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Heterogeneous infectiousness in mathematical models of tuberculosis: A systematic review

机译:结核数学模型中的异质传染性:系统评价

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TB mathematical models employ various assumptions and approaches in dealing with the heterogeneous infectiousness of persons with active TB. We reviewed existing approaches and considered the relationship between them and existing epidemiological evidence. We searched the following electronic bibliographic databases from inception to 9 October 2018: MEDLINE, EMBASE, Biosis, Global Health and Scopus. Two investigators extracted data using a standardised data extraction tool. We included in the review any transmission dynamic model of M. tuberculosis transmission explicitly simulating heterogeneous infectiousness of person with active TB. We extracted information including: study objective, model structure, number of active TB compartments, factors used to stratify the active TB compartment, relative infectiousness of each active TB compartment and any intervention evaluated in the model. Our search returned 1899 unique references, of which the full text of 454 records were assessed for eligibility, and 99 studies met the inclusion criteria. Of these, 89 used compartmental models implemented with ordinary differential equations, while the most common approach to stratification of the active TB compartment was to incorporate two levels of infectiousness. However, various clinical characteristics were used to stratify the active TB compartments, and models differed as to whether they permitted transition between these states. Thirty-four models stratified the infectious compartment according to sputum smear status or pulmonary involvement, while 18 models stratified based on health care-related factors. Variation in infectiousness associated with drug-resistant M. tuberculosis was the rationale for stratifying active TB in 33 models, with these models consistently assuming that drug-resistant active TB cases were less infectious. Given the evidence of extensive heterogeneity in infectiousness of individuals with active TB, an argument exists for incorporating heterogeneous infectiousness, although this should be considered in light of the objectives of the study and the research question. PROSPERO Registration: CRD42019111936.
机译:TB数学模型采用各种假设和方法,用于处理有活性TB的人的异质传染性。我们审查了现有的方法,并考虑了它们与现有流行病学证据之间的关系。我们从2018年10月9日开始搜查了以下电子书目数据库:Medline,Embase,Biosis,全球健康和Scopus。两位调查人员使用标准化的数据提取工具提取数据。我们包括在审查中的任何传播动态模型的肺结核传播中的任何传播动态模型明确地模拟了活性结核病的异质传染性。我们提取信息包括:研究目标,模型结构,有源TB隔室的数量,用于分层有源TB隔室的因素,每个活性TB隔室的相对传染性以及在模型中评估的任何干预。我们的搜索返回了1899年的独特参考,其中评估了454条记录的全文,以获得资格,99项研究达到了纳入标准。其中89种二手隔间模型用常微分方程实现,而活性TB隔室的分层的最常见方法是掺入两种水平的传染病。然而,各种临床特征用于分层活性TB隔室,并且模型不同于它们是否允许在这些状态之间转换。三十四个模型根据痰涂片状况或肺部受累分析了传染性隔室,而基于医疗保健相关因素分层的18种模型。与耐药M.结核病相关的传染病变异是在33种型号中分层活性TB的基本原理,这些模型一致地假设耐药活性TB病例不太感染。鉴于具有活性结核病的个体传染性的广泛异质性的证据,存在掺入异质传染病的论据,尽管这应该考虑到研究的目标和研究问题。 Prospero注册:CRD42019111936。

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