An Integrated Approach to Rapid Diagnosis of Tuberculosis and Multidrug Resistance Using Liquid Culture and Molecular Methods in Russia

被引:44
作者
Balabanova, Yanina
Drobniewski, Francis
Nikolayevskyy, Vladyslav
Kruuner, Annika
Malomanova, Nadezhda
Simak, Tatyana
Ilyina, Nailya
Zakharova, Svetlana
Lebedeva, Natalya
Alexander, Heather L.
O'Brien, Rick
Sohn, Hojoon
Shakhmistova, Anastasia
Fedorin, Ivan
机构
[1] National Mycobacterium Reference Laboratory, Institute of Cell and Molecular Sciences, University of London, London
[2] Samara Oblast Tuberculosis Dispensary, Samara
[3] Samara City Tuberculosis Service, Samara
[4] Foundation for Innovative New Diagnostic, Cointrin, Geneva
[5] US Centers for Disease Control and Prevention, Division of TB Elimination, Atlanta, GA
来源
PLOS ONE | 2009年 / 4卷 / 09期
关键词
D O I
10.1371/journal.pone.0007129
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective: To analyse the feasibility, cost and performance of rapid tuberculosis (TB) molecular and culture systems, in a high multidrug-resistant TB (MDR TB) middle-income region (Samara, Russia) and provide evidence for WHO policy change. Methods: Performance and cost evaluation was conducted to compare the BACTEC (TM) MGIT (TM) 960 system for culture and drug susceptibility testing (DST) and molecular systems for TB diagnosis, resistance to isoniazid and rifampin, and MDR TB identification compared to conventional Lowenstein-Jensen culture assays. Findings: 698 consecutive patients (2487 sputum samples) with risk factors for drug-resistant tuberculosis were recruited. Overall M. tuberculosis complex culture positivity rates were 31.6% (787/2487) in MGIT and 27.1% (675/2487) in LJ (90.5% and 83.2% for smear-positive specimens). In total, 809 cultures of M. tuberculosis complex were isolated by any method. Median time to detection was 14 days for MGIT and 36 days for LJ (10 and 33 days for smear positive specimens) and indirect DST in MGIT took 9 days compared to 21 days on LJ. There was good concordance between DST on LJ and MGIT (96.8% for rifampin and 95.6% for isoniazid). Both molecular hybridization assay results correlated well with MGIT DST results, although molecular assays generally yielded higher rates of resistance (by approximately 3% for both isoniazid and rifampin). Conclusion: With effective planning and logistics, the MGIT 960 and molecular based methodologies can be successfully introduced into a reference laboratory setting in a middle incidence country. High rates of MDR TB in the Russian Federation make the introduction of such assays particularly useful.
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页数:9
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