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10.3390/pathogens10060658

http://scihub22266oqcxt.onion/10.3390/pathogens10060658
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34073618!8228578!34073618
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suck abstract from ncbi


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pmid34073618      Pathogens 2021 ; 10 (6): ä
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  • Performance of the LIAISON((R)) SARS-CoV-2 Antigen Assay vs SARS-CoV-2-RT-PCR #MMPMID34073618
  • Fiedler M; Holtkamp C; Dittmer U; Anastasiou OE
  • Pathogens 2021[May]; 10 (6): ä PMID34073618show ga
  • We aimed to evaluate the LIAISON((R)) SARS-CoV-2 antigen assay (DiaSorin), comparing its performance to real-time polymerase chain reaction (RT-PCR) for the detection of SARS-CoV-2 RNA. 182 (110 PCR-positive and 72 PCR-negative) nasopharyngeal swab samples were taken for the detection of SARS-CoV-2. RT-PCR and antigen assay were performed using the same material. The sensitivity and specificity of the antigen assay were calculated for different cut-offs, with RT-PCR serving as the reference method. Stored clinical samples that were positive for other respiratory viruses were tested to evaluate cross-reactivity. One third (33/110, 30%) were falsely classified as negative, while no false positives were found using the 200 TCID(50)/mL cut-off for the SARS-CoV-2 antigen as proposed by the manufacturer. This corresponded to a sensitivity of 70% (60-78%) and a specificity of 100% (94-100%). Lowering the cut-off for positivity of the antigen assay to 22.79 or 57.68 TCID(50)/mL increased the sensitivity of the method, reaching a sensitivity of 92% (85-96%) vs. 79% (70-86%) and a specificity of 81% (69-89%) vs. 99% (91-100%), respectively. The antigen assay reliably detected samples with high SARS-CoV-2 viral loads (>/=10(6) copies SARS-CoV-2/mL), while it cannot differentiate between negative and low positive samples. Cross-reactivity toward other respiratory viruses was not detected.
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