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Performance Evaluation of STANDARD Q COVID/FLU Ag Combo for Detection of SARS-CoV-2 and Influenza A/B
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Widyasari, K. | - |
| dc.contributor.author | Kim, S. | - |
| dc.contributor.author | Kim, S. | - |
| dc.contributor.author | Lim, C.S. | - |
| dc.date.accessioned | 2023-01-18T07:58:00Z | - |
| dc.date.available | 2023-01-18T07:58:00Z | - |
| dc.date.issued | 2023-01 | - |
| dc.identifier.issn | 2075-4418 | - |
| dc.identifier.issn | 2075-4418 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/30113 | - |
| dc.description.abstract | We evaluated the performance of the STANDARD Q COVID/FLU Ag Combo test (Q Ag combo test) for the detection of SARS-CoV-2, influenza A, and influenza B using a single point-of-care device compared with real-time PCR. A total of 408 individuals, 55 positives with SARS-CoV-2, 90 with influenza A, 68 with influenza B, and 195 negatives for all viruses, participated. The Q Ag combo test demonstrated a high level of sensitivity of 92.73% and a specificity of 99.49% for the detection of SARS-CoV-2. When the number of days from symptom onset (DSO) was restricted to 0 < DSO ≤ 6, the sensitivity of the Q Ag combo test to detect SARS-CoV-2 was 100%, and when the Ct value of RdRp was ≤20, the sensitivity to detect SARS-CoV-2 was 93.10%. The Q Ag combo test results also demonstrated a sensitivity of 92.22% and a specificity of 100% for influenza A, a sensitivity of 91.18%, and a specificity of 99.49% for influenza B. The agreement analysis of the Q Ag combo test with the RT-PCR results demonstrated excellent outcomes, making it useful and efficient for the detection of SARS-CoV-2, influenza A, and influenza B. © 2022 by the authors. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | MDPI | - |
| dc.title | Performance Evaluation of STANDARD Q COVID/FLU Ag Combo for Detection of SARS-CoV-2 and Influenza A/B | - |
| dc.type | Article | - |
| dc.publisher.location | 스위스 | - |
| dc.identifier.doi | 10.3390/diagnostics13010032 | - |
| dc.identifier.scopusid | 2-s2.0-85145918360 | - |
| dc.identifier.wosid | 000908825600001 | - |
| dc.identifier.bibliographicCitation | Diagnostics, v.13, no.1 | - |
| dc.citation.title | Diagnostics | - |
| dc.citation.volume | 13 | - |
| dc.citation.number | 1 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | General & Internal Medicine | - |
| dc.relation.journalWebOfScienceCategory | Medicine, General & Internal | - |
| dc.subject.keywordAuthor | influenza A | - |
| dc.subject.keywordAuthor | influenza B | - |
| dc.subject.keywordAuthor | point-of-care | - |
| dc.subject.keywordAuthor | rapid antigen test | - |
| dc.subject.keywordAuthor | SARS-CoV-2 | - |
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