Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, USA.
Desmond Tutu Tuberculosis Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Clin Infect Dis. 2021 Aug 16;73(4):e904-e912. doi: 10.1093/cid/ciab018.
Limitations in the sensitivity and accessibility of diagnostic tools for childhood tuberculosis contribute to the substantial gap between estimated cases and cases notified to national tuberculosis programs. Thus, tools to make accurate and rapid clinical diagnoses are necessary to initiate antituberculosis treatment in more children.
We analyzed data from a prospective cohort of children <13 years old being routinely evaluated for pulmonary tuberculosis in Cape Town, South Africa, from March 2012 to November 2017. We developed a regression model to describe the contributions of baseline clinical evaluation to the diagnosis of tuberculosis using standardized, retrospective case definitions. We included baseline chest radiographic and Xpert MTB/RIF assay results to the model to develop an algorithm with ≥90% sensitivity in predicting tuberculosis.
Data from 478 children being evaluated for pulmonary tuberculosis were analyzed (median age, 16.2 months; interquartile range, 9.8-30.9 months); 242 (50.6%) were retrospectively classified with tuberculosis, bacteriologically confirmed in 104 (43.0%). The area under the receiver operating characteristic curve for the final model was 0.87. Clinical evidence identified 71.4% of all tuberculosis cases in this cohort, and inclusion of baseline chest radiographic results increased the proportion to 89.3%. The algorithm was 90.1% sensitive and 52.1% specific, and maintained a sensitivity of >90% among children <2 years old or with low weight for age.
Clinical evidence alone was sufficient to make most clinical antituberculosis treatment decisions. The use of evidence-based algorithms may improve decentralized, rapid treatment initiation, reducing the global burden of childhood mortality.
儿童结核病诊断工具的敏感性和可及性有限,这导致了估计病例数与向国家结核病规划报告的病例数之间存在巨大差距。因此,需要能够准确快速做出临床诊断的工具,以便在更多儿童中启动抗结核治疗。
我们分析了 2012 年 3 月至 2017 年 11 月期间在南非开普敦常规评估儿童肺结核的前瞻性队列研究数据。我们开发了一个回归模型,使用标准化的回顾性病例定义来描述基线临床评估对结核病诊断的贡献。我们将基线胸部 X 光和 Xpert MTB/RIF 检测结果纳入模型,以开发一种预测结核病的算法,其灵敏度≥90%。
对 478 名正在接受肺结核评估的儿童进行了数据分析(中位数年龄为 16.2 个月;四分位距为 9.8-30.9 个月);242 名(50.6%)儿童被回顾性诊断为结核病,104 名(43.0%)经细菌学证实。最终模型的受试者工作特征曲线下面积为 0.87。该队列中,临床证据识别了所有结核病病例的 71.4%,纳入基线胸部 X 光结果后,这一比例增加到 89.3%。该算法的灵敏度为 90.1%,特异性为 52.1%,在年龄<2 岁或体重不足的儿童中,其灵敏度仍保持在>90%。
仅凭临床证据就足以做出大多数临床抗结核治疗决策。使用基于证据的算法可以改善分散的快速治疗启动,从而降低儿童死亡率的全球负担。