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Xpert MTB/RIF Ultra 检测在比利时布鲁塞尔多中心医院实验室使用一年后的肺结核和肺外结核诊断性能。

Performance of Xpert MTB/RIF Ultra for diagnosis of pulmonary and extra-pulmonary tuberculosis, one year of use in a multi-centric hospital laboratory in Brussels, Belgium.

机构信息

Department of Microbiology, Laboratoire Hospitalier Universitaire de Bruxelles-Universitair Laboratorium Brussel (LHUB-ULB), Brussels, Belgium.

Pediatric Department, CHU Saint Pierre, Université Libre de Bruxelles, Brussels, Belgium.

出版信息

PLoS One. 2021 Apr 8;16(4):e0249734. doi: 10.1371/journal.pone.0249734. eCollection 2021.

Abstract

Among the challenges in controlling tuberculosis, a rapid and accurate diagnostic test for the detection of Mycobacterium tuberculosis complex (MTBc) and its resistance to first line therapies is crucial. We evaluated the performance of the Xpert MTB/RIF Ultra assay (Xpert Ultra) for the rapid detection of MTBc and rifampicin resistance (RR) in 1120 pulmonary and 461 extra-pulmonary clinical specimens and compared it with conventional phenotypic techniques. The Xpert Ultra assay detected MTBc in 223 (14.1%) samples with an overall sensitivity and specificity, using culture as the "gold standard", of 91.1% (95% CI, 85.6-95.1) and 94.5% (95% CI, 93.1-95.6), respectively. The sensitivity of the Xpert Ultra test for smear-negative extra-pulmonary specimens was high (87.1%), even higher than with smear-negative pulmonary specimens (81.8%). But this enhanced sensitivity came with a low overall specificity of smear-negative extra-pulmonary specimens (66.7%). For 73 patients, 79/1423 (3.4%) negative mycobacterial culture samples were found to be positive with Xpert Ultra. Clinical data was necessary to correctly interpret potential false-positive results, especially trace-positive results. Sensitivity of the Xpert Ultra to detect RR compared to drug susceptibility testing was 100% (95% CI, 29.2-100) and specificity was 99.2% (95% CI, 95.8-100). We concluded that the Xpert Ultra test is able to provide a reliable TB diagnosis within a significantly shorter turnaround time than culture. This is especially true for paucibacillary samples such as smear-negative pulmonary specimens and extra-pulmonary specimens.

摘要

在控制结核病的挑战中,快速准确地检测结核分枝杆菌复合体(MTBc)及其对一线治疗药物的耐药性的诊断测试至关重要。我们评估了 Xpert MTB/RIF Ultra assay(Xpert Ultra)快速检测 MTBc 和利福平耐药性(RR)在 1120 例肺部和 461 例肺外临床标本中的性能,并将其与传统表型技术进行了比较。Xpert Ultra assay 检测到 223 份(14.1%)培养物作为“金标准”的 MTBc 样本,总体敏感性和特异性分别为 91.1%(95%置信区间,85.6-95.1)和 94.5%(95%置信区间,93.1-95.6)。Xpert Ultra 试验对涂片阴性肺外标本的敏感性较高(87.1%),甚至高于涂片阴性的肺部标本(81.8%)。但这种增强的敏感性伴随着涂片阴性肺外标本总体特异性较低(66.7%)。对于 73 例患者,在 1423 份负培养物的标本中,79/73(3.4%)份 Xpert Ultra 检测为阳性。临床数据对于正确解释潜在的假阳性结果,尤其是痕量阳性结果,是必要的。Xpert Ultra 检测 RR 的敏感性与药敏试验相比为 100%(95%置信区间,29.2-100),特异性为 99.2%(95%置信区间,95.8-100)。我们得出结论,与培养相比,Xpert Ultra 试验能够在明显更短的周转时间内提供可靠的结核病诊断。对于如涂片阴性的肺部标本和肺外标本等少菌标本,情况更是如此。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be2/8031447/ca7ea28a13f6/pone.0249734.g001.jpg

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