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Protocol describes pediatric TB diagnostic study evaluating non-sputum assays in Kenyan children

Protocol describes pediatric TB diagnostic study evaluating non-sputum assays in Kenyan children
Photo by Dmytro Vynohradov / Unsplash
Key Takeaway
Note: This is a study protocol; no diagnostic performance or outcome data are available.

This publication describes the protocol for the Pediatric Diagnostic Biomarkers for Tuberculosis (PDTBDx) study, a prospective observational cohort study. The study aims to enroll >400 children under 15 years of age presenting with TB symptoms at inpatient and outpatient clinical sites in Nairobi, Kenya. The protocol focuses on evaluating non-sputum-based TB diagnostics for both initial diagnosis and monitoring treatment response. No diagnostic accuracy data, treatment outcomes, or results of any kind are presented in this protocol paper.

The planned intervention is the evaluation of non-sputum-based TB diagnostic assays. A specific comparator is not reported. Participants are scheduled for follow-up visits at week 2, and months 1, 2, 4, 6, 12, and 24. The primary outcome is the evaluation of these diagnostics for diagnosis and treatment response monitoring in children.

Safety and tolerability data are not reported, as this is a protocol description. Key limitations inherent to this publication type include the absence of any results, efficacy data, or safety findings. The protocol states that assays evaluated may guide improved diagnostic strategies, but this is a forward-looking statement pending study completion.

Practice relevance is currently theoretical. The protocol's stated goal is to generate evidence that could inform future pediatric TB diagnostic strategies. Clinicians should recognize this as a study plan, not an evidence report, and await the publication of completed study results before considering any changes to practice.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
Tuberculosis (TB) is a significant cause of morbidity and mortality in children and adolescents, causing 172,000 deaths in 2024 in children and adolescents worldwide. Diagnostic challenges are pronounced in pediatrics, in which collecting respiratory specimens is challenging and TB is often paucibacillary, leading to delayed diagnosis and increased mortality. We describe the protocol and methodology of the Pediatric TB Diagnostic (PDTBDx) cohort, a study with the primary aim of evaluating non-sputum-based TB diagnostics for diagnosis and treatment response in children. This is a prospective observational cohort study of >400 children recruited from inpatient and outpatient clinical sites in Nairobi, Kenya. Children <15 years presenting to study clinical sites with TB symptoms will be considered for enrollment as symptomatic participants. Enrolled participants will undergo rigorous clinical assessment and longitudinal follow-up to ensure appropriate diagnostic classification by NIH consensus statement guidelines for pediatric TB. Baseline evaluation includes symptom assessment, chest x-ray, HIV testing, respiratory TB culture and GeneXpert Ultra, and urine LAM. Subsequent visits occur at week 2, months 1, 2, 4, 6,12 and 24. Blood and urine specimens will be collected at baseline and at follow-up visits for storage for evaluation of novel diagnostic assays, including exosome-based and CRISPR-based TB biomarkers. This large, prospective cohort of pediatric participants with and without TB follows a consistent and rigorous protocol for diagnosing childhood TB, in concordance with internationally recognized guidelines. Assays evaluated in PDTBDx will guide improved diagnostic strategies for pediatric TB.
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