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dc.contributor.authorBerk, RH
dc.contributor.authorYazici, M
dc.contributor.authorAtabey, N
dc.contributor.authorOzdamar, OS
dc.contributor.authorPabuccuoglu, U
dc.contributor.authorAlici, E
dc.date.accessioned2020-06-21T15:53:38Z
dc.date.available2020-06-21T15:53:38Z
dc.date.issued1996
dc.identifier.issn0362-2436
dc.identifier.issn1528-1159
dc.identifier.urihttps://doi.org/10.1097/00007632-199609010-00011
dc.identifier.urihttps://hdl.handle.net/20.500.12712/22712
dc.descriptionberk, rasim haluk/0000-0003-0402-3608; Atabey, Nese/0000-0003-4966-2980; Alici, Evren/0000-0001-5307-6648en_US
dc.descriptionWOS: A1996VG51700011en_US
dc.descriptionPubMed: 8883200en_US
dc.description.abstractStudy Design. Twenty-five formaldehyde solution-fixed, paraffin-embedded tissue blocks from vertebral biopsy specimen materials with presumptive diagnosis of tuberculous spondylitis and nonspecific vertebral osteomyelitis were studied. Objectives. To evaluate the sensitivity and specificity of polymerase chain reaction in detecting Mycobacterium tuberculosis in formaldehyde solution-fixed, paraffin-embedded tissue samples from histologically proved tuberculous spondylitis. Summary of Background Data. Diagnosis of a mycobacterial infection is a long and tedious process; because of the slow growth rate of mycobacteria on solid media, identification and antibiotic sensitivity testing can take up to 10 weeks, but the sensitivity of culture can be as low as 50%. Direct microscopy is insensitive because clinical samples may contain only few organisms. Recently, polymerase chain reaction has been applied in the rapid amplification and identification of many organisms, including mycobacteria. Methods. The DNAs were extracted from 25 paraffin-embedded tissue blocks. An insertion element IS 6110 (integrated DNA Tec. Inc., Corrallville, IA), a DNA sequence unique to Mycobacterium complex (M. tuberculosis and the subspecies Mycobacterium bovis), was amplified by polymerase chain reaction. Polymerase chain reaction results were compared with those of Mycobacterium culture, acid-fast bacilli staining, and histologic findings. Results. Polymerase chain reaction was positive in 18 cases of 19 tuberculous spondylitis. Three of the polymerase chain reaction test results were positive with concomitant negative culture and positive acid-fast bacilli staining. There were six chronic nonspecific infections, and polymerase chain reaction results were negative in five cases; in the single positive case, DNA amplification results remained positive even after three repeated tests. Conclusion. Polymerase chain reaction has a sensitivity of 94.7%, specificity of 83.3%, positive predictive value of 94.7%, and a negative predictive value of 83.3%. Accuracy was calculated as 92%.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/00007632-199609010-00011en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectinfectionen_US
dc.subjectpolymerase chain reactionen_US
dc.subjectspineen_US
dc.subjecttuberculosisen_US
dc.titleDetection of Mycobacterium tuberculosis in formaldehyde solution-fixed, paraffin-embedded tissue by polymerase chain reaction in Pott's diseaseen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume21en_US
dc.identifier.issue17en_US
dc.identifier.startpage1991en_US
dc.identifier.endpage1995en_US
dc.relation.journalSpineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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