Enhanced surveillance of COVID-19 in Scotland: population-based seroprevalence surveillance for SARS-CoV-2 during the first wave of the epidemic.


Journal

Public health
ISSN: 1476-5616
Titre abrégé: Public Health
Pays: Netherlands
ID NLM: 0376507

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 03 11 2020
accepted: 17 11 2020
pubmed: 17 1 2021
medline: 3 2 2021
entrez: 16 1 2021
Statut: ppublish

Résumé

The impact of the COVID-19 pandemic in Scotland has been amongst the most severe in Europe. Serological surveillance is critical to determine the overall extent of infection across populations and to inform the public health response. This study aimed to estimate the proportion of people who have antibodies to SARS-CoV-2 ('seroprevalence') in the general population of Scotland and to see if this changes over time. Between International Organization for Standardization (ISO) week 17 (i.e. week commencing 20th April) and ISO week 25 (week commencing 15 June), 4751 residual blood samples were obtained from regional biochemistry laboratories in six participating regional health authority areas covering approximately 75% of the Scottish population. Samples were tested for the presence of anti-SARS-CoV-2 IgG antibodies using the LIAISON®SARS-CoV-2 S1/S2 IgG assay (DiaSorin, Italy). Seroprevalence rates were adjusted for the sensitivity and specificity of the assay using Bayesian methods. The combined adjusted seroprevalence across the study period was 4.3% (95% confidence interval: 4.2%-4.5%). The proportion varied each week between 1.9% and 6.8% with no difference in antibody positivity by age, sex or geographical area. At the end of the first wave of the COVID-19 pandemic, only a small fraction of the Scottish population had antibodies to SARS-CoV-2. Control of COVID-19 requires the ability to detect asymptomatic and mild infections that would otherwise remain undetected through existing surveillance systems. This is important to determine the true number of infections within the general population which, in turn, can help to understand transmission, inform control measures and provide a denominator for the estimation of severity measures such as the proportion of infected people who have been hospitalised and/or have died.

Identifiants

pubmed: 33453689
pii: S0033-3506(20)30502-3
doi: 10.1016/j.puhe.2020.11.014
pmc: PMC7685039
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

132-134

Informations de copyright

Copyright © 2020 The Royal Society for Public Health. Published by Elsevier Ltd. All rights reserved.

Références

N Engl J Med. 2020 Oct 29;383(18):1782-1784
pubmed: 32871061
Nat Med. 2020 Aug;26(8):1200-1204
pubmed: 32555424
Lancet. 2020 Aug 1;396(10247):313-319
pubmed: 32534626
Euro Surveill. 2020 Oct;25(42):
pubmed: 33094713
Lancet. 2020 Aug 22;396(10250):535-544
pubmed: 32645347

Auteurs

E Dickson (E)

Public Health Scotland, Glasgow, UK.

N E Palmateer (NE)

Public Health Scotland, Glasgow, UK; School of Health and Life Sciences, Glasgow Caledonian University, UK.

J Murray (J)

Public Health Scotland, Glasgow, UK.

C Robertson (C)

Public Health Scotland, Glasgow, UK; Department of Mathematics and Statistics, University of Strathclyde, UK.

C Waugh (C)

Public Health Scotland, Glasgow, UK.

L A Wallace (LA)

Public Health Scotland, Glasgow, UK.

L Mathie (L)

Public Health Scotland, Glasgow, UK.

K Heatlie (K)

Public Health Scotland, Glasgow, UK.

S Mavin (S)

Scottish Microbiology Reference Laboratory, NHS Highland, Inverness, UK.

P Gousias (P)

Public Health Scotland, Glasgow, UK.

B Von Wissman (B)

Public Health Scotland, Glasgow, UK.

D J Goldberg (DJ)

Public Health Scotland, Glasgow, UK; School of Health and Life Sciences, Glasgow Caledonian University, UK.

A McAuley (A)

Public Health Scotland, Glasgow, UK; School of Health and Life Sciences, Glasgow Caledonian University, UK. Electronic address: Andy.Mcauley@phs.scot.

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