The rapid molecular test Xpert MTB/RIF ultra: towards improved tuberculosis diagnosis and rifampicin resistance detection  O. Opota, J. Mazza-Stalder,

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The rapid molecular test Xpert MTB/RIF ultra: towards improved tuberculosis diagnosis and rifampicin resistance detection  O. Opota, J. Mazza-Stalder, G. Greub, K. Jaton  Clinical Microbiology and Infection  DOI: 10.1016/j.cmi.2019.03.021 Copyright © 2019 The Authors Terms and Conditions

Fig. 1 Improved sensitivity of Xpert MTB/RIF Ultra as compared to Xpert MTB/RIF especially for paucibacillary samples. The data represent the difference in sensitivity (delta = Ultra – Xpert) for different patients and different clinical conditions on respiratory specimens with the exception of tuberculous meningitis which corresponds to CSF. Each dot represents data retrieved from publications comparing the performances of both tests used in the same study. The graph represents the Median with 95% confidence interval. Clinical Microbiology and Infection DOI: (10.1016/j.cmi.2019.03.021) Copyright © 2019 The Authors Terms and Conditions

Fig. 2 Performance of Xpert MTB/RIF and Xpert MTB/RIF Ultra. Representation of the performance of some microbial diagnostic tests for tuberculosis. Clinical Microbiology and Infection DOI: (10.1016/j.cmi.2019.03.021) Copyright © 2019 The Authors Terms and Conditions

Fig. 3 Correlation between DNA burden and smear microscopy results. The semi-quantitative results of Xpert and Ultra high, medium, low, very low (trace for Ultra only) and negative were found to positively correlate with acid-fast bacilli detection (smear microscopy) and could be used to evaluate patient's transmission potential and guide isolation decision in smear-independent algorithms. Patients with negative Xpert could be considered poorly infectious, whereas patients with positive results high and medium should be considered as the most infectious; patients with Xpert low, very low or trace should be considered as potentially infectious and other clinical information should be considered to guide isolation measures. This algorithm may apply for any quantitative or semi-quantitative nucleic acid amplification test. Clinical Microbiology and Infection DOI: (10.1016/j.cmi.2019.03.021) Copyright © 2019 The Authors Terms and Conditions