Diagnostic prediction models for bacterial meningitis in children with a suspected central nervous system infection:

Nina S Groeneveld1, Merijn W Bijlsma2, Ingeborg E van Zeggeren1

  • 1Department of Neurology, Amsterdam UMC Location AMC, Amsterdam, The Netherlands.

BMJ Open
|August 8, 2024
PubMed
Abstract

Insights

Diagnostic prediction models effectively help rule out bacterial meningitis (BM) in children with suspected central nervous system (CNS) infections. These models show good to excellent accuracy but should complement, not replace, clinical evaluation.

Area of Science:

  • Pediatric infectious diseases
  • Clinical epidemiology
  • Diagnostic test evaluation

Background:

  • Bacterial meningitis (BM) poses a significant risk in children with suspected central nervous system (CNS) infections.
  • Existing diagnostic prediction models aim to assess the probability of BM in pediatric patients.

Purpose of the Study:

  • To externally validate existing diagnostic prediction models for bacterial meningitis (BM) in a broad pediatric population.
  • To evaluate the diagnostic accuracy and calibration of these models in children with suspected CNS infections.

Main Methods:

  • Systematic literature review in Medline to identify relevant prediction models for BM.
  • External validation of identified models in a prospective cohort of 450 children (0-18 years) with suspected CNS infections (2012-2015).
  • Calculation of sensitivity, specificity, predictive values, AUC, and calibration assessment.

Main Results:

  • 23 prediction models were validated. 17% of patients had CNS infections, with 7% diagnosed with BM.
  • Overall AUCs ranged from 0.69 to 0.94 (median 0.83).
  • Models demonstrated good to excellent performance, particularly in children aged ≥28 days (median AUC 0.89).

Conclusions:

  • Diagnostic prediction models exhibit good to excellent test characteristics for excluding BM in pediatric patients.
  • These models can aid in the diagnostic workup of suspected CNS infections in children.
  • Models should be used in conjunction with thorough clinical assessment and ancillary testing, not as a replacement.

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