Clinical severity of COVID-19 in patients admitted to hospital during the omicron wave in South Africa: a retrospective observational study

被引:131
作者
Jassat, Waasila [1 ,2 ]
Karim, Salim S. Abdool [3 ,4 ]
Mudara, Caroline [1 ]
Welch, Richard [1 ]
Ozougwu, Lovelyn [1 ]
Groome, Michelle J. [1 ,5 ]
Govender, Nevashan [1 ]
von Gottberg, Anne [1 ,5 ]
Wolter, Nicole [1 ,5 ]
Wolmarans, Milani [7 ]
Rousseau, Petro [7 ]
Blumberg, Lucille [1 ,2 ]
Cohen, Cheryl [1 ,6 ]
机构
[1] Natl Inst Communicable Dis, Natl Hlth Lab Serv, Johannesburg, South Africa
[2] Right Care, Centurion, South Africa
[3] Blumberg Ctr AIDS Programme Res South Africa, Durban, South Africa
[4] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA
[5] Univ Witwatersrand, Fac Hlth Sci, Sch Pathol, Johannesburg, South Africa
[6] Univ Witwatersrand, Fac Hlth Sci, Sch Publ Hlth, Johannesburg, South Africa
[7] Natl Dept Hlth, Pretoria, South Africa
来源
LANCET GLOBAL HEALTH | 2022年 / 10卷 / 07期
关键词
D O I
10.1016/S2214-109X(22)00114-0
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Up to the end of January, 2022, South Africa has had four recognisable COVID-19 pandemic waves, each predominantly dominated by one variant of concern: the ancestral strain with an Asp614Gly mutation during the first wave, the beta variant (B.1.351) during the second wave, the delta variant (B.1.617.2) during the third wave, and lastly, the omicron variant (B.1.1.529) during the fourth wave. We aimed to assess the clinical disease severity of patients admitted to hospital with SARS-CoV-2 infection during the omicron wave and compare the findings with those of the preceding three pandemic waves in South Africa. Methods We defined the start and end of each pandemic wave as the crossing of the threshold of weekly incidence of 30 laboratory-confirmed SARS-CoV-2 cases per 100 000 population. Hospital admission data were collected through an active national COVID-19-specific surveillance programme. We compared disease severity across waves by postimputation random effect multivariable logistic regression models. Severe disease was defined as one or more of the following: acute respiratory distress, receipt of supplemental oxygen or mechanical ventilation, admission to intensive care, or death. Findings We analysed 335 219 laboratory-confirmed SARS-CoV-2 hospital admissions with a known outcome, constituting 10.4% of 3 216 179 cases recorded during the four waves. During the omicron wave, 52 038 (8.3%) of 629 617 cases were admitted to hospital, compared with 71 411 (12.9%) of 553 530 in the Asp614Gly wave, 91 843 (12.6%) of 726 772 in the beta wave, and 131 083 (10.0%) of 1 306 260 in the delta wave (p<0.0001). During the omicron wave, 15 421 (33.6%) of 45 927 patients admitted to hospital had severe disease, compared with 36 837 (52.3%) of 70 424 in the Asp614Gly wave, 57 247 (63.4%) of 90 310 in the beta wave, and 81 040 (63.0%) of 128 558 in the delta wave (p<0.0001). The in-hospital case-fatality ratio during the omicron wave was 10.7%, compared with 21.5% during the Asp614Gly wave, 28.8% during the beta wave, and 26.4% during the delta wave (p<0.0001). Compared with those admitted to hospital during the omicron wave, patients admitted during the other three waves had more severe clinical presentations (adjusted odds ratio 2.07 [95% CI 2.01-2.13] in the Asp614Gly wave, 3.59 [3.49-3.70] in the beta wave, and 3.47 [3.38-3.57] in the delta wave). Interpretation The trend of increasing cases and admissions across South Africa's first three waves shifted in the omicron wave, with a higher and quicker peak but fewer patients admitted to hospital, less clinically severe illness, and a lower case-fatality ratio compared with the preceding three waves. Omicron marked a change in the SARSCoV-2 epidemic curve, clinical profile, and deaths in South Africa. Extrapolations to other populations should factor in differing vaccination and previous infection levels. Copyright (C) 2022 The Author(s). Published by Elsevier Ltd.
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页码:E961 / E969
页数:9
相关论文
共 30 条
[1]   New SARS-CoV-2 Variants - Clinical, Public Health, and Vaccine Implications [J].
Abdool Karim, Salim S. ;
de Oliveira, Tulio .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (19) :1866-1868
[2]   Severity of SARS-CoV-2 Reinfections as Compared with Primary Infections [J].
Abu-Raddad, Laith J. ;
Chemaitelly, Hiam ;
Bertollini, Roberto .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (26) :2487-2489
[3]  
Bager P, 2022, LANCET INFECT DIS, DOI [10.2139/ssrn.4008930, DOI 10.2139/SSRN.4008930]
[4]  
Bentley E., 2021, Microbiology, DOI DOI 10.1101/2021.12.26.474085
[5]   Omicron extensively but incompletely escapes Pfizer BNT162b2 neutralization [J].
