Related Experiment Video
Updated: Jun 26, 2025

The MODS method for diagnosis of tuberculosis and multidrug resistant tuberculosis
Published on: August 11, 2008
Multidrug-resistant tuberculosis in children: A practical update on epidemiology, diagnosis, treatment and prevention
James T Gaensbauer1,2, Nabaneeta Dash3, Sanjay Verma4
1Mayo Clinic Center for Tuberculosis, Mayo Clinic, Rochester, MN, USA.
Insights
Pediatric multidrug-resistant tuberculosis (MDR-TB) diagnosis and treatment face challenges, but new rapid tests and shorter, all-oral drug regimens offer hope for better outcomes in children. Further pediatric trials are needed for optimal management.
Area of Science:
- Pediatric infectious diseases
- Mycobacteriology
- Global health
Background:
- Pediatric multidrug-resistant tuberculosis (MDR-TB) is a critical global health issue with significant diagnostic and treatment barriers.
- Less than 5% of estimated annual pediatric MDR-TB cases are microbiologically confirmed, leading to poor outcomes and increased mortality.
- Traditional MDR-TB treatment regimens are lengthy, involve multiple drugs, and often include toxic injectable agents.
Purpose of the Study:
- To review recent advances in diagnostics and treatment for pediatric MDR-TB.
- To highlight challenges in identifying, confirming, and managing MDR-TB in children.
- To discuss the potential of new drugs and regimens to improve outcomes for children with MDR-TB.
Main Methods:
- Review of current literature on pediatric MDR-TB diagnostics and therapeutics.
- Case examples illustrating management challenges and potential successes.
- Discussion of emerging rapid molecular tests and novel drug regimens.
Main Results:
- Rapid molecular tests for rifampin susceptibility are becoming available but face sample collection and paucibacillary nature challenges in children.
- New drugs like bedaquiline, delamanid, clofazimine, and linezolid enable shorter, all-oral MDR-TB treatment regimens.
- Insufficient data currently exists for short, all-oral regimens including pretomanid in young children.
Conclusions:
- Advances in diagnostics and therapeutics offer promise for improving pediatric MDR-TB management.
- There is a critical need for pediatric clinical trials to evaluate novel drugs and MDR-TB treatment regimens.
- Optimizing diagnosis and treatment is essential to reduce mortality and improve outcomes for children with MDR-TB.
Abstract:
Pediatric multidrug-resistant tuberculosis (MDR-TB) remains a significant global problem, and there are numerous barriers preventing children with MDR-TB from being identified, confirmed with microbiologic tests, and treated with a safe, practical, and effective regimen. However, several recent advances in diagnostics and treatment regimens have the promise to improve outcomes for children with MDR-TB. We introduce this review with two cases that exemplify both the challenges in management of MDR-TB in children, but also the potential to achieve a positive outcome. More than 30,000 cases of MDR-TB per year are believed to occur in children but less than 5% are confirmed microbiologically, contributing to poorer outcomes and excess mortality. Rapid molecular-based testing that provides information on rifampin susceptibility is increasingly globally available and recommended for all children suspected of TB disease--but remains limited by challenges obtaining appropriate samples and the paucibacillary nature of most pediatric TB. More complex assays allowing better characterization of drug-resistant isolates are emerging. For children diagnosed with MDR-TB, treatment regimens have traditionally been long and utilize multiple drugs associated with significant side effects, particularly injectable agents. Several new or repurposed drugs including bedaquiline, delamanid, clofazimine and linezolid now allow most treatment regimens to be shorter and all-oral. Yet data to support short, all-oral, novel regimens for young children containing pretomanid remain insufficient at present, and there is a compelling need to conduct pediatric trials of promising therapeutics and MDR-TB treatment regimens.
More Related Videos
10:04Analysis of 18FDG PET/CT Imaging as a Tool for Studying Mycobacterium tuberculosis Infection and Treatment in Non-human Primates
Published on: September 5, 2017
10:29A High-throughput Compatible Assay to Evaluate Drug Efficacy against Macrophage Passaged Mycobacterium tuberculosis
Published on: March 24, 2017
Related Concept Videos
Pulmonary Tuberculosis V
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the...
Pulmonary Tuberculosis IV
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
Pulmonary Tuberculosis I
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
Pulmonary Tuberculosis III
The first classification is based on the development of the disease, and it includes the following categories:
Pulmonary Tuberculosis II
Here is a detailed explanation of its pathophysiology:
Transmission: The process begins when a person inhales droplet nuclei containing M. tuberculosis. These are typically released into the air when an individual with pulmonary or...
Transmission-based Precautions II: Airborne and Protective Environment
Airborne precautions:
Use airborne precautions when treating patients known or suspected to have diseases that spread through the air—for example, tuberculosis or measles. These organisms are present in smaller droplets expelled by an infected person and...