Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/36873
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dc.contributor.authorSheikh, Azizen_UK
dc.contributor.authorKerr, Stevenen_UK
dc.contributor.authorWoolhouse, Marken_UK
dc.contributor.authorMcMenamin, Jimen_UK
dc.contributor.authorRobertson, Chrisen_UK
dc.contributor.authorEAVE II Collaborators,en_UK
dc.date.accessioned2025-03-19T01:06:58Z-
dc.date.available2025-03-19T01:06:58Z-
dc.date.issued2022-07en_UK
dc.identifier.urihttp://hdl.handle.net/1893/36873-
dc.description.abstractBackground Since its emergence in November, 2021, in southern Africa, the SARS-CoV-2 omicron variant of concern (VOC) has rapidly spread across the world. We aimed to investigate the severity of omicron and the extent to which booster vaccines are effective in preventing symptomatic infection. Methods In this study, using the Scotland-wide Early Pandemic Evaluation and Enhanced Surveillance of COVID-19 (EAVE II) platform, we did a cohort analysis with a nested test-negative design incident case-control study covering the period Nov 1–Dec 19, 2021, to provide initial estimates of omicron severity and the effectiveness of vaccine boosters against symptomatic disease relative to 25 weeks or more after the second vaccine dose. Primary care data derived from 940 general practices across Scotland were linked to laboratory data and hospital admission data. We compared outcomes between infection with the delta VOC (defined as S-gene positive) and the omicron VOC (defined as S-gene negative). We assessed effectiveness against symptomatic SARS-CoV-2 infection, with infection confirmed through a positive RT-PCR. Findings By Dec 19, 2021, there were 23 840 S-gene-negative cases in Scotland, which were predominantly among those aged 20–39 years (11 732 [49·2%]). The proportion of S-gene-negative cases that were possible reinfections was more than ten times that of S-gene-positive cases (7·6% vs 0·7%; p<0·0001). There were 15 hospital admissions in S-gene-negative individuals, giving an adjusted observed-to-expected admissions ratio of 0·32 (95% CI 0·19–0·52). The booster vaccine dose was associated with a 57% (54–60) reduction in the risk of symptomatic S-gene-negative infection relative to individuals who tested positive 25 weeks or more after the second vaccine dose. Interpretation These early national data suggest that omicron is associated with a two-thirds reduction in the risk of COVID-19 hospitalisation compared with delta. Although offering the greatest protection against delta, the booster dose of vaccination offers substantial additional protection against the risk of symptomatic COVID-19 for omicron compared with 25 weeks or more after the second vaccine dose.en_UK
dc.language.isoenen_UK
dc.publisherElsevier BVen_UK
dc.relationSheikh A, Kerr S, Woolhouse M, McMenamin J, Robertson C & EAVE II Collaborators (2022) Severity of omicron variant of concern and effectiveness of vaccine boosters against symptomatic disease in Scotland (EAVE II): a national cohort study with nested test-negative design. <i>The Lancet Infectious Diseases</i>, 22 (7), pp. 959-966. https://doi.org/10.1016/s1473-3099%2822%2900141-4en_UK
dc.rightsThis is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You are not required to obtain permission to reuse this article.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.titleSeverity of omicron variant of concern and effectiveness of vaccine boosters against symptomatic disease in Scotland (EAVE II): a national cohort study with nested test-negative designen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1016/s1473-3099(22)00141-4en_UK
dc.identifier.pmid35468332en_UK
dc.citation.jtitleLancet Infectious Diseasesen_UK
dc.citation.issn1474-4457en_UK
dc.citation.issn1473-3099en_UK
dc.citation.volume22en_UK
dc.citation.issue7en_UK
dc.citation.spage959en_UK
dc.citation.epage966en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailelliott.hall@stir.ac.uken_UK
dc.citation.date22/04/2022en_UK
dc.description.notesEAVE II Collaborators: Colin Richard Simpson,Tristan Millington, Ting Shi, Utkarsh Agrawal, Safraj Shahul Hameed, Elliott Hall, Igor Rudan, Syed Ahmar Shah, Lewis Ritchie, Sarah Stock, Colin McCowanen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationPublic Health Scotlanden_UK
dc.contributor.affiliationPublic Health Scotlanden_UK
dc.contributor.affiliationSporten_UK
dc.identifier.isiWOS:000833382700039en_UK
dc.identifier.scopusid2-s2.0-85132311297en_UK
dc.identifier.wtid2084560en_UK
dc.date.accepted2022-04-22en_UK
dcterms.dateAccepted2022-04-22en_UK
dc.date.filedepositdate2024-12-19en_UK
dc.subject.tagCOVID-19en_UK
rioxxterms.apcnot chargeden_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorSheikh, Aziz|en_UK
local.rioxx.authorKerr, Steven|en_UK
local.rioxx.authorWoolhouse, Mark|en_UK
local.rioxx.authorMcMenamin, Jim|en_UK
local.rioxx.authorRobertson, Chris|en_UK
local.rioxx.authorEAVE II Collaborators, |en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2025-02-26en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2025-02-26|en_UK
local.rioxx.filenameSheikh et al. (2022) Severity of omicron variant.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1474-4457en_UK
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