Associations between SARS-CoV-2 variants and risk of COVID-19 hospitalization among confirmed cases in Washington State: a retrospective cohort study

The COVID-19 pandemic is dominated by variant viruses; the resulting impact on disease severity remains unclear. Using a retrospective cohort study, we assessed the hospitalization risk following infection with seven SARS-CoV-2 variants. Our study includes individuals with positive SARS-CoV-2 RT-PCR...

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Hauptverfasser: Paredes, Miguel I, Lunn, Stephanie M, Famulare, Michael, Frisbie, Lauren A, Painter, Ian, Burstein, Roy, Roychoudhury, Pavitra, Xie, Hong, Mohamed Bakhash, Shah A, Perez, Ricardo, Lukes, Maria, Ellis, Sean, Sathees, Saraswathi, Mathias, Patrick C, Greninger, Alexander, Starita, Lea M, Frazar, Chris D, Ryke, Erica, Zhong, Weizhi, Gamboa, Luis, Threlkeld, Machiko, Lee, Jover, McDermot, Evan, Truong, Melissa, Nickerson, Deborah A, Bates, Daniel L, Hartman, Matthew E, Haugen, Eric, Nguyen, Truong N, Richards, Joshua D, Rodriguez, Jacob L, Stamatoyannopoulos, John A, Thorland, Eric, Melly, Geoff, Dykema, Philip E, MacKellar, Drew C, Gray, Hannah K, Singh, Avi, Peterson, JohnAric M, Russell, Denny, Marcela Torres, Laura, Lindquist, Scott, Bedford, Trevor, Allen, Krisandra J, Oltean, Hanna N
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container_title Clinical infectious diseases
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creator Paredes, Miguel I
Lunn, Stephanie M
Famulare, Michael
Frisbie, Lauren A
Painter, Ian
Burstein, Roy
Roychoudhury, Pavitra
Xie, Hong
Mohamed Bakhash, Shah A
Perez, Ricardo
Lukes, Maria
Ellis, Sean
Sathees, Saraswathi
Mathias, Patrick C
Greninger, Alexander
Starita, Lea M
Frazar, Chris D
Ryke, Erica
Zhong, Weizhi
Gamboa, Luis
Threlkeld, Machiko
Lee, Jover
McDermot, Evan
Truong, Melissa
Nickerson, Deborah A
Bates, Daniel L
Hartman, Matthew E
Haugen, Eric
Nguyen, Truong N
Richards, Joshua D
Rodriguez, Jacob L
Stamatoyannopoulos, John A
Thorland, Eric
Melly, Geoff
Dykema, Philip E
MacKellar, Drew C
Gray, Hannah K
Singh, Avi
Peterson, JohnAric M
Russell, Denny
Marcela Torres, Laura
Lindquist, Scott
Bedford, Trevor
Allen, Krisandra J
Oltean, Hanna N
description The COVID-19 pandemic is dominated by variant viruses; the resulting impact on disease severity remains unclear. Using a retrospective cohort study, we assessed the hospitalization risk following infection with seven SARS-CoV-2 variants. Our study includes individuals with positive SARS-CoV-2 RT-PCR in the Washington Disease Reporting System with available viral genome data, from December 1, 2020 to January 14, 2022. The analysis was restricted to cases with specimens collected through sentinel surveillance. Using a Cox proportional hazards model with mixed effects, we estimated hazard ratios (HR) for hospitalization risk following infection with a variant, adjusting for age, sex, calendar week, and vaccination. 58,848 cases were sequenced through sentinel surveillance, of which 1705 (2.9%) were hospitalized due to COVID-19. Higher hospitalization risk was found for infections with Gamma (HR 3.20, 95%CI 2.40-4.26), Beta (HR 2.85, 95%CI 1.56-5.23), Delta (HR 2.28 95%CI 1.56-3.34) or Alpha (HR 1.64, 95%CI 1.29-2.07) compared to infections with ancestral lineages; Omicron (HR 0.92, 95%CI 0.56-1.52) showed no significant difference in risk. Following Alpha, Gamma, or Delta infection, unvaccinated patients show higher hospitalization risk, while vaccinated patients show no significant difference in risk, both compared to unvaccinated, ancestral lineage cases. Hospitalization risk following Omicron infection is lower with vaccination. Infection with Alpha, Gamma, or Delta results in a higher hospitalization risk, with vaccination attenuating that risk. Our findings support hospital preparedness, vaccination, and genomic surveillance.
doi_str_mv 10.1093/cid/ciac279
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Using a retrospective cohort study, we assessed the hospitalization risk following infection with seven SARS-CoV-2 variants. Our study includes individuals with positive SARS-CoV-2 RT-PCR in the Washington Disease Reporting System with available viral genome data, from December 1, 2020 to January 14, 2022. The analysis was restricted to cases with specimens collected through sentinel surveillance. Using a Cox proportional hazards model with mixed effects, we estimated hazard ratios (HR) for hospitalization risk following infection with a variant, adjusting for age, sex, calendar week, and vaccination. 58,848 cases were sequenced through sentinel surveillance, of which 1705 (2.9%) were hospitalized due to COVID-19. Higher hospitalization risk was found for infections with Gamma (HR 3.20, 95%CI 2.40-4.26), Beta (HR 2.85, 95%CI 1.56-5.23), Delta (HR 2.28 95%CI 1.56-3.34) or Alpha (HR 1.64, 95%CI 1.29-2.07) compared to infections with ancestral lineages; Omicron (HR 0.92, 95%CI 0.56-1.52) showed no significant difference in risk. Following Alpha, Gamma, or Delta infection, unvaccinated patients show higher hospitalization risk, while vaccinated patients show no significant difference in risk, both compared to unvaccinated, ancestral lineage cases. Hospitalization risk following Omicron infection is lower with vaccination. Infection with Alpha, Gamma, or Delta results in a higher hospitalization risk, with vaccination attenuating that risk. 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Higher hospitalization risk was found for infections with Gamma (HR 3.20, 95%CI 2.40-4.26), Beta (HR 2.85, 95%CI 1.56-5.23), Delta (HR 2.28 95%CI 1.56-3.34) or Alpha (HR 1.64, 95%CI 1.29-2.07) compared to infections with ancestral lineages; Omicron (HR 0.92, 95%CI 0.56-1.52) showed no significant difference in risk. Following Alpha, Gamma, or Delta infection, unvaccinated patients show higher hospitalization risk, while vaccinated patients show no significant difference in risk, both compared to unvaccinated, ancestral lineage cases. Hospitalization risk following Omicron infection is lower with vaccination. Infection with Alpha, Gamma, or Delta results in a higher hospitalization risk, with vaccination attenuating that risk. 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Higher hospitalization risk was found for infections with Gamma (HR 3.20, 95%CI 2.40-4.26), Beta (HR 2.85, 95%CI 1.56-5.23), Delta (HR 2.28 95%CI 1.56-3.34) or Alpha (HR 1.64, 95%CI 1.29-2.07) compared to infections with ancestral lineages; Omicron (HR 0.92, 95%CI 0.56-1.52) showed no significant difference in risk. Following Alpha, Gamma, or Delta infection, unvaccinated patients show higher hospitalization risk, while vaccinated patients show no significant difference in risk, both compared to unvaccinated, ancestral lineage cases. Hospitalization risk following Omicron infection is lower with vaccination. Infection with Alpha, Gamma, or Delta results in a higher hospitalization risk, with vaccination attenuating that risk. 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title Associations between SARS-CoV-2 variants and risk of COVID-19 hospitalization among confirmed cases in Washington State: a retrospective cohort study
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