The evaluation of FASTPlaqueTB™ test for the rapid diagnosis of tuberculosis

被引:27
作者
Albay, A [1 ]
Kisa, O [1 ]
Baylan, O [1 ]
Doganci, L [1 ]
机构
[1] Gulhane Mil Med Acad, Dept Microbiol & Clin Microbiol, Ankara, Turkey
关键词
D O I
10.1016/S0732-8893(03)00048-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
FASTPlaqueTB(TM) (Biotec Laboratories Ltd., Ipswich, UK) is a rapid test which utilizes bacteriophage amplification technology for the detection of viable Mycobacterium tuberculosis in clinical specimens. We evaluated performance of the FASTPlaqueTB(TM) test by comparing with BACTEC 460 TB culture system (Becton Dickinson Co., Maryland, USA), polymerase chain reaction (PCR) and acid fast bacilli (AFB) smear methods. We investigated 192 sputum specimens collected from the patients suspected of having pulmonary TB by AFB smear, BACTEC 460 TB culture system, PCR and FASTPlaqueTB(TM) test. The sensitivity of AFB smear, PCR and FASTPlaqueTB(TM) test were 57.8%, 84.4% and 87.5% respectively when we accepted BACTEC 460 TB culture system as gold standard. We conclude that FASTPlaqueTB(TM) test has a good potential for rapid diagnosis of Mycobacterium tuberculosis as a result of the evaluation of these three tests by comparison to the BACTEC 460 TB culture system. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:211 / 215
页数:5
相关论文
共 23 条
[11]   DETECTION OF MYCOBACTERIUM-TUBERCULOSIS IN SPUTUM SAMPLES USING A POLYMERASE CHAIN-REACTION [J].
EISENACH, KD ;
SIFFORD, MD ;
CAVE, MD ;
BATES, JH ;
CRAWFORD, JT .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 144 (05) :1160-1163
[12]   Evaluation of reverse transcription-PCR and a bacteriophage-based assay far rapid phenotypic detection of rifampin resistance in clinical isolates of Mycobacterium tuberculosis [J].
Eltringham, IJ ;
Drobniewski, FA ;
Mangan, JA ;
Butcher, PD ;
Wilson, SM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3524-3527
[13]   Comparative evaluation of initial and new versions of the Gen-Probe amplified Mycobacterium Tuberculosis Direct Test for direct detection of Mycobacterium tuberculosis in respiratory and nonrespiratory specimens [J].
Gamboa, F ;
Fernandez, G ;
Padilla, E ;
Manterola, JM ;
Lonca, J ;
Cardona, PJ ;
Matas, L ;
Ausina, V .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :684-689
[14]  
KENT BD, 1985, PUBLIC HLTH MYCOBACT, P1
[15]  
REVATHI G, 2001, 11 EUR C CLIN MICR I
[16]   Comparison of enhanced Mycobacterium tuberculosis amplified direct test with COBAS AMPLICOR Mycobacterium tuberculosis assay for direct detection of Mycobacterium tuberculosis complex in respiratory and extrapulmonary specimens [J].
Scarparo, C ;
Piccoli, P ;
Rigon, A ;
Ruggiero, G ;
Scagnelli, M ;
Piersimoni, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (04) :1559-1562
[17]  
SHULTZ EK, 1999, TIETZ TXB, P310
[18]  
SIDDIQI SH, 1996, BACTEC TB SYSTEM PRO
[19]  
Somoskövi A, 1999, J CLIN MICROBIOL, V37, P1366
[20]   US hospital mycobacteriology laboratories: Status and comparison with state public health department laboratories [J].
Tokars, JI ;
Rudnick, JR ;
Kroc, K ;
Manangan, L ;
Pugliese, G ;
Huebner, RE ;
Chan, JL ;
Jarvis, WR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (03) :680-685