Impact of CSF Meningitis and Encephalitis Panel on Resource Use for Febrile Well-Appearing Infants

Angelica W DesPain1, Ryan Pearman2, Rana F Hamdy3,4

  • 1Division of Emergency Medicine, The Children's Hospital of San Antonio, San Antonio, Texas.

Hospital Pediatrics
|October 6, 2022
PubMed
Abstract

Insights

The BioFire FilmArray Meningitis/Encephalitis (ME) panel did not reduce hospital length of stay or antibiotic use in febrile infants. However, ME panel testing was linked to increased acyclovir initiation in this patient group.

Area of Science:

  • Pediatric Infectious Diseases
  • Clinical Diagnostics
  • Healthcare Resource Utilization

Background:

  • Febrile infants require prompt diagnosis to rule out serious infections like meningitis and encephalitis.
  • The BioFire FilmArray Meningitis/Encephalitis (ME) panel offers rapid results (1-2 hours) for pathogen identification.
  • Potential benefits include reduced length of stay (LOS) and antimicrobial use.

Purpose of the Study:

  • To evaluate the association between BioFire FilmArray ME panel use and resource utilization in febrile infants.
  • To determine if ME panel testing impacts hospital LOS, antibiotic duration, or acyclovir use.

Main Methods:

  • Retrospective cohort study of febrile infants (≤60 days) from July 2017 to April 2019.
  • Examined ME panel use, hospital LOS, and antibiotic/antiviral initiation and duration.
  • Nonparametric tests used for median duration comparisons.

Main Results:

  • ME panel was used in 36% of 237 infants.
  • No significant difference in median hospital LOS between ME panel and non-ME panel groups (40-42 hours).
  • Antibiotic initiation was high (>97%) in both groups; ME panel use was associated with increased acyclovir initiation (33% vs 18%) but not duration.

Conclusions:

  • BioFire FilmArray ME panel use was not associated with reduced hospital LOS or antibiotic use in febrile infants.
  • ME panel testing was associated with increased initiation of acyclovir.
  • Further research may be needed to optimize the clinical utility of the ME panel in febrile infants.