Predictors of Severe Acute Respiratory Syndrome Coronavirus 2 Infection Following High-Risk Exposure.

SARS-CoV-2 face masks non-pharmaceutical interventions vaccination

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
24 08 2022
Historique:
received: 20 10 2021
pubmed: 22 12 2021
medline: 30 8 2022
entrez: 21 12 2021
Statut: ppublish

Résumé

Non-pharmaceutical interventions (NPIs) are recommended for COVID-19 prevention. However, the effectiveness of NPIs in preventing SARS-CoV-2 transmission remains poorly quantified. We conducted a test-negative design case-control study enrolling cases (testing positive for SARS-CoV-2) and controls (testing negative) with molecular SARS-CoV-2 diagnostic test results reported to California Department of Public Health between 24 February-12 November, 2021. We used conditional logistic regression to estimate adjusted odds ratios (aORs) of case status among participants who reported contact with an individual known or suspected to have been infected with SARS-CoV-2 ("high-risk exposure") ≤14 days before testing. 751 of 1448 cases (52%) and 255 of 1443 controls (18%) reported high-risk exposures ≤14 days before testing. Adjusted odds of case status were 3.02-fold (95% confidence interval: 1.75-5.22) higher when high-risk exposures occurred with household members (vs. other contacts), 2.10-fold (1.05-4.21) higher when exposures occurred indoors (vs. outdoors only), and 2.15-fold (1.27-3.67) higher when exposures lasted ≥3 hours (vs. shorter durations) among unvaccinated and partially-vaccinated individuals; excess risk associated with such exposures was mitigated among fully-vaccinated individuals. Cases were less likely than controls to report mask usage during high-risk exposures (aOR = 0.50 [0.29-0.85]). The adjusted odds of case status was lower for fully-vaccinated (aOR = 0.25 [0.15-0.43]) participants compared to unvaccinated participants. Benefits of mask usage were greatest among unvaccinated and partially-vaccinated participants, and in interactions involving non-household contacts or interactions occurring without physical contact. NPIs reduced the likelihood of SARS-CoV-2 infection following high-risk exposure. Vaccine effectiveness was substantial for partially and fully vaccinated persons.

Sections du résumé

BACKGROUND
Non-pharmaceutical interventions (NPIs) are recommended for COVID-19 prevention. However, the effectiveness of NPIs in preventing SARS-CoV-2 transmission remains poorly quantified.
METHODS
We conducted a test-negative design case-control study enrolling cases (testing positive for SARS-CoV-2) and controls (testing negative) with molecular SARS-CoV-2 diagnostic test results reported to California Department of Public Health between 24 February-12 November, 2021. We used conditional logistic regression to estimate adjusted odds ratios (aORs) of case status among participants who reported contact with an individual known or suspected to have been infected with SARS-CoV-2 ("high-risk exposure") ≤14 days before testing.
RESULTS
751 of 1448 cases (52%) and 255 of 1443 controls (18%) reported high-risk exposures ≤14 days before testing. Adjusted odds of case status were 3.02-fold (95% confidence interval: 1.75-5.22) higher when high-risk exposures occurred with household members (vs. other contacts), 2.10-fold (1.05-4.21) higher when exposures occurred indoors (vs. outdoors only), and 2.15-fold (1.27-3.67) higher when exposures lasted ≥3 hours (vs. shorter durations) among unvaccinated and partially-vaccinated individuals; excess risk associated with such exposures was mitigated among fully-vaccinated individuals. Cases were less likely than controls to report mask usage during high-risk exposures (aOR = 0.50 [0.29-0.85]). The adjusted odds of case status was lower for fully-vaccinated (aOR = 0.25 [0.15-0.43]) participants compared to unvaccinated participants. Benefits of mask usage were greatest among unvaccinated and partially-vaccinated participants, and in interactions involving non-household contacts or interactions occurring without physical contact.
CONCLUSIONS
NPIs reduced the likelihood of SARS-CoV-2 infection following high-risk exposure. Vaccine effectiveness was substantial for partially and fully vaccinated persons.

Identifiants

pubmed: 34932817
pii: 6473597
doi: 10.1093/cid/ciab1040
pmc: PMC8903328
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e276-e288

Subventions

Organisme : NCEZID CDC HHS
ID : U01 CK000539
Pays : United States
Organisme : ACL HHS
ID : U01CK000539
Pays : United States

Investigateurs

Helia Samani (H)
Nikolina Walas (N)
Erin Xavier (E)
Diana J Poindexter (DJ)
Najla Dabbagh (N)
Michelle M Spinosa (MM)
Shrey Saretha (S)
Adrian F Cornejo (AF)
Hyemin Park (H)
Miriam I Bermejo (MI)
Amanda Lam (A)
Amandeep Kaur (A)
Ashly Dyke (A)
Diana Felipe (D)
Maya Spencer (M)
Savannah Corredor (S)
Yasmine Abdulrahim (Y)

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Kristin L Andrejko (KL)

Division of Epidemiology and Biostatistics, School of Public Health, University of California, Berkeley, California, USA.

Jake Pry (J)

California Department of Public Health, Richmond, California, USA.

Jennifer F Myers (JF)

California Department of Public Health, Richmond, California, USA.

John Openshaw (J)

California Department of Public Health, Richmond, California, USA.

James Watt (J)

California Department of Public Health, Richmond, California, USA.

Nozomi Birkett (N)

California Department of Public Health, Richmond, California, USA.

Jennifer L DeGuzman (JL)

California Department of Public Health, Richmond, California, USA.

Camilla M Barbaduomo (CM)

California Department of Public Health, Richmond, California, USA.

Zheng N Dong (ZN)

California Department of Public Health, Richmond, California, USA.

Anna T Fang (AT)

California Department of Public Health, Richmond, California, USA.

Paulina M Frost (PM)

California Department of Public Health, Richmond, California, USA.

Timothy Ho (T)

California Department of Public Health, Richmond, California, USA.

Mahsa H Javadi (MH)

California Department of Public Health, Richmond, California, USA.

Sophia S Li (SS)

California Department of Public Health, Richmond, California, USA.

Vivian H Tran (VH)

California Department of Public Health, Richmond, California, USA.

Christine Wan (C)

California Department of Public Health, Richmond, California, USA.

Seema Jain (S)

California Department of Public Health, Richmond, California, USA.

Joseph A Lewnard (JA)

Division of Epidemiology and Biostatistics, School of Public Health, University of California, Berkeley, California, USA.
Division of Infectious Diseases & Vaccinology, School of Public Health, University of California, Berkeley, California, USA.
Center for Computational Biology, College of Engineering, University of California, Berkeley, California, USA.

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