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Published on: April 21, 2019
Pediatric drug allergy: a retrospective analysis of clinical features, laboratory parameters, and systemic
Filiz Demir Şahin1, Ozan Kapçay2, Mehmet Kılıç2
1Department of Pediatric Immunology and Allergy, Faculty of Medicine, Fırat University, Elâzığ, Turkey; fdsahin@firat.edu.tr.
Insights
Hematological parameters like neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII) may help predict drug hypersensitivity reactions (DHRs) in children. These inflammatory indices require further validation in larger studies.
Area of Science:
- Pediatric Allergy and Immunology
- Hematology
- Clinical Biomarkers
Background:
- Drug hypersensitivity reactions (DHRs) pose a significant challenge in pediatric care.
- Identifying reliable biomarkers for early detection and risk stratification of DHRs is crucial.
Purpose of the Study:
- To evaluate the potential of hematological parameters and systemic inflammatory indices as predictive biomarkers for DHRs in pediatric patients.
- To analyze specific indices like neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), eosinophil-to-lymphocyte ratio (ELR), and systemic immune-inflammation index (SII).
Main Methods:
- Retrospective review of medical records of children with suspected DHRs at a Pediatric Allergy and Immunology Clinic.
- Analysis of demographic data, clinical features, complete blood counts, and total immunoglobulin E (IgE) levels.
- Calculation and comparison of inflammatory indices (NLR, PLR, ELR, SII) between patients with confirmed DHRs and controls.
Main Results:
- Drug allergy was confirmed in 31.1% of the 45 included children.
- Significantly higher monocyte counts and elevated NLR, PLR, and SII were observed in children with confirmed DHRs.
- Significantly lower lymphocyte and basophil counts were noted in the patient group, while eosinophil counts were higher in controls.
Conclusions:
- Elevated NLR, PLR, and SII may serve as potential indicators for DHRs in pediatric patients.
- These hematological indices offer a promising avenue for hypothesis generation and tentative risk stratification.
- Further validation in larger, prospective studies is essential to confirm these preliminary findings.
Background:
This study aimed to investigate the potential utility of hematological parameters and systemic inflammatory indices as predictive biomarkers in pediatric patients with drug hypersensitivity reactions (DHRs).
Methods:
We performed a retrospective review of medical records of children presenting to the Pediatric Allergy and Immunology Clinic at Fırat University Hospital, Turkey, between January 2019 and July 2025 with suspected DHRs. Demographic characteristics, clinical manifestations, reaction phenotypes, complete blood counts, and total immunoglobulin E (IgE) levels were analyzed. Inflammatory indices, such as neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), eosinophil-to-lymphocyte ratio (ELR), and systemic immune-inflammation index (SII), were calculated subsequently.
Results:
Among the 45 children included, drug allergy was confirmed in 14 (31.1%) children. Total IgE levels did not differ significantly between groups (P = 0.712). Monocyte counts were significantly higher in the patient group (P = 0.039), whereas eosinophil counts were elevated in the control group (P = 0.026). Lymphocyte (P = 0.002) and basophil counts (P = 0.002) were significantly lower in the patient cohort. No significant differences were observed in neutrophil or platelet counts. Regarding inflammatory indices, NLR (P = 0.007), PLR (P = 0.006), and SII (P = 0.007) were significantly increased in the patient group, whereas ELR did not differ significantly (P = 0.073).
Conclusion:
In this small, single-center cohort (n = 45; confirmed DHR, n = 14), higher NLR, PLR, and SII were observed among children with confirmed DHRs. These preliminary findings suggest that readily available hematological indices may aid hypothesis generation and tentative risk stratification; however, they should be interpreted cautiously and require confirmation in larger prospective studies.
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