P-1906. Early COVID-19 and Severity of Subsequent Omicron Infection in Ontario, Canada

Abstract Background As SARS-CoV-2 evolves, assessing changes in COVID-19 severity over time, and the impact of prior infection on repeat infection, is important. We determined whether developing COVID-19 early in the pandemic was associated with reduced severity of subsequent infection with Omicron sub-lineages. Methods We evaluated COVID-19 severity among patients infected during the Omicron wave. Severity was measured in 3 ways:(1) an ordinal measure combining activities of daily living (ADL) and presence of fever,(2) healthcare required (yes/no),(3) an ordinal measure of illness duration. We compared these outcomes in a study of age and time-period matched cohorts in Toronto, Canada: one with symptomatic COVID-19 between Mar 1 & Sep 30/2020 ('early COVID-19') and another who did not test positive for SARS-CoV-2 during the same period. Participants completed baseline, then biweekly surveys to identify SARS-CoV-2 infection episodes from Jan 2020 to Jan 2023. Multivariable binary and ordinal logistic regression models were used to construct ORs and 95% CI for impact of early COVID-19 on severity, adjusted for social/demographic characteristics, comorbidities, COVID-19 vaccination status, and time from early COVID-19 to first Omicron infection. Results Of 261 participants with COVID-19 due to Omicron (Table 1), 177 had early COVID-19 at a median of 26 months prior. In adjusted analyses, those with early COVID-19 occurring < 24 months prior to their Omicron infection had lower odds of having severe Omicron-related illness; OR 0.35 (95%CI 0.15-0.80); with non-significant lower odds of requirement for healthcare (OR 0.49,95%CI 0.14-1.8) and illness duration (OR 0.80, 95%CI 0.32-2.0) (Table 2). Immunocompromise was associated with more severe illness based on all 3 outcomes; other non-immunocompromising comorbidities were associated with requiring healthcare and longer illness duration, and females reported longer illness duration (Table 2). Conclusion Developing COVID-19 early in the pandemic was associated with reduced severity of first Omicron infection if it occurred < 24 months later. Immunocompromise and the presence of other underlying comorbidities were associated with increased severity, and women reported longer duration of illness. Disclosures Moe H. Kyaw, PhD, Pfizer: Employee Catherine Martin, PhD, Pfizer: employee|Pfizer: Stocks/Bonds (Private Company) Maria Major, B.Sc., M.P.H., Pfizer: Employee Samira Mubareka, MD, Pfizer: Grant/Research Support Srinivas Valluri, PhD, Pfizer: Employee John M. McLaughlin, PhD, Pfizer: Employee|Pfizer: Stocks/Bonds (Public Company) Allison McGeer, MD, AstraZeneca: Honoraria|GSK: Honoraria|Merck: Honoraria|Moderna: Honoraria|Novavax: Honoraria|Pfizer: Grant/Research Support|Pfizer: Honoraria|Roche: Honoraria|Seqirus: Grant/Research Support|Seqirus: Honoraria

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Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.2067
Primary Topic
COVID-19 Clinical Research Studies
Type
article
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article

P-1906. Early COVID-19 and Severity of Subsequent Omicron Infection in Ontario, Canada

Allison McGeer, Srinivas Rao Valluri, Maria Major, Altynay Shigayeva et al.
Open Forum Infectious Diseases
COVID-19 Clinical Research Studies
article

P-1906. Early COVID-19 and Severity of Subsequent Omicron Infection in Ontario, Canada

Allison McGeer, Srinivas Rao Valluri, Maria Major, Altynay Shigayeva, Brenda L. Coleman, Caroline Kassee, Christopher Kandel, Lubna Farooqi, Samira Mubareka, Wayne L. Gold, Catherine Martin, Moe H. Kyaw, Zoë Zhong, John M. McLaughlin
article en

Abstract

Abstract Background As SARS-CoV-2 evolves, assessing changes in COVID-19 severity over time, and the impact of prior infection on repeat infection, is important. We determined whether developing COVID-19 early in the pandemic was associated with reduced severity of subsequent infection with Omicron sub-lineages. Methods We evaluated COVID-19 severity among patients infected during the Omicron wave. Severity was measured in 3 ways:(1) an ordinal measure combining activities of daily living (ADL) and presence of fever,(2) healthcare required (yes/no),(3) an ordinal measure of illness duration. We compared these outcomes in a study of age and time-period matched cohorts in Toronto, Canada: one with symptomatic COVID-19 between Mar 1 & Sep 30/2020 ('early COVID-19') and another who did not test positive for SARS-CoV-2 during the same period. Participants completed baseline, then biweekly surveys to identify SARS-CoV-2 infection episodes from Jan 2020 to Jan 2023. Multivariable binary and ordinal logistic regression models were used to construct ORs and 95% CI for impact of early COVID-19 on severity, adjusted for social/demographic characteristics, comorbidities, COVID-19 vaccination status, and time from early COVID-19 to first Omicron infection. Results Of 261 participants with COVID-19 due to Omicron (Table 1), 177 had early COVID-19 at a median of 26 months prior. In adjusted analyses, those with early COVID-19 occurring < 24 months prior to their Omicron infection had lower odds of having severe Omicron-related illness; OR 0.35 (95%CI 0.15-0.80); with non-significant lower odds of requirement for healthcare (OR 0.49,95%CI 0.14-1.8) and illness duration (OR 0.80, 95%CI 0.32-2.0) (Table 2). Immunocompromise was associated with more severe illness based on all 3 outcomes; other non-immunocompromising comorbidities were associated with requiring healthcare and longer illness duration, and females reported longer illness duration (Table 2). Conclusion Developing COVID-19 early in the pandemic was associated with reduced severity of first Omicron infection if it occurred < 24 months later. Immunocompromise and the presence of other underlying comorbidities were associated with increased severity, and women reported longer duration of illness. Disclosures Moe H. Kyaw, PhD, Pfizer: Employee Catherine Martin, PhD, Pfizer: employee|Pfizer: Stocks/Bonds (Private Company) Maria Major, B.Sc., M.P.H., Pfizer: Employee Samira Mubareka, MD, Pfizer: Grant/Research Support Srinivas Valluri, PhD, Pfizer: Employee John M. McLaughlin, PhD, Pfizer: Employee|Pfizer: Stocks/Bonds (Public Company) Allison McGeer, MD, AstraZeneca: Honoraria|GSK: Honoraria|Merck: Honoraria|Moderna: Honoraria|Novavax: Honoraria|Pfizer: Grant/Research Support|Pfizer: Honoraria|Roche: Honoraria|Seqirus: Grant/Research Support|Seqirus: Honoraria

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Sunnybrook Health Science Centre (CA), Pfizer (United States) (US), University of Toronto (CA), Sinai Hospital (US), Toronto East General Hospital (CA), Health Sciences Centre (CA), Pfizer (France) (FR), Pfizer (Canada) (CA)
Openalex Percentile: Top 98%
COVID-19 Clinical Research Studies
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