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01 · ABSTRACT

Abstract

Rapid Antigen Detection Tests can be a good approach to in time SARS-CoV-2 detection as they are easy to use and provide a result in few minutes. However, they have shown to have lower sensitivities than desirable for a diagnostic technique that has come to be used for mass screening. With the aim of continuing to define the limits of RAgDT, their possible variability of sensitivity has been analysed against different variants of SARS-CoV-2.

In this study, three different Tests from different manufacturers (Abbott, Roche and Lambra) were tested with a set of 100 nasopharyngeal samples, of which 93 were determined as positive by RT-qPCR and 7 as negative.

Total sensitivities were: 72.04% for Abbott and 59.14% both for Roche and Lambra. Attending to variants, the three with higher sensitivity were: Alfa, Omicron and Delta (Abbott); Alfa, Omicron and Mu (Roche) and Alfa, Beta and Gamma (Lambra).

Results show great variability between the tests analysed, which reinforces the idea that any negative diagnosis made with them should be taken with caution, especially in seasons of alternating circulation of variants.

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02 · PUBLICATION RECORD

Article details

JournalMedical Research Archives
IssueVol 11 No 2 (2023): February Issue, Vol.11 Issue 2
SectionResearch Articles
Published13 March 2023
DOI10.18103/mra.v11i2.3381
ISSN2375-1924
03 · RIGHTS & REUSE

Rights & reuse

This article is published under a Creative Commons Attribution License (CC BY 3.0) and may be shared or distributed by anyone as long as attribution is given to the journal.

Authors & affiliations

GM

Gabriel Martin

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

ZP

Zulema Pérez-Martínez

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

SR

Susana Rojo-Alba

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

JG

Jose María González-Alba

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

MR

Mercedes Rodríguez-Pérez

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

JB

Jose Antonio Boga

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

SM

Santiago Melón

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

Marta Elena Álvarez-Argüelles

Grupo de Microbiología Traslacional, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA); Oviedo, Asturias; Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA); Oviedo, Asturias

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