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- W4319461256 abstract "Objective To rapidly screen patients with novel coronavirus pneumonia (COVID-19) infection including asymptomatic ones. Method Established a rapid detection test kit, and evaluated analytical and clinical performance of it. Result The minimum limit of detection of the reagent was 9.75×102 TCID50/mL; there was no cross-reaction and interference in the high-concentration samples of 29 common respiratory pathogens tested. The diagnostic sensitivity of clinical samples was 98.56%, specificity was 99.00%, and the total coincidence rate was 98.85%; the consistency test Kappa value is 0.974 5. The stratified analysis of positive samples with different Ct values showed that the coincidence rate within each stratum was greater than 95%. Conclusion This COVID-19 antigen test kit with excellent detection performance, fast detection speed, and portable operation. It can be used as a supplementary method for existing nucleic acid detection methods for early screening of new coronavirus." @default.
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- W4319461256 date "2023-01-30" @default.
- W4319461256 modified "2023-09-23" @default.
- W4319461256 title "[Evaluation of COVID-19 Antigen Test Kit Assay Analytical and Clinical Performance]." @default.
- W4319461256 doi "https://doi.org/10.3969/j.issn.1671-7104.2023.01.018" @default.
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