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Clinical significance of negative BioFire® pneumonia panel in ICU: Diagnosis, management, and outcomes
Thibault Nardy1, Emilie Rondinaud2, Julien Dessajan1
1Medical and Infectious Diseases Intensive Care Unit, Hospital Bichat-Claude Bernard, Université Paris Cité, AP-HP, Paris, France.
Objectives:
This study assessed the clinical significance of negative BioFire® FilmArray® Pneumonia Panel (FA-PP) results in ICU patients with suspected hospital-acquired (HAP) or ventilator-associated pneumonia (VAP), evaluating its impact on diagnosis, antimicrobial management, and outcomes, and identifying factors associated with false-negative results.
Methods:
A retrospective single-center study (April 2021 to July 2023) included 190 critically ill patients with negative FA-PP results on deep respiratory samples. Patients with microbiologically confirmed HAP/VAP were compared to those without.
Results:
Among 190 patients, 69 (36%) had culture-confirmed HAP/VAP. Gram-negative bacilli (GNB) on Gram stain independently predicted true infection (OR = 3.08, 95% CI [1.47-6.45], P = 0.003). The false-negative rate for FA-PP-detectable bacteria was 12% (31/251), mainly Klebsiella pneumoniae and Pseudomonas aeruginosa. Nontargeted GNBs accounted for 27% (19/69) of confirmed cases. Recent broad-spectrum antibiotic exposure (≤3 months) reduced confirmed infection likelihood (OR = 0.28, 95% CI [0.13-0.6], P < 0.001). No inappropriate antibiotic de-escalation occurred, but 6% (7/121) of noninfected patients had antibiotics withdrawn based solely on FA-PP negativity.
Conclusions:
Negative FA-PP results do not exclude HAP/VAP, especially with nontargeted GNBs or recent antibiotic exposure. Gram stain remains a valuable complementary tool. Integrated diagnostic approaches are essential for optimal antimicrobial stewardship in ICU settings.
Insights
Negative results from the BioFire® FilmArray® Pneumonia Panel (FA-PP) do not rule out hospital-acquired (HAP) or ventilator-associated pneumonia (VAP) in ICU patients. Gram stain is crucial for accurate diagnosis and antimicrobial stewardship.
Area of Science:
- Critical Care Medicine
- Clinical Microbiology
- Infectious Diseases
Background:
- Hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) are significant challenges in intensive care units (ICUs).
- The BioFire® FilmArray® Pneumonia Panel (FA-PP) is a multiplex PCR test used for rapid pathogen detection in suspected pneumonia.
- Understanding the clinical utility of negative FA-PP results is crucial for appropriate patient management and antimicrobial stewardship.
Purpose of the Study:
- To assess the clinical significance of negative FA-PP results in ICU patients with suspected HAP/VAP.
- To evaluate the impact of negative FA-PP results on diagnosis, antimicrobial management, and patient outcomes.
- To identify factors associated with false-negative FA-PP results in this patient population.
Main Methods:
- A retrospective single-center study was conducted from April 2021 to July 2023.
- Included were 190 critically ill patients with negative FA-PP results from deep respiratory samples.
- Patients with microbiologically confirmed HAP/VAP were compared to those without confirmed infections.
Main Results:
- Of 190 patients, 36% had culture-confirmed HAP/VAP. Gram-negative bacilli (GNB) on Gram stain predicted true infection (OR=3.08).
- The FA-PP false-negative rate for detectable bacteria was 12%, primarily Klebsiella pneumoniae and Pseudomonas aeruginosa.
- Non-targeted GNBs comprised 27% of confirmed cases. Recent broad-spectrum antibiotic exposure reduced infection likelihood (OR=0.28).
Conclusions:
- Negative FA-PP results do not exclude HAP/VAP, particularly when non-targeted GNBs are involved or with prior antibiotic exposure.
- Gram stain remains a valuable complementary diagnostic tool alongside molecular testing.
- Integrated diagnostic strategies are essential for optimizing antimicrobial stewardship in ICU settings.
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