Prospective, clinical comparison of self-collected throat-bilateral nares swabs and saline gargle compared to health care provider collected nasopharyngeal swabs among symptomatic outpatients with potential SARS-CoV-2 infection.

Q3 Medicine
JAMMI Pub Date : 2024-01-16 eCollection Date: 2024-01-01 DOI:10.3138/jammi-2023-0002
Eric M Hempel, Aamir Bharmal, Guiyun Li, Aileen Minhas, Ramndip Manan, Kathy Doull, Lynsey Hamilton, Branco Cheung, Michael Chan, Kingsley Gunadasa, Ron Chow, Tracy Lee, Frankie Tsang, Mel Krajden, Karen Mooder, Trushna Kassan, Natalie Prystajecky, Agatha Jassem, Linda Mn Hoang
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引用次数: 0

Abstract

Background: In British Columbia (BC), self-collected saline gargle (SG) is the only alternative to health care provider (HCP)-collected nasopharyngeal (NP) swabs to detect SARS-CoV-2 in an outpatient setting by polymerase chain reaction (PCR). However, some individuals cannot perform a SG. Our study aimed to assess combined throat-bilateral nares (TN) swabbing as a swab-based alternative.

Methods: Symptomatic individuals greater than 12 years of age seeking a COVID-19 PCR test at one of two COVID-19 collection centres in Metro Vancouver were asked to participate in this study. Participants provided a HCP-collected NP sample and a self-collected SG and TN sample for PCR testing, which were either HCP observed or unobserved.

Results: Three-hundred and eleven individuals underwent all three collections. Compared against HCP-NP, SG was 99% sensitive and 98% specific (kappa 0.97) and TN was 99% sensitive and 99% specific (kappa 0.98). Using the final clinical test interpretation as the reference standard, NP was 98% sensitive and 100% specific (kappa 0.98), and both SG and TN were 99% sensitive and 100% specific (both kappa 0.99). Mean cycle threshold values for each viral target were higher in SG specimens compared to the other sample types; however, this did not significantly impact the clinical performance, because the positivity rates were similar. The clinical performance of all specimen types was comparable within the first 7 days of symptom onset, regardless of the observation method. SG self-collections were rated the most acceptable, followed by TN.

Conclusions: TN provides another less invasive self-collection modality for symptomatic outpatient SARS-CoV-2 PCR testing.

在可能感染 SARS-CoV-2 的有症状门诊患者中,自取咽喉-双侧鼻腔拭子和生理盐水漱口与医护人员采集鼻咽拭子的前瞻性临床比较。
背景:在不列颠哥伦比亚省(BC),自取生理盐水漱口(SG)是在门诊环境中通过聚合酶链反应(PCR)检测 SARS-CoV-2 的唯一替代方法,而不是由医疗保健提供者(HCP)采集鼻咽(NP)拭子。然而,有些人无法进行 SG 检测。我们的研究旨在评估将咽喉-双侧鼻孔(TN)联合拭子法作为一种基于拭子的替代方法:方法:大温地区的两个 COVID-19 采集中心之一邀请 12 岁以上有症状的人参加本研究,寻求 COVID-19 PCR 检测。参与者提供一份由 HCP 采集的 NP 样本和一份自采的 SG 和 TN 样本进行 PCR 检测,这些样本可以是 HCP 观察到的,也可以是未观察到的:有 311 人进行了所有三种样本的采集。与 HCP-NP 相比,SG 的敏感性为 99%,特异性为 98%(kappa 0.97),TN 的敏感性为 99%,特异性为 99%(kappa 0.98)。以最终的临床检验解释作为参考标准,NP 的敏感性为 98%,特异性为 100%(kappa 0.98),SG 和 TN 的敏感性为 99%,特异性为 100%(kappa 均为 0.99)。与其他样本类型相比,SG 标本中每种病毒靶标的平均周期阈值较高;但是,由于阳性率相似,这并不会对临床性能产生显著影响。无论采用哪种观察方法,所有样本类型在症状出现后 7 天内的临床表现都相当。SG自取标本的可接受性最高,其次是 TN:结论:TN为有症状的门诊SARS-CoV-2 PCR检测提供了另一种侵入性较小的自采样方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JAMMI
JAMMI Medicine-Infectious Diseases
CiteScore
3.80
自引率
0.00%
发文量
48
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