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Febrile illness in high-risk children: a prospective, international observational study
Fabian J S van der Velden1,2, Gabriella de Vries1,3, Alexander Martin1,2
1Paediatric Immunology, Infectious Diseases & Allergy, Great North Children's Hospital, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Insights
Febrile illness in immunocompromised children has diverse causes, with bacterial infections being common but often unidentified. While standard antibiotic treatment is effective, better diagnostic tools are needed for this high-risk group.
Area of Science:
- Pediatrics
- Infectious Diseases
- Immunology
Background:
- Immunocompromised children face high risks of serious bacterial and viral infections, often presenting solely with fever.
- Current diagnostic methods lack specificity for bacterial infections in this population, with low microbiological culture positivity rates.
Purpose of the Study:
- To investigate the causes and management of febrile illness in children with primary or acquired immunodeficiency at high risk for serious bacterial infection.
- To identify predictive features for bacterial or viral infections in immunocompromised children presenting with fever.
Main Methods:
- Prospective data analysis from the 'Biomarker Validation in HR patients' database in PERFORM across 16 European and African hospitals.
- Analysis included demographics, clinical features, investigations, microbiology, management, and outcomes of 599 febrile episodes in 482 immunocompromised children (<18 years).
- Logistic regression was employed to determine the effect size of predictive features for proven/presumed bacterial or viral infections.
Main Results:
- Bacterial infections accounted for 29.0% of episodes, viral infections for 21.0%, unknown infections for 31.7%, and non-infectious causes for 18.1%.
- Ill appearance (OR 3.1) and HIV (OR 10.4) were predictive of bacterial infection, while ill appearance reduced the odds of viral infection (OR 0.5).
- Empirical antibiotics were initiated in 82.1% of cases; mortality was 1.9%, with 87.1% achieving full recovery.
Conclusions:
- The etiology of febrile illness in immunocompromised children is varied, with a significant proportion having unidentified causes.
- Standard empirical intravenous antibiotic treatment is effective but debatable, highlighting the need for improved clinical decision-making tools and biomarkers.
- Developing pathways for early discharge or antibiotic cessation requires further research into better diagnostic strategies for this vulnerable population.
Abstract:
To assess and describe the aetiology and management of febrile illness in children with primary or acquired immunodeficiency at high risk of serious bacterial infection, as seen in emergency departments in tertiary hospitals. Prospective data on demographics, presenting features, investigations, microbiology, management, and outcome of patients within the 'Biomarker Validation in HR patients' database in PERFORM, were analysed. Immunocompromised children (< 18 years old) presented to fifteen European hospitals in nine countries, and one Gambian hospital, with fever or suspected infection and clinical indication for blood investigations. Febrile episodes were assigned clinical phenotypes using the validated PERFORM algorithm. Logistic regression was used to assess the effect size of predictive features of proven/presumed bacterial or viral infection. A total of 599 episodes in 482 children were analysed. Seventy-eight episodes (13.0%) were definite bacterial, 67 episodes probable bacterial (11.2%), and 29 bacterial syndrome (4.8%). Fifty-five were definite viral (9.2%), 49 probable viral (8.2%), and 23 viral syndrome (3.8%). One hundred ninety were unknown bacterial or viral infections (31.7%), and 108 had inflammatory or other non-infectious causes of fever (18.1%). Predictive features of proven/presumed bacterial infection were ill appearance (OR 3.1 (95% CI 2.1-4.6)) and HIV (OR 10.4 (95% CI 2.0-54.4)). Ill appearance reduced the odds of having a proven/presumed viral infection (OR 0.5 (95% CI 0.3-0.9)). A total of 82.1% had new empirical antibiotics started on admission (N = 492); 94.3% proven/presumed bacterial (N = 164), 66.1% proven/presumed viral (N = 84), and 93.2% unknown bacterial or viral infections (N = 177). Mortality was 1.9% (N = 11) and 87.1% made full recovery (N = 522). Conclusion: The aetiology of febrile illness in immunocompromised children is diverse. In one-third of cases, no cause for the fever will be identified. Justification for standard intravenous antibiotic treatment for every febrile immunocompromised child is debatable, yet effective. Better clinical decision-making tools and new biomarkers are needed for this population. What is Known: • Immunosuppressed children are at high risk for morbidity and mortality of serious bacterial and viral infection, but often present with fever as only clinical symptom. • Current diagnostic measures in this group are not specific to rule out bacterial infection, and positivity rates of microbiological cultures are low. What is New: • Febrile illness and infectious complications remain a significant cause of mortality and morbidity in HR children, yet management is effective. • The aetiology of febrile illness in immunocompromised children is diverse, and development of pathways for early discharge or cessation of intravenous antibiotics is debatable, and requires better clinical decision-making tools and biomarkers.
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