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Updated: Feb 27, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
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.
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.
Background:
Improving the diagnosis of serious bacterial infections (SBIs) in the children's emergency department is a clinical priority. Early recognition reduces morbidity and mortality, and supporting clinicians in ruling out SBIs may limit unnecessary admissions and antibiotic use.
Methods:
A prospective, diagnostic accuracy study of clinical and biomarker variables in the diagnosis of SBIs (pneumonia or other SBI) in febrile children <16 years old. A diagnostic model was derived by using multinomial logistic regression and internally validated. External validation of a published model was undertaken, followed by model updating and extension by the inclusion of procalcitonin and resistin.
Results:
There were 1101 children studied, of whom 264 had an SBI. A diagnostic model discriminated well between pneumonia and no SBI (concordance statistic 0.84, 95% confidence interval 0.78-0.90) and between other SBIs and no SBI (0.77, 95% confidence interval 0.71-0.83) on internal validation. A published model discriminated well on external validation. Model updating yielded good calibration with good performance at both high-risk (positive likelihood ratios: 6.46 and 5.13 for pneumonia and other SBI, respectively) and low-risk (negative likelihood ratios: 0.16 and 0.13, respectively) thresholds. Extending the model with procalcitonin and resistin yielded improvements in discrimination.
Conclusions:
Diagnostic models discriminated well between pneumonia, other SBIs, and no SBI in febrile children in the emergency department. Improvements in the classification of nonevents have the potential to reduce unnecessary hospital admissions and improve antibiotic prescribing. The benefits of this improved risk prediction should be further evaluated in robust impact studies.
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