Infectious Disease Research Centre, Massey University, Palmerston North, New Zealand.
School of Fundamental Science, Massey University, PO Box 11222, Palmerston North, New Zealand.
BMC Infect Dis. 2021 Oct 30;21(1):1119. doi: 10.1186/s12879-021-06810-4.
Diagnostic testing using PCR is a fundamental component of COVID-19 pandemic control. Criteria for determining who should be tested by PCR vary between countries, and ultimately depend on resource constraints and public health objectives. Decisions are often based on sets of symptoms in individuals presenting to health services, as well as demographic variables, such as age, and travel history. The objective of this study was to determine the sensitivity and specificity of sets of symptoms used for triaging individuals for confirmatory testing, with the aim of optimising public health decision making under different scenarios.
Data from the first wave of COVID-19 in New Zealand were analysed; comprising 1153 PCR-confirmed and 4750 symptomatic PCR negative individuals. Data were analysed using Multiple Correspondence Analysis (MCA), automated search algorithms, Bayesian Latent Class Analysis, Decision Tree Analysis and Random Forest (RF) machine learning.
Clinical criteria used to guide who should be tested by PCR were based on a set of mostly respiratory symptoms: a new or worsening cough, sore throat, shortness of breath, coryza, anosmia, with or without fever. This set has relatively high sensitivity (> 90%) but low specificity (< 10%), using PCR as a quasi-gold standard. In contrast, a group of mostly non-respiratory symptoms, including weakness, muscle pain, joint pain, headache, anosmia and ageusia, explained more variance in the MCA and were associated with higher specificity, at the cost of reduced sensitivity. Using RF models, the incorporation of 15 common symptoms, age, sex and prioritised ethnicity provided algorithms that were both sensitive and specific (> 85% for both) for predicting PCR outcomes.
If predominantly respiratory symptoms are used for test-triaging, a large proportion of the individuals being tested may not have COVID-19. This could overwhelm testing capacity and hinder attempts to trace and eliminate infection. Specificity can be increased using alternative rules based on sets of symptoms informed by multivariate analysis and automated search algorithms, albeit at the cost of sensitivity. Both sensitivity and specificity can be improved through machine learning algorithms, incorporating symptom and demographic data, and hence may provide an alternative approach to test-triaging that can be optimised according to prevailing conditions.
PCR 检测是 COVID-19 大流行控制的基本组成部分。决定谁应该接受 PCR 检测的标准因国家而异,最终取决于资源限制和公共卫生目标。决策通常基于向卫生服务机构就诊的个体的一组症状以及人口统计学变量,如年龄和旅行史。本研究的目的是确定用于对个体进行确证性检测进行分诊的症状集的敏感性和特异性,目的是在不同情况下优化公共卫生决策。
分析了新西兰 COVID-19 第一波的数据;包括 1153 例 PCR 确诊和 4750 例有症状但 PCR 阴性的个体。使用多变量对应分析(MCA)、自动搜索算法、贝叶斯潜在类别分析、决策树分析和随机森林(RF)机器学习对数据进行了分析。
用于指导谁应该接受 PCR 检测的临床标准基于一组主要是呼吸道症状:新的或恶化的咳嗽、喉咙痛、呼吸急促、鼻塞、嗅觉丧失,伴有或不伴有发热。使用 PCR 作为准金标准,该组具有相对较高的敏感性(>90%)但特异性低(<10%)。相比之下,一组主要是非呼吸道症状,包括乏力、肌肉疼痛、关节疼痛、头痛、嗅觉丧失和味觉丧失,在 MCA 中解释了更多的方差,并且与更高的特异性相关,但其敏感性降低。使用 RF 模型,纳入 15 种常见症状、年龄、性别和优先族裔,提供了既敏感又特异(>85%)的预测 PCR 结果的算法。
如果主要使用呼吸道症状进行测试分诊,那么接受测试的个体中可能有很大一部分没有 COVID-19。这可能会使测试能力不堪重负,并阻碍追踪和消除感染的努力。可以使用基于多元分析和自动搜索算法提供的症状集的替代规则来提高特异性,尽管是以敏感性为代价。通过结合症状和人口统计学数据的机器学习算法可以提高敏感性和特异性,因此可能为测试分诊提供一种替代方法,可以根据流行情况进行优化。