Department of Mathematics and Statistics, Radford University, Radford, Virginia, USA.
Department of Statistics, University of South Carolina, Columbia, South Carolina, USA.
Biom J. 2023 Oct;65(7):e2200270. doi: 10.1002/bimj.202200270. Epub 2023 May 16.
When screening a population for infectious diseases, pooling individual specimens (e.g., blood, swabs, urine, etc.) can provide enormous cost savings when compared to testing specimens individually. In the biostatistics literature, testing pools of specimens is commonly known as group testing or pooled testing. Although estimating a population-level prevalence with group testing data has received a large amount of attention, most of this work has focused on applications involving a single disease, such as human immunodeficiency virus. Modern methods of screening now involve testing pools and individuals for multiple diseases simultaneously through the use of multiplex assays. Hou et al. (2017, Biometrics, 73, 656-665) and Hou et al. (2020, Biostatistics, 21, 417-431) recently proposed group testing protocols for multiplex assays and derived relevant case identification characteristics, including the expected number of tests and those which quantify classification accuracy. In this article, we describe Bayesian methods to estimate population-level disease probabilities from implementing these protocols or any other multiplex group testing protocol which might be carried out in practice. Our estimation methods can be used with multiplex assays for two or more diseases while incorporating the possibility of test misclassification for each disease. We use chlamydia and gonorrhea testing data collected at the State Hygienic Laboratory at the University of Iowa to illustrate our work. We also provide an online R resource practitioners can use to implement the methods in this article.
在对传染病进行人群筛查时,与逐个检测样本(例如血液、拭子、尿液等)相比,将个体样本合并为样本池可以节省大量成本。在生物统计学文献中,对样本池进行检测通常被称为分组检测或混合检测。尽管使用分组检测数据来估计人群水平的流行率已经受到了广泛关注,但这些工作大多集中在涉及单一疾病的应用上,例如人类免疫缺陷病毒。现代筛查方法现在通过使用多重检测同时对多个疾病进行样本池和个体检测。Hou 等人(2017 年,《生物统计学》,73,656-665)和 Hou 等人(2020 年,《生物统计学》,21,417-431)最近提出了用于多重检测的分组检测方案,并推导出了相关的病例识别特征,包括预期的检测次数和量化分类准确性的那些。在本文中,我们描述了从实施这些方案或任何其他可能在实践中进行的多重分组检测方案中估计人群疾病概率的贝叶斯方法。我们的估计方法可以用于两种或更多种疾病的多重检测,同时考虑每种疾病的检测错误分类的可能性。我们使用爱荷华州立卫生实验室收集的衣原体和淋病检测数据来说明我们的工作。我们还提供了一个在线 R 资源,从业者可以使用该资源来实现本文中的方法。