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Clinical prediction models for young febrile infants at the emergency department: an international validation study
Evelien de Vos-Kerkhof1, Borja Gomez2,3, Karen Milcent4
1Department of General Paediatrics, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
Insights
Four clinical prediction models (CPMs) effectively identify serious bacterial infections in febrile infants. These models, incorporating clinical signs, symptoms, and lab markers, serve as valuable adjunctive tools for risk assessment in young children.
Area of Science:
- Pediatrics
- Infectious Diseases
- Clinical Diagnostics
Background:
- Febrile young infants are at risk for serious bacterial infections (SBIs).
- Clinical prediction models (CPMs) are statistically derived tools to aid diagnosis.
- Assessing the diagnostic value of existing CPMs is crucial for timely intervention.
Purpose of the Study:
- To evaluate the diagnostic accuracy of established CPMs for identifying SBIs in febrile infants.
- To determine the performance of CPMs across different age groups and clinical settings.
Main Methods:
- Systematic literature review to identify eight relevant CPMs.
- Validation of selected CPMs using four independent cohorts of febrile infants (<3 months and 1-12 months).
- Performance assessment using sensitivity, specificity, area under the receiver operating characteristic curve (AUC), and calibration.
Main Results:
- Four CPMs demonstrated moderate to excellent performance (AUC 0.68-0.94) in validation cohorts.
- Models incorporating clinical signs, symptoms, urine dipstick, and laboratory markers showed best results.
- Specificities generally exceeded sensitivities in validation cohorts, particularly for infants <3 months.
Conclusions:
- Four CPMs, utilizing clinical and laboratory data, can assist clinicians in diagnosing SBIs in febrile infants.
- CPMs should be employed as adjunctive tools for risk stratification in this vulnerable population.
Objective:
To assess the diagnostic value of existing clinical prediction models (CPM; ie, statistically derived) in febrile young infants at risk for serious bacterial infections.
Methods:
A systematic literature review identified eight CPMs for predicting serious bacterial infections in febrile children. We validated these CPMs on four validation cohorts of febrile children in Spain (age <3 months), France (age <3 months) and two cohorts in the Netherlands (age 1-3 months and >3-12 months). We evaluated the performance of the CPMs by sensitivity/specificity, area under the receiver operating characteristic curve (AUC) and calibration studies.
Results:
The original cohorts in which the prediction rules were developed (derivation cohorts) ranged from 381 to 15 781 children, with a prevalence of serious bacterial infections varying from 0.8% to 27% and spanned an age range of 0-16 years. All CPMs originally performed moderately to very well (AUC 0.60-0.93). The four validation cohorts included 159-2204 febrile children, with a median age range of 1.8 (1.2-2.4) months for the three cohorts <3 months and 8.4 (6.0-9.6) months for the cohort >3-12 months of age. The prevalence of serious bacterial infections varied between 15.1% and 17.2% in the three cohorts <3 months and was 9.8% for the cohort >3-12 months of age. Although discriminative values varied greatly, best performance was observed for four CPMs including clinical signs and symptoms, urine dipstick analyses and laboratory markers with AUC ranging from 0.68 to 0.94 in the three cohorts <3 months (ranges sensitivity: 0.48-0.94 and specificity: 0.71-0.97). For the >3-12 months' cohort AUC ranges from 0.80 to 0.89 (ranges sensitivity: 0.70-0.82 and specificity: 0.78-0.90). In general, the specificities exceeded sensitivities in our cohorts, in contrast to derivation cohorts with high sensitivities, although this effect was stronger in infants <3 months than in infants >3-12 months.
Conclusion:
We identified four CPMs, including clinical signs and symptoms, urine dipstick analysis and laboratory markers, which can aid clinicians in identifying serious bacterial infections. We suggest clinicians should use CPMs as an adjunctive clinical tool when assessing the risk of serious bacterial infections in febrile young infants.
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