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Saliva-based PCR tests for SARS-CoV-2 detection.用于检测新型冠状病毒的唾液聚合酶链反应检测
J Oral Sci. 2020;62(3):350-351. doi: 10.2334/josnusd.20-0267.
2
Detection of SARS-CoV-2 by bronchoscopy after negative nasopharyngeal testing: Stay vigilant for COVID-19.鼻咽检测呈阴性后通过支气管镜检查检测严重急性呼吸综合征冠状病毒2:对2019冠状病毒病保持警惕。
Respir Med Case Rep. 2020 Jun 8;30:101120. doi: 10.1016/j.rmcr.2020.101120. eCollection 2020.
3
Swabs Collected by Patients or Health Care Workers for SARS-CoV-2 Testing.患者或医护人员采集的用于新型冠状病毒检测的拭子。
N Engl J Med. 2020 Jul 30;383(5):494-496. doi: 10.1056/NEJMc2016321. Epub 2020 Jun 3.
4
Variation in False-Negative Rate of Reverse Transcriptase Polymerase Chain Reaction-Based SARS-CoV-2 Tests by Time Since Exposure.基于时间的暴露后,逆转录聚合酶链反应(RT-PCR)检测 SARS-CoV-2 的假阴性率的变化。
Ann Intern Med. 2020 Aug 18;173(4):262-267. doi: 10.7326/M20-1495. Epub 2020 May 13.
5
Comparison of Two High-Throughput Reverse Transcription-PCR Systems for the Detection of Severe Acute Respiratory Syndrome Coronavirus 2.两种用于检测严重急性呼吸综合征冠状病毒2的高通量逆转录聚合酶链反应系统的比较
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6
Comparison of Commercially Available and Laboratory-Developed Assays for Detection of SARS-CoV-2 in Clinical Laboratories.临床实验室中用于检测新型冠状病毒2的商用检测方法与实验室自行开发检测方法的比较
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7
Comparison of Four Molecular Diagnostic Assays for the Detection of SARS-CoV-2 in Nasopharyngeal Specimens.四种用于检测鼻咽标本中新型冠状病毒(SARS-CoV-2)的分子诊断检测方法的比较。
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8
Clinical Evaluation of Three Sample-to-Answer Platforms for Detection of SARS-CoV-2.三种用于检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的样本到答案平台的临床评估
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Comparison of Abbott ID Now and Abbott m2000 Methods for the Detection of SARS-CoV-2 from Nasopharyngeal and Nasal Swabs from Symptomatic Patients.雅培ID Now与雅培m2000方法用于检测有症状患者鼻咽拭子和鼻拭子中新型冠状病毒的比较。
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Viral dynamics of SARS-CoV-2 across a spectrum of disease severity in COVID-19.新型冠状病毒肺炎中不同疾病严重程度下的严重急性呼吸综合征冠状病毒2病毒动力学
J Infect. 2020 Aug;81(2):318-356. doi: 10.1016/j.jinf.2020.04.014. Epub 2020 Apr 18.

SARS-CoV-2 PCR 循环阈值分布为有症状患者的整体和目标特异性灵敏度提供了实用见解。

Distribution of SARS-CoV-2 PCR Cycle Threshold Values Provide Practical Insight Into Overall and Target-Specific Sensitivity Among Symptomatic Patients.

机构信息

Department of Pathology, The Medical College of Wisconsin, Milwaukee.

Department of Microbiology and Molecular Diagnostics, Wisconsin Diagnostic Laboratories, Milwaukee.

出版信息

Am J Clin Pathol. 2020 Sep 8;154(4):479-485. doi: 10.1093/ajcp/aqaa133.

DOI:10.1093/ajcp/aqaa133
PMID:32687186
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7454307/
Abstract

OBJECTIVES

We examined the distribution of reverse transcription polymerase chain reaction (RT-PCR) cycle threshold (CT) values obtained from symptomatic patients being evaluated for coronavirus disease 2019 (COVID-19) to determine the proportion of specimens containing a viral load near the assay limit of detection (LoD) to gain practical insight to the risk of false-negative results. We also examined the relationship between CT value and patient age to determine any age-dependent difference in viral load or test sensitivity.

METHODS

We collected CT values obtained from the cobas severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) assay corresponding to 1,213 combined nasopharyngeal-oropharyngeal specimens obtained from symptomatic individuals that were reported as positive or presumptive positive for SARS-CoV-2. CT values were stratified by SARS-CoV target and patient age group.

RESULTS

In total, 93.3% to 98.4% of specimens demonstrated CT values greater than 3× the assay LoD, at which point false-negative results would not be expected. The mean of CT values between age groups was statistically equivalent with the exception of patients in age group 80 to 89 years, which demonstrated slightly lower CTs.

CONCLUSIONS

Based on the distribution of observed CT values, including the small proportion of specimens with values near the assay LoD, there is a low risk of false-negative RT-PCR results in combined nasopharyngeal-oropharyngeal specimens obtained from symptomatic individuals.

摘要

目的

我们研究了接受新型冠状病毒病 2019(COVID-19)评估的有症状患者的逆转录聚合酶链反应(RT-PCR)循环阈值(CT)值的分布,以确定接近检测限(LoD)的病毒载量的标本比例,从而深入了解假阴性结果的风险。我们还研究了 CT 值与患者年龄之间的关系,以确定病毒载量或检测敏感性是否存在任何年龄依赖性差异。

方法

我们收集了来自 1213 例联合鼻咽或口咽标本的 CT 值,这些标本来自被报告为新型冠状病毒 2(SARS-CoV-2)阳性或疑似阳性的有症状个体,这些标本是使用 cobas SARS-CoV-2 检测获得的。按 SARS-CoV 靶标和患者年龄组对 CT 值进行分层。

结果

总共有 93.3%至 98.4%的标本的 CT 值大于 3×检测 LoD,此时不应出现假阴性结果。除了 80 至 89 岁年龄组的患者外,各年龄组之间的 CT 值平均值无统计学差异,这些患者的 CT 值略低。

结论

根据观察到的 CT 值分布情况,包括接近检测 LoD 的标本比例很小,因此从有症状的个体中获得的联合鼻咽或口咽标本中,RT-PCR 结果出现假阴性的风险较低。