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Published on: March 1, 2011
Inflammatory Cytokine and Chemokine Patterns in Paediatric Patients with Suspected Serious Bacterial Infection
Linda Rautiainen1,2, Jana Pavare3, Ilze Grope4
1Lapland Central Hospital, Department of Paediatrics, Rovaniemi 96101, Finland. linda.rautiainen@lshp.fi.
Insights
Early inflammatory cytokine panels, including granulocyte colony-stimulating factor (G-CSF), may help diagnose severe bacterial infections (SBI) in children admitted to the emergency department. This aids in identifying critical cases needing prompt treatment.
Area of Science:
- Pediatrics
- Infectious Diseases
- Clinical Immunology
Background:
- Acute infections are a leading cause of pediatric emergency department visits.
- Severe bacterial infections (SBI) in children carry significant mortality risk.
- Accurate early diagnosis of SBI is crucial when clinical suspicion is high but admission is not warranted.
Purpose of the Study:
- To evaluate the utility of early inflammatory cytokine and chemokine panels in diagnosing SBI in hospitalized children.
- To assess the potential of these panels in evaluating early therapeutic responses.
- To improve diagnostic accuracy for febrile infections in pediatric emergency care.
Main Methods:
- A cohort of 51 febrile children admitted to the emergency department was studied.
- Patients were classified into SBI (n=21) and non-SBI (n=30) groups based on established diagnostic criteria.
- Inflammatory cytokine and chemokine levels were measured from blood samples at admission and 24 hours.
Main Results:
- Granulocyte colony-stimulating factor (G-CSF) and Eotaxin showed significant differences between SBI and non-SBI groups at admission.
- Receiver operator characteristic analysis indicated an Area Under the Curve (AUC) of 0.679 for G-CSF in predicting SBI.
- Other tested cytokines and chemokines did not show statistically significant differences.
Conclusions:
- Inflammatory cytokine profiles, particularly G-CSF, may offer valuable adjunctive information for the early diagnosis of SBI in children.
- Further research can explore the integration of cytokine panels into diagnostic algorithms for febrile children.
- Early cytokine analysis shows promise in enhancing the diagnostic capabilities in pediatric emergency settings.
Abstract:
Background and objectives: In children, acute infection is the most common cause of visits to the emergency department. Although most of them are self-limiting, mortality due to severe bacterial infections (SBI) in developed countries is still high. When the risk of serious bacterial infection is too high to ignore, yet too low to justify admission and hospital observation, clinicians try to improve diagnostic accuracy by performing various laboratory tests. The aim of the study was to investigate whether an early inflammatory cytokine and chemokine panel can add information in diagnostics of SBI and assessment of efficacy of early therapies in hospitalized children with fever. Methods: This study included 51 children with febrile infections that were admitted to the emergency department (ED). Clinical examination and microbiological and radiological tests were used as reference standards for the definition of SBI. Study population was categorized into two groups: (1) patients with SBI (n = 21); (2) patients without SBI (n = 30). Inflammatory cytokine and chemokine panels were analyzed from the first routine blood samples at hospital admission and after 24 h. Results: Out of 12 cytokines and chemokines, only Eotaxin and granulocyte colony-stimulating factor (G-CSF) had statistically significant differences between groups at the time of inclusion. Receiver operator characteristic analysis to predict SBI showed an area under the curve (AUC) of 0.679 for G-CSF. Conclusions: Analysis of inflammatory cytokine profiles may provide additional information in early diagnostics of SBI.
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