Service de Biostatistique et d'Épidémiologie, Institut Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette Cedex, France.
PLoS One. 2021 Jun 10;16(6):e0253007. doi: 10.1371/journal.pone.0253007. eCollection 2021.
Diagnosis of COVID-19 in symptomatic patients and screening of populations for SARS-CoV-2 infection require access to straightforward, low-cost and high-throughput testing. The recommended nasopharyngeal swab tests are limited by the need of trained professionals and specific consumables and this procedure is poorly accepted as a screening method In contrast, saliva sampling can be self-administered.
In order to compare saliva and nasopharyngeal/oropharyngeal samples for the detection of SARS-CoV-2, we designed a meta-analysis searching in PubMed up to December 29th, 2020 with the key words "(SARS-CoV-2 OR COVID-19 OR COVID19) AND (salivary OR saliva OR oral fluid)) NOT (review[Publication Type]) NOT (PrePrint[Publication Type])" applying the following criteria: records published in peer reviewed scientific journals, in English, with at least 15 nasopharyngeal/orapharyngeal swabs and saliva paired samples tested by RT-PCR, studies with available raw data including numbers of positive and negative tests with the two sampling methods. For all studies, concordance and sensitivity were calculated and then pooled in a random-effects model.
A total of 377 studies were retrieved, of which 50 were eligible, reporting on 16,473 pairs of nasopharyngeal/oropharyngeal and saliva samples. Meta-analysis showed high concordance, 92.5% (95%CI: 89.5-94.7), across studies and pooled sensitivities of 86.5% (95%CI: 83.4-89.1) and 92.0% (95%CI: 89.1-94.2) from saliva and nasopharyngeal/oropharyngeal swabs respectively. Heterogeneity across studies was 72.0% for saliva and 85.0% for nasopharyngeal/oropharyngeal swabs.
Our meta-analysis strongly suggests that saliva could be used for frequent testing of COVID-19 patients and "en masse" screening of populations.
对有症状的新冠病毒肺炎(COVID-19)患者进行诊断,以及对 SARS-CoV-2 感染人群进行筛查,都需要采用简单、经济、高通量的检测方法。推荐的鼻咽拭子检测受到需要专业人员和特定耗材的限制,作为筛查方法,这种检测方法很难被接受。相比之下,唾液采样可以由患者自行完成。
为了比较唾液和鼻咽/口咽样本检测 SARS-CoV-2 的效果,我们设计了一项荟萃分析,于 2020 年 12 月 29 日在 PubMed 上检索了关键词为“(SARS-CoV-2 或 COVID-19 或 COVID19) AND (salivary 或 saliva 或 oral fluid)) NOT (review[Publication Type]) NOT (PrePrint[Publication Type])”的文献,并应用以下标准进行筛选:发表在同行评审的科学期刊上、使用 RT-PCR 对至少 15 例鼻咽/口咽拭子和唾液配对样本进行检测、研究有可供分析的原始数据,包括两种采样方法的阳性和阴性检测例数。对所有研究,我们计算了一致性和敏感度,并在随机效应模型中进行了汇总。
共检索到 377 项研究,其中 50 项符合条件,共报告了 16473 对鼻咽/口咽和唾液样本。荟萃分析显示,研究间的一致性很高,为 92.5%(95%CI:89.5-94.7),从唾液和鼻咽/口咽拭子中分别汇总得到的敏感度为 86.5%(95%CI:83.4-89.1)和 92.0%(95%CI:89.1-94.2)。研究间的异质性在唾液样本中为 72.0%,在鼻咽/口咽拭子中为 85.0%。
我们的荟萃分析强烈提示,唾液可以用于对 COVID-19 患者进行频繁检测,也可以用于对人群进行“大规模”筛查。