Evidence map›Paper›PMID 36484987›Full record

ArticleJAMA network open2022

Trends in Risk Factors and Symptoms Associated With SARS-CoV-2 and Rhinovirus Test Positivity in King County, Washington, June 2020 to July 2022.

Chelsea Hansen, Amanda C Perofsky, Roy Burstein, Michael Famulare, Shanda Boyle, Robin Prentice, Cooper Marshall, Benjamin J J McCormick, David Reinhart, Ben Capodanno and 20 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 8 institutions in 1 country.

Chelsea HansenBrotman Baty Institute, University of Washington, Seattle.
Amanda C PerofskyBrotman Baty Institute, University of Washington, Seattle.
Roy BursteinInstitute for Disease Modeling, Bill & Melinda Gates Foundation, Seattle, Washington.
Michael FamulareInstitute for Disease Modeling, Bill & Melinda Gates Foundation, Seattle, Washington.
Shanda BoyleBrotman Baty Institute, University of Washington, Seattle.
Robin PrenticeBrotman Baty Institute, University of Washington, Seattle.
Cooper MarshallBrotman Baty Institute, University of Washington, Seattle.
Benjamin J J McCormickFogarty International Center, National Institutes of Health, Bethesda, Maryland.
David ReinhartBrotman Baty Institute, University of Washington, Seattle.
Ben CapodannoBrotman Baty Institute, University of Washington, Seattle.
Melissa TruongBrotman Baty Institute, University of Washington, Seattle.
Kristen Schwabe-FryBrotman Baty Institute, University of Washington, Seattle.
Kayla KuchtaBrotman Baty Institute, University of Washington, Seattle.
Brian PfauBrotman Baty Institute, University of Washington, Seattle.
Zack AckerBrotman Baty Institute, University of Washington, Seattle.
Jover LeeVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Thomas R SibleyVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Evan McDermotBrotman Baty Institute, University of Washington, Seattle.
Leslie Rodriguez-SalasBrotman Baty Institute, University of Washington, Seattle.
Jeremy StoneBrotman Baty Institute, University of Washington, Seattle.
Luis GamboaBrotman Baty Institute, University of Washington, Seattle.
Peter D HanBrotman Baty Institute, University of Washington, Seattle.
Jeffery S DuchinPublic Health Seattle and King County, Seattle, Washington.
Alpana WaghmareVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Janet A EnglundBrotman Baty Institute, University of Washington, Seattle.
Jay ShendureBrotman Baty Institute, University of Washington, Seattle.
Trevor BedfordBrotman Baty Institute, University of Washington, Seattle.
Helen Y ChuDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle.
Lea M StaritaBrotman Baty Institute, University of Washington, Seattle.
Cécile ViboudFogarty International Center, National Institutes of Health, Bethesda, Maryland.
Brotman Baty Institute · USUniversity of Washington · USFogarty International Center · USFred Hutch Cancer Center · USBill & Melinda Gates Foundation · USHoward Hughes Medical Institute · USInstitute for Disease Modeling · USPublic Health – Seattle & King County · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Importance: Few US studies have reexamined risk factors for SARS-CoV-2 positivity in the context of widespread vaccination and new variants or considered risk factors for cocirculating endemic viruses, such as rhinovirus. Objectives: To evaluate how risk factors and symptoms associated with SARS-CoV-2 test positivity changed over the course of the pandemic and to compare these with the risk factors associated with rhinovirus test positivity. Design, Setting, and Participants: This case-control study used a test-negative design with multivariable logistic regression to assess associations between SARS-CoV-2 and rhinovirus test positivity and self-reported demographic and symptom variables over a 25-month period. The study was conducted among symptomatic individuals of all ages enrolled in a cross-sectional community surveillance study in King County, Washington, from June 2020 to July 2022. Exposures: Self-reported data for 15 demographic and health behavior variables and 16 symptoms. Main Outcomes and Measures: Reverse transcription-polymerase chain reaction-confirmed SARS-CoV-2 or rhinovirus infection. Results: Analyses included data from 23 498 individuals. The median (IQR) age of participants was 34.33 (22.42-45.08) years, 13 878 (59.06%) were female, 4018 (17.10%) identified as Asian, 654 (2.78%) identified as Black, and 2193 (9.33%) identified as Hispanic. Close contact with an individual with SARS-CoV-2 (adjusted odds ratio [aOR], 3.89; 95% CI, 3.34-4.57) and loss of smell or taste (aOR, 3.49; 95% CI, 2.77-4.41) were the variables most associated with SARS-CoV-2 test positivity, but both attenuated during the Omicron period. Contact with a vaccinated individual with SARS-CoV-2 (aOR, 2.03; 95% CI, 1.56-2.79) was associated with lower odds of testing positive than contact with an unvaccinated individual with SARS-CoV-2 (aOR, 4.04; 95% CI, 2.39-7.23). Sore throat was associated with Omicron infection (aOR, 2.27; 95% CI, 1.68-3.20) but not Delta infection. Vaccine effectiveness for participants fully vaccinated with a booster dose was 93% (95% CI, 73%-100%) for Delta, but not significant for Omicron. Variables associated with rhinovirus test positivity included being younger than 12 years (aOR, 3.92; 95% CI, 3.42-4.51) and experiencing a runny or stuffy nose (aOR, 4.58; 95% CI, 4.07-5.21). Black race, residing in south King County, and households with 5 or more people were significantly associated with both SARS-CoV-2 and rhinovirus test positivity. Conclusions and Relevance: In this case-control study of 23 498 symptomatic individuals, estimated risk factors and symptoms associated with SARS-CoV-2 infection changed over time. There was a shift in reported symptoms between the Delta and Omicron variants as well as reductions in the protection provided by vaccines. Racial and sociodemographic disparities persisted in the third year of SARS-CoV-2 circulation and were also present in rhinovirus infection. Trends in testing behavior and availability may influence these results.

Indexed as

COVID-19SARS-CoV-2AdultCase-Control StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedRhinovirusRisk Factors

Identifiers

PMID36484987
PMCPMC9856230
OpenAlexW4312013621

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.