Fluorescein diacetate and rapid molecular testing for the early identification of rifampicin resistance in Mali
0303 health sciences
Sputum
Mycobacterium tuberculosis
Fluoresceins
Mali
Sensitivity and Specificity
3. Good health
03 medical and health sciences
Molecular Diagnostic Techniques
Drug Resistance, Bacterial
Tuberculosis, Multidrug-Resistant
Humans
Human medicine
Rifampin
DOI:
10.5588/ijtld.19.0698
Publication Date:
2020-09-11T04:47:38Z
AUTHORS (28)
ABSTRACT
BACKGROUND: Non-conversion on auramine smear microscopy indicates a lack of treatment response, possibly associated with initial rifampicin-resistant tuberculosis (RR-TB). However, dead bacteria still stain positive and may be detected. Fluorescein diacetate (FDA) shows live mycobacteria only. Therefore, we studied the potential 2-month (2M) FDA for identification RR-TB. METHODS: Between 2015 2018, enrolled new smear-positive pulmonary TB patients from five local centres in Bamako, Mali. After baseline screening, sputum samples were collected at 1M, 2M, 5M 18M. We used rpo B sequencing to identify RESULTS: Of 1359 enrolled, 1019 (75%) had results. Twenty-six (2.6%, 95%CI: 1.7–3.7) mutations conferring rifampicin resistance. Most frequent located codons Asp435Val (42.4%) Ser450Leu (34.7%). Among RR-TB, 72.2% FDA-negative 2M ( P = 0.2). The negative predictive value culture-based failure was respectively 20.0% 94.7%. CONCLUSION: did not majority RR-TB or failure. As full spectrum identified using Xpert, our data support its rapid universal implementation
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