Cited by 1,221SARS-CoV-2 and COVID-19 ResearchCOVID-19 Clinical Research StudiesCOVID-19 epidemiological studies

Comparative analysis of the risks of hospitalisation and death associated with SARS-CoV-2 omicron (B.1.1.529) and delta (B.1.617.2) variants in England: a cohort study

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Nyberg, Tommy, Ferguson, Neil M, Nash, Sophie G, Webster, Harriet H, Flaxman, Seth, Andrews, Nick, Hinsley, Wes, Bernal, Jamie Lopez +44 more·2022·The Lancet

Abstract

BACKGROUND: The omicron variant (B.1.1.529) of SARS-CoV-2 has demonstrated partial vaccine escape and high transmissibility, with early studies indicating lower severity of infection than that of the delta variant (B.1.617.2). We aimed to better characterise omicron severity relative to delta by assessing the relative risk of hospital attendance, hospital admission, or death in a large national cohort. METHODS: Individual-level data on laboratory-confirmed COVID-19 cases resident in England between Nov 29, 2021, and Jan 9, 2022, were linked to routine datasets on vaccination status, hospital attendance and admission, and mortality. The relative risk of hospital attendance or admission within 14 days, or death within 28 days after confirmed infection, was estimated using proportional hazards regression. Analyses were stratified by test date, 10-year age band, ethnicity, residential region, and vaccination status, and were further adjusted for sex, index of multiple deprivation decile, evidence of a previous infection, and year of age within each age band. A secondary analysis estimated variant-specific and vaccine-specific vaccine effectiveness and the intrinsic relative severity of omicron infection compared with delta (ie, the relative risk in unvaccinated cases). FINDINGS: The adjusted hazard ratio (HR) of hospital attendance (not necessarily resulting in admission) with omicron compared with delta was 0·56 (95% CI 0·54-0·58); for hospital admission and death, HR estimates were 0·41 (0·39-0·43) and 0·31 (0·26-0·37), respectively. Omicron versus delta HR estimates varied with age for all endpoints examined. The adjusted HR for hospital admission was 1·10 (0·85-1·42) in those younger than 10 years, decreasing to 0·25 (0·21-0·30) in 60-69-year-olds, and then increasing to 0·47 (0·40-0·56) in those aged at least 80 years. For both variants, past infection gave some protection against death both in vaccinated (HR 0·47 [0·32-0·68]) and unvaccinated (0·18 [0·06-0·57]) cases. In vaccinated cases, past infection offered no additional protection against hospital admission beyond that provided by vaccination (HR 0·96 [0·88-1·04]); however, for unvaccinated cases, past infection gave moderate protection (HR 0·55 [0·48-0·63]). Omicron versus delta HR estimates were lower for hospital admission (0·30 [0·28-0·32]) in unvaccinated cases than the corresponding HR estimated for all cases in the primary analysis. Booster vaccination with an mRNA vaccine was highly protective against hospitalisation and death in omicron cases (HR for hospital admission 8-11 weeks post-booster vs unvaccinated: 0·22 [0·20-0·24]), with the protection afforded after a booster not being affected by the vaccine used for doses 1 and 2. INTERPRETATION: The risk of severe outcomes following SARS-CoV-2 infection is substantially lower for omicron than for delta, with higher reductions for more severe endpoints and significant variation with age. Underlying the observed risks is a larger reduction in intrinsic severity (in unvaccinated individuals) counterbalanced by a reduction in vaccine effectiveness. Documented previous SARS-CoV-2 infection offered some protection against hospitalisation and high protection against death in unvaccinated individuals, but only offered additional protection in vaccinated individuals for the death endpoint. Booster vaccination with mRNA vaccines maintains over 70% protection against hospitalisation and death in breakthrough confirmed omicron infections. FUNDING: Medical Research Council, UK Research and Innovation, Department of Health and Social Care, National Institute for Health Research, Community Jameel, and Engineering and Physical Sciences Research Council.

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  • Omicron cases had greater infectivity and the highest hospital admission frequency, but severe illness was lower than Delta and Alpha variants.

    “Omicron cases had greater infectivity and the highest hospital admission frequency, but severe illness was lower than Delta and Alpha variants.”

    From COVID-19, Myocarditis and Pericarditis (2023) · cites this paper as [100]

    The Discussion reports that omicron cases had a 59% lower risk of hospital admission and a 69% lower risk of death than delta cases, and the Introduction describes a rapid rise in omicron cases. But the paper does not establish that omicron had the highest hospital admission frequency or that its illness was less severe than alpha; its severity analysis compares omicron with delta. (LLM, conf=0.87)

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Research works printed but not linked: 22

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Authors
Nyberg, T., Ferguson, N. M., Nash, S. G., Webster, H. H., Flaxman, S., Andrews, N., Hinsley, W., Bernal, J. L., Kall, M., Bhatt, S., Blomquist, P., Zaidi, A., Volz, E., Aziz, N. A., Harman, K., Funk, S., Abbott, S., Nyberg, T., Ferguson, N. M., Nash, S. G., Webster, H. H., Flaxman, S., Andrews, N., Hinsley, W., Lopez Bernal, J., Kall, M., Bhatt, S., Blomquist, P., Zaidi, A., Volz, E., Abdul Aziz, N., Harman, K., Funk, S., Abbott, S., Hope, R., Charlett, A., Chand, M., Ghani, A. C., Seaman, S. R., Dabrera, G., De Angelis, D., Presanis, A. M., Thelwall, S., Hope, R., Charlett, A., Chand, M., Ghani, A. C., Seaman, S. R., Dabrera, G., De Angelis, D., Presanis, A. M., & Thelwall, S.
Venue
The Lancet
Publisher
Elsevier BV
Published
2022-04
Volume
399
Issue
10332
Pages
1303-1312
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
OpenAlex
W4220777055
Cited by
1,221
References
2
Citations by year
2026: 71 · 2025: 127 · 2024: 232 · 2023: 430 · 2022: 360 · 2021: 1
FWCI
140.56
Type
journal article
Language
en
Open access
Locations
  • The Lancet (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
  • Explore Bristol Research (submittedVersion, cc-by)
  • Spiral (Imperial College London) (submittedVersion, other-oa)
Funders
  • Wellcome Trust (210758/Z/18/Z, 210758)
  • Government of the United Kingdom
  • UK Research and Innovation (MR/V038109/1)
  • National Institute for Health and Care Research (MR/R015600/1, (NIHR200908))
  • Department of Health and Social Care
  • Academy of Medical Sciences (AMS-CSF4-Torok)
  • Medical Research Council (MC_UU_00002/11, MR/R015600/1, MR/V038109/1, NIHR200908, MC_PC_19012, COVID-19)
  • Engineering and Physical Sciences Research Council (EP/V002910/2)
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
  • Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
Keywords
Omicron variant, Delta variant, COVID-19 severity, hospitalization, COVID-19 mortality, relative risk, vaccine effectiveness, vaccination status, England, COVID-19 pandemic
MeSH terms
COVID-19, SARS-CoV-2, mRNA Vaccines, England, Hospitalization, Humans, Vaccines, Synthetic, Cohort Studies

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