Associations Between Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants and Risk of Coronavirus Disease 2019 (COVID-19) Hospitalization Among Confirmed Cases in Washington State: A Retrospective Cohort Study

M. Paredes, Stephanie M Lunn, M. Famulare, L. Frisbie, I. Painter, R. Burstein, Pavitra Roychoudhury, H. Xie, S. A. Mohamed Bakhash, R. Perez, Maria Lukes, S. Ellis, Saraswathi Sathees, P. Mathias, A. Greninger, L. Starita, C. Frazar, E. Ryke, W. Zhong, L. Gamboa, M. Threlkeld, Jover Lee, E. McDermot, M. Truong, D. Nickerson, Daniel L Bates, M. Hartman, E. Haugen, Truong Nguyen, J. Richards, Jacob L Rodriguez, J. Stamatoyannopoulos, Eric Thorland, G. Melly, P. Dykema, Drew Mackellar, Hannah K. Gray, Avi Singh, J. Peterson, Denny Russell, L. M. Torres, S. Lindquist, T. Bedford, Krisandra J. Allen, H. Oltean
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引用次数: 22

Abstract

Abstract Background The coronavirus disease 2019 (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 7 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants. Methods Our study includes individuals with positive SARS-CoV-2 reverse transcription polymerase chain reaction (RT-PCR) in the Washington Disease Reporting System with available viral genome data, from 1 December 2020 to 14 January 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. Results In total, 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% confidence interval [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 .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. Conclusions 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.
华盛顿州确诊病例中严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)变异与2019冠状病毒病(COVID-19)住院风险之间的关系:一项回顾性队列研究
背景2019冠状病毒病(COVID-19)大流行以变异病毒为主;由此产生的对疾病严重程度的影响尚不清楚。通过一项回顾性队列研究,我们评估了感染7种严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)变体后的住院风险。方法研究对象为华盛顿疾病报告系统中具有可用病毒基因组数据的SARS-CoV-2逆转录聚合酶链反应(RT-PCR)阳性个体,时间为2020年12月1日至2022年1月14日。分析仅限于通过哨点监测收集标本的病例。使用混合效应的Cox比例风险模型,在调整了年龄、性别、日历周和疫苗接种等因素后,我们估计了感染变异后住院风险的风险比(HR)。结果通过哨点监测共获得58 848例病例,其中1705例(2.9%)因COVID-19住院。与具有祖先血统的感染相比,Gamma (HR 3.20, 95%可信区间[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)或Alpha (HR 1.64, 95% CI 1.29-2.07)感染的住院风险更高;Omicron组(HR 0.92, 95% CI 0.56 ~ 1.52)的风险差异无统计学意义。在Alpha、Gamma或Delta感染后,未接种疫苗的患者显示出更高的住院风险,而接种疫苗的患者与未接种疫苗的祖系病例相比,在风险方面没有显着差异。接种疫苗后,感染欧米克隆后住院的风险较低。结论:α、γ或Delta感染可导致较高的住院风险,接种疫苗可降低这种风险。我们的研究结果支持医院准备、疫苗接种和基因组监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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