» Articles » PMID: 37455844

Pooled Analysis of Diagnostic Performance of the Instrument-read Quidel Sofia SARS Antigen Fluorescent Immunoassay (FIA)

Overview
Journal EJIFCC
Specialty Biochemistry
Date 2023 Jul 17
PMID 37455844
Authors
Affiliations
Soon will be listed here.
Abstract

Background: This article presents a critical literature review and meta-analysis of diagnostic performance of Quidel Sofia SARS antigen Fluorescent Immunoassay (FIA), a rapid diagnostic antigen test (RDT-Ag) adapted for automatic reading with portable instruments, thus potentially combining the advantages of point-of-care testing with those of a laboratory-based immunoassay.

Methods: We conducted an electronic search in PubMed and Scopus with the keywords "Quidel" OR "SOFIA" AND "Antigen" AND "SARS-CoV-2" OR "COVID-19" up to March 24, 2023, for identifying articles containing data on accuracy of Quidel Sofia SARS antigen FIA for diagnosing acute SARS-CoV-2 infections. We selected those where test accuracy was compared to that of a reference SARS-CoV-2 molecular assay, and with sufficient information for constructing a 2×2 table.

Results: A total number of 18 articles (48165 samples; 9.8% positive at molecular testing) were included in this meta-analysis, averaging 24 sample cohorts. The diagnostic accuracy (summary area under the curve), sensitivity and specificity were 0.980, 0.76 and 1.00 in all samples, 0.981, 0.81 and 0.99 in samples collected from symptomatic patients, 0.931, 0.55 and 1.00 in those taken from asymptomatic patients, and 0.960, 0.77 and 0.99 in samples from mixed cohorts of patients, respectively. Minor and clinically negligible differences of accuracy could be found by comparing test results in nasal and nasopharyngeal swabs.

Conclusion: Quidel Sofia SARS Ag FIA meets the minimum performance criteria of accuracy for SARS-CoV-2 antigenic testing, thus combining satisfactory diagnostic performance with the advantages of being potentially used as a portable device.

Citing Articles

Performance of rapid antigen tests to detect SARS-CoV-2 variant diversity and correlation with viral culture positivity: implication for diagnostic development and future public health strategies.

Goux H, Green J, Wilson A, Sozhamannan S, Richard S, Colombo R mBio. 2024; 15(12):e0273724.

PMID: 39480114 PMC: 11633148. DOI: 10.1128/mbio.02737-24.

References
1.
Zamora J, Abraira V, Muriel A, Khan K, Coomarasamy A . Meta-DiSc: a software for meta-analysis of test accuracy data. BMC Med Res Methodol. 2006; 6:31. PMC: 1552081. DOI: 10.1186/1471-2288-6-31. View

2.
Ang G, Chan K, Yean Yean C, Yu C . Lateral Flow Immunoassays for SARS-CoV-2. Diagnostics (Basel). 2022; 12(11). PMC: 9689684. DOI: 10.3390/diagnostics12112854. View

3.
Al-Alawi S, Al-Hinai H, Al-Kindi N, Al-Rashidi M, Al-Kindi H, Al-Shukri I . Evaluation of Four Rapid Antigen Tests for Detection of SARS-CoV-2 virus. Oman Med J. 2021; 36(5):e297. PMC: 8491111. DOI: 10.5001/omj.2021.106. View

4.
Han A, Toporowski A, Sacks J, Perkins M, Briand S, Van Kerkhove M . SARS-CoV-2 diagnostic testing rates determine the sensitivity of genomic surveillance programs. Nat Genet. 2023; 55(1):26-33. PMC: 9839449. DOI: 10.1038/s41588-022-01267-w. View

5.
Mitchell S, Orris S, Freeman T, Freeman M, Adam M, Axe M . Performance of SARS-CoV-2 antigen testing in symptomatic and asymptomatic adults: a single-center evaluation. BMC Infect Dis. 2021; 21(1):1071. PMC: 8521263. DOI: 10.1186/s12879-021-06716-1. View