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Published on: January 21, 2018
The differential burden of acute rhinovirus infections in children with underlying conditions
María Isabel Sánchez Códez1, Isabel Benavente Fernández2,3,4, Katherine Moyer5
1Division of Pediatric Infectious Diseases, Puerta del Mar, Cadiz, Spain.
Insights
Rhinovirus infections in children are often linked to underlying conditions like asthma, prematurity, and congenital heart disease, leading to severe outcomes. Higher viral loads and bacterial co-infections also worsen clinical results in pediatric patients.
Area of Science:
- Pediatric Infectious Diseases
- Respiratory Viral Infections
- Clinical Outcomes Research
Background:
- Rhinoviruses (RVs) are established triggers for wheezing in asthmatic children.
- The impact of RV infections on other pediatric chronic medical conditions remains less understood.
Purpose of the Study:
- To investigate the prevalence of comorbidities in children hospitalized or seen as outpatients with symptomatic RV infection.
- To identify associations between underlying conditions, RV loads, co-infections, and clinical outcomes.
Main Methods:
- Retrospective analysis of 1,899 pediatric patients with symptomatic RV infection (2011-2013).
- Categorization by underlying disease, comparison of clinical parameters, RV loads (CT values), and co-infections.
- Multivariable analyses to determine comorbidities linked to oxygen requirement, PICU admission, and prolonged hospitalization.
Main Results:
- 77.7% of children had comorbidities; asthma/atopy (36.8%), prematurity (7.7%), congenital heart disease (CHD, 3.2%), and immunocompromised hosts (ICH, 1.4%) were common.
- Asthma/atopy, prematurity, CHD, and bacterial co-infections were consistently associated with severe outcomes (oxygen requirement, PICU admission, prolonged hospitalization).
- Higher RV loads and bacterial co-infections, though infrequent, correlated with worse outcomes.
Conclusions:
- Comorbidities are highly prevalent in pediatric RV infections.
- Asthma/atopy, prematurity, and CHD are key risk factors for severe RV disease in children.
- Understanding these phenotypes is crucial for developing targeted interventions for pediatric RV infections.
Introduction:
Rhinoviruses (RVs) are a well-known trigger of wheezing episodes in children with asthma. Their role in other pediatric chronic medical conditions is not fully known.
Methods:
Patients ≤21 years hospitalized or evaluated as outpatients with symptomatic RV infection were identified from 2011-2013. Patients were categorized based on the type of underlying disease and differences in clinical parameters, RV loads (CT values), viral, bacterial and fungal co-infections and clinical outcomes were compared between groups. Multivariable analyses were performed to identify the comorbidities associated with oxygen requirement, PICU admission, and prolonged hospitalization.
Results:
Of 1,899 children identified, 77.7% (n = 1477) had an underlying comorbidity including asthma/atopy (36.8%), prematurity (7.7%), chronic respiratory diseases (6.4%), congenital heart disease (CHD, 3.2%), immunocompromised hosts (ICH; 1.4%) and others (22.2%). Prevalence of comorbidities increased with age (70%, infants vs 84%-87%, children >1 year; p < 0.0001). Median RV loads were intermediate-high (24-26 CT values), irrespective of the underlying disease. RV/viral co-detections were identified in 11% of ICH vs 20%- 30% in all other children whereas bacterial co-infections were identified in 2.9% of children. Multivariable models identified asthma/atopy, prematurity, CHD and bacterial co-infections consistently associated with all three clinical outcomes (p < 0.0001). Older age and higher RV loads were also associated with increased odds of PICU admission.
Conclusions:
The prevalence of comorbidities was high in children with RV infections. Of those, asthma/atopy, prematurity and CHD were consistently associated with severe disease. Higher RV loads and bacterial co-infections, although infrequent, were also associated with worse clinical outcomes, suggesting the importance of defining clinical phenotypes for future targeted interventions.
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