Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14295
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dc.contributor.authorLinasmita P.
dc.contributor.authorSrisangkaew S.
dc.contributor.authorWongsuk T.
dc.contributor.authorBhongmakapat T.
dc.contributor.authorWatcharananan S.P.
dc.date.accessioned2021-04-05T03:34:01Z-
dc.date.available2021-04-05T03:34:01Z-
dc.date.issued2012
dc.identifier.issn10584838
dc.identifier.other2-s2.0-84863924847
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14295-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84863924847&doi=10.1093%2fcid%2fcis401&partnerID=40&md5=b6e68055764108bdd319c405532b7a97
dc.description.abstractBackground.Tuberculous lymphadenitis (TBL) is the most common form of extrapulmonary tuberculosis. Currently, the standard diagnostic test for TBL is culture, which takes more than several weeks to yield results. We studied a real-time polymerase chain reaction (PCR) for rapid detection of Mycobacterium tuberculosis in cervical lymph node specimens obtained from patients in a country where the tuberculosis incidence is high.Methods.Patients with cervical lymphadenopathy were prospectively enrolled between April 2009 and March 2010. Clinical specimens obtained through fine-needle aspiration (FNA) and excisional biopsy were tested for M. tuberculosis by the COBAS TaqMan MTB Test, a real-time PCR assay for detecting the 16S ribosomal RNA gene of M. tuberculosis. Mycobacterial culture and histopathological findings from tissue biopsy specimens were used as a reference standard for sensitivity and specificity calculations.Results.Of 73 patients, 41 received a diagnosis of TBL. For biopsy specimens, the sensitivity of real-time PCR was 63.4, and the specificity was 96.9. For FNA specimens, the sensitivity was 17.1, and the specificity was 100. The sensitivity of real-time PCR of biopsy specimens was comparable to that of tissue culture but significant lower than that of histopathological examination (P <. 01).Conclusions.Real-time PCR did not increase the yield for rapid diagnosis of TBL. © 2012 The Author.
dc.subjectRNA 16S
dc.subjecttuberculostatic agent
dc.subjectadult
dc.subjectarticle
dc.subjectaspiration biopsy
dc.subjectcervical lymph node
dc.subjectcross-sectional study
dc.subjectfemale
dc.subjecthistopathology
dc.subjecthuman
dc.subjecthuman tissue
dc.subjectlymph node biopsy
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectMycobacterium tuberculosis
dc.subjectpriority journal
dc.subjectprospective study
dc.subjectreal time polymerase chain reaction
dc.subjectsensitivity and specificity
dc.subjecttuberculous lymphadenitis
dc.subjectAdult
dc.subjectBacteriological Techniques
dc.subjectBiopsy
dc.subjectBiopsy, Fine-Needle
dc.subjectCross-Sectional Studies
dc.subjectFemale
dc.subjectHistocytochemistry
dc.subjectHumans
dc.subjectIncidence
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectMolecular Diagnostic Techniques
dc.subjectMycobacterium tuberculosis
dc.subjectProspective Studies
dc.subjectReal-Time Polymerase Chain Reaction
dc.subjectRNA, Bacterial
dc.subjectRNA, Ribosomal, 16S
dc.subjectSensitivity and Specificity
dc.subjectTuberculosis, Lymph Node
dc.titleEvaluation of real-time polymerase chain reaction for detection of the 16s ribosomal RNA gene of mycobacterium tuberculosis and the diagnosis of cervical tuberculous lymphadenitis in a country with a high tuberculosis incidence
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationClinical Infectious Diseases. Vol 55, No.3 (2012), p.313-321
dc.identifier.doi10.1093/cid/cis401
Appears in Collections:Scopus 1983-2021

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