儿童结核病的非痰分诊和确证性诊断试验。

IJTLD open Pub Date : 2025-03-12 eCollection Date: 2025-03-01 DOI:10.5588/ijtldopen.24.0484
A Drane, A Molkenthin, M Gassama, S Pouzol, P Vanhems, J Hoffmann
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引用次数: 0

摘要

背景:非痰检分诊和确认性检查对于儿童早期结核发现和及时治疗至关重要。方法:从2022年1月至2024年5月进行了一项小型综述,评估了5项儿童结核病非痰基础检测的研究。使用微生物学和临床参考标准来评估诊断准确性和分诊潜力。结果:在验证性试验中,只有胃吸入试验与基于墨盒的核酸扩增试验(CBNAAT)符合WHO目标产品简介标准。然而,这种方法仍然是侵入性的,不适合即时检测。通过气相色谱-质谱(GC/MS)或C-ELISA (BJ76/A194)进行尿液检测显示出高性能,但在资源有限的环境中缺乏点护理适用性。粪便检测CBNAAT是一种可行的替代方法,具有高特异性但低敏感性。对于分诊,尿脂阿拉伯糖甘露聚糖测试和血液MTB-HR测试基于特异性、实用性、成本和周转时间显示出前景。结论:本综述强调了儿童结核病非痰基础检测的性能及其作为分诊工具的潜力。虽然其他一些创新显示出对成人结核病进行分类和/或诊断的希望,但需要进一步研究以评估这些检测在儿科人群中的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-sputum-based triage and confirmatory diagnostic tests for pediatric TB.

Background: Non-sputum-based triage and confirmatory tests are essential for early TB detection and timely treatment in children.

Methods: A mini-review was conducted from January 2022 to May 2024, evaluating five studies on non-sputum-based assays for childhood TB diagnosis. Both Microbiological and Clinical Reference Standards were used to assess diagnostic accuracy and triage potential.

Results: Among the confirmatory tests, only the gastric aspiration test with cartridge-based nucleic acid amplification tests (CBNAAT) met the WHO Target Product Profile criteria. However, this method remains invasive and is not suitable for point-of-care testing. Urine testing by gas chromatography-mass spectrometry (GC/MS) or C-ELISA (BJ76/A194) demonstrated high performance but lacked point-of-care applicability in resource-limited settings. Stool testing with CBNAAT is a viable alternative with high specificity but low sensitivity. For triage, urine lipoarabinomannan tests and blood MTB-HR tests show promise based on specificity, practicality, cost, and turnaround time.

Conclusion: This review highlights the performance of non-sputum-based assays for childhood TB and their potential as triage tools. While some other innovations show promise for the triage and/or diagnosis of TB in adults, further studies are needed to evaluate the performance of these tests in pediatric populations.

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