An assessment of nucleic acid amplification testing for active mycobacterial infection



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Figure 13 LR scattergram for diagnosis of MTB infection by AFB plus NAAT compared with culture in studies using either in-house NAAT or commercial Xpert NAAT

AFB microscopy plus NAAT was most effective at confirming and excluding the presence of culture-positive disease in sputum specimens but could only confidently exclude culture-positive disease in non-sputum specimens (Figure 13B and C). When studies using either an in-house NAAT or the commercial NAAT in combination with AFB were analysed separately, the summary LR+ and LR– estimates for the AFB plus commercial NAAT were more effective at confirming the presence of culture-positive disease than AFB plus in-house NAAT for all specimen types. Furthermore, in non-sputum specimens a positive AFB or in-house NAAT result did not provide any useful information, most likely due to the 14% false-positive rate in this population. A negative AFB and commercial NAAT result was only able to confidently exclude the presence of culture-positive disease in non-sputum specimens.

The SROC curve shows no threshold effect when AFB microscopy is combined with either in-house NAAT or commercial NAAT (Figure 14). The SROC curves also show that when AFB microscopy plus NAAT was conducted in countries with a high incidence of TB, the results were less sensitive in sputum specimens and less specific in non-sputum specimens than when conducted in countries with an intermediate or low incidence of TB. The area under the curve (AUC) for AFB microscopy plus NAAT (0.97; 95%CI 0.95, 0.98) indicated that AFB plus NAAT performs well in predicting culture positivity (AUC > 0.9).



SROC curve for all studies investigating the sensitivity and specificity of AFB plus NAAT versus culture in the diagnosis of TB for all studies based on NAAT methodology (A), and for sputum (B) and non-sputum (C) specimens based on incidence of TB



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