Operational Usability Evaluation of the LIAISON® QuantiFERON®-TB Gold Plus Solution in a High Volume Laboratory Setting
- PMID: 33180418
- DOI: 10.7754/Clin.Lab.2020.200338
Operational Usability Evaluation of the LIAISON® QuantiFERON®-TB Gold Plus Solution in a High Volume Laboratory Setting
Abstract
Background: Screening for latent tuberculosis infection (LTBI) using interferon gamma release assays has become commonplace for a variety of reasons. Given the high test volume, automated platforms are highly desired.
Methods: To this end, we performed an operational usability study using a newly FDA-approved, fully automated, random-access platform.
Results & conclusions: Our results showed that this platform can save time and labor and will be a potential useful addition to streamline LTBI screening. Studies to verify performance characteristics are warranted.
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