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Rapid Antigen Test LumiraDx TM vs. Real Time Polymerase Chain Reaction for the Diagnosis of SARS-CoV-2 Infection: A Retrospective Cohort Study

Author

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  • Anna Maria Cattelan

    (Infectious and Tropical Diseases Unit, Azienda Ospedale Università di Padova, 35128 Padova, Italy)

  • Lolita Sasset

    (Infectious and Tropical Diseases Unit, Azienda Ospedale Università di Padova, 35128 Padova, Italy)

  • Federico Zabeo

    (Department of Cardiac Thoracic and Vascular Sciences and Public Health, University of Padova, 35127 Padova, Italy)

  • Anna Ferrari

    (Infectious and Tropical Diseases Unit, Azienda Ospedale Università di Padova, 35128 Padova, Italy)

  • Lucia Rossi

    (Microbiology Department, Azienda Ospedale Università di Padova, 35128 Padova, Italy)

  • Maria Mazzitelli

    (Infectious and Tropical Diseases Unit, Azienda Ospedale Università di Padova, 35128 Padova, Italy)

  • Silvia Cocchio

    (Department of Cardiac Thoracic and Vascular Sciences and Public Health, University of Padova, 35127 Padova, Italy)

  • Vincenzo Baldo

    (Department of Cardiac Thoracic and Vascular Sciences and Public Health, University of Padova, 35127 Padova, Italy)

Abstract

Background: Real time reverse transcription polymerase chain reaction (real time RT-PCR) testing is the gold standard for the diagnosis of SARS-CoV-2 infections. However, to expand the testing capacity, new SARS-CoV-2 rapid antigen tests (Ag-RDTs) have been implemented. Ag-RDTs are more rapid, but less reliable in terms of sensitivity, and real-life data on their performance in comparison with the real time RT-PCR test are lacking. Methods: We aimed at assessing the diagnostic performance of the third-generation antigenic swab LumiraDx™ compared with real time RT-PCR in a retrospective cohort study at the Infectious Diseases Unit of Padua. All of the patients who were consecutively tested for SARS-CoV-2 in our centre (by both real time RT-PCR and Ag-RTD LumiraDx TM ) from 19 January to 30 May 2021, were included. Cycle-threshold (Ct) values of positive real time RT-PCR were recorded as well as the number of days from symptoms’ onset to testing. Results: Among the 282 patients included, 80.9% (N = 228) tested positive to real time RT-PCR, and among these, 174 tested positive also to LumiraDx™. Compared with real time RT-PCR, which is considered as the gold standard for the assessment of the presence/absence of SARS-CoV-2 infection, LumiraDx™ showed an overall sensitivity of 76.3% and specificity of 94.4%. Sensitivity increased to 91% when testing was performed <10 days from symptoms’ onset, and to 95% when considering Ct < 25. Multivariable binomial logistic regression showed that false negative LumiraDx™ results were significantly associated with high Ct values, and with further testing from symptoms’ onset. Conclusions: The results of our study suggested that the LumiraDx™ SARS-CoV-2 antigen assay may be appropriate for the detection of SARS-CoV-2 infection, especially in its early phase when the test largely meets the performance requirements of the European Centre for Disease Prevention and Control (ECDC).

Suggested Citation

  • Anna Maria Cattelan & Lolita Sasset & Federico Zabeo & Anna Ferrari & Lucia Rossi & Maria Mazzitelli & Silvia Cocchio & Vincenzo Baldo, 2022. "Rapid Antigen Test LumiraDx TM vs. Real Time Polymerase Chain Reaction for the Diagnosis of SARS-CoV-2 Infection: A Retrospective Cohort Study," IJERPH, MDPI, vol. 19(7), pages 1-12, March.
  • Handle: RePEc:gam:jijerp:v:19:y:2022:i:7:p:3826-:d:777946
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    1. Jing Qi & Jia Neng Tan & Soh Heng Hui & Neoh Choo Lim & Titus Lau & Sabrina Haroon, 2022. "The Implementation and Role of Antigen Rapid Test for COVID-19 in Hemodialysis Units," IJERPH, MDPI, vol. 19(22), pages 1-10, November.

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