Abstract

The 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.

Highlights

  • The high transmissibility of SARS-CoV2, even in asymptomatic patients, indicates that diagnosis based on symptoms and contact tracing alone is insufficient to contain the COVID-19 pandemic

  • We considered an incorrect use of the self-test when sending a second kit was necessary, the control band did not appear in the rapid test picture sent, and specialized healthcare personnel assisted in its performance

  • Around one half of participants reported symptoms suggestive of COVID-19 in the past three months, but only 79 (7.7%) participants were previously subjected to molecular testing to detect SARS-CoV2 infection, of whom four (5%) had a positive result

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Summary

Introduction

The high transmissibility of SARS-CoV2, even in asymptomatic patients, indicates that diagnosis based on symptoms and contact tracing alone is insufficient to contain the COVID-19 pandemic. Detection of viral genome by reverse transcription polymerase chain reaction (RT-PCR) performed with respiratory specimens, especially with nasopharyngeal swabs, are the cornerstone of SARS-CoV2 infection diagnostic ­testing[3]. These techniques require specialized healthcare personnel, centralized laboratory facilities, and time to provide results; the widespread use of these techniques has economic and logistical limitations. Recent studies showed that saliva is useful in diagnosing COVID-1910 This has the advantage of being self-collected by the subject. The simplicity and low cost of these rapid tests greatly

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