help button home button
AJRCCM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by JOUVESHOMME, S.
Right arrow Articles by GROSSET, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by JOUVESHOMME, S.
Right arrow Articles by GROSSET, J.

Am. J. Respir. Crit. Care Med., Volume 158, Number 4, October 1998, 1096-1101

Clinical Utility of an Amplification Test Based on Ligase Chain Reaction in Pulmonary Tuberculosis

STÉPHANE JOUVESHOMME, EMMANUELLE CAMBAU, DAVID TRYSTRAM, MICHEL SZPYTMA, WLADIMIR SOUGAKOFF, JEAN-PHILIPPE DERENNE, and JACQUES GROSSET

Service de Pneumologie et de Réanimation Respiratoire and Service de Bactériologie-Hygiène Hôpital Pitié-Salpêtrière, National Reference Centre for Surveillance of Mycobacterial Diseases and Drug Resistance, Paris, France

We evaluated the sensitivity and specificity of a new semiautomated direct amplification test (DAT), the LCx-MTB, for the diagnosis of pulmonary tuberculosis (TB) and assessed its positive predictive value by focusing on patients with high clinical and radiologic suspicion of pulmonary TB. Respiratory tract specimens from 32 consecutive patients with high suspicion of active pulmonary TB (case patients) and from 204 control patients were cultured for Mycobacterium tuberculosis and tested by LCx-MTB. Sensitivity and specificity of LCx-MTB when compared with culture was, respectively, 80 and 98%. Pulmonary TB was confirmed in the 32 case patients without knowledge of the LCx results: 18 patients were smear- and culture-positive for M. tuberculosis, and all gave at least one specimen that was LCx-positive. Eight patients were smear-negative culture-positive, and seven gave at least one LCx-positive specimen. LCx-MTB was negative in all the specimens obtained from six patients with smear- and culture-negative TB. A positive LCx-MTB result in a smear negative specimen was 100% predictive that at least one of the case patients' specimens would yield M. tuberculosis. As a consequence, knowledge of the LCx-MTB results at the time of specimen collection could have hastened the start of the antituberculosis therapy in three (21%) smear-negative case patients and could have avoided unnecessary invasive diagnostic procedures in four (29%). We conclude that the sensitivity of LCx-MTB in detecting M. tuberculosis DNA in respiratory tract specimens is similar to other DATs, that LCx-MTB is a reliable test for confirmation of TB in smear-positive patients and that LCx-MTB could be beneficial as a diagnostic step in smear-negative patients with a high suspicion of pulmonary TB.




This article has been cited by other articles:


Home page
ThoraxHome page
S Greco, E Girardi, A Navarra, and C Saltini
Current evidence on diagnostic accuracy of commercially based nucleic acid amplification tests for the diagnosis of pulmonary tuberculosis
Thorax, September 1, 2006; 61(9): 783 - 790.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
S. Chakravorty and J. S. Tyagi
Novel Multipurpose Methodology for Detection of Mycobacteria in Pulmonary and Extrapulmonary Specimens by Smear Microscopy, Culture, and PCR
J. Clin. Microbiol., June 1, 2005; 43(6): 2697 - 2702.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
G. Torrea, P. Van de Perre, M. Ouedraogo, A. Zougba, A. Sawadogo, B. Dingtoumda, B. Diallo, M. C. Defer, I. Sombie, S. Zanetti, et al.
PCR-based detection of the Mycobacterium tuberculosis complex in urine of HIV-infected and uninfected pulmonary and extrapulmonary tuberculosis patients in Burkina Faso
J. Med. Microbiol., January 1, 2005; 54(1): 39 - 44.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
N. Lemaitre, S. Armand, A. Vachee, O. Capilliez, C. Dumoulin, and R. J. Courcol
Comparison of the Real-Time PCR Method and the Gen-Probe Amplified Mycobacterium tuberculosis Direct Test for Detection of Mycobacterium tuberculosis in Pulmonary and Nonpulmonary Specimens
J. Clin. Microbiol., September 1, 2004; 42(9): 4307 - 4309.
[Abstract] [Full Text] [PDF]


Home page
ChestHome page
T. K. Lim, A. Gough, N.-K. Chin, and G. Kumarasinghe
Relationship Between Estimated Pretest Probability and Accuracy of Automated Mycobacterium tuberculosis Assay in Smear-Negative Pulmonary Tuberculosis
Chest, September 1, 2000; 118(3): 641 - 647.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
E. Cambau, C. Wichlacz, C. Truffot-Pernot, and V. Jarlier
Evaluation of the New MB Redox System for Detection of Growth of Mycobacteria
J. Clin. Microbiol., June 1, 1999; 37(6): 2013 - 2015.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Cell Mol. Biol.
Copyright © 1998 American Thoracic Society
  ATS Coding and Billing Quarterly