Clinical and Financial Impact of a Diagnostic Stewardship Program for Children with Suspected Central Nervous System

Kevin Messacar1, Claire Palmer2, LiseAnne Gregoire3

  • 1Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO; Children's Hospital Colorado, Aurora, CO.

The Journal of Pediatrics
|February 12, 2022
PubMed
Abstract

Insights

Implementing the FilmArray Meningitis Encephalitis Panel (MEP) with diagnostic stewardship significantly reduced time to optimal antimicrobials for children with suspected central nervous system infections. This approach improved antimicrobial use and diagnostic speed without increasing overall hospital costs.

Area of Science:

  • Clinical Microbiology
  • Infectious Diseases
  • Pediatric Neurology

Background:

  • Central nervous system infections in children require rapid diagnosis and appropriate antimicrobial treatment.
  • The FilmArray Meningitis Encephalitis Panel (MEP) offers multiplex polymerase chain reaction (PCR) testing for cerebrospinal fluid (CSF).
  • Optimizing the implementation of advanced diagnostic tools like MEP is crucial for improving patient outcomes and resource utilization.

Purpose of the Study:

  • To evaluate the clinical and financial impacts of implementing the FilmArray Meningitis Encephalitis Panel (MEP) in children with suspected central nervous system infections.
  • To assess the effectiveness of a rapid CSF diagnostic stewardship program integrated with MEP testing.
  • To determine if MEP implementation influences antimicrobial prescribing patterns and patient outcomes.

Main Methods:

  • A pre-post quasiexperimental cohort study design was employed at Children's Hospital Colorado.
  • MEP testing was guided by electronic medical record indications for high-yield pediatric populations.
  • Antimicrobial stewardship provided real-time decision support for positive MEP results, comparing preimplementation (2015-2016) and postimplementation (2017-2018) cohorts.

Main Results:

  • Time to optimal antimicrobials decreased significantly from 28 to 18 hours post-MEP implementation (P < .0001).
  • Time to positive CSF results was faster (4.8 vs 9.6 hours, P < .0001), and intravenous antimicrobial duration was shorter (24 vs 36 hours, P = .004).
  • Infectious neurologic diagnoses were identified more frequently (15% vs 10%, P = .03), with no significant changes in overall hospital costs.

Conclusions:

  • MEP implementation, coupled with a diagnostic stewardship program, enhances antimicrobial use and diagnostic efficiency in pediatric CNS infections.
  • Targeted MEP testing for high-yield indications optimizes antimicrobial therapy and leads to faster results.
  • This integrated approach achieves improved clinical outcomes with stable overall hospital expenditures.

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