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Infection . Evaluation of accuracy, exclusivity, limit-of-detection and ease-of-use of LumiraDx™: An antigen-detecting point-of-care device for SARS-CoV-2

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  • Infection . Evaluation of accuracy, exclusivity, limit-of-detection and ease-of-use of LumiraDx™: An antigen-detecting point-of-care device for SARS-CoV-2


    Infection


    . 2021 Aug 12.
    doi: 10.1007/s15010-021-01681-y. Online ahead of print.
    Evaluation of accuracy, exclusivity, limit-of-detection and ease-of-use of LumiraDx™: An antigen-detecting point-of-care device for SARS-CoV-2


    Lisa J Krüger 1 , Julian A F Klein 1 , Frank Tobian 1 , Mary Gaeddert 1 , Federica Lainati 1 , Sarah Klemm 2 , Paul Schnitzler 2 , Ralf Bartenschlager 3 4 , Berati Cerikan 3 , Christopher J Neufeldt 3 , Olga Nikolai 5 , Andreas K Lindner 5 , Frank P Mockenhaupt 5 , Joachim Seybold 6 , Terry C Jones 7 8 9 , Victor M Corman 7 8 , Nira R Pollock 10 , Britta Knorr 11 , Andreas Welker 11 , Margaretha de Vos 12 , Jilian A Sacks 12 , Claudia M Denkinger 13 14 , ACE-IT Study Group



    Collaborators, Affiliations

    Abstract

    Purpose: Rapid antigen-detecting tests (Ag-RDTs) for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can transform pandemic control. Thus far, sensitivity (≤ 85%) of lateral-flow assays has limited scale-up. Conceivably, microfluidic immunofluorescence Ag-RDTs could increase sensitivity for SARS-CoV-2 detection.
    Methods: This multi-centre diagnostic accuracy study investigated performance of the microfluidic immunofluorescence LumiraDx™ assay, enrolling symptomatic and asymptomatic participants with suspected SARS-CoV-2 infection. Participants collected a supervised nasal mid-turbinate (NMT) self-swab for Ag-RDT testing, in addition to a professionally collected nasopharyngeal (NP) swab for routine testing with reverse transcriptase polymerase chain reaction (RT-PCR). Results were compared to calculate sensitivity and specificity. Sub-analyses investigated the results by viral load, symptom presence and duration. An analytical study assessed exclusivity and limit-of-detection (LOD). In addition, we evaluated ease-of-use.
    Results: The study was conducted between November 2nd 2020 and 4th of December 2020. 761 participants were enrolled, with 486 participants reporting symptoms on testing day. 120 out of 146 RT-PCR positive cases were detected positive by LumiraDx™, resulting in a sensitivity of 82.2% (95% CI 75.2-87.5%). Specificity was 99.3% (CI 98.3-99.7%). Sensitivity was increased in individuals with viral load ≥ 7 log10 SARS-CoV2 RNA copies/ml (93.8%; CI 86.2-97.3%). Testing against common respiratory commensals and pathogens showed no cross-reactivity and LOD was estimated to be 2-56 PFU/mL. The ease-of-use-assessment was favourable for lower throughput settings.
    Conclusion: The LumiraDx™ assay showed excellent analytical sensitivity, exclusivity and clinical specificity with good clinical sensitivity using supervised NMT self-sampling.
    Trial registration number and registration date: DRKS00021220 and 01.04.2020.

    Keywords: Antigen-detecting diagnostics; Covid-19; Diagnostic accuracy; Point-of-care; SARS-CoV-2.

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