Cele, Sandile ;
Jackson, Laurelle ;
Khoury, David S. ;
Khan, Khadija ;
Moyo-Gwete, Thandeka ;
Tegally, Houriiyah ;
San, James Emmanuel ;
Cromer, Deborah ;
Scheepers, Cathrine ;
Amoako, Daniel G. ;
Karim, Farina ;
Bernstein, Mallory ;
Lustig, Gila ;
Archary, Derseree ;
Smith, Muneerah ;
Ganga, Yashica ;
Jule, Zesuliwe ;
Reedoy, Kajal ;
Hwa, Shi-Hsia ;
Giandhari, Jennifer ;
Blackburn, Jonathan M. ;
Gosnell, Bernadett, I ;
Karim, Salim S. Abdool ;
Hanekom, Willem ;
von Gottberg, Anne ;
Bhiman, Jinal N. ;
Lessells, Richard J. ;
Moosa, Mahomed-Yunus S. ;
Davenport, Miles P. ;
de Oliveira, Tulio ;
Moore, Penny L. ;
Sigal, Alex .
NATURE, 2022, 602 (7898) :654-+
[6]   Effectiveness of BNT162b2 Vaccine against Omicron Variant in South Africa [J].
Collie, Shirley ;
Champion, Jared ;
Moultrie, Harry ;
Bekker, Linda-Gail ;
Gray, Glenda .
NEW ENGLAND JOURNAL OF MEDICINE, 2022, 386 (05) :494-496
[7]   Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection [J].
Dan, Jennifer M. ;
Mateus, Jose ;
Kato, Yu ;
Hastie, Kathryn M. ;
Yu, Esther Dawen ;
Faliti, Caterina E. ;
Grifoni, Alba ;
Ramirez, Sydney, I ;
Haupt, Sonya ;
Frazier, April ;
Nakao, Catherine ;
Rayaprolu, Vamseedhar ;
Rawlings, Stephen A. ;
Peters, Bjoern ;
Krammer, Florian ;
Simon, Viviana ;
Saphire, Erica Ollmann ;
Smith, Davey M. ;
Weiskopf, Daniela ;
Sette, Alessandro ;
Crotty, Shane .
SCIENCE, 2021, 371 (6529) :587-+
[8]  
Geary W, 2021, Geocoding with Google sheets-API
[9]   SARS-CoV-2 Omicron virus causes attenuated disease in mice and hamsters [J].
Halfmann, Peter J. ;
Iida, Shun ;
Iwatsuki-Horimoto, Kiyoko ;
Maemura, Tadashi ;
Kiso, Maki ;
Scheaffer, Suzanne M. ;
Darling, Tamarand L. ;
Joshi, Astha ;
Loeber, Samantha ;
Singh, Gagandeep ;
Foster, Stephanie L. ;
Ying, Baoling ;
Case, James Brett ;
Chong, Zhenlu ;
Whitener, Bradley ;
Moliva, Juan ;
Floyd, Katharine ;
Ujie, Michiko ;
Nakajima, Noriko ;
Ito, Mutsumi ;
Wright, Ryan ;
Uraki, Ryuta ;
Warang, Prajakta ;
Gagne, Matthew ;
Li, Rong ;
Sakai-Tagawa, Yuko ;
Liu, Yanan ;
Larson, Deanna ;
Osorio, Jorge E. ;
Hernandez-Ortiz, Juan P. ;
Henry, Amy R. ;
Ciuoderis, Karl ;
Florek, Kelsey R. ;
Patel, Mit ;
Odle, Abby ;
Wong, Lok-Yin Roy ;
Bateman, Allen C. ;
Wang, Zhongde ;
Edara, Venkata-Viswanadh ;
Chong, Zhentu ;
Franks, John ;
Jeevan, Trushar ;
Fabrizio, Thomas ;
DeBeauchamp, Jennifer ;
Kercher, Lisa ;
Seiler, Patrick ;
Gonzalez-Reiche, Ana Silvia ;
Sordillo, Emilia Mia ;
Chang, Lauren A. ;
van Baker, Harm .
NATURE, 2022, 603 (7902) :687-+
[10]   SARS-CoV-2 Omicron variant replication in human bronchus and lung ex vivo [J].
Hui, Kenrie P. Y. ;
Ho, John C. W. ;
Cheung, Man-chun ;
Ng, Ka-chun ;
Ching, Rachel H. H. ;
Lai, Ka-ling ;
Kam, Tonia Tong ;
Gu, Haogao ;
Sit, Ko-Yung ;
Hsin, Michael K. Y. ;
Au, Timmy W. K. ;
Poon, Leo L. M. ;
Peiris, Malik ;
Nicholls, John M. ;
Chan, Michael C. W. .
NATURE, 2022, 603 (7902) :715-+