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Published on: April 9, 2012
Novel and optimized diagnostics for pediatric TB in endemic countries: NOD-pedFEND study protocol
Rinn Song1, Else Margreet Bijker2,3, Grace Kisitu4
1Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK. rinn.song@paediatrics.ox.ac.uk.
Insights
Accurate diagnosis of pediatric tuberculosis (TB) is crucial. This large study in young children aims to improve diagnostic tests for TB, especially using non-sputum samples, to aid treatment and public health efforts.
Area of Science:
- Global Health
- Infectious Diseases
- Pediatric Medicine
Background:
- Pediatric tuberculosis (TB) poses a significant global health challenge.
- Accurate diagnosis is a major barrier to effective treatment in children.
- Current diagnostic studies are limited by small sample sizes and few confirmed cases.
Purpose of the Study:
- To evaluate existing and novel diagnostic assays for pediatric tuberculosis.
- To enroll one of the largest cohorts of children at high risk for TB.
- To improve diagnostic capabilities, particularly in children under five years of age.
Main Methods:
- Prospective observational cohort study in Uganda and Peru.
- Enrollment of children under five with suspected TB symptoms.
- Comprehensive baseline workup including microbiological tests, chest X-ray, and sample collection for investigational tests.
Main Results:
- This section is not applicable for the protocol description.
- This section is not applicable for the protocol description.
- This section is not applicable for the protocol description.
Conclusions:
- This large cohort study will significantly contribute to evaluating new pediatric TB diagnostics.
- The established biorepository will facilitate assessment of novel tests.
- Findings will aid in identifying and treating children with tuberculosis more effectively.
Background:
Pediatric tuberculosis is a major global public health challenge, with reliable diagnosis being a main obstacle to identifying and treating affected children. New and improved diagnostics, ideally on non-sputum samples, are urgently required, especially in the most vulnerable group of children under five years of age. Studies to date have been limited by small sample sizes and few bacteriologically-confirmed cases. Here, we describe the study protocol of the NIH-funded NOD-pedFEND study, which will be one of the largest diagnostic studies to date of children at greatest risk of tuberculosis.
Methods:
In this prospective observational cohort study, we aim to evaluate existing and novel diagnostic assays, including pathogen- and host-based tests and combinations of tests. A consecutive cohort of children under five years of age with signs and symptoms of tuberculosis is enrolled in Uganda and Peru. All children undergo an extensive baseline workup with signs- and symptoms recording, microbiological reference tests, chest X-ray and tuberculin skin test for rigorous classification according to internationally recognized microbiological, composite reference and strict standards. An array of samples is collected for investigational tests. Follow-up visits are conducted at 2 weeks, 2 months and 6 months. A small cohort of healthy controls is enrolled to evaluate the specificity of selected diagnostics. The study has been approved by the relevant institutional review boards.
Discussion:
With this large cohort study of children under five years of age, we aim to make an important contribution to the evaluation of new diagnostics for pediatric tuberculosis. By establishing a comprehensive biorepository, the study will also enable the assessment of novel tests as they become available during and after the study.
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