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Progression from latent infection to active disease in dynamic tuberculosis transmission models: a systematic review of the validity of modelling assumptions

机译:动态肺结核传播模型中从潜在感染到活动性疾病的进展:对模型假设有效性的系统评价

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摘要

Mathematical modelling is commonly used to evaluate infectious disease control policy and is influential in shaping policy and budgets. Mathematical models necessarily make assumptions about disease natural history and, if these assumptions are not valid, the results of these studies can be biased. We did a systematic review of published tuberculosis transmission models to assess the validity of assumptions about progression to active disease after initial infection (PROSPERO ID CRD42016030009). We searched PubMed, Web of Science, Embase, Biosis, and Cochrane Library, and included studies from the earliest available date (Jan 1, 1962) to Aug 31, 2017. We identified 312 studies that met inclusion criteria. Predicted tuberculosis incidence varied widely across studies for each risk factor investigated. For population groups with no individual risk factors, annual incidence varied by several orders of magnitude, and 20-year cumulative incidence ranged from close to 0% to 100%. A substantial proportion of modelled results were inconsistent with empirical evidence: for 10-year cumulative incidence, 40% of modelled results were more than double or less than half the empirical estimates. These results demonstrate substantial disagreement between modelling studies on a central feature of tuberculosis natural history. Greater attention to reproducing known features of epidemiology would strengthen future tuberculosis modelling studies, and readers of modelling studies are recommended to assess how well those studies demonstrate their validity.
机译:数学建模通常用于评估传染病控制政策,并且在制定政策和预算方面具有影响力。数学模型必须对疾病的自然史做出假设,如果这些假设无效,则这些研究的结果可能会产生偏差。我们对已发表的结核病传播模型进行了系统的综述,以评估有关初始感染后进展为活动性疾病的假设的有效性(PROSPERO ID CRD42016030009)。我们搜索了PubMed,Web of Science,Embase,Biosis和Cochrane图书馆,并纳入了最早的可用日期(1962年1月1日)至2017年8月31日的研究。我们确定了312项符合纳入标准的研究。在每个研究的危险因素中,结核病的预测发病率差异很大。对于没有个人危险因素的人群,年发病率变化了几个数量级,而20年累积发病率的范围从接近0%到100%。很大一部分模拟结果与经验证据不一致:对于10年累积发生率,40%的模拟结果是经验估计的两倍以上或不到一半。这些结果表明,在关于结核病自然史的主要特征的模型研究之间存在实质性分歧。对复制流行病学已知特征的更多关注将加强未来的结核病建模研究,建议建模研究的读者评估这些研究证明其有效性的程度。

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