Performance of the extended use of the FilmArray® BCID panel kit for bronchoalveolar lavage analysis

Maxime Sansot1, Eugénie Fradin2, Rachel Chenouard1

  • 1Laboratoire de Bactériologie, CHU Angers, 4 rue Larrey, 49933, Angers cedex, France.

Molecular Biology Reports
|February 25, 2019
PubMed

Insights

The FilmArray® BCID panel shows good performance in detecting bacteria causing ventilator-associated pneumonia (VAP) from bronchoalveolar lavage fluid. This molecular test aids in early antimicrobial therapy adaptation for improved patient outcomes.

Area of Science:

  • Clinical Microbiology
  • Infectious Diseases
  • Critical Care Medicine

Background:

  • Ventilator-associated pneumonia (VAP) significantly increases patient morbidity, mortality, and hospital stays.
  • Early and accurate diagnosis of VAP is critical for effective antimicrobial therapy and improved clinical outcomes.
  • Multiplex PCR kits offer potential for rapid pathogen identification.

Purpose of the Study:

  • To evaluate the diagnostic performance of the FilmArray® BCID panel for detecting bacterial pathogens in bronchoalveolar lavage (BAL) fluid from VAP patients.
  • To compare the FilmArray® BCID panel results against conventional culture-based methods.

Main Methods:

  • A prospective study involving 50 BAL samples from intensive care unit patients.
  • Samples were analyzed using the FilmArray® BCID panel and standard culture methods.
  • Performance metrics including sensitivity and specificity were calculated.

Main Results:

  • The FilmArray® BCID panel demonstrated high specificity (98.9%) for VAP detection in BAL fluid.
  • Sensitivity varied: 67.2% overall, 88.6% for cultures >10^4 CFU/mL, and 94.7% for positive direct examination.
  • The panel provided reliable results early, especially with positive direct examination findings.

Conclusions:

  • The FilmArray® BCID panel exhibits good performance for analyzing BAL fluid in VAP diagnosis.
  • Early results from the panel, particularly when direct examination is positive, facilitate timely antimicrobial treatment adjustments.
  • This molecular approach supports rapid adaptation of therapy, potentially improving VAP patient management.

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