WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Lancet Infect Dis. 2021 Sep;21(9):1233-1245. doi: 10.1016/S1473-3099(21)00146-8. Epub 2021 Apr 12.
The comparative performance of different clinical sampling methods for diagnosis of SARS-CoV-2 infection by RT-PCR among populations with suspected infection remains unclear. This meta-analysis aims to systematically compare the diagnostic performance of different clinical specimen collection methods.
In this systematic review and meta-analysis, we systematically searched PubMed, Embase, MEDLINE, Web of Science, medRxiv, bioRxiv, SSRN, and Research Square from Jan 1, 2000, to Nov 16, 2020. We included original clinical studies that examined the performance of nasopharyngeal swabs and any additional respiratory specimens for the diagnosis of SARS-CoV-2 infection among individuals presenting in ambulatory care. Studies without data on paired samples, or those that only examined different samples from confirmed SARS-CoV-2 cases were not useful for examining diagnostic performance of a test and were excluded. Diagnostic performance, including sensitivity, specificity, positive predictive value, and negative predictive value, was examined using random effects models and double arcsine transformation.
Of the 5577 studies identified in our search, 23 studies including 7973 participants with 16 762 respiratory samples were included. Respiratory specimens examined in these studies included 7973 nasopharyngeal swabs, 1622 nasal swabs, 6110 saliva samples, 338 throat swabs, and 719 pooled nasal and throat swabs. Using nasopharyngeal swabs as the gold standard, pooled nasal and throat swabs gave the highest sensitivity of 97% (95% CI 93-100), whereas lower sensitivities were achieved by saliva (85%, 75-93) and nasal swabs (86%, 77-93) and a much lower sensitivity by throat swabs (68%, 35-94). A comparably high positive predictive value was obtained by pooled nasal and throat (97%, 90-100) and nasal swabs (96%, 87-100) and a slightly lower positive predictive value by saliva (93%, 88-97). Throat swabs have the lowest positive predictive value of 75% (95% CI 45-96). Comparably high specificities (range 97-99%) and negative predictive value (range 95-99%) were observed among different clinical specimens. Comparison between health-care-worker collection and self-collection for pooled nasal and throat swabs and nasal swabs showed comparable diagnostic performance. No significant heterogeneity was observed in the analysis of pooled nasal and throat swabs and throat swabs, whereas moderate to substantial heterogeneity (I ≥30%) was observed in studies on saliva and nasal swabs.
Our review suggests that, compared with the gold standard of nasopharyngeal swabs, pooled nasal and throat swabs offered the best diagnostic performance of the alternative sampling approaches for diagnosis of SARS-CoV-2 infection in ambulatory care. Saliva and nasal swabs gave comparable and very good diagnostic performance and are clinically acceptable alternative specimen collection methods. Throat swabs gave a much lower sensitivity and positive predictive value and should not be recommended. Self-collection for pooled nasal and throat swabs and nasal swabs was not associated with any significant impairment of diagnostic accuracy. Our results also provide a useful reference framework for the proper interpretation of SARS-CoV-2 testing results using different clinical specimens.
Hong Kong Research Grants Council.
在疑似感染人群中,不同临床采样方法对 RT-PCR 检测 SARS-CoV-2 感染的比较性能仍不清楚。本荟萃分析旨在系统比较不同临床标本采集方法的诊断性能。
在这项系统评价和荟萃分析中,我们系统地检索了 2000 年 1 月 1 日至 2020 年 11 月 16 日的 PubMed、Embase、MEDLINE、Web of Science、medRxiv、bioRxiv、SSRN 和 Research Square。我们纳入了原临床研究,这些研究检查了鼻咽拭子和任何其他呼吸道标本在门诊护理中检测 SARS-CoV-2 感染的性能。没有配对样本数据的研究,或仅检查确诊 SARS-CoV-2 病例的不同样本的研究,对检查试验的诊断性能没有帮助,因此被排除在外。使用随机效应模型和双反正弦变换检查诊断性能,包括敏感性、特异性、阳性预测值和阴性预测值。
在我们的搜索中,共确定了 5577 项研究,其中包括 23 项研究,共纳入了 7973 名参与者和 16762 个呼吸道样本。这些研究中检查的呼吸道标本包括 7973 个鼻咽拭子、1622 个鼻拭子、6110 个唾液样本、338 个咽拭子和 719 个鼻咽和咽拭子混合样本。使用鼻咽拭子作为金标准,鼻咽和咽拭子混合样本的敏感性最高,为 97%(95%CI 93-100),而唾液(85%,75-93)和鼻拭子(86%,77-93)的敏感性较低,咽拭子的敏感性要低得多(68%,35-94)。鼻咽和咽拭子混合样本(97%,90-100)和鼻拭子(96%,87-100)获得了类似的高阳性预测值,唾液的阳性预测值略低(93%,88-97)。咽拭子的阳性预测值最低,为 75%(95%CI 45-96)。不同临床标本的特异性(范围为 97-99%)和阴性预测值(范围为 95-99%)均较高。对混合鼻咽和咽拭子以及鼻拭子的医护人员采集和自我采集进行比较,结果显示诊断性能相当。在分析混合鼻咽和咽拭子以及咽拭子时,未观察到明显的异质性,而在唾液和鼻拭子的研究中观察到中度至高度异质性(I≥30%)。
我们的综述表明,与鼻咽拭子的金标准相比,混合鼻咽和咽拭子在门诊护理中诊断 SARS-CoV-2 感染的替代采样方法中提供了最佳的诊断性能。唾液和鼻拭子具有相当好的诊断性能,是可接受的替代标本采集方法。咽拭子的敏感性和阳性预测值较低,因此不推荐使用。混合鼻咽和咽拭子以及鼻拭子的自我采集不会对诊断准确性造成任何显著损害。我们的结果还为使用不同临床标本正确解释 SARS-CoV-2 检测结果提供了有用的参考框架。
香港研究资助局。