AI Article Synopsis

  • There are two tests for diagnosing latent tuberculosis infection (LTBI), the Tuberculin Skin Test (TST) and Interferon Gamma Release Assays (IGRA), but their effectiveness in high TB-burden areas is still debated.
  • A study followed 1,511 household contacts of TB patients for two years to compare the two tests, finding that both methods did not significantly predict the development of active TB.
  • Despite both tests' limitations, TST is recommended for diagnosing LTBI in resource-limited settings due to cost and logistical factors.

Article Abstract

Background: There are currently two tests for diagnosing latent tuberculosis infection (LTBI); TST and IGRA. However, it is still unclear that which one of these tests performs better in high TB-burden settings.

Methods: 1511 household contacts of pulmonary TB patients were enrolled to compare the performance of TST and IGRA for LTBI. At baseline all participant underwent testing for IGRA [QuantiFERON-TB® Gold In-tube (QFT-GIT) assay] and TST [2 tuberculin unit (TU), purified protein derivative (PPD), RT23, Staten Serum Institute (SSI), Copenhagen, Denmark]. All the household contacts were followed-up for two years for incident TB cases.

Results: Active TB was diagnosed in 76 household contacts at an incidence rate of 2.14 per 1000 person-years. Both, TST [Hazard Ratio (HR): 1.14, 95% confidence interval (CI): 0.72-1.79, p = 0.57], as well as QFT-GIT assay (HR: 1.66, 95% CI: 0.97-2.84, p = 0.06) results at baseline were not significantly associated with subsequent development of active TB among household contacts of pulmonary TB patients.

Conclusion: Neither TST nor IGRA predicted subsequent development of active TB among household contacts of pulmonary TB patients during follow-up. However, keeping in view the cost, and other logistics, TST remains the most preferred method for LTBI diagnosis in resource-limited, high TB-burden settings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218498PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0169539PLOS

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