Simon Ching Lam , Jing Jing Su , Shun Wa Tsang , Anna On Na Wong , Vivian Ching Man Pang , Jessie Yuk Seng Chung , Shun Chan , Rick Yiu Cho Kwan , Lorna Kwai Ping Suen
{"title":"Diagnostic accuracy of point-of-care testing methods for SARS-CoV-2 detection in community quarantine and isolation settings","authors":"Simon Ching Lam , Jing Jing Su , Shun Wa Tsang , Anna On Na Wong , Vivian Ching Man Pang , Jessie Yuk Seng Chung , Shun Chan , Rick Yiu Cho Kwan , Lorna Kwai Ping Suen","doi":"10.1016/j.infpip.2025.100496","DOIUrl":null,"url":null,"abstract":"<div><div>Reverse transcriptase polymerase chain reaction (RT-PCR) testing has been regarded as the gold standard for the diagnosis of coronavirus disease 2019 (COVID-19). In response to the sudden surge in cases that overwhelmed the healthcare system in Hong Kong, several point-of-care testing (POCT) methods have been developed for rapid COVID-19 screening. However, the diagnostic accuracy of these methods remains inadequately established.</div><div>COVID-19–positive patients and negative control subjects were recruited from a community isolation centre and individuals under home quarantine. Four nasal swab samples were collected by trained operators from each subject. Three swab samples were immediately tested using conventional COVID-19 rapid antigen test (RAT), fluorescence-based RAT (Fluorescent-RAT) and POCT quantitative polymerase chain reaction (qPCR). The fourth swab sample was submitted to a certified laboratory for standard RT-PCR analysis. The sensitivity and specificity of the three rapid testing methods were evaluated against the results obtained from the certified laboratory-based RT-PCR, which served as the reference standard.</div><div>The performance of the three diagnostic methods was assessed in 186 valid cases, which comprised 86 RT-PCR–confirmed positive cases and 100 negative cases. The participants' age ranged from 3 years to 94 years. The sensitivity of the Fluorescent-RAT (87.21%, 95% confidence interval [CI]:80.15%–94.27%) and the POCT qPCR (84.27%, 95% CI:76.71%–91.83%) was comparable and significantly higher than that of the conventional RAT (51.69%, 95% CI:41.30%–62.07%). All three methods demonstrated high specificity. The RAT and POCT qPCR exhibited 100% specificity (95% CI:100%), and the Fluorescent-RAT showed a specificity of 97.06% (95% CI:93.78%–100%).</div><div>This study demonstrated that the Fluorescent-RAT and POCT qPCR can serve as reliable alternatives to RT-PCR for COVID-19 diagnosis, offering improved performance compared with the conventional RAT.</div></div>","PeriodicalId":33492,"journal":{"name":"Infection Prevention in Practice","volume":"8 1","pages":"Article 100496"},"PeriodicalIF":2.6000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection Prevention in Practice","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590088925000605","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/11/17 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Reverse transcriptase polymerase chain reaction (RT-PCR) testing has been regarded as the gold standard for the diagnosis of coronavirus disease 2019 (COVID-19). In response to the sudden surge in cases that overwhelmed the healthcare system in Hong Kong, several point-of-care testing (POCT) methods have been developed for rapid COVID-19 screening. However, the diagnostic accuracy of these methods remains inadequately established.
COVID-19–positive patients and negative control subjects were recruited from a community isolation centre and individuals under home quarantine. Four nasal swab samples were collected by trained operators from each subject. Three swab samples were immediately tested using conventional COVID-19 rapid antigen test (RAT), fluorescence-based RAT (Fluorescent-RAT) and POCT quantitative polymerase chain reaction (qPCR). The fourth swab sample was submitted to a certified laboratory for standard RT-PCR analysis. The sensitivity and specificity of the three rapid testing methods were evaluated against the results obtained from the certified laboratory-based RT-PCR, which served as the reference standard.
The performance of the three diagnostic methods was assessed in 186 valid cases, which comprised 86 RT-PCR–confirmed positive cases and 100 negative cases. The participants' age ranged from 3 years to 94 years. The sensitivity of the Fluorescent-RAT (87.21%, 95% confidence interval [CI]:80.15%–94.27%) and the POCT qPCR (84.27%, 95% CI:76.71%–91.83%) was comparable and significantly higher than that of the conventional RAT (51.69%, 95% CI:41.30%–62.07%). All three methods demonstrated high specificity. The RAT and POCT qPCR exhibited 100% specificity (95% CI:100%), and the Fluorescent-RAT showed a specificity of 97.06% (95% CI:93.78%–100%).
This study demonstrated that the Fluorescent-RAT and POCT qPCR can serve as reliable alternatives to RT-PCR for COVID-19 diagnosis, offering improved performance compared with the conventional RAT.