Abstract

The efficacy of Quantiferon-TB gold test (QFT-GIT) remains to be documented in pediatric population. Tuberculin skin test (TST) is a conventional test available for the diagnosis of latent tuberculosis infection (LTBI). We aimed to investigate the concordance between QFT-GIT and TST in children with and without tuberculosis infection. Ninety-seven patients, aged 3 months–14 years, admitted to pediatric outpatient clinics of Dr. Sadi Konuk Training Hospital Bakırköy, Turkey between March 2008 and April 2009 were recruited. Demographic features, TST results, history of exposure to active tuberculosis (TB), chest X-ray findings, clinical history, presence of Bacillus Calmette Guerin (BCG) vaccination scar were recorded. Patients were categorized into four groups namely, active TB, LTBI, no TB and healthy. It was found that BCG scar positivity did not influence QFT-GIT results. There was a statistically significant agreement between QFT-GIT and TST results (κ = 0.486; p < 0.01). In patients ≥5 years of age, TST positivity and QFT positivity had a significant relationship (p < 0.01). In all patient groups, sensitivity and specificity was 65.85 % and 82.14 %, respectively. In active TB group, TST and QFT-GIT results demonstrated significant agreement ratio of 40.8 % (κ = 0.364; p < 0.01). Sensitivity and specificity was 100 % and 30 %, respectively. Utilization of QFT-GIT in the diagnosis of LTBI reduces false-positive results and prevents unnecessary treatment with INH and its adverse effects.

Highlights

  • Number of cases with tuberculosis infection increased at the beginning of 21st century

  • Identification of Early Secreted Antigenic Target6 kD protein (ESAT-6) and Culture Filtrate Protein-10 kD (CFT-10) has been a promising development in the diagnosis of TB. These antigenic proteins are encoded within the region of difference 1 (RD 1) of the M. tuberculosis genome

  • We aimed to investigate the agreement between QFT-GIT and TST results in children with and without tuberculosis infection

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Summary

Introduction

Number of cases with tuberculosis infection increased at the beginning of 21st century. It is documented that over 1 million new cases of tuberculosis is diagnosed in children younger than 15 years of age annually and active disease accounts. TB is diagnosed by combining patient’s history of exposure to active disease, tuberculin skin test (TST) results, clinical and radiological findings. Microbiologic tests yield positive results in only 30–40 % of cases [2]. Identification of Early Secreted Antigenic Target kD protein (ESAT-6) and Culture Filtrate Protein-10 kD (CFT-10) has been a promising development in the diagnosis of TB. These antigenic proteins are encoded within the region of difference 1 (RD 1) of the M. tuberculosis genome. This article is published with open access at Springerlink.com

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