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在乌干达使用鼻咽样本对 SARS-CoV-2 抗原快速诊断检测的性能进行现场评估。

Field evaluation of the performance of a SARS-CoV-2 antigen rapid diagnostic test in Uganda using nasopharyngeal samples.

机构信息

Uganda Virus Research Institute, P.O. Box 49, Plot 51-59, Nakiwogo Road, Entebbe, Uganda.

Uganda Virus Research Institute, P.O. Box 49, Plot 51-59, Nakiwogo Road, Entebbe, Uganda; Medical Research Council/Uganda Virus Research Institute & London School of Hygiene and Tropical Medicine, Uganda Research Unit, P.O. Box 49, Plot 51-59, Nakiwogo Road, Entebbe, Uganda.

出版信息

Int J Infect Dis. 2021 Mar;104:282-286. doi: 10.1016/j.ijid.2020.10.073. Epub 2020 Oct 30.

Abstract

OBJECTIVES

There is a high demand for SARS-CoV-2 testing to identify COVID-19 cases. Real-time quantitative PCR (qRT-PCR) is the recommended diagnostic test but a number of constraints prevent its widespread implementation, including cost. The aim of this study was to evaluate a low cost and easy to use rapid antigen test for diagnosing COVID-19 at the point of care.

METHODS

Nasopharyngeal swabs from suspected COVID-19 cases and low-risk volunteers were tested with the STANDARD Q COVID-19 Ag Test and the results were compared with the qRT-PCR results.

RESULTS

In total, 262 samples were collected, including 90 qRT-PCR positives. The majority of samples were from males (89%) with a mean age of 34 years and only 13 (14%) of the positives were mildly symptomatic. The sensitivity and specificity of the antigen test were 70.0% (95% confidence interval (CI): 60-79) and 92% (95% CI: 87-96), respectively, and the diagnostic accuracy was 84% (95% CI: 79-88). The antigen test was more likely to be positive for samples with qRT-PCR Ct values ≤29, with a sensitivity of 92%.

CONCLUSIONS

The STANDARD Q COVID-19 Ag Test performed less than optimally in this evaluation. However, the test may still have an important role to play early in infection when timely access to molecular testing is not available but the results should be confirmed by qRT-PCR.

摘要

目的

目前对 SARS-CoV-2 检测的需求很高,以识别 COVID-19 病例。实时定量 PCR(qRT-PCR)是推荐的诊断检测方法,但由于成本等诸多限制,其广泛实施受到阻碍。本研究旨在评估一种低成本、易于使用的即时抗原检测方法,以便在护理点诊断 COVID-19。

方法

对疑似 COVID-19 病例和低风险志愿者的鼻咽拭子进行 STANDARD Q COVID-19 Ag 检测,并将结果与 qRT-PCR 结果进行比较。

结果

共采集 262 份样本,其中 90 份 qRT-PCR 阳性。大多数样本来自男性(89%),平均年龄为 34 岁,仅有 13 例(14%)阳性者症状轻微。抗原检测的敏感性和特异性分别为 70.0%(95%置信区间:60-79)和 92%(95%置信区间:87-96),诊断准确性为 84%(95%置信区间:79-88)。抗原检测对于 qRT-PCR Ct 值≤29 的样本更有可能呈阳性,敏感性为 92%。

结论

在本评估中,STANDARD Q COVID-19 Ag 检测的性能不尽如人意。然而,当无法及时进行分子检测但需要及时获得检测结果时,该检测可能仍然具有重要作用,但结果应通过 qRT-PCR 进行确认。

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