Performance of the BioFire FilmArray Pneumonia Panel Plus Compared to Standard Microbiology in Lung Transplant Donor
Andrea Lombardi1,2, Giulia Renisi1, Lorenzo Rosso2,3
1SC Malattie Infettive, Fondazione IRCCS Ospedale Maggiore Policlinico, Milan, Lombardy, Italy.
Background:
Lung transplantation (LuTx) is hampered by infectious risks. Perioperative antibiotic prophylaxis (PAP) is widely used; however, real-time adjustment is hindered by the timing of standard microbiology. Syndromic molecular panels offer rapid results, yet their integration into PAP strategies remains unclear.
Methods:
We conducted a prospective cohort study comparing the BioFire FilmArray Pneumonia Panel Plus (PNplus) with standard of care (SOC) on bronchoalveolar lavage (BAL) samples obtained from donors at procurement and from recipients 72 h after LuTx. Concordance between PNplus and SOC was assessed for bacterial species and antimicrobial resistance genes.
Results:
Fifty-three donor-recipient pairs were analyzed. In donor BAL, PNplus identified at least one pathogen in 67.9% (36/53) of cases versus 63.5% (33/53) by SOC, with a markedly shorter time to result (221 min vs. 5.3 days). Concordance between PNplus and SOC for bacterial species was substantial (Cohen's κ = 0.654), particularly for Staphylococcus aureus (Cohen's κ = 0.689), Streptococcus pneumoniae (Cohen's κ = 0.658), and Pseudomonas aeruginosa (Cohen's κ = 0.731). In recipient BAL, PNplus detected pathogens in 61.5% (32/53) compared to 47.2% (25/53) with SOC, but overall concordance was only moderate (κ = 0.365). Resistance gene concordance was minimal, with PNplus often identifying additional determinants not confirmed by SOC. Viruses were detected exclusively by PNplus, while fungi were identified only by SOC.
Conclusion:
PNplus provides rapid, clinically relevant pathogen detection in LuTx, showing substantial agreement with SOC in donor samples and offering potential to support PAP adjustment. In early post-transplant recipient BAL, interpretation requires caution, and SOC remains indispensable, particularly for detecting fungi and confirming phenotypic resistance.
Insights
Rapid molecular panels like BioFire FilmArray Pneumonia Panel Plus (PNplus) show promise for guiding perioperative antibiotic prophylaxis (PAP) in lung transplantation (LuTx). While effective in donor samples, caution is advised for recipient samples due to moderate concordance with standard methods.
Area of Science:
- Infectious disease diagnostics
- Transplant medicine
- Molecular microbiology
Background:
- Lung transplantation (LuTx) faces significant infectious risks.
- Perioperative antibiotic prophylaxis (PAP) is standard but lacks real-time pathogen data.
- Molecular panels offer rapid results, but their role in PAP adjustment is unclear.
Purpose of the Study:
- To evaluate the BioFire FilmArray Pneumonia Panel Plus (PNplus) for pathogen detection in lung transplant recipients.
- To compare PNplus performance against standard of care (SOC) microbiology.
- To assess the utility of PNplus for guiding perioperative antibiotic prophylaxis (PAP).
Main Methods:
- Prospective cohort study comparing PNplus and SOC on bronchoalveolar lavage (BAL) samples.
- Samples collected from donors at procurement and recipients 72 hours post-LuTx.
- Assessed concordance for bacterial species and antimicrobial resistance genes.
Main Results:
- PNplus detected pathogens faster than SOC in donor BAL (221 min vs. 5.3 days) with substantial species agreement (κ=0.654).
- In recipient BAL, PNplus showed moderate concordance (κ=0.365) with SOC, detecting more pathogens but with lower agreement.
- PNplus exclusively detected viruses, while SOC exclusively detected fungi; resistance gene concordance was minimal.
Conclusions:
- PNplus offers rapid pathogen detection in lung transplant donors, potentially aiding PAP adjustment.
- Early post-transplant recipient BAL analysis with PNplus requires caution; SOC is essential for fungal detection and resistance confirmation.
- Molecular diagnostics show promise but need further integration and validation in transplant infectious disease management.
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