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Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study
The Omicron variant has been associated with reduced vaccine effectiveness (VE) against mild disease with rapid waning. Meanwhile Omicron has also been associated with milder disease. Protection against severe disease has been substantially higher than protection against infection with previous vari...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523190/ https://www.ncbi.nlm.nih.gov/pubmed/36180428 http://dx.doi.org/10.1038/s41467-022-33378-7 |
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author | Stowe, Julia Andrews, Nick Kirsebom, Freja Ramsay, Mary Bernal, Jamie Lopez |
author_facet | Stowe, Julia Andrews, Nick Kirsebom, Freja Ramsay, Mary Bernal, Jamie Lopez |
author_sort | Stowe, Julia |
collection | PubMed |
description | The Omicron variant has been associated with reduced vaccine effectiveness (VE) against mild disease with rapid waning. Meanwhile Omicron has also been associated with milder disease. Protection against severe disease has been substantially higher than protection against infection with previous variants. We used a test-negative case-control design to estimate VE against hospitalisation with the Omicron and Delta variants using PCR testing linked to hospital records. We investigated the impact of increasing the specificity and severity of hospitalisation definitions on VE. Among 18–64-year-olds using cases admitted via emergency care, VE after a 3rd dose peaked at 82.4% and dropped to 53.6% by 15+ weeks after the 3rd dose; using all admissions for > = 2 days stay with a respiratory code in the primary diagnostic field VE ranged from 90.9% to 67.4%; further restricting to those on oxygen/ventilated/intensive care VE ranged from 97.1% to 75.9%. Among 65+ year olds the equivalent VE estimates were 92.4% to 76.9%; 91.3% to 85.3% and 95.8% to 86.8%. Here we show that with milder Omicron disease contamination of hospitalisations with incidental cases is likely to reduce VE estimates. VE estimates increase, and waning is reduced, when specific hospitalisation definitions are used. |
format | Online Article Text |
id | pubmed-9523190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95231902022-09-30 Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study Stowe, Julia Andrews, Nick Kirsebom, Freja Ramsay, Mary Bernal, Jamie Lopez Nat Commun Article The Omicron variant has been associated with reduced vaccine effectiveness (VE) against mild disease with rapid waning. Meanwhile Omicron has also been associated with milder disease. Protection against severe disease has been substantially higher than protection against infection with previous variants. We used a test-negative case-control design to estimate VE against hospitalisation with the Omicron and Delta variants using PCR testing linked to hospital records. We investigated the impact of increasing the specificity and severity of hospitalisation definitions on VE. Among 18–64-year-olds using cases admitted via emergency care, VE after a 3rd dose peaked at 82.4% and dropped to 53.6% by 15+ weeks after the 3rd dose; using all admissions for > = 2 days stay with a respiratory code in the primary diagnostic field VE ranged from 90.9% to 67.4%; further restricting to those on oxygen/ventilated/intensive care VE ranged from 97.1% to 75.9%. Among 65+ year olds the equivalent VE estimates were 92.4% to 76.9%; 91.3% to 85.3% and 95.8% to 86.8%. Here we show that with milder Omicron disease contamination of hospitalisations with incidental cases is likely to reduce VE estimates. VE estimates increase, and waning is reduced, when specific hospitalisation definitions are used. Nature Publishing Group UK 2022-09-30 /pmc/articles/PMC9523190/ /pubmed/36180428 http://dx.doi.org/10.1038/s41467-022-33378-7 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Stowe, Julia Andrews, Nick Kirsebom, Freja Ramsay, Mary Bernal, Jamie Lopez Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study |
title | Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study |
title_full | Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study |
title_fullStr | Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study |
title_full_unstemmed | Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study |
title_short | Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study |
title_sort | effectiveness of covid-19 vaccines against omicron and delta hospitalisation, a test negative case-control study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523190/ https://www.ncbi.nlm.nih.gov/pubmed/36180428 http://dx.doi.org/10.1038/s41467-022-33378-7 |
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