Infectious meningitis/encephalitis: evaluation of a rapid and fully automated multiplex PCR in the microbiological

Giulia Piccirilli1, Angela Chiereghin1, Liliana Gabrielli2

  • 1Department of Specialized, Experimental and Diagnostic Medicine, Operative Unit of Clinical Microbiology, St.Orsola-Malpighi Polyclinic, University of Bologna.

Insights

Rapid multiplex PCR testing for central nervous system (CNS) infections like meningitis/encephalitis (ME) significantly improves pathogen identification. This automated test offers faster results than conventional methods, aiding quicker patient management.

Area of Science:

  • Clinical Microbiology
  • Infectious Diseases
  • Molecular Diagnostics

Background:

  • Central nervous system (CNS) infections, including meningitis and encephalitis (ME), necessitate prompt etiological diagnosis for effective treatment.
  • Conventional microbiological procedures (CMP) for diagnosing ME can be time-consuming, potentially delaying critical patient care.
  • The development of rapid, automated diagnostic tools is crucial for improving the management of suspected CNS infections.

Purpose of the Study:

  • To evaluate the analytical performance and clinical utility of a fully automated multiplex PCR test, the FilmArray™ (FA) ME Panel.
  • To assess the FA ME Panel's ability to improve the microbiological diagnostic workup for patients with suspected ME.
  • To compare the diagnostic speed and accuracy of the FA ME Panel against conventional microbiological procedures (CMP).

Main Methods:

  • Seventy-seven cerebrospinal fluid (CSF) samples from patients with suspected ME were analyzed using the FA ME Panel.
  • Results from the FA ME Panel were compared with those obtained from CMP.
  • Assay validity was further confirmed using 5 pooled CSF samples containing known pathogens.

Main Results:

  • A high concordance rate of 90.9% was observed between the FA ME Panel and CMP.
  • Discrepancies were noted in samples with low viral loads and in patients receiving antifungal therapy.
  • The FA ME Panel demonstrated significantly faster detection of bacterial and viral pathogens compared to CMP (P<0.001).

Conclusions:

  • The automated FA ME Panel exhibits good analytical performance and clinical utility for diagnosing ME.
  • This multiplex PCR test provides a faster microbiological diagnosis, potentially enhancing patient management strategies.
  • Implementation of the FA ME Panel can streamline the diagnostic workflow for suspected CNS infections.

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