Author:
Iruzubieta Paula,Fernández-Lanas Tatiana,Rasines Laura,Cayon Lorena,Álvarez-Cancelo Ana,Santos-Laso Alvaro,García-Blanco Agustín,Curiel-Olmo Soraya,Cabezas Joaquín,Wallmann Reinhard,Fábrega Emilio,Martínez-Taboada Víctor M.,Hernández José L.,López-Hoyos Marcos,Lazarus Jeffrey V.,Crespo Javier
Abstract
AbstractThe simplicity and low cost of rapid point-of-care tests greatly facilitate large-scale population testing, which can contribute to controlling the spread of the COVID-19 virus. We evaluated the applicability of a self-testing strategy for SARS-CoV2 in a population-based, cross-sectional study in Cantabria, Spain, between April and May 2020. For the self-testing strategy, participants received the necessary material for the self-collection of blood and performance of a rapid antibody test using lateral flow immunoassay at home without the supervision of healthcare personnel. A total of 1,022 participants were enrolled. Most participants correctly performed the COVID-19 self-test the first time (91.3% [95% CI 89.4–92.9]). Only a minority of the participants (0.7%) needed the help of healthcare personnel, while 6.9% required a second kit delivery, for a total valid test result in 96.9% of the participants. Incorrect use of the self-test was not associated with the educational level, age over 65, or housing area. Prevalence of IgG antibodies against SARS-CoV2 for subjects with a valid rapid test result was 3.1% (95% CI 2.2–4.4), similar to the seroprevalence result obtained using a conventional approach carried out by healthcare professionals. In conclusion, COVID-19 self-testing should be considered as a screening tool.
Publisher
Springer Science and Business Media LLC
Cited by
18 articles.
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