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Published on: November 5, 2019
Clinical phenotypes and household structure in pediatric invasive meningococcal disease: A retrospective cohort study
Kubra Boydag Guvenc1, Cansu Durak1, Nihal Akcay2
1Ministry of Health Sancaktepe Sehit Prof Dr Ilhan Varank Training and Research Hospital, Department of Pediatric Intensive Care, Istanbul, Turkey, Istanbul.
Insights
Meningococcal sepsis in children presents more severe symptoms and higher mortality than meningitis. Early identification of sepsis phenotype aids critical care management for invasive meningococcal disease.
Area of Science:
- Pediatric critical care medicine
- Infectious diseases
- Clinical epidemiology
Background:
- Invasive meningococcal disease (IMD) has varied presentations, with phenotype-specific severity in critically ill children not fully understood.
- Differences in clinical phenotypes of IMD can impact disease severity and patient outcomes.
- Understanding these differences is crucial for effective management in pediatric intensive care units.
Purpose of the Study:
- To evaluate the association between clinical phenotypes of IMD and early disease severity.
- To assess the impact of different IMD phenotypes on outcomes in critically ill children.
- To inform risk stratification and management strategies for pediatric IMD.
Main Methods:
- Retrospective cohort study of 42 children with IMD admitted to a tertiary pediatric intensive care unit (PICU) from 2006-2020.
- Patients classified into two groups: meningococcal sepsis without meningitis and meningococcal meningitis.
- Disease severity assessed using Pediatric Risk of Mortality III (PRISM III) score; demographic, clinical, and household data analyzed.
Main Results:
- Meningococcal sepsis without meningitis occurred in 54.8% of patients, associated with higher PRISM III scores (median 20 vs. 11), increased lactate, lower platelets, and more organ support.
- The sepsis phenotype showed significantly higher mortality (34.8% vs. 5.3%, p=0.023) compared to the meningitis phenotype.
- Extended family living was more common in the meningitis group (26.3% vs. 4.3%, p=0.043); Serogroup B was predominant.
Conclusions:
- Meningococcal sepsis without meningitis is linked to greater early severity and higher mortality in a PICU cohort compared to meningococcal meningitis.
- Phenotype-based early risk assessment can aid in managing critically ill children with IMD.
- Household structure findings require further investigation.
Background:
Invasive meningococcal disease is a rapidly progressive infection with heterogeneous clinical presentations. Phenotype-related severity differences in critically ill children remain incompletely defined. We evaluated the association between clinical phenotypes, early disease severity, and outcomes in a pediatric intensive care unit cohort.
Methods:
This retrospective study included 42 children admitted to a tertiary pediatric intensive care unit with invasive meningococcal disease between 2006 and 2020. Patients were classified as meningococcal sepsis without meningitis or meningococcal meningitis. Disease severity was assessed using the Pediatric Risk of Mortality III score. Demographic, clinical, microbiological, and selected household characteristics were analyzed.
Results:
Twenty-three patients (54.8%) had meningococcal sepsis without meningitis and 19 patients (45.2%) had meningococcal meningitis. The overall mortality was 21.4%. The sepsis phenotype was associated with higher Pediatric Risk of Mortality III scores (median 20 vs. 11, p=0.007), higher lactate, lower platelet counts, more organ support, and higher mortality (34.8% vs. 5.3%, p=0.023). Extended family living was more frequent in the meningitis group (26.3% vs. 4.3%, p=0.043). Serogroup data were available in 40.5% of cases, with serogroup B predominating.
Conclusions:
In this pediatric intensive care unit cohort, meningococcal sepsis without meningitis was associated with greater early severity and higher mortality than meningococcal meningitis. Household-structure findings should be considered exploratory. Early phenotype-based risk assessment may support the management of critically ill children with invasive meningococcal disease.
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