Assay Integrity of a PCR Influenza Point-of-Care Test Remains Following Artificial System Contamination
Author(s) -
Jamie E. Phillips,
Stephen McCune,
Corinne R. Fantz,
Julia Engstrom-Melnyk,
J Osiecki
Publication year - 2019
Publication title -
the journal of applied laboratory medicine
Language(s) - English
Resource type - Journals
eISSN - 2576-9456
pISSN - 2475-7241
DOI - 10.1373/jalm.2018.028639
Subject(s) - contamination , point of care testing , test (biology) , virology , medicine , environmental science , reliability engineering , microbiology and biotechnology , biology , engineering , pathology , ecology
Healthcare providers who have access to tests at the point of care (POC) are increasingly requesting the same performance from the POC test as they expect from the laboratory. With the introduction of the cobas ® Liat instrument, highly sensitive molecular diagnostic testing can be performed closer to the patient in CLIA-waived, POC settings. As more sensitive tests become available, there is concern regarding contamination of instrumentation owing to improper handling, mistakes made when processing, or environmental contamination. Recent concerns were raised when a nurse performed environmental surveillance for flu A/B by inserting a dry swab into the cobas Liat instrument and then ran it as a sample on the instrument, generating a positive result. This finding stimulated questions about the possibility of system contamination contributing to false-positive results, ultimately leading to the possibility of providing incorrect treatment to patients.
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