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African Journal of Laboratory Medicine
On-line version ISSN 2225-2010
Print version ISSN 2225-2002
Abstract
MOLAUDZI, Mulalo and MOLEPO, Julitha. The use of real-time polymerase chain reaction and an adenosine deaminase assay for diagnosing pleural tuberculosis. Afr. J. Lab. Med. [online]. 2019, vol.8, n.1, pp.1-5. ISSN 2225-2010. http://dx.doi.org/10.4102/ajlm.v8i1.731.
BACKGROUND: The diagnosis of pleural tuberculosis remains a challenge, because the most widely used conventional diagnostic tools are unable to rapidly detect Mycobacterium tuberculosis in pleural fluid with sufficient sensitivity. OBJECTIVES: The aim of this study was to evaluate the usefulness of an adenosine deaminase assay and real-time polymerase chain reaction (qPCR) in diagnosing pleural tuberculosis. METHODS: One hundred and five consecutive pleural fluid specimens collected between August 2008 and March 2009 were assessed. Among the 105 specimens, 50 (48%) were unconfirmed tuberculosis cases, 21 (20%) were confirmed tuberculosis cases and 34 (32%) were non-tuberculosis cases (controls). Real-time PCR was performed using the Light Cycler Mycobacterium detection kit according to the manufacturer's instructions (Roche Diagnostics). An adenosine deaminase assay was carried out using a commercial colorimetric assay kit as a user-defined method on a Beckman DxC 600 Synchron analyser. RESULTS: The sensitivity of the qPCR was 67% and specificity was 100%. The sensitivity of the adenosine deaminase assay was 80% and specificity was 94%. CONCLUSION: The findings show that the adenosine deaminase assay had higher sensitivity than qPCR. Real-time PCR had 100% specificity, thus a combination of the two methods may be useful for the diagnosis of pleural tuberculosis.
Keywords : Pleural tuberculosis; adenosine deaminase assay; qPCR; real-time polymerase chain reaction.