Literature DB >> 10092966

Multicenter evaluation of two commercial amplification kits (Amplicor, Roche and LCx, Abbott) for direct detection of Mycobacterium tuberculosis in pulmonary and extrapulmonary specimens.

E Tortoli1, M Tronci, C P Tosi, C Galli, F Lavinia, S Natili, A Goglio.   

Abstract

Direct detection of Mycobacterium tuberculosis was performed in parallel with the Amplicor M. tuberculosis test (Roche Diagnostic System, USA) and the LCx M. tuberculosis (Abbott Diagnostic Division, USA) on 697 samples, collected from 481 patients, in three different Italian laboratories. Though both systems are licensed only for pulmonary specimens, 113 extrapulmonary specimens (represented mainly by pleural fluids, cerebrospinal fluids and urines) were included in the study. Amplification results were compared with acid-fast microscopy, culture, and identification of isolates. Final clinical diagnosis was used to resolve discrepant results. M. tuberculosis was detected in 105 specimens by both assays, whereas 561 were agreeing negatives; 21 and 6 of the remaining true-positive samples scored positive with LCx only and with Amplicor only, respectively. There were three false-positives with LCx and one false-positive with Amplicor. The diagnostic sensitivity of both methods was significantly better when only respiratory specimens were considered (78% versus 59% in nonrespiratory samples with Amplicor, and 88% versus 65% with LCx). Our data reveal a significantly better sensitivity of the LCx (p = 0.026) and a slight better specificity of the Amplicor assay. It is noteworthy that 16 of the 21 Amplicor-negative specimens in which LCx detected M. tuberculosis were culture negative, thus suggesting that the higher diagnostic sensitivity of the latter assay is attributable to its better analytical sensitivity. However, the majority of such samples originated from patients under antimicrobial treatment, which makes uncertain the clinical significance of such increased sensitivity. Considering true-positive for LCx and true-negative for Amplicor, the 16 culture-negative/LCx-positive/Amplicor-negative specimens resulted true-positives after the resolution of discrepancies, the final overall sensitivity and specificity values of the LCx assay were not significantly different from the ones of the Amplicor assay.

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Year:  1999        PMID: 10092966     DOI: 10.1016/s0732-8893(98)00097-2

Source DB:  PubMed          Journal:  Diagn Microbiol Infect Dis        ISSN: 0732-8893            Impact factor:   2.803


  9 in total

Review 1.  Relevance of commercial amplification methods for direct detection of Mycobacterium tuberculosis complex in clinical samples.

Authors:  Claudio Piersimoni; Claudio Scarparo
Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

2.  Clinical evaluation of the polymerase chain reaction for the rapid diagnosis of tuberculosis.

Authors:  V C C Cheng; W C Yam; I F N Hung; P C Y Woo; S K P Lau; B S F Tang; K Y Yuen
Journal:  J Clin Pathol       Date:  2004-03       Impact factor: 3.411

Review 3.  Molecular Mycobacteriology and Expansion in Disease Diagnosis.

Authors:  Narotam Sharma; R K Singh; Praveen Sharma
Journal:  Indian J Clin Biochem       Date:  2015-04-28

4.  Detection and identification of Mycobacterium spp. in clinical specimens by combining the Roche Cobas Amplicor Mycobacterium tuberculosis assay with Mycobacterium genus detection and nucleic acid sequencing.

Authors:  S Peter-Getzlaff; J Lüthy; A Voit; G V Bloemberg; E C Böttger
Journal:  J Clin Microbiol       Date:  2010-09-08       Impact factor: 5.948

5.  Evaluation of Cobas TaqMan MTB for direct detection of the Mycobacterium tuberculosis complex in comparison with Cobas Amplicor MTB.

Authors:  Guido V Bloemberg; Antje Voit; Claudia Ritter; Vanessa Deggim; Erik C Böttger
Journal:  J Clin Microbiol       Date:  2013-04-24       Impact factor: 5.948

6.  Four-year experience of use of the Cobas Amplicor system for rapid detection of Mycobacterium tuberculosis complex in respiratory and nonrespiratory specimens in Greece.

Authors:  S Levidiotou; G Vrioni; E Galanakis; E Gesouli; C Pappa; D Stefanou
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2003-06-03       Impact factor: 3.267

7.  Development and evaluation of a molecular assay for detection of nontuberculous mycobacteria by use of the cobas amplicor platform.

Authors:  S Peter-Getzlaff; J Lüthy; B Böddinghaus; E C Böttger; B Springer
Journal:  J Clin Microbiol       Date:  2008-10-22       Impact factor: 5.948

8.  Comparison of diagnostic performance of three real-time PCR kits for detecting Mycobacterium species.

Authors:  Sun Young Cho; Min Jin Kim; Jin-Tae Suh; Hee Joo Lee
Journal:  Yonsei Med J       Date:  2011-03       Impact factor: 2.759

9.  Commercial nucleic-acid amplification tests for diagnosis of pulmonary tuberculosis in respiratory specimens: meta-analysis and meta-regression.

Authors:  Daphne I Ling; Laura L Flores; Lee W Riley; Madhukar Pai
Journal:  PLoS One       Date:  2008-02-06       Impact factor: 3.240

  9 in total

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