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干扰素-γ 释放对儿童结核病预测模型无附加价值。

No added value of interferon-γ release to a prediction model for childhood tuberculosis.

机构信息

Vaccines and Immunity Theme, Medical Research Council (MRC) Unit, Banjul, The Gambia

Vaccines and Immunity Theme, Medical Research Council (MRC) Unit, Banjul, The Gambia.

出版信息

Eur Respir J. 2016 Jan;47(1):223-32. doi: 10.1183/13993003.00890-2015. Epub 2015 Oct 22.

Abstract

The predictive value of a combination of clinical and radiological features with interferon-γ release assay (IGRA) for diagnosis of active tuberculosis (TB) disease among TB-exposed children is unknown.150 symptomatic HIV-negative children (aged 3 months to 14 years), prospectively recruited through active contact tracing, were included. Backward stepwise logistic regression and bootstrapping techniques were used for the development and internal validation of a clinical prediction model for active TB disease. Model discrimination and incremental value of a positive IGRA test were assessed by area under the receiver operating characteristic curve (AUC).35 (23%) children were diagnosed with active TB disease and started on treatment and 115 (77%) had other respiratory tract infections. A final parsimonious clinical model, comprising age <5 years (adjusted (a)OR 4.8, 95% CI 2.0-11.5) and lymphadenopathy on clinical examination (aOR 4.9, 95% CI 1.8-13.0) discriminated active TB disease from other disease with an AUC of 0.70 (95% CI 0.61-0.80). A positive IGRA result did not improve the discriminatory ability of the clinical model (c-statistic 0.72 versus 0.70; p=0.644).A clinical algorithm, including age <5 years and lymphadenopathy classified 70% of active TB disease among symptomatic TB-exposed children. IGRA does not add any discriminatory value to this prediction model.

摘要

一项结合临床和影像学特征与干扰素-γ释放试验(IGRA)对暴露于结核病(TB)儿童中活动性结核病(TB)疾病的预测价值尚不清楚。150 名有症状的 HIV 阴性儿童(3 个月至 14 岁)通过主动接触追踪前瞻性招募,纳入研究。采用后退逐步逻辑回归和自举技术建立和内部验证用于活动性 TB 疾病的临床预测模型。通过接受者操作特征曲线(ROC)下面积(AUC)评估模型鉴别力和阳性 IGRA 检测的增量价值。35 名(23%)儿童被诊断为活动性 TB 疾病并开始治疗,115 名(77%)患有其他呼吸道感染。最终简化的临床模型包括年龄<5 岁(调整后的(a)OR 4.8,95%CI 2.0-11.5)和临床检查中的淋巴结病(aOR 4.9,95%CI 1.8-13.0),区分活动性 TB 疾病和其他疾病的 AUC 为 0.70(95%CI 0.61-0.80)。IGRA 结果并未提高临床模型的鉴别能力(c 统计量为 0.72 与 0.70;p=0.644)。一个包含年龄<5 岁和淋巴结病的临床算法将 70%的有症状 TB 暴露儿童的活动性 TB 疾病进行了分类。IGRA 对该预测模型没有增加任何鉴别价值。

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