Diagnosis of Helicobacter pylori gastritis in children using the 13C urea breath test
Related Experiment Video
Updated: Aug 13, 2026

Quantitative Polymerase Chain Reaction (qPCR)-Based Rapid Diagnosis of Helicobacter pylori Infection and Antibiotic Resistance
Published on: July 28, 2023
M Eltumi1, M J Brueton, N Francis
1Academic Department of Child Health, Imperial College School of Medicine, Chelsea and Westminster Hospital, London, United Kingdom.
Insights
The 13C urea breath test (13C-UBT) accurately diagnoses Helicobacter pylori infection in children with recurrent abdominal pain. This noninvasive test shows high sensitivity and specificity, aiding clinical decisions.
Area of Science:
- Pediatric Gastroenterology
- Infectious Diseases
- Diagnostic Medicine
Background:
- Recurrent abdominal pain in children often presents diagnostic challenges.
- Clinical recognition of Helicobacter pylori gastritis is difficult in pediatric patients.
- Endoscopy is invasive and reserved for specific indications.
Purpose of the Study:
- To evaluate the diagnostic value of a simplified 13C urea breath test (13C-UBT) in children with recurrent abdominal pain.
- To compare the accuracy of 13C-UBT with histology, urease test, and serology for H. pylori detection.
- To assess the reliability of 13C-UBT as a noninvasive diagnostic tool.
Main Methods:
- Prospective study of 50 children with recurrent abdominal pain meeting endoscopy criteria.
- Gastric antral biopsies analyzed histologically and by quick urease test.
- Comparison of histological results with H. pylori serology and 13C-UBT.
Main Results:
- 32 patients had gastritis; 19 had H. pylori gastritis confirmed histologically.
- 17 of 19 patients with H. pylori gastritis tested positive via 13C-UBT.
- 13C-UBT demonstrated 89% sensitivity and 90% specificity versus histology.
- 13C-UBT showed higher specificity than H. pylori serology.
Conclusions:
- The simplified 13C-UBT is a reliable, noninvasive method for diagnosing H. pylori infection in children.
- 13C-UBT offers a valuable alternative to invasive procedures for H. pylori diagnosis in this population.
- The test aids in managing pediatric patients with recurrent abdominal pain potentially linked to H. pylori gastritis.
Abstract:
The clinical recognition of Helicobacter pylori gastritis in children with recurrent abdominal pain is difficult. We assessed the value of a simplified 13C urea breath test (13C-UBT) in a selected group of children with nocturnal waking and disruptive recurrent abdominal pain who fulfilled criteria for endoscopy. Gastric antral biopsies were examined histologically and by the quick urease test and were compared with H. pylori serology and the 13C-UBT in a prospective study of 50 children referred to a tertiary center. Thirty-two patients had gastritis and of these, 19 had histologically proven H. pylori gastritis. Seventeen of these 19 patients had a positive 13C-UBT. The sensitivity and specificity of the 13C-UBT compared with the histologic diagnosis of H. pylori was 89 and 90% respectively. The 13C-UBT was more specific than the H. pylori serology. The 13C-UBT using two breath collections is a reliable and noninvasive diagnostic test for H. pylori infection in children.
More Related Videos
04:56Detection of Helicobacter pylori Infection and Antibiotic Resistance via Stool Quantitative Polymerase Chain Reaction Analysis
Published on: May 16, 2025
03:33Rapid Detection of Fecal Antigen of Helicobacter pylori Infection Based on Double Antibody Sandwich Detection Technology
Published on: May 23, 2025
Related Concept Videos
Treating Helicobacter pylori in Peptic Ulcers: Antimicrobial Therapy
Peptic Ulcer Disease III: Clinical Manifestations and Diagnostic Studies
Few clinical manifestations differentiate gastric ulcers from duodenal ulcers. Distinctions in the location, timing, and pain relief are crucial for healthcare providers in differentiating between gastric and duodenal ulcers during clinical assessments.
Serum Laboratory Studies, Stool Test, Breath Test
Peptic Ulcer
Gastritis II: Pathophysiology
Peptic Ulcer Disease II: Pathophysiology