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.

Abstract

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.