A Multisite Assessment of the Quantitative Capabilities of the Xpert MTB/RIF Assay

被引:102
作者
Blakemore, Robert [1 ]
Nabeta, Pamela [13 ]
Davidow, Amy L. [2 ,3 ]
Vadwai, Viral [7 ,8 ]
Tahirli, Rasim [11 ]
Munsamy, Vanisha [10 ]
Nicol, Mark [5 ,6 ]
Jones, Martin [12 ]
Persing, David H. [12 ]
Hillemann, Doris [4 ]
Ruesch-Gerdes, Sabine [4 ]
Leisegang, Felicity [5 ,6 ]
Zamudio, Carlos [9 ]
Rodrigues, Camilla [7 ,8 ]
Boehme, Catharina C. [13 ]
Perkins, Mark D. [13 ]
Alland, David [1 ]
机构
[1] Univ Med & Dent New Jersey, Div Infect Dis, Dept Med, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, Dept Prevent Med & Community Hlth, Newark, NJ 07103 USA
[3] Global TB Inst, Newark, NJ USA
[4] Forschungszentrum Borstel, Borstel, Germany
[5] Univ Cape Town, Dept Clin Lab Sci, ZA-7925 Cape Town, South Africa
[6] Natl Hlth Lab Serv, Cape Town, South Africa
[7] PD Hinduja Natl Hosp, Bombay, Maharashtra, India
[8] Med Res Ctr Hinduja, Bombay, Maharashtra, India
[9] Univ Peruana Cayetano Heredia, Inst Med Trop Alexander von Humboldt, Lima, Peru
[10] S African MRC, Unit Clin & Biomed TB Res, Durban, South Africa
[11] Special Treatment Inst Detainees TB, Baku, Azerbaijan
[12] Cepheid, Sunnyvale, CA USA
[13] Fdn Innovat New Diagnost, Geneva, Switzerland
基金
美国国家卫生研究院;
关键词
tuberculosis; molecular diagnostics; diagnostic techniques and procedures; diagnosis; clinical trial; MYCOBACTERIUM-TUBERCULOSIS; PULMONARY TUBERCULOSIS; TIME; TRANSMISSION; DIAGNOSIS; LOAD;
D O I
10.1164/rccm.201103-0536OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: The Xpert MTB/RIF is an automated molecular test for Mycobacterium tuberculosis that estimates bacterial burden by measuring the threshold-cycle (Ct) of its M. tuberculosis-specific real-time polymerase chain reaction. Bacterial burden is an important biomarker for disease severity, infection control risk, and response to therapy. Objectives: Evaluate bacterial load quantitation by Xpert MTB/RIF compared with conventional quantitative methods. Methods: Xpert MTB/RIF results were compared with smear-microscopy, semiquantiative solid culture, and time-to-detection in liquid culture for 741 patients and 2,008 samples tested in a multisite clinical trial. An internal control real-time polymerase chain reaction was evaluated for its ability to identify inaccurate quantitative Xpert MTB/RIF results. Measurements and Main Results: Assays with an internal control Ct greater than 34 were likely to be inaccurately quantitated; this represented 15% of M. tuberculosis-positive tests. Excluding these, decreasing M. tuberculosis Ct was associated with increasing smear microscopy grade for smears of concentrated sputum pellets (r(s) = -0.77) and directly from sputum (r(s) = -0.71). A Ct cutoff of approximately 27.7 best predicted smear-positive status. The association between M. tuberculosis Ct and time-to-detection in liquid culture (r(s) = 0.68) and semiquantitative colony counts (r(s) = -0.56) was weaker than smear. Tests of paired same-patient sputum showed that high-viscosity sputum samples contained X32 more M. tuberculosis than nonviscous samples. Comparisons between the grade of the acid-fast bacilli smear and Xpert MTB/RIF quantitative data across study sites enabled us to identify a site outlier in microscopy. Conclusions: Xpert MTB/RIF quantitation offers a new, standardized approach to measuring bacterial burden in the sputum of patients with tuberculosis.
引用
收藏
页码:1076 / 1084
页数:9
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