Models and interaction terms assessed to estimate the adjusted relative risk describing SARS-CoV-2 transmission among household contacts controlling for SARS-CoV-2 variant, index case characteristics and household contact characteristics.

<p>Abbreviations: Ref, reference group; RR, relative risk; CI, confidence interval, <sup>a</sup> Final model shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0313680#pone.0313680.t002" target="_blank">Table 2</a>. <sup>b</sup> Data shown are the exponentiated interaction terms (ratio of Delta:Omicron relative risks). An interaction term was included in the final model if the term was significant at the α = 0.05 level (i.e. the 95% confidence interval did not include the null). For multilevel variables, an interaction term was included if it was significant at the α = 0.05 level for any level of the variable. <sup>c</sup> Vaccination status was defined as of the index case date and was categorized as unvaccinated (never received a COVID-19 vaccine), partially vaccinated (completed part of a COVID-19 vaccine series or completed the primary series <14 days prior), fully vaccinated (completed the primary series ≥14 days prior or received a booster dose <7 days prior), or boosted (received an additional vaccine dose beyond the primary series ≥7 days prior). <sup>d</sup> Number of prior immunologic experiences combined previous infection and vaccination doses to estimate the number of times a person’s immune system had been exposed to SARS-CoV-2 or the vaccine. The possible range of values was zero to four exposures and could be any combination of infection and vaccination. Those with unknown previous infection status were considered to have no previous infection for this composite variable.</p> <p>(DOCX)</p>

Publication Details

Journal
Figshare
Published
2025-01-09
DOI
https://doi.org/10.1371/journal.pone.0313680.s001
Primary Topic
COVID-19 epidemiological studies
Type
article
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article

Models and interaction terms assessed to estimate the adjusted relative risk describing SARS-CoV-2 transmission among household contacts controlling for SARS-CoV-2 variant, index case characteristics and household contact characteristics.

Figshare
COVID-19 epidemiological studies
article

Models and interaction terms assessed to estimate the adjusted relative risk describing SARS-CoV-2 transmission among household contacts controlling for SARS-CoV-2 variant, index case characteristics and household contact characteristics.

article en

Abstract

<p>Abbreviations: Ref, reference group; RR, relative risk; CI, confidence interval, <sup>a</sup> Final model shown in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0313680#pone.0313680.t002" target="_blank">Table 2</a>. <sup>b</sup> Data shown are the exponentiated interaction terms (ratio of Delta:Omicron relative risks). An interaction term was included in the final model if the term was significant at the α = 0.05 level (i.e. the 95% confidence interval did not include the null). For multilevel variables, an interaction term was included if it was significant at the α = 0.05 level for any level of the variable. <sup>c</sup> Vaccination status was defined as of the index case date and was categorized as unvaccinated (never received a COVID-19 vaccine), partially vaccinated (completed part of a COVID-19 vaccine series or completed the primary series <14 days prior), fully vaccinated (completed the primary series ≥14 days prior or received a booster dose <7 days prior), or boosted (received an additional vaccine dose beyond the primary series ≥7 days prior). <sup>d</sup> Number of prior immunologic experiences combined previous infection and vaccination doses to estimate the number of times a person’s immune system had been exposed to SARS-CoV-2 or the vaccine. The possible range of values was zero to four exposures and could be any combination of infection and vaccination. Those with unknown previous infection status were considered to have no previous infection for this composite variable.</p> <p>(DOCX)</p>

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COVID-19 epidemiological studies
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