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Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area

BACKGROUND: Diagnosis of Mycobacterium tuberculosis (MTB) infection can be confirmed by Xpert assays within hours. However, when sample size does not allow performing both culture and Xpert, or if Xpert is negative, then formal diagnosis of MTB relies on culture and time to detection of growth (TDG)...

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Autores principales: Vongthilath-Moeung, Rechana, Poncet, Antoine, Renzi, Gesuele, Schrenzel, Jacques, Janssens, Jean-Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418320/
https://www.ncbi.nlm.nih.gov/pubmed/34490143
http://dx.doi.org/10.3389/fcimb.2021.704169
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author Vongthilath-Moeung, Rechana
Poncet, Antoine
Renzi, Gesuele
Schrenzel, Jacques
Janssens, Jean-Paul
author_facet Vongthilath-Moeung, Rechana
Poncet, Antoine
Renzi, Gesuele
Schrenzel, Jacques
Janssens, Jean-Paul
author_sort Vongthilath-Moeung, Rechana
collection PubMed
description BACKGROUND: Diagnosis of Mycobacterium tuberculosis (MTB) infection can be confirmed by Xpert assays within hours. However, when sample size does not allow performing both culture and Xpert, or if Xpert is negative, then formal diagnosis of MTB relies on culture and time to detection of growth (TDG) becomes critical for clinical management. OBJECTIVES: To determine TDG in Xpert negative samples, or in samples in which Xpert could not be performed, in a low-incidence area for MTB. METHODS: Retrospective analysis (2015-2020) of a database including all cultures for mycobacteria in a University Hospital covering approximately 500’000 inhabitants. Analysis was restricted to culture positive (C+) samples for MTB for which 1/Xpert was negative or could not be performed because of limited sample volume, and 2/collected from subjects treated less than 24 hours. TDG was analyzed according to microscopy, origin of sample (pulmonary or not) and presence of cavitation. RESULTS: Among 837 C+ samples for MTB, 236 samples (80% of respiratory origin) from 147 patients fulfilled study criteria; 78 samples (49 patients, 33%) were acid-fast bacilli (AFB) positive. Median (IQR) TDG was 25 (17; 40) days for all samples. TDG exceeded 28 days in 43% of samples and was significantly shorter in AFB+ vs AFB- samples, and samples from cavitary vs non cavitary or extra-thoracic disease. CONCLUSIONS: In Xpert negative samples, or samples for which Xpert could not be performed, TDG exceeded 4 weeks in 43% of samples. AFB+ and samples from cavitary lung disease had a significantly shorter TDG.
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spelling pubmed-84183202021-09-05 Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area Vongthilath-Moeung, Rechana Poncet, Antoine Renzi, Gesuele Schrenzel, Jacques Janssens, Jean-Paul Front Cell Infect Microbiol Cellular and Infection Microbiology BACKGROUND: Diagnosis of Mycobacterium tuberculosis (MTB) infection can be confirmed by Xpert assays within hours. However, when sample size does not allow performing both culture and Xpert, or if Xpert is negative, then formal diagnosis of MTB relies on culture and time to detection of growth (TDG) becomes critical for clinical management. OBJECTIVES: To determine TDG in Xpert negative samples, or in samples in which Xpert could not be performed, in a low-incidence area for MTB. METHODS: Retrospective analysis (2015-2020) of a database including all cultures for mycobacteria in a University Hospital covering approximately 500’000 inhabitants. Analysis was restricted to culture positive (C+) samples for MTB for which 1/Xpert was negative or could not be performed because of limited sample volume, and 2/collected from subjects treated less than 24 hours. TDG was analyzed according to microscopy, origin of sample (pulmonary or not) and presence of cavitation. RESULTS: Among 837 C+ samples for MTB, 236 samples (80% of respiratory origin) from 147 patients fulfilled study criteria; 78 samples (49 patients, 33%) were acid-fast bacilli (AFB) positive. Median (IQR) TDG was 25 (17; 40) days for all samples. TDG exceeded 28 days in 43% of samples and was significantly shorter in AFB+ vs AFB- samples, and samples from cavitary vs non cavitary or extra-thoracic disease. CONCLUSIONS: In Xpert negative samples, or samples for which Xpert could not be performed, TDG exceeded 4 weeks in 43% of samples. AFB+ and samples from cavitary lung disease had a significantly shorter TDG. Frontiers Media S.A. 2021-08-19 /pmc/articles/PMC8418320/ /pubmed/34490143 http://dx.doi.org/10.3389/fcimb.2021.704169 Text en Copyright © 2021 Vongthilath-Moeung, Poncet, Renzi, Schrenzel and Janssens https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Vongthilath-Moeung, Rechana
Poncet, Antoine
Renzi, Gesuele
Schrenzel, Jacques
Janssens, Jean-Paul
Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area
title Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area
title_full Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area
title_fullStr Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area
title_full_unstemmed Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area
title_short Time to Detection of Growth for Mycobacterium tuberculosis in a Low Incidence Area
title_sort time to detection of growth for mycobacterium tuberculosis in a low incidence area
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418320/
https://www.ncbi.nlm.nih.gov/pubmed/34490143
http://dx.doi.org/10.3389/fcimb.2021.704169
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