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赞比亚和乌干达5岁以下因重度急性营养不良住院儿童结核病治疗决策算法的制定:一项前瞻性诊断队列研究

Development of tuberculosis treatment decision algorithms in children below 5 years hospitalised with severe acute malnutrition in Zambia and Uganda: a prospective diagnostic cohort study.

作者信息

Chabala Chishala, Roucher Clémentine, Ton Nu Nguyet Minh Huyen, Babirekere Esther, Inambao Muleya, Businge Gerald, Kapula Chifunda, Shankalala Perfect, Nduna Bwendo, Mulenga Veronica, Graham Stephen, Wobudeya Eric, Bonnet Maryline, Marcy Olivier

机构信息

School of Medicine, University of Zambia, Lusaka, Zambia.

University Teaching Hospitals-Children's Hospital, Lusaka, Zambia.

出版信息

EClinicalMedicine. 2024 Jun 20;73:102688. doi: 10.1016/j.eclinm.2024.102688. eCollection 2024 Jul.

Abstract

BACKGROUND

In children with severe acute malnutrition (SAM) tuberculosis is common, challenging to diagnose, and often fatal. We developed tuberculosis treatment decision algorithms (TDAs) for children under the age of 5 years with SAM.

METHODS

In this prospective diagnostic study, we enrolled and followed up children aged <60 months hospitalised with SAM at three tertiary hospitals in Zambia and Uganda from 4 November 2019 to 20 June 2022. We included children aged 2-59 months with SAM as defined by WHO and hospitalised following the WHO clinical criteria. We excluded children with current or history of antituberculosis treatment within the preceding 3 months. They underwent tuberculosis symptom screening, clinical assessment, chest X-ray, abdominal ultrasound, Xpert MTB/RIF Ultra (Ultra) and culture on respiratory and stool samples with 6 months follow-up. Tuberculosis was retrospectively defined using the 2015 standard case definition for childhood tuberculosis. We used logistic regression to develop diagnostic prediction models for a one-step diagnosis and a two-step screening and diagnostic approaches. We derived scores from models using WHO-recommended thresholds for sensitivity and proposed TDAs. This study is registered with ClinicalTrials.gov, NCT04240990.

FINDINGS

Of 1906 children hospitalised with SAM during the study period, 1230 were screened, 1152 were eligible and 603 were enrolled. Of the 603 children enrolled-median age 15 (inter-quartile range (IQR): 11-20) months and 65 (11.0%) living with HIV-114 (18.9%) were diagnosed with tuberculosis, including 51 (8.5%) with microbiological confirmation and 104 (17.2%) initiated treatment at a median of 6(IQR: 2-10) days after inclusion. 108 children were retrospectively classified as having tuberculosis resulting in a prevalence of 17.9% (95% confidence intervals (CI): 15.1; 21.2). 75 (69.4%) children with tuberculosis reported cough of any duration, 32 (29.6%) cough ≥2 weeks and 11 (10.2%) tuberculosis contact history. 535 children had complete data and were included in the diagnostic prediction model. The one-step diagnostic model had 15 predictors, including Ultra, clinical, radiographic, and abdominal features, an area under the receiving operating curve (AUROC) of 0.910, and derived TDA sensitivity of 86.14% (95% CI: 78.07-91.56) and specificity of 80.88% (95% CI: 76.91-84.30). The two-step model had AUROCs of 0.750 and 0.912 for screening and diagnosis, respectively, and derived combined TDA sensitivity of 79.21% (95% CI: 70.30-85.98) and a specificity of 83.64% (95% CI: 79.87-86.82).

INTERPRETATION

Tuberculosis prevalence was high among hospitalised children with SAM, with atypical clinical features. TDAs achieved satisfactory diagnostic accuracy and could be used to improve diagnosis in this vulnerable group.

FUNDING

Unitaid.

摘要

背景

在重度急性营养不良(SAM)儿童中,结核病很常见,诊断具有挑战性,且往往是致命的。我们为5岁以下的SAM儿童开发了结核病治疗决策算法(TDA)。

方法

在这项前瞻性诊断研究中,我们于2019年11月4日至2022年6月20日在赞比亚和乌干达的三家三级医院招募并随访了年龄小于60个月因SAM住院的儿童。我们纳入了年龄在2至59个月、符合世界卫生组织(WHO)定义的SAM且按照WHO临床标准住院的儿童。我们排除了在过去3个月内有当前或既往抗结核治疗史的儿童。他们接受了结核病症状筛查、临床评估、胸部X光检查、腹部超声检查、Xpert MTB/RIF Ultra(Ultra)检测以及呼吸道和粪便样本培养,并进行了6个月的随访。结核病是根据2015年儿童结核病标准病例定义进行回顾性定义的。我们使用逻辑回归来开发一步诊断和两步筛查及诊断方法的诊断预测模型。我们根据模型得出分数,并使用WHO推荐的敏感性阈值和提议的TDA。本研究已在ClinicalTrials.gov注册,注册号为NCT04240990。

结果

在研究期间因SAM住院的1906名儿童中,1230名接受了筛查,1152名符合条件,603名被纳入研究。在纳入的603名儿童中,中位年龄为15(四分位间距(IQR):11 - 20)个月,65名(11.0%)感染HIV - 114名(18.9%)被诊断为结核病,其中51名(8.5%)经微生物学确诊,104名(17.2%)在纳入后中位6(IQR:2 - 10)天开始治疗。108名儿童经回顾性分类为患有结核病,患病率为17.9%(95%置信区间(CI):15.1;21.2)。75名(69.4%)患有结核病的儿童报告了任何持续时间的咳嗽,32名(29.6%)咳嗽≥2周,11名(10.2%)有结核病接触史。535名儿童有完整数据并被纳入诊断预测模型。一步诊断模型有15个预测因素,包括Ultra、临床、影像学和腹部特征,接受者操作曲线下面积(AUROC)为0.910,得出的TDA敏感性为86.14%(95% CI:78.07 - 91.56),特异性为80.88%(95% CI:76.91 - 84.30)。两步模型的筛查和诊断AUROC分别为0.750和0.912,得出的联合TDA敏感性为79.21%(95% CI:70.30 - 85.98),特异性为83.64%(95% CI:79.87 - 86.82)。

解读

住院的SAM儿童中结核病患病率很高,且具有非典型临床特征。TDA取得了令人满意的诊断准确性,可用于改善这一弱势群体的诊断。

资助

国际药品采购机制(Unitaid)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b39f/11245985/beca6f7f1361/gr1.jpg

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