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A combined risk modeling strategy for clinical prediction of beta-lactam allergies in children
Ali Demirhan1, Didem D Yildirim2, Tugba Arikoglu1
1From the Department of Pediatric Allergy and Clinical Immunology, Faculty of Medicine, Mersin University, Mersin, Turkey, and.
Insights
A new clinical model identifies children at low risk for beta-lactam (BL) allergy, enabling safe drug provocation testing (DPT) without skin tests. Key factors include family history, anaphylaxis, atopy, and reaction timing.
Area of Science:
- Pediatric Allergy and Immunology
- Clinical Risk Prediction
- Drug Hypersensitivity
Background:
- Drug provocation testing (DPT) is increasingly used for children with low-risk beta-lactam (BL) allergies.
- Clear definitions for low-risk patients are lacking, creating uncertainty in clinical practice.
Purpose of the Study:
- To develop a clinical predictive model for identifying children at low risk for BL allergy.
- To enable safe direct DPT in a carefully selected pediatric population.
Main Methods:
- Analysis of clinical data from 204 children undergoing a full diagnostic algorithm for suspected BL allergy.
- Construction of a mathematical predictive model using logistic regression.
- External validation of the model using a new prospective cohort.
Main Results:
- Confirmed BL allergy in 15.7% of suspected cases; anaphylaxis occurred in 5.9%.
- Significant predictors for confirmed BL allergy included family history, anaphylaxis, other atopic diseases, and early reaction interval (0-6 hours).
- The combined model achieved 77.8% sensitivity and 94.3% negative predictive value, validated in a new cohort.
Conclusions:
- Population-specific predictive models incorporating key risk factors are superior to empiric approaches for defining BL allergy risk.
- Accurate risk stratification using such models can safely guide direct DPT in children.
Abstract:
Background: Drug provocation test (DPT) without skin tests is increasingly recommended in the evaluation of children with low-risk beta-lactam (BL) allergies. However, risk definitions are unclear. Objective: The aim of this study was to compose a clinical predictive model that could identify the children at low risk who could safely undergo direct DPT. Methods: The clinical data of 204 children who underwent a full diagnostic algorithm for suspected BL allergy were analyzed. Clinical data were used to construct mathematical predictive model for confirmed BL allergies. A prospective new sample was used for external validation of the final model. Results: The presentations during the index reaction were anaphylaxis in 5.9% and cutaneous reactions in the majority. BL allergy was confirmed in 15.7% of suspected cases. A backward multiple logistic regression model showed that a family history of drug allergy (adjusted odds ratio [aOR], 5.52), anaphylaxis (aOR, 5.14), any atopic disease other than asthma (aOR, 4.38), and a reaction interval of 0-6 hours during the index reaction (aOR, 5.32) were significantly associated with a confirmed BL allergy. A mathematical combined model based on these factors showed a sensitivity of 77.8% and a negative predictive value (NPV) of 94.3%. The validation study replicated sensitivity and NPV values of the main cohort. Conclusion: The risk definition in BL allergies should depend on population-specific predictive models, including a combination of significant risk factors rather than empiric risk approaches. This may help to accurately determinate children at low risk who may safely proceed to direct DPT.
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