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ABSTRACT: Objectives
We determined the performance of a sensor array (an electronic nose) made of 8 metalloporphyrins coated quartz microbalances sensors for the diagnosis and prognosis of pulmonary tuberculosis (TB) using exhaled breath samples.Methods
TB cases and healthy controls were prospectively enrolled. Signals from volatile organic compounds (VOCs) in breath samples were measured at days 0, 2, 7, 14, and 30 of TB therapy and correlated with clinical and microbiological measurements.Results
Fifty one pulmonary TB cases and 20 healthy HIV-uninfected controls were enrolled in the study. 31 (61%) of the 51 pulmonary TB cases were coinfected with HIV. At day 0 (before TB treatment initiation) the sensitivity of our device was estimated at 94.1% (95% confidence interval [CI], 83.8-98.8%) and specificity was 90.0% (95% CI, 68.3-98.8%) for distinguishing TB cases from controls. Time-dependent changes in the breath signals were identified as time on TB treatment progressed. Time-dependent signal changes were more pronounced among HIV-uninfected patients.Conclusion
The identification of VOCs' signals in breath samples using a sensor array achieved high sensitivity and specificity for the diagnosis of TB and allowed following signal changes during TB treatment.
SUBMITTER: Zetola NM
PROVIDER: S-EPMC5337142 | biostudies-literature | 2017 Apr
REPOSITORIES: biostudies-literature
Zetola Nicola M NM Modongo Chawangwa C Matsiri Ogopotse O Tamuhla Tsaone T Mbongwe Bontle B Matlhagela Keikantse K Sepako Enoch E Catini Alexandro A Sirugo Giorgio G Martinelli Eugenio E Paolesse Roberto R Di Natale Corrado C
The Journal of infection 20161222 4
<h4>Objectives</h4>We determined the performance of a sensor array (an electronic nose) made of 8 metalloporphyrins coated quartz microbalances sensors for the diagnosis and prognosis of pulmonary tuberculosis (TB) using exhaled breath samples.<h4>Methods</h4>TB cases and healthy controls were prospectively enrolled. Signals from volatile organic compounds (VOCs) in breath samples were measured at days 0, 2, 7, 14, and 30 of TB therapy and correlated with clinical and microbiological measurement ...[more]