Clinical outcomes associated with SARS-CoV-2 Omicron (B.1.1.529) variant and BA.1/BA.1.1 or BA.2 subvariant infection in Southern California

被引:225
作者
Lewnard, Joseph A. [1 ,2 ,3 ]
Hong, Vennis X. [4 ]
Patel, Manish M. [5 ]
Kahn, Rebecca [5 ]
Lipsitch, Marc [5 ]
Tartof, Sara Y. [4 ,6 ]
机构
[1] Univ Calif Berkeley, Sch Publ Hlth, Div Epidemiol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Sch Publ Hlth, Div Infect Dis & Vaccinol, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Coll Engn, Ctr Computat Biol, Berkeley, CA 94720 USA
[4] Kaiser Permanente Southern Calif, Dept Res & Evaluat, Pasadena, CA 91188 USA
[5] Ctr Dis Control & Prevent, COVID 19 Response Team, Atlanta, GA USA
[6] Kaiser Permanente Bernard J Tyson Sch Med, Dept Hlth Syst Sci, Pasadena, CA 91101 USA
基金
美国国家卫生研究院;
关键词
DISEASE SEVERITY; UNITED-STATES; IMPACT;
D O I
10.1038/s41591-022-01887-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Comparison of outcomes of SARS-CoV-2 Delta and Omicron infections shows reduced severity of Omicron infections, most notably in unvaccinated individuals, and no differential risk of severe outcomes between subvariants BA.1 and BA.2. The findings highlight the importance of continual assessment of clinical outcomes associated with SARS-CoV-2 variants of concern to inform both medical interventions and healthcare resource management. Epidemiologic surveillance has revealed decoupling of Coronavirus Disease 2019 (COVID-19) hospitalizations and deaths from case counts after emergence of the Omicron (B.1.1.529) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant globally. However, assessment of the relative severity of Omicron variant infections presents challenges because of differential acquired immune protection against Omicron and prior variants and because longer-term changes have occurred in testing and healthcare practices. Here we show that Omicron variant infections were associated with substantially reduced risk of progression to severe clinical outcomes relative to time-matched Delta (B.1.617.2) variant infections within a large, integrated healthcare system in Southern California. Adjusted hazard ratios (aHRs) for any hospital admission, symptomatic hospital admission, intensive care unit admission, mechanical ventilation and death comparing individuals with Omicron versus Delta variant infection were 0.59 (95% confidence interval: 0.51-0.69), 0.59 (0.51-0.68), 0.50 (0.29-0.87), 0.36 (0.18-0.72) and 0.21 (0.10-0.44), respectively. This reduced severity could not be explained by differential history of prior infection among individuals with Omicron or Delta variant infection and was starkest among individuals not previously vaccinated against COVID-19 (aHR = 0.40 (0.33-0.49) for any hospital admission and 0.14 (0.07-0.28) for death). Infections with the Omicron BA.2 subvariant were not associated with differential risk of severe outcomes in comparison to BA.1/BA.1.1 subvariant infections. Lower risk of severe clinical outcomes among individuals with Omicron variant infection should inform public health response amid establishment of the Omicron variant as the dominant SARS-CoV-2 lineage globally.
引用
收藏
页码:1933 / +
页数:17
相关论文
共 59 条
  • [1] The omicron (B.1.1.529) SARS-CoV-2 variant of concern does not readily infect Syrian hamsters
    Abdelnabi, Rana
    Foo, Caroline S.
    Zhang, Xin
    Lemmens, Viktor
    Maes, Piet
    Slechten, Bram
    Raymenants, Joren
    Andr, Emmanuel
    Weynand, Birgit
    Dallmeier, Kai
    Neyts, Johan
    [J]. ANTIVIRAL RESEARCH, 2022, 198
  • [2] Protection against the Omicron Variant from Previous SARS-CoV-2 Infection
    Altarawneh, Heba N.
    Chemaitelly, Hiam
    Hasan, Mohammad R.
    Ayoub, Houssein H.
    Qassim, Suelen
    AlMukdad, Sawsan
    Coyle, Peter
    Yassine, Hadi M.
    Al-Khatib, Hebah A.
    Benslimane, Fatiha M.
    Al-Kanaani, Zaina
    Al-Kuwari, Einas
    Jeremijenko, Andrew
    Kaleeckal, Anvar H.
    Latif, Ali N.
    Shaik, Riyazuddin M.
    Abdul-Rahim, Hanan F.
    Nasrallah, Gheyath K.
    Al-Kuwari, Mohamed G.
    Butt, Adeel A.
    Al-Romaihi, Hamad E.
    Al-Thani, Mohamed H.
    Al-Khal, Abdullatif
    Bertollini, Roberto
    Tang, Patrick
    Abu-Raddad, Laith J.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2022, 386 (13) : 1288 - 1290
  • [3] Prevention of Coronavirus Disease 2019 (COVID-19) by mRNA-Based Vaccines Within the General Population of California
    Andrejko, Kristin L.
    Pry, Jake
    Myers, Jennifer F.
    Jewell, Nicholas P.
    Openshaw, John
    Watt, James
    Jain, Seema
    Lewnard, Joseph A.
    [J]. CLINICAL INFECTIOUS DISEASES, 2022, 74 (08) : 1382 - 1389
  • [4] Andrews N, 2022, NEW ENGL J MED, V386, P1532, DOI [10.1016/S1473-3099(22)00309-7, 10.1056/NEJMoa2119451]
  • [5] BAGER P, 2022, LANCERT INFECT DIS
  • [6] Challenges in Inferring Intrinsic Severity of the SARS-CoV-2 Omicron Variant
    Bhattacharyya, Roby P.
    Hanage, William P.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2022, 386 (07)
  • [7] Multimodel inference - understanding AIC and BIC in model selection
    Burnham, KP
    Anderson, DR
    [J]. SOCIOLOGICAL METHODS & RESEARCH, 2004, 33 (02) : 261 - 304
  • [8] California Department of Public Health, VAR CAL COVID 19 RES
  • [9] Activity of convalescent and vaccine serum against SARS-CoV-2 Omicron
    Carreno, Juan Manuel
    Alshammary, Hala
    Tcheou, Johnstone
    Singh, Gagandeep
    Raskin, Ariel J.
    Kawabata, Hisaaki
    Sominsky, Levy A.
    Clark, Jordan J.
    Adelsberg, Daniel C.
    Bielak, Dominika A.
    Gonzalez-Reiche, Ana Silvia
    Dambrauskas, Nicholas
    Vigdorovich, Vladimir
    Srivastava, Komal
    Sather, D. Noah
    Sordillo, Emilia Mia
    Bajic, Goran
    van Bakel, Harm
    Simon, Viviana
    Krammer, Florian
    [J]. NATURE, 2022, 602 (7898) : 682 - +
  • [10] Clarke KEN, 2022, MMWR-MORBID MORTAL W, V71, P606, DOI 10.15585/mmwr.mm7117e3