Predicting Risk of Serious Bacterial Infections in Febrile Children in the Emergency Department

Adam D Irwin1, Alison Grant2, Rhian Williams2

  • 1Institute of Infection and Global Health, adam.irwin@nhs.net.

Pediatrics
|July 7, 2017
PubMed

Insights

This study developed diagnostic models to accurately identify serious bacterial infections (SBIs) in children, aiming to reduce unnecessary hospital admissions and antibiotic use in emergency departments.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Clinical Diagnostics

Background:

  • Accurate diagnosis of serious bacterial infections (SBIs) in pediatric emergency departments is crucial for patient outcomes.
  • Early identification of SBIs can decrease morbidity, mortality, and inappropriate antibiotic prescribing.
  • Developing improved diagnostic tools is a clinical priority to support clinicians in ruling out SBIs.

Purpose of the Study:

  • To derive and validate diagnostic models for identifying SBIs in febrile children.
  • To assess the accuracy of existing models and improve them with novel biomarkers.
  • To enhance the classification of children without SBIs to reduce unnecessary hospitalizations.

Main Methods:

  • Prospective diagnostic accuracy study involving febrile children under 16.
  • Development and internal validation of a diagnostic model using multinomial logistic regression.
  • External validation of a published model, followed by updating with procalcitonin and resistin.

Main Results:

  • The derived model showed good discrimination for pneumonia and other SBIs (concordance statistics 0.84 and 0.77).
  • External validation confirmed the performance of a published model.
  • Model updating with procalcitonin and resistin improved discrimination and provided reliable risk stratification.

Conclusions:

  • Diagnostic models effectively differentiate between pneumonia, other SBIs, and no SBI in febrile children.
  • Improved classification of non-SBI cases can lead to reduced hospital admissions and optimized antibiotic use.
  • Further impact studies are recommended to evaluate the clinical benefits of these risk prediction models.
Abstract

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