Performance of stool-based molecular tests and processing methods for paediatric tuberculosis diagnosis: a systematic review and meta-analysis.

IF 20.9 1区 生物学 Q1 INFECTIOUS DISEASES
Lucía Carratalà-Castro, Shilzia Munguambe, Belén Saavedra-Cervera, Petra de Haas, Alexander Kay, Olivier Marcy, Pamela Nabeta, Willy Ssengooba, Elisabetta Ghimenton-Walters, Sozinho Acácio, Maryline Bonnet, Joanna Ehrlich, Andrew R DiNardo, Anca Vasiliu, Christoph Lange, Sabine Hermans, Anna M Mandalakas, Elisa López-Varela, Alberto L García-Basteiro
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引用次数: 0

Abstract

Background: There has been a global pursuit to improve the diagnosis of tuberculosis in young children by applying diagnostic methods on accessible biospecimens such as stool. We aimed to conduct a systematic review on the accuracy of stool-based molecular tests for tuberculosis diagnosis in children and to assess the impact of the available pre-processing methods and other design characteristics.

Methods: In this systematic review and meta-analysis, we evaluated studies in children younger than 16 years with presumptive tuberculosis that were published in English, Spanish, French, and Portuguese from Jan 1, 2000, to May 3, 2024, in MEDLINE, Embase, and Embase Classic, comparing the molecular detection of Mycobacterium tuberculosis DNA in stool with microbiological tests on other samples or a clinical diagnosis. We did not exclude studies based on geographical location, sample size, or study design if they were reporting primary data. Two independent reviewers (LC-C and SM) screened titles, abstracts, and full-text articles for eligibility and extracted data on study characteristics, study population, and diagnostic performance. If information relevant to the main analysis was not reported in the article, the corresponding authors were contacted. Point estimates and 95% CIs were calculated for sensitivity and specificity for each study and for the different molecular tests (Xpert MTB/RIF, Xpert Ultra MTB/RIF [Cepheid, Sunnyvale, CA, USA], and other tests) versus a reference standard (culture only, any bacteriological confirmation, and tuberculosis case definition). Sensitivity and specificity were stratified by the stool processing method. We also quantified the additionality of stool Xpert Ultra tests for tuberculosis bacteriological confirmation. The protocol was registered with PROSPERO, CRD42022341514.

Findings: A total of 4521 records were identified through the database search, one record was identified from an article bibliography, and 67 studies were retained for full-text reading. 39 studies were included in the qualitative synthesis, 35 of which were included in the meta-analyses. When using any bacteriological confirmation from a respiratory sample as the reference standard, stool Xpert sensitivity was 0·60 (95% CI 0·48-0·71), stool Xpert Ultra sensitivity was 0·73 (0·63-0·81), and sensitivity was 0·44 (0·29-0·60) for other in-house molecular methods combined. When using tuberculosis case definition as the reference standard, stool Xpert sensitivity was 0·23 (0·11-0·41), stool Xpert Ultra sensitivity was 0·38 (0·22-0·56), and sensitivity was 0·17 (0·09-0·23) for other in-house molecular methods. The addition of stool Xpert Ultra increased bacteriological confirmation of tuberculosis by 38·6% overall. Further, the utilisation of centrifuge-free simplified methods improved the sensitivity of stool Xpert Ultra when using any bacteriological confirmation as a reference standard (0·77 [0·66-0·85] for centrifuge-free methods vs 0·61 [0·41-0·78] for non-centrifuge-free methods).

Interpretation: This systematic review and meta-analysis supports the use of Xpert Ultra in stool samples as a diagnostic tool for paediatric tuberculosis diagnosis. Stool-based Xpert Ultra can contribute to increase the bacteriological confirmation in this population, even when respiratory specimens are also tested.

Funding: The EDCTP2 programme supported by the EU via Stool4TB Project and the European Society of Pediatric Infectious Diseases.

用于儿科结核病诊断的粪便分子检验和处理方法的性能:系统综述和荟萃分析。
背景:全球都在寻求通过对粪便等可获取的生物样本采用诊断方法来改进幼儿结核病的诊断。我们旨在对基于粪便的分子检测诊断儿童结核病的准确性进行系统综述,并评估现有预处理方法和其他设计特征的影响:在本系统综述和荟萃分析中,我们评估了 2000 年 1 月 1 日至 2024 年 5 月 3 日期间在 MEDLINE、Embase 和 Embase Classic 中以英语、西班牙语、法语和葡萄牙语发表的针对 16 岁以下儿童推定肺结核的研究,这些研究比较了粪便中结核分枝杆菌 DNA 的分子检测与其他样本的微生物检测或临床诊断。如果研究报告的是主要数据,我们不会根据地理位置、样本大小或研究设计排除这些研究。两名独立审稿人(LC-C 和 SM)筛选了文章的标题、摘要和全文,并提取了有关研究特征、研究人群和诊断效果的数据。如果文章中没有报告与主要分析相关的信息,则会联系相应的作者。计算了每项研究以及不同分子检验(Xpert MTB/RIF、Xpert Ultra MTB/RIF [Cepheid, Sunnyvale, CA, USA]和其他检验)相对于参考标准(仅培养、任何细菌学确证和结核病例定义)的敏感性和特异性的点估计值和 95% CI。灵敏度和特异性按粪便处理方法分层。我们还量化了粪便 Xpert Ultra 检测对结核病细菌学确诊的额外性。该方案已在 PROSPERO 注册,编号为 CRD42022341514:通过数据库检索共找到 4521 条记录,从文章书目中找到一条记录,保留 67 项研究进行全文阅读。39项研究被纳入定性综合,其中35项被纳入荟萃分析。当以呼吸道样本的任何细菌学确认作为参考标准时,粪便 Xpert 的灵敏度为 0-60(95% CI 0-48-0-71),粪便 Xpert Ultra 的灵敏度为 0-73(0-63-0-81),其他内部分子方法的综合灵敏度为 0-44(0-29-0-60)。以肺结核病例定义作为参考标准时,粪便 Xpert 的灵敏度为 0-23(0-11-0-41),粪便 Xpert Ultra 的灵敏度为 0-38(0-22-0-56),其他内部分子方法的灵敏度为 0-17(0-09-0-23)。粪便 Xpert Ultra 的加入使结核病的细菌学确诊率总体提高了 38-6%。此外,在使用任何细菌学确认作为参考标准时,使用免离心简化方法提高了粪便 Xpert Ultra 的灵敏度(免离心方法为 0-77 [0-66-0-85] vs 非免离心方法为 0-61 [0-41-0-78]):本系统综述和荟萃分析支持将粪便样本中的 Xpert Ultra 用作儿科结核病诊断工具。即使同时检测呼吸道标本,粪便样本中的 Xpert Ultra 仍有助于提高这一人群的细菌学确诊率:EDCTP2项目由欧盟通过Stool4TB项目和欧洲儿科传染病学会提供支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lancet Microbe
Lancet Microbe Multiple-
CiteScore
27.20
自引率
0.80%
发文量
278
审稿时长
6 weeks
期刊介绍: The Lancet Microbe is a gold open access journal committed to publishing content relevant to clinical microbiologists worldwide, with a focus on studies that advance clinical understanding, challenge the status quo, and advocate change in health policy.
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