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Comparison of five SARS-CoV-2 rapid antigen detection tests in a hospital setting and performance of one antigen assay in routine practice: a useful tool to guide isolation precautions?
Van Honacker, E; Van Vaerenbergh, K; Boel, A; De Beenhouwer, H; Leroux-Roels, I; Cattoir, L.
Afiliação
  • Van Honacker E; Clinical Laboratory of Microbiology, OLVZ Aalst, Aalst, Belgium. Electronic address: eveline.vanhonacker@ugent.be.
  • Van Vaerenbergh K; Clinical Laboratory of Microbiology, OLVZ Aalst, Aalst, Belgium; Department of Infection Control, OLVZ Aalst, Aalst, Belgium.
  • Boel A; Clinical Laboratory of Microbiology, OLVZ Aalst, Aalst, Belgium.
  • De Beenhouwer H; Clinical Laboratory of Microbiology, OLVZ Aalst, Aalst, Belgium.
  • Leroux-Roels I; Department of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium; Department of Infection Control, Ghent University Hospital, Ghent, Belgium.
  • Cattoir L; Clinical Laboratory of Microbiology, OLVZ Aalst, Aalst, Belgium; Department of Infection Control, OLVZ Aalst, Aalst, Belgium.
J Hosp Infect ; 114: 144-152, 2021 Aug.
Article em En | MEDLINE | ID: mdl-33785377
ABSTRACT

BACKGROUND:

In a hospital setting, there is a need for rapid detection of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) to guide isolation measures and targeted admission.

AIM:

To evaluate the diagnostic performance of five SARS-CoV-2 rapid nucleocapsid protein antigen detection (RAD) assays (Biosynex, Biotical, Orient Gene, Panbio and SD Biosensor), and describe the performance and impact of implementation of the SD Biosensor assay in an emergency department.

METHODS:

Sensitivity and specificity of the five RAD assays were analysed on 100 respiratory samples 60 real-time reverse transcriptase polymerase chain reaction (rRT-PCR)-confirmed SARS-CoV-2-positive samples, 24 SARS-CoV-2 RNA-negative samples and 16 samples positive for other respiratory pathogens. The manufacturer's protocol was adapted to validate the antigen tests on transport media used for rRT-PCR in the authors' routine practice. The SD Biosensor RAD assay was implemented as a screening method for rapid diagnosis and targeted admission.

FINDINGS:

Sensitivity of the five RAD assays ranged from 88.9% to 100% for samples with cycle threshold values <26, and specificity ranged from 46.2% to 100%. During the implementation period, 4195 RAD tests were performed. Due to the rapid RAD result, 157 patients were transferred directly to the coronavirus disease 2019 (COVID-19) cohort ward instead of the regular ward (N=47) or the temporary COVID-19 ward (N=110).

CONCLUSION:

The SD Biosensor, Biotical and Panbio SARS-CoV-2 antigen tests showed acceptable overall performance, and identified the majority of contagious patients. In the context of high prevalence of SARS-CoV-2, RAD tests can be used as a rapid screening tool to guide infection prevention measures and aid targeted admission.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teste para COVID-19 / COVID-19 / Antígenos Virais Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Hosp Infect Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teste para COVID-19 / COVID-19 / Antígenos Virais Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Hosp Infect Ano de publicação: 2021 Tipo de documento: Article