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Updated: Jan 28, 2026

Bronchoalveolar Lavage BAL for Research; Obtaining Adequate Sample Yield
Published on: March 24, 2014
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.
Abstract:
Ventilator-associated pneumonia (VAP) are responsible for an increase in morbidity, mortality, and prolonged hospital stay. A multiplex PCR kit such as the FilmArray® BCID panel could allow early adaptation of antimicrobial therapy, which is crucial for clinical outcomes. The purpose of this study was to test the performances of FilmArray® BCID panel for the detection of bacteria producing VAP. We tested the FilmArray® BCID panel on 50 bronchoalveolar lavages (BALs), from patients hospitalized in two intensive care units at the Angers university hospital, compared to the conventional culture-based method. The sensitivity and the specificity of the FilmArray® BCID panel were 67.2% and 98.9% respectively. They were 88.6% and 98.3% respectively when considering BALs with a positive culture > 104 CFU/mL, and 94.7% and 99.6% respectively if considering BALs with a positive direct examination. This study underlines the good performance of the FilmArray® BCID panel for BAL fluid analysis. In case of positive direct examination, this test allows reliable results that can be obtained at an early stage, facilitating the early adaptation of antimicrobial therapy.
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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