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新型冠状病毒肺炎快速抗原检测的诊断性能以及病毒载量、采样时间、受试者临床和实验室参数对检测准确性的影响。

Diagnostic performance of rapid antigen test for COVID-19 and the effect of viral load, sampling time, subject's clinical and laboratory parameters on test accuracy.

作者信息

Amer Rania M, Samir Mohamed, Gaber Osama A, El-Deeb Nahawand A, Abdelmoaty Ahmed A, Ahmed Alshymaa A, Samy Walaa, Atta Amal H, Walaa Mohammad, Anis Reham H

机构信息

Medical Microbiology and Immunology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt; Zagazig Scientific and Medical Research Center, Faculty of Medicine, Zagazig University, Zagazig, Egypt.

Department of Zoonoses, Faculty of Veterinary Medicine, Zagazig University, Zagazig, Egypt.

出版信息

J Infect Public Health. 2021 Oct;14(10):1446-1453. doi: 10.1016/j.jiph.2021.06.002. Epub 2021 Jun 11.

Abstract

BACKGROUND

Egypt was among the first 10 countries in Africa that experienced COVID-19 cases. The sudden surge in the number of cases is overwhelming the capacity of the national healthcare system, particularly in developing countries. Central to the containment of the ongoing pandemic is the availability of rapid and accurate diagnostic tests that could pinpoint patients at early disease stages. In the current study, we aimed to (1) Evaluate the diagnostic performance of the rapid antigen test (RAT) "Standard™ Q COVID-19 Ag" against reverse transcriptase quantitative real-time PCR (RT-qPCR) in eighty-three swabs collected from COVID-19 suspected individuals showing various demographic features, clinical and radiological findings. (2) Test whether measuring laboratory parameters in participant's blood would enhance the predictive accuracy of RAT. (3) Identify the most important features that determine the results of both RAT and RT-qPCR.

METHODS

Diagnostic measurements (e.g. sensitivity, specificity, etc.) and receiver operating characteristic curve were used to assess the clinical performance of "Standard™ Q COVID-19 Ag". We used the support vector machine (SVM) model to investigate whether measuring laboratory indices would enhance the accuracy of RAT. Moreover, a random forest classification model was used to determine the most important determinants of the results of RAT and RT-qPCR for COVID-19 diagnosis.

RESULTS

The sensitivity, specificity, and accuracy of RAT were 78.2, 64.2, and 75.9%, respectively. Samples with high viral load and those that were collected within one-week post-symptoms showed the highest sensitivity and accuracy. The SVM modeling showed that measuring laboratory indices did not enhance the predictive accuracy of RAT.

CONCLUSION

"Standard™ Q COVID-19 Ag" should not be used alone for COVID-19 diagnosis due to its low diagnostic performance relative to the RT-qPCR. RAT is best used at the early disease stage and in patients with high viral load.

摘要

背景

埃及是非洲最早出现新冠病毒病例的10个国家之一。病例数的突然激增使国家医疗系统不堪重负,尤其是在发展中国家。控制当前疫情的关键在于能否获得快速、准确的诊断检测方法,以便在疾病早期阶段确定患者。在本研究中,我们旨在:(1)评估快速抗原检测(RAT)“标准™Q新冠病毒抗原”针对逆转录酶定量实时聚合酶链反应(RT-qPCR)在从83份新冠病毒疑似个体采集的拭子中的诊断性能,这些个体呈现出不同的人口统计学特征、临床和影像学表现。(2)测试测量参与者血液中的实验室参数是否会提高RAT的预测准确性。(3)确定决定RAT和RT-qPCR结果的最重要特征。

方法

使用诊断测量指标(如敏感性、特异性等)和受试者工作特征曲线来评估“标准™Q新冠病毒抗原”的临床性能。我们使用支持向量机(SVM)模型来研究测量实验室指标是否会提高RAT的准确性。此外,使用随机森林分类模型来确定用于新冠病毒诊断的RAT和RT-qPCR结果的最重要决定因素。

结果

RAT的敏感性、特异性和准确性分别为78.2%、64.2%和75.9%。病毒载量高的样本以及在症状出现后一周内采集的样本显示出最高的敏感性和准确性。SVM建模表明,测量实验室指标并未提高RAT的预测准确性。

结论

由于“标准™Q新冠病毒抗原”相对于RT-qPCR的诊断性能较低,不应单独用于新冠病毒诊断。RAT最适合在疾病早期阶段和病毒载量高的患者中使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83da/8192262/624bee406b3e/gr1_lrg.jpg

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