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Evaluation of four laboratory-based high-throughput SARS-CoV-2 automated antigen tests compared to RT-PCR on nasal and oropharyngeal samples.
Leineweber, Thomas Daell; Ghathian, Khaled; Lisby, Jan Gorm; Friis-Hansen, Lennart; Afzal, Shoaib; Ellermann-Eriksen, Svend; Ma, Chih Man German; Cohen, Arieh S; Jørgensen, Rikke Lind; Hansen, Matilde Bøgelund; Kamstrup, Pia Rørbæk; Larsen, Helene; Steenhard, Nina; Jensen, Christel Barker; Kallemose, Thomas; Forsberg, Maria Wendelboe; Kirkby, Nikolai Søren; Schneider, Uffe Vest.
  • Leineweber TD; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Ghathian K; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Lisby JG; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Friis-Hansen L; Copenhagen University Hospital Bispebjerg and Frederiksberg, Department of Clinical Biochemistry, Nielsine Nielsens Vej 4B, 2400, Copenhagen, Denmark.
  • Afzal S; Copenhagen University Hospital Herlev and Gentofte, Department of Clinical Biochemistry, Borgmester Ib Juuls Vej 52, 2730, Herlev, Denmark.
  • Ellermann-Eriksen S; Aarhus University Hospital, Department of Clinical Microbiology, Palle Juul-Jensens Boulevard 99, Skejby, 8200, Aarhus N., Denmark.
  • Ma CMG; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Cohen AS; Danish National Test Center, Statens Serum Institut, Artillerivej 5, 2300, Copenhagen, Denmark.
  • Jørgensen RL; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Hansen MB; Copenhagen University Hospital Herlev and Gentofte, Department of Clinical Microbiology, Borgmester Ib Juuls Vej 52, 2730, Herlev, Denmark.
  • Kamstrup PR; Copenhagen University Hospital Herlev and Gentofte, Department of Clinical Biochemistry, Borgmester Ib Juuls Vej 52, 2730, Herlev, Denmark.
  • Larsen H; Technical University of Denmark - DTU, Centre for Diagnostics Department of Health Technology, Henrik Dams Allé, 2800, Kgs Lyngby, Denmark.
  • Steenhard N; Danish National Test Center, Statens Serum Institut, Artillerivej 5, 2300, Copenhagen, Denmark.
  • Jensen CB; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Kallemose T; Copenhagen University Hospital Hvidovre, Department of Clinical Research, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Forsberg MW; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark.
  • Kirkby NS; Rigshospitalet, Department of Clinical Microbiology, Henrik Harpestrengsvej 4A, 2100, Copenhagen, Denmark.
  • Schneider UV; Copenhagen University Hospital Hvidovre, Department of Clinical Microbiology, Kettegaard Alle 30, 2650, Hvidovre, Denmark. Electronic address: UFVS@ssi.dk.
J Clin Virol ; 164: 105472, 2023 07.
Article in English | MEDLINE | ID: covidwho-2309511
ABSTRACT

BACKGROUND:

The demand for RT-PCR testing has been unprecedented during the SARS-CoV-2 pandemic. Fully automated antigen tests (AAT) are less cumbersome than RT-PCR, but data on performance compared to RT-PCR are scarce.

METHODS:

The study consists of two parts. A retrospective analytical part, comparing the performance of four different AAT on 100 negative and 204 RT-PCR positive deep oropharyngeal samples divided into four groups based on RT-PCR cycle of quantification levels. In the prospective clinical part, 206 individuals positive for and 199 individuals negative for SARS-CoV-2 were sampled from either the anterior nasal cavity (mid-turbinate) or by deep oropharyngeal swabs or both. The performance of AATs was compared to RT-PCR.

RESULTS:

The overall analytical sensitivity of the AATs differed significantly from 42% (95% CI 35-49) to 60% (95% CI 53-67) with 100% analytical specificity. Clinical sensitivity of the AATs differed significantly from 26% (95% CI 20-32) to 88% (95% CI 84-93) with significant higher sensitivity for mid-turbinate nasal swabs compared to deep oropharyngeal swabs. Clinical specificity varied from 97% to 100%.

CONCLUSION:

All AATs were highly specific for detection of SARS-CoV-2. Three of the four AATs were significantly more sensitive than the fourth AAT both in terms of analytical and clinical sensitivity. Anatomical test location significantly influenced the clinical sensitivity of AATs.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: J Clin Virol Journal subject: Virology Year: 2023 Document Type: Article Affiliation country: J.jcv.2023.105472

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: J Clin Virol Journal subject: Virology Year: 2023 Document Type: Article Affiliation country: J.jcv.2023.105472