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Article Synopsis
  • Drug-resistant tuberculosis (TB) poses a significant public health issue, particularly in low-income areas, where resistance rates can exceed 25%, and treatment can last 9-12 months with less favorable outcomes.
  • Conventional treatments for drug-resistant TB face challenges such as poor drug delivery to the lungs, drug interactions, and severe side effects, highlighting the need for more effective delivery methods.
  • Inhalable formulations, particularly those using repurposed drugs, present a promising strategy to improve treatment outcomes by targeting the infection directly at the site in the lungs, although research in this area is still limited.
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Article Synopsis
  • This study aimed to evaluate targeted next-generation sequencing (NGS) as a method for diagnosing drug-resistant tuberculosis by reviewing existing data on its effectiveness and prevalence in detecting mutations across different gene targets.
  • The researchers conducted a systematic review and meta-analysis of various sources for publications related to targeted NGS from 2005 to 2022, focusing on studies that utilized the technique for drug resistance prediction in tuberculosis.
  • They assessed the diagnostic accuracy of targeted NGS by analyzing sensitivity and specificity compared to traditional drug susceptibility testing methods, using a Bayesian model for comprehensive results.
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Article Synopsis
  • Whole genome sequencing (WGS) can be used to predict drug resistance in tuberculosis either through a catalog-based method that identifies specific mutations or a noncatalog approach using advanced algorithms like machine learning.
  • A systematic review analyzed 44 studies with nearly 17,000 specimens, revealing excellent test accuracy for isoniazid and rifampicin, very good accuracy for several other drugs, and good accuracy for a few more.
  • Both catalog-based and noncatalog-based methods demonstrated similar effectiveness in predicting drug susceptibility using WGS results.
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Background: Advances in drug therapy for pulmonary tuberculosis have had an extraordinary impact on the incidence of tuberculosis in the United States in the past century, which has decreased from 113/100,000 persons in 1920 to 2.2/100,000 in 2020. Modern treatments have contributed to a remarkable decrease in hospitalizations and mortality and have had a significant impact on the duration and severity of illness, quality of life, and work potential of affected persons.

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Background: The WHO End TB Strategy requires drug susceptibility testing and treatment of all people with tuberculosis, but second-line diagnostic testing with line-probe assays needs to be done in experienced laboratories with advanced infrastructure. Fewer than half of people with drug-resistant tuberculosis receive appropriate treatment. We assessed the diagnostic accuracy of the rapid Xpert MTB/XDR automated molecular assay (Cepheid, Sunnyvale, CA, USA) to overcome these limitations.

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