Self-Collected Oral Fluid Saliva Is Insensitive Compared With Nasal-Oropharyngeal Swabs in the Detection of Severe Acute Respiratory Syndrome Coronavirus 2 in Outpatients.

Self-Collected Oral Fluid Saliva Is Insensitive Compared With Nasal-Oropharyngeal Swabs in the Detection of Severe Acute Respiratory Syndrome Coronavirus 2 in Outpatients.
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在门诊患者中,与鼻-口咽拭子相比,自采集口腔液唾液检测严重急性呼吸综合征冠状病毒2不敏感。

DOI:
10.1093/ofid/ofaa648
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发表时间:
2021-03
影响因子:
4.2
通讯作者:
Ambulatory COVID Team
Ambulatory COVID Team
中科院分区:
医学3区
文献类型:
--
作者:
Manabe YC;Reuland C;Yu T;Azamfirei R;Hardick JP;Church T;Brown DM;Sewell TT;Antar A;Blair PW;Heaney CD;Pekosz A;Thomas DL;Ambulatory COVID Team

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控制严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)大流行将需要广泛获得准确诊断。唾液取样绕过了拭子供应链瓶颈,易于自我收集,与鼻咽拭子相比,在收集过程中产生气溶胶的可能性更小。我们比较了来自2019冠状病毒病(COVID-19)非住院门诊队列患者多个时间点的匹配唾液唾液液(Oracol设备中收集的牙龈沟液)和鼻-口咽(OP)自采标本的实时逆转录聚合酶链反应雅培m2000结果。这两句话应该放在结果的开头。共有171对匹配的标本。与鼻拭子相比,41.6%的口腔液标本呈阳性。将唾液添加到口腔液百分比收集装置中,将阳性同意率从37.2%(43人中16人)提高到44.6%(65人中29人)。在出现症状后的前5天,阳性同意率最高,此后下降。所有传染性鼻- op样本(VeroE6 TMPRSS2细胞培养阳性)均具有匹配的SARS-CoV-2阳性口腔液样本。在这项对非住院sars - cov -2感染者的研究中,我们发现,与鼻腔- op标本相比,自采口腔液的诊断敏感性较低,这种差异在症状出现后5天以上尤为突出。这些数据并不能证明常规使用口腔液体采集来诊断SARS-CoV-2是合理的,尽管收集起来更容易。它还强调了考虑唾液标本采集方法和时间从症状发作的重要性,特别是在门诊人群。在一项对未住院的COVID-19患者的研究中,口腔液体唾液样本类型与鼻- op样本类型相比总体不敏感,但随着唾液的加入而改善,并且在症状出现后的前5天最敏感。
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic control will require widespread access to accurate diagnostics. Salivary sampling circumvents swab supply chain bottlenecks, is amenable to self-collection, and is less likely to create an aerosol during collection compared with the nasopharyngeal swab. We compared real-time reverse-transcription polymerase chain reaction Abbott m2000 results from matched salivary oral fluid (gingival crevicular fluid collected in an Oracol device) and nasal-oropharyngeal (OP) self-collected specimens in viral transport media from a nonhospitalized, ambulatory cohort of coronavirus disease 2019 (COVID-19) patients at multiple time points. These 2 sentences should be at the beginning of the results. There were 171 matched specimen pairs. Compared with nasal-OP swabs, 41.6% of the oral fluid samples were positive. Adding spit to the oral fluid percent collection device increased the percent positive agreement from 37.2% (16 of 43) to 44.6% (29 of 65). The positive percent agreement was highest in the first 5 days after symptoms and decreased thereafter. All of the infectious nasal-OP samples (culture positive on VeroE6 TMPRSS2 cells) had a matched SARS-CoV-2 positive oral fluid sample. In this study of nonhospitalized SARS-CoV-2-infected persons, we demonstrate lower diagnostic sensitivity of self-collected oral fluid compared with nasal-OP specimens, a difference that was especially prominent more than 5 days from symptom onset. These data do not justify the routine use of oral fluid collection for diagnosis of SARS-CoV-2 despite the greater ease of collection. It also underscores the importance of considering the method of saliva specimen collection and the time from symptom onset especially in outpatient populations. In a study of nonhospitalized COVID-19 patients, the oral fluid salivary sample type was insensitive compared to nasal-OP specimen types overall, but was improved with the addition of spit and most sensitive in the first 5 days after symptom onset.
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