyngeal reverse-transcription polymerase chain reaction (RT-PCR) between March 13 and April 16, 2020. In multivariable analysis, employees of Hispanic ethnicity (odds ratio [OR], 2.01; 95% confidence interval [CI], 1.22-3.46) and those working in environmental services, food services, or patient transport (OR, 4.81; 95% CI, 2.08-10.30) were at increased risk for seropositivity compared to other groups. Employees reporting a household contact with COVID-19 were also at higher risk for seropositivity (OR, 3.25; 95% CI, 1.47-6.44), but those with a work, exposure alone were not (OR, 1.27; 95% CI, 0.58-2.47). Importantly, one-third of seropositive individuals reported no prior symptoms, no suspected exposures, and no prior positive RT-PCR test.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">In this study, SARS-CoV-2 seropositivity among HCP early in the northern California epidemic appeared to be quite low and was more likely attributable to community rather than occupational exposure.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Rosser</LastName>
<ForeName>Joelle I</ForeName>
<Initials>JI</Initials>
<Identifier Source="ORCID">https://orcid.org/0000-0001-7803-9333</Identifier>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Röltgen</LastName>
<ForeName>Katharina</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Dymock</LastName>
<ForeName>Melissa</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Stanford Health Care, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Shepard</LastName>
<ForeName>John</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Stanford Health Care, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Martin</LastName>
<ForeName>Andrew</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Stanford Health Care, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hogan</LastName>
<ForeName>Catherine A</ForeName>
<Initials>CA</Initials>
<AffiliationInfo>
<Affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Blomkalns</LastName>
<ForeName>Andra</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Emergency Medicine, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mathew</LastName>
<ForeName>Roshni</ForeName>
<Initials>R</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Parsonnet</LastName>
<ForeName>Julie</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, California.</Affiliation>
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<Author ValidYN="Y">
<LastName>Pinsky</LastName>
<ForeName>Benjamin A</ForeName>
<Initials>BA</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Maldonado</LastName>
<ForeName>Yvonne A</ForeName>
<Initials>YA</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Boyd</LastName>
<ForeName>Scott D</ForeName>
<Initials>SD</Initials>
<AffiliationInfo>
<Affiliation>Department of Pathology, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chang</LastName>
<ForeName>Sang-Ick</ForeName>
<Initials>SI</Initials>
<AffiliationInfo>
<Affiliation>Stanford Health Care, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Holubar</LastName>
<ForeName>Marisa</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Division of Infectious Diseases & Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Stanford Health Care, Stanford, California.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<CollectiveName>Stanford Healthcare COVID-19 Workforce Response Group</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2020</Year>
<Month>12</Month>
<Day>09</Day>
</ArticleDate>
</Article>
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<Country>United States</Country>
<MedlineTA>Infect Control Hosp Epidemiol</MedlineTA>
<NlmUniqueID>8804099</NlmUniqueID>
<ISSNLinking>0899-823X</ISSNLinking>
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