Xpert MTB/RIF Testing in a Low Tuberculosis Incidence, High-Resource Setting: Limitations in Accuracy and Clinical Impact

被引:74
|
作者
Sohn, Hojoon [1 ,2 ,3 ]
Aero, Abebech D. [1 ,2 ,3 ]
Menzies, Dick [1 ,2 ,3 ]
Behr, Marcel [1 ,2 ,3 ]
Schwartzman, Kevin [1 ,2 ,3 ]
Alvarez, Gonzalo G. [1 ,2 ,4 ]
Dan, Andrei [1 ,2 ]
McIntosh, Fiona [1 ,2 ,3 ]
Pai, Madhukar [1 ,2 ,3 ]
Denkinger, Claudia M. [1 ,2 ,5 ]
机构
[1] McGill Univ, McGill Int TB Ctr, Montreal, PQ H3A 1A2, Canada
[2] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ H3A 1A2, Canada
[3] Montreal Chest Inst, Resp Epidemiol & Clin Res Unit, Montreal, PQ, Canada
[4] Univ Ottawa, Ottawa Hosp Res Inst, Ottawa, ON K1N 6N5, Canada
[5] Beth Israel Deaconess Med Ctr, Div Infect Dis, Boston, MA 02215 USA
基金
加拿大健康研究院;
关键词
tuberculosis; diagnostics; molecular testing; point-of-care; MYCOBACTERIUM-TUBERCULOSIS; PULMONARY TUBERCULOSIS; ASSAY; DIAGNOSIS; TIME; TRANSMISSION; RESISTANCE;
D O I
10.1093/cid/ciu022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Xpert MTB/RIF, the first automated molecular test for tuberculosis, is transforming the diagnostic landscape in low-income countries. However, little information is available on its performance in low-incidence, high-resource countries. Methods. We evaluated the accuracy of Xpert in a university hospital tuberculosis clinic in Montreal, Canada, for the detection of pulmonary tuberculosis on induced sputum samples, using mycobacterial cultures as the reference standard. We also assessed the potential reduction in time to diagnosis and treatment initiation. Results. We enrolled 502 consecutive patients who presented for evaluation of possible active tuberculosis (most with abnormal chest radiographs, only 18% symptomatic). Twenty-five subjects were identified to have active tuberculosis by culture. Xpert had a sensitivity of 46% (95% confidence interval [CI], 26%-67%) and specificity of 100% (95% CI, 99%-100%) for detection of Mycobacterium tuberculosis. Sensitivity was 86% (95% CI, 42%-100%) in the 7 subjects with smear-positive results, and 28% (95% CI, 10%-56%) in the remaining subjects with smear-negative, culture-positive results; in this latter group, positive Xpert results were obtained a median 12 days before culture results. Subjects with positive cultures but negative Xpert results had minimal disease: 11 of 13 had no symptoms on presentation, and mean time to positive liquid culture results was 28 days (95% CI, 25-47 days) compared with 14 days (95% CI, 8-21 days) in Xpert/culture-positive cases. Conclusions. Our findings suggest limited potential impact of Xpert testing in high-resource, low-incidence ambulatory settings due to lower sensitivity in the context of less extensive disease, and limited potential to expedite diagnosis beyond what is achieved with the existing, well-performing diagnostic algorithm.
引用
收藏
页码:970 / 976
页数:7
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