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Xpert MTB/RIF Ultra 检测在被动和主动发现病例情况下对结核病诊断的性能。

Performance of Xpert MTB/RIF Ultra for tuberculosis diagnosis in the context of passive and active case finding.

机构信息

Centro de Investigação em Saúde de Manhiça (CISM), Maputo, Mozambique.

ISGlobal, Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.

出版信息

Eur Respir J. 2021 Dec 23;58(6). doi: 10.1183/13993003.00257-2021. Print 2021 Dec.

Abstract

AIMS

We present a field evaluation of the diagnostic accuracy of Xpert MTB/RIF ("Xpert") and Xpert MTB/RIF Ultra ("Ultra") using two cohorts in a high tuberculosis/HIV burden setting in Southern Mozambique.

METHODS

Single respiratory specimens from symptomatic adults accessing healthcare services (passive case finding (PCF) cohort) and from household and community close contacts (active case finding (ACF) cohort) were tested by smear microscopy, culture, Xpert and Ultra. Liquid and solid culture served as a composite reference standard. We explored the impact of trace results on specificity their recategorisation to negative (in all and just among those previously treated individuals).

RESULTS

1419 and 252 participants were enrolled in the PCF and ACF cohorts, respectively. For the PCF cohort, Ultra showed higher sensitivity than Xpert overall (0.95 (95% CI 0.90-0.98) 0.88 (96% CI 0.82-0.93); p<0.001) and among smear-negative patients (0.84 (96% CI 0.71-0.93) 0.63 (96% CI 0.48-0.76)). Ultra's specificity was lower than Xpert's (0.96 (96% CI 0.95-0.97) 0.98 (96% CI 0.97-0.99); p=0.008). For ACF, sensitivities were the same (0.67 (95% CI 0.22-0.96) for both tests), although Ultra detected a higher number of microbiologically confirmed samples than Xpert (4.7% (12 out of 252) 2.7% (seven out of 252)). Conditional recategorisation of trace results among previously treated participants maintained differences in specificity in the PCF cohort.

CONCLUSION

These results add evidence on the improved sensitivity of Ultra and support its use in different case finding scenarios.

摘要

目的

我们在莫桑比克南部一个结核病/艾滋病负担较高的地区,使用两个队列评估 Xpert MTB/RIF(“Xpert”)和 Xpert MTB/RIF Ultra(“Ultra”)的诊断准确性。

方法

来自就诊于医疗机构的有症状成年人(被动病例发现(PCF)队列)和来自家庭和社区密切接触者的单个呼吸道标本(主动病例发现(ACF)队列)通过涂片显微镜检查、培养、Xpert 和 Ultra 进行检测。液体和固体培养作为复合参考标准。我们探讨了痕量结果对特异性的影响——将其重新归类为阴性(在所有患者和仅在那些先前接受过治疗的患者中)。

结果

PCF 队列和 ACF 队列分别纳入了 1419 名和 252 名参与者。对于 PCF 队列,Ultra 的总体敏感性高于 Xpert(0.95(95%置信区间 0.90-0.98)比 0.88(96%置信区间 0.82-0.93);p<0.001),并且在涂片阴性患者中也是如此(0.84(96%置信区间 0.71-0.93)比 0.63(96%置信区间 0.48-0.76))。Ultra 的特异性低于 Xpert(0.96(96%置信区间 0.95-0.97)比 0.98(96%置信区间 0.97-0.99);p=0.008)。对于 ACF,两种检测的敏感性相同(均为 0.67(95%置信区间 0.22-0.96)),尽管 Ultra 检测到的微生物学确认样本数量多于 Xpert(4.7%(12 例 252 例)比 2.7%(7 例 252 例))。在 PCF 队列中,对先前治疗过的参与者的痕量结果进行条件重新分类,维持了特异性方面的差异。

结论

这些结果提供了关于 Ultra 提高敏感性的证据,并支持在不同病例发现情况下使用它。

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