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Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates

CONTEXT: The treatment of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB) is consistently difficult. Besides resistances, drug availability can be problematic and costs for therapy are high. AIMS: Our aim was to evaluate alternatives in treatment of MDR and XDR TB ot...

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Autores principales: Schönfeld, Nicolas, Bergmann, Thorsten, Vesenbeckh, Silvan, Mauch, Harald, Bettermann, Gudrun, Bauer, Torsten T., Rüssmann, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519013/
https://www.ncbi.nlm.nih.gov/pubmed/23243341
http://dx.doi.org/10.4103/0970-2113.102794
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author Schönfeld, Nicolas
Bergmann, Thorsten
Vesenbeckh, Silvan
Mauch, Harald
Bettermann, Gudrun
Bauer, Torsten T.
Rüssmann, Holger
author_facet Schönfeld, Nicolas
Bergmann, Thorsten
Vesenbeckh, Silvan
Mauch, Harald
Bettermann, Gudrun
Bauer, Torsten T.
Rüssmann, Holger
author_sort Schönfeld, Nicolas
collection PubMed
description CONTEXT: The treatment of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB) is consistently difficult. Besides resistances, drug availability can be problematic and costs for therapy are high. AIMS: Our aim was to evaluate alternatives in treatment of MDR and XDR TB other than using second-line drugs. MATERIALS AND METHODS: We analyzed retrospectively the minimal inhibitory concentrations (MICs) of first-line drugs for 44 multidrug–resistant Mycobacterium tuberculosis isolates determined in our institute over a period of 20 years (1990 - 2010, n = 44). Drug susceptibility testing (DST) was performed using the proportion method on Lowenstein–Jensen Medium or Middlebrook 7H10 agar. MICs were defined as the lowest drug concentration after two-fold serially diluted concentration of the drugs that inhibits growth of more than 99.0% of a bacterial proportion of the tested M. tuberculosis within 14 to 21 days of incubation at 37°C. STATISTICAL ANALYSIS USED: Summation. RESULTS: The MICs of isoniazid and ethambutol were equal or slightly above the critical concentration in most of the strains (92% and 84%, respectively), defined as “low-level resistance”. Rifampicin and streptomycin exhibited very high MICs in most of the strains (100% and 77%, respectively), indicating a “high-level resistance”. CONCLUSION: Our results indicate that isoniazid and ethambutol could still play a role in treating MDR and XDR TB patients if low-level resistance is detected. Quantitative DST seems to be promising for the recognition of residual drug activity, but has to be confirmed by clinical studies.
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spelling pubmed-35190132012-12-14 Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates Schönfeld, Nicolas Bergmann, Thorsten Vesenbeckh, Silvan Mauch, Harald Bettermann, Gudrun Bauer, Torsten T. Rüssmann, Holger Lung India Original Article CONTEXT: The treatment of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB) is consistently difficult. Besides resistances, drug availability can be problematic and costs for therapy are high. AIMS: Our aim was to evaluate alternatives in treatment of MDR and XDR TB other than using second-line drugs. MATERIALS AND METHODS: We analyzed retrospectively the minimal inhibitory concentrations (MICs) of first-line drugs for 44 multidrug–resistant Mycobacterium tuberculosis isolates determined in our institute over a period of 20 years (1990 - 2010, n = 44). Drug susceptibility testing (DST) was performed using the proportion method on Lowenstein–Jensen Medium or Middlebrook 7H10 agar. MICs were defined as the lowest drug concentration after two-fold serially diluted concentration of the drugs that inhibits growth of more than 99.0% of a bacterial proportion of the tested M. tuberculosis within 14 to 21 days of incubation at 37°C. STATISTICAL ANALYSIS USED: Summation. RESULTS: The MICs of isoniazid and ethambutol were equal or slightly above the critical concentration in most of the strains (92% and 84%, respectively), defined as “low-level resistance”. Rifampicin and streptomycin exhibited very high MICs in most of the strains (100% and 77%, respectively), indicating a “high-level resistance”. CONCLUSION: Our results indicate that isoniazid and ethambutol could still play a role in treating MDR and XDR TB patients if low-level resistance is detected. Quantitative DST seems to be promising for the recognition of residual drug activity, but has to be confirmed by clinical studies. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3519013/ /pubmed/23243341 http://dx.doi.org/10.4103/0970-2113.102794 Text en Copyright: © Lung India http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Schönfeld, Nicolas
Bergmann, Thorsten
Vesenbeckh, Silvan
Mauch, Harald
Bettermann, Gudrun
Bauer, Torsten T.
Rüssmann, Holger
Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
title Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
title_full Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
title_fullStr Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
title_full_unstemmed Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
title_short Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
title_sort minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519013/
https://www.ncbi.nlm.nih.gov/pubmed/23243341
http://dx.doi.org/10.4103/0970-2113.102794
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