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Predictors of bacterial meningitis in the era after Haemophilus influenzae

S B Freedman1, A Marrocco, J Pirie

  • 1Department of Pediatrics, Faculty of Medicine, University of Toronto, Ontario.

Insights

In children, a cerebrospinal fluid (CSF) white blood cell (WBC) count of 30 or less indicates a low risk for bacterial meningitis. Other clinical factors are crucial for managing suspected cases, potentially avoiding unnecessary hospital admission and antibiotics.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Clinical Microbiology

Background:

  • The incidence of bacterial meningitis has changed since the introduction of Haemophilus influenzae type b vaccines.
  • Accurate risk stratification is essential for managing children with suspected bacterial meningitis.

Purpose of the Study:

  • To evaluate the utility of cerebrospinal fluid (CSF) white blood cell (WBC) count in stratifying children with suspected bacterial meningitis into low- and high-risk groups.
  • To determine if CSF WBC count alone is sufficient for risk assessment in the post-Hib vaccine era.

Main Methods:

  • Retrospective analysis of 1617 atraumatic CSF samples from children aged 2 months to 17 years.
  • Evaluation of predictive values for CSF WBC count, differential, protein, and glucose in diagnosing bacterial meningitis.
  • Inclusion of children without prior neurologic or immunologic disease.

Main Results:

  • A CSF WBC count of 30 or less had a 99.3% negative predictive value for bacterial meningitis.
  • CSF samples with >30 WBCs/µL had a likelihood ratio of 10.3 for bacterial meningitis.
  • Age, CSF glucose, protein, gram stain, CSF-serum glucose ratio, and peripheral blood band count were also significant predictors.

Conclusions:

  • Bacterial meningitis can occur in children without CSF pleocytosis, necessitating consideration of additional factors.
  • Children over 6 months with CSF WBC count ≤30/µL are generally low-risk.
  • Hospital admission and empiric antibiotics may be unnecessary for stable, low-risk children without other concerning laboratory markers.
Abstract

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