Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Dec 9;13(12):1198.
doi: 10.3390/antibiotics13121198.

BioFire® Joint Infection Panel for Samples Other than Synovial Fluid

Affiliations

BioFire® Joint Infection Panel for Samples Other than Synovial Fluid

Nicola Benvenuto et al. Antibiotics (Basel). .

Abstract

Objectives: The early identification of infection-causing microorganisms through multiplex PCR panels enables prompt and targeted antibiotic therapy. This study aimed to assess the performance of the BioFire® Joint Infection Panel (BF-JIP) in analysing non-synovial fluid samples. Methods: We conducted a retrospective cohort study at Trieste University Hospital, Italy, on hospitalised adults with non-synovial fluid samples tested by both BF-JIP and traditional culture methods (November 2022-April 2024). Results: We evaluated 48 samples from 45 patients, including 24 abscess drainage fluids and 10 tissue samples. The BF-JIP showed high concordance (85.4%) and enhanced detection (4.3%) compared to culture methods. The BF-JIP excelled in cerebrospinal fluid (CSF) (100% accuracy and concordance) and in abscess drainage fluid (accuracy: 95.8%; concordance: 91.7%) identification and maintained high performance rates in patients under antibiotics. Conclusions: These findings suggest that BF-JIP is a valuable tool for accurate pathogen detection in various clinical samples, offering the additional advantage of being a rapid method.

Keywords: BioFire® Joint Infection Panel; culture-based diagnosis; diagnosis; diagnostic microbiology; multiplex PCR panels.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Figure 1
Figure 1
BF-JIP results.

References

    1. Muzzi M., Viaggi B., Fabbri S., Bechi L., Scirè-Calabrisotto C., Villa G., Romagnoli S. The Impact of Fast Microbiology in Intensive Care Units in the Era of Antibiotic Resistance: An Observational Retrospective Study. Curr. Microbiol. 2022;31:79. doi: 10.1007/s00284-022-02773-0. - DOI - PubMed
    1. Botan A., Campisciano G., Zerbato V., Di Bella S., Simonetti O., Busetti M., Toc D.A., Luzzati R., Comar M. Performance of 16S rRNA Gene Next-Generation Sequencing and the Culture Method in the Detection of Bacteria in Clinical Specimens. Diagnostics. 2024;14:1318. doi: 10.3390/diagnostics14131318. - DOI - PMC - PubMed
    1. Lagier J.-C., Edouard S., Pagnier I., Mediannikov O., Drancourt M., Raoult D. Current and Past Strategies for Bacterial Culture in Clinical Microbiology. Clin. Microbiol. Rev. 2015;28:208–236. doi: 10.1128/CMR.00110-14. - DOI - PMC - PubMed
    1. Miller J.M., Binnicker M.J., Campbell S., Carroll K.C., Chapin K.C., Gonzalez M.D., Harrington A., Jerris R.C., Kehl S.C., Leal S.M., et al. Guide to Utilization of the Microbiology Laboratory for Diagnosis of Infectious Diseases: 2024 Update by the Infectious Diseases Society of America (IDSA) and the American Society for Microbiology (ASM) Clin. Infect. Dis. 2024;67:e1–e94. doi: 10.1093/cid/ciy381. - DOI - PMC - PubMed
    1. Hawkins S.F.C., Guest P.C. Methods in Molecular Biology. Volume 1546. Springer; Berlin/Heidelberg, Germany: 2017. Multiplex Analyses Using Real-Time Quantitative PCR. - DOI - PubMed

LinkOut - more resources