Rapid point-of-care testing for SARS-CoV-2 in a community screening setting shows low sensitivity.


Journal

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

Informations de publication

Date de publication:
May 2020
Historique:
received: 03 04 2020
accepted: 06 04 2020
pubmed: 26 4 2020
medline: 2 6 2020
entrez: 26 4 2020
Statut: ppublish

Résumé

With the current SARS-CoV2 outbreak, countless tests need to be performed on potential symptomatic individuals, contacts and travellers. The gold standard is a quantitative polymerase chain reaction (qPCR)-based system taking several hours to confirm positivity. For effective public health containment measures, this time span is too long. We therefore evaluated a rapid test in a high-prevalence community setting. Thirty-nine randomly selected individuals at a COVID-19 screening centre were simultaneously tested via qPCR and a rapid test. Ten previously diagnosed individuals with known SARS-CoV-2 infection were also analysed. The evaluated rapid test is an IgG/IgM-based test for SARS-CoV-2 with a time to result of 20 min. Two drops of blood are needed for the test performance. Of 49 individuals, 22 tested positive by repeated qPCR. In contrast, the rapid test detected only eight of those positive correctly (sensitivity: 36.4%). Of the 27 qPCR-negative individuals, 24 were detected correctly (specificity: 88.9%). Given the low sensitivity, we recommend not to rely on an antibody-based rapid test for public health measures such as community screenings.

Identifiants

pubmed: 32334183
pii: S0033-3506(20)30114-1
doi: 10.1016/j.puhe.2020.04.009
pmc: PMC7165286
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

170-172

Commentaires et corrections

Type : CommentIn

Informations de copyright

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

Références

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Auteurs

M Döhla (M)

Institute for Hygiene and Public Health, One Health Department, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany. Electronic address: manuel.doehla@ukbonn.de.

C Boesecke (C)

Clinic for Internal Medicine, Infectious Diseases Department, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

B Schulte (B)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

C Diegmann (C)

Institute for Hygiene and Public Health, One Health Department, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

E Sib (E)

Institute for Hygiene and Public Health, One Health Department, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

E Richter (E)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

M Eschbach-Bludau (M)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

S Aldabbagh (S)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

B Marx (B)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

A-M Eis-Hübinger (AM)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

R M Schmithausen (RM)

Institute for Hygiene and Public Health, One Health Department, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

H Streeck (H)

Institute of Virology, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.

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Classifications MeSH