Performance evaluation of STANDARD Q COVID-19 Ag home test for the diagnosis of COVID-19 during early symptom onset
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Shin, Hyoshim | - |
dc.contributor.author | Lee, Seungjun | - |
dc.contributor.author | Widyasari, Kristin | - |
dc.contributor.author | Yi, Jongyoun | - |
dc.contributor.author | Bae, Eunsin | - |
dc.contributor.author | Kim, Sunjoo | - |
dc.date.accessioned | 2022-12-26T06:41:02Z | - |
dc.date.available | 2022-12-26T06:41:02Z | - |
dc.date.issued | 2022-06 | - |
dc.identifier.issn | 0887-8013 | - |
dc.identifier.issn | 1098-2825 | - |
dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/1212 | - |
dc.description.abstract | Background Surveillance and control of SARS-CoV-2 outbreak through gold standard detection, that is, real-time polymerase chain reaction (RT-PCR), become a great obstacle, especially in overwhelming outbreaks. In this study, we aimed to analyze the performance of rapid antigen home test (RAHT) as an alternative detection method compared with RT-PCR. Methods In total, 79 COVID-19-positive and 217 COVID-19-negative patients confirmed by RT-PCR were enrolled in this study. A duration from symptom onset to COVID-19 confirmation of <5 days was considered a recruiting criterion for COVID-19-positive cases. A nasal cavity specimen was collected for the RAHT, and a nasopharyngeal swab specimen was collected for RT-PCR. Results Sensitivity of the STANDARD Q COVID-19 Ag Home Test (SD Biosensor, Korea), compared with RT-PCR, was 94.94% (75/79) (95% [confidence interval] CI, 87.54%-98.60%), and specificity was 100%. Sensitivity was significantly higher in symptomatic patients (98.00%) than in asymptomatic (89.66%) patients (p-value = 0.03). There was no difference in sensitivity according to the duration of symptom onset to confirmation (100% for 0-2 days and 96.97% for 3-5 days, respectively) (p-value = 1.00). The RAHT detected all 51 COVID-19 patients whose Ct values were <= 25 (100%), whereas sensitivity was 73.33% (11/15) among patients with Ct values >25 (p-value = 0.01). Conclusion The RAHT showed an excellent sensitivity for COVID-19-confirmed cases, especially for those with symptoms. There was a decrease in sensitivity when the Ct value is over 25, indicating that RAHT screening may be useful during the early phase of symptom onset, when the viral numbers are higher and it is more transmissible. | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | John Wiley & Sons Inc. | - |
dc.title | Performance evaluation of STANDARD Q COVID-19 Ag home test for the diagnosis of COVID-19 during early symptom onset | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1002/jcla.24410 | - |
dc.identifier.scopusid | 2-s2.0-85128345199 | - |
dc.identifier.wosid | 000783786300001 | - |
dc.identifier.bibliographicCitation | Journal of Clinical Laboratory Analysis, v.36, no.6 | - |
dc.citation.title | Journal of Clinical Laboratory Analysis | - |
dc.citation.volume | 36 | - |
dc.citation.number | 6 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Medical Laboratory Technology | - |
dc.relation.journalWebOfScienceCategory | Medical Laboratory Technology | - |
dc.subject.keywordAuthor | COVID-19 testing | - |
dc.subject.keywordAuthor | diagnosis | - |
dc.subject.keywordAuthor | point of care | - |
dc.subject.keywordAuthor | SARS-CoV-2 | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
Gyeongsang National University Central Library, 501, Jinju-daero, Jinju-si, Gyeongsangnam-do, 52828, Republic of Korea+82-55-772-0533
COPYRIGHT 2022 GYEONGSANG NATIONAL UNIVERSITY LIBRARY. ALL RIGHTS RESERVED.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.