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Xpert MTB/RIF Results in Patients With Previous Tuberculosis: Can We Distinguish True From False Positive Results?
被引:103
|作者:
Theron, Grant
[1
,2
,3
,4
]
Venter, Rouxjeane
[3
,4
]
Calligaro, Greg
[1
,2
]
Smith, Liezel
[1
,2
]
Limberis, Jason
[1
,2
]
Meldau, Richard
[1
,2
]
Chanda, Duncan
[1
,2
,5
]
Esmail, Aliasgar
[1
,2
]
Peter, Jonny
[1
,2
]
Dheda, Keertan
[1
,2
,6
]
机构:
[1] Univ Cape Town, Lung Infect & Immun Unit, Div Pulmonol, Tygerberg, South Africa
[2] Univ Cape Town, Lung Inst, Dept Med, Tygerberg, South Africa
[3] Univ Stellenbosch, DST NRF Excellence Biomed TB Res, ZA-7505 Tygerberg, South Africa
[4] Univ Stellenbosch, MRC Ctr Mol & Cellular Biol, Div Mol Biol & Human Genet, Fac Med & Hlth Sci, ZA-7505 Tygerberg, South Africa
[5] Inst Med Res & Training, Lusaka, Zambia
[6] Univ Cape Town, Inst Infect Dis & Mol Med, ZA-7925 Observatory, South Africa
基金:
英国医学研究理事会;
英国惠康基金;
关键词:
tuberculosis;
diagnosis;
Xpert;
false positivity;
PULMONARY TUBERCULOSIS;
BACTERIAL LOAD;
DIAGNOSIS;
ASSAY;
PERFORMANCE;
GENEXPERT;
BIOMARKER;
SPECIFICITY;
ACCURACY;
D O I:
10.1093/cid/civ1223
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. Patients with previous tuberculosis may have residual DNA in sputum that confounds nucleic acid amplification tests such as Xpert MTB/RIF. Little is known about the frequency of Xpert-positive, culture-negative ("false positive") results in retreatment patients, whether these are distinguishable from true positives, and whether Xpert's automated filter-based wash step reduces false positivity by removing residual DNA associated with nonintact cells. Methods. Pretreatment patients (n= 2889) with symptoms of tuberculosis from Cape Town, South Africa, underwent a sputum-based liquid culture and Xpert. We also compared Xpert results from dilutions of intact or heat-lysed and mechanically lysed bacilli. Results. Retreatment cases were more likely to be Xpert false-positive (45/321 Xpert-positive retreatment cases were false-positive) than new cases (40/461) (14% [95% confidence interval {CI}, 10%-18%]vs 8% [95% CI, 6%-12%]; P=.018). Fewer years since treatment completion (adjusted odds ratio [aOR], 0.85 [95% CI,.73-. 99]), less mycobacterial DNA (aOR, 1.14 [95% CI, 1.03-1.27]per cycle threshold [C-T]), and a chest radiograph not suggestive of active tuberculosis (aOR, 0.22 [95% CI,.06-. 82]) were associated with false positivity. C-T had suboptimal accuracy for false positivity: 46% of Xpert-positives with C-T > 30 would be false positive, although 70% of false positives would be missed. C-T's predictive ability (area under the curve, 0.83 [95% CI,.76-. 90]) was not improved by additional variables. Xpert detected nonviable, nonintact bacilli without a change in C-T vs controls. Conclusions. One in 7 Xpert-positive retreatment patients were culture negative and potentially false positive. False positivity was associated with recent previous tuberculosis, high C-T, and a chest radiograph not suggestive of active tuberculosis. Clinicians may consider awaiting confirmatory testing in retreatment patients with C-T > 30; however, most false positives fall below this cut-point. Xpert can detect DNA from nonviable, nonintact bacilli.
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页码:995 / 1001
页数:7
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