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Pulmonary Sequelae of Severe Acute COVID-19 and Multisystem Inflammatory Syndrome (MIS-C) in Dutch Children
Lieke C E Noij1, Caroline L H Brackel2, Mariëlle W Pijnenburg3
1Department of Pediatrics, Division of Pediatric Pulmonology and Allergy, Emma Children's Hospital, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Insights
Children hospitalized with COVID-19 or Multisystem Inflammatory Syndrome in Children (MIS-C) can experience long-term respiratory issues. COVID-19 survivors reported more symptoms and lower quality of life than MIS-C patients.
Area of Science:
- Pediatric critical care medicine
- Infectious disease epidemiology
- Pulmonary rehabilitation
Background:
- COVID-19 can cause severe respiratory illness or Multisystem Inflammatory Syndrome in Children (MIS-C), necessitating hospitalization.
- Long-term health outcomes, particularly respiratory morbidity, following severe pediatric COVID-19 or MIS-C require further investigation.
Purpose of the Study:
- To assess respiratory morbidity and health-related quality of life (HRQoL) in children 5-12 months post-hospitalization for MIS-C or COVID-19.
- To compare the prevalence and nature of long-term symptoms between children who had MIS-C and those who had COVID-19.
Main Methods:
- A multi-center, prospective cohort study involving children (0-17 years) hospitalized for MIS-C or COVID-19 in Dutch hospitals.
- Follow-up assessments included clinical evaluation, HRQoL questionnaires, spirometry, and cardiopulmonary exercise testing (CPET).
Main Results:
- 19% of 72 children reported persistent respiratory symptoms (dyspnea, cough) at a median of 8 months post-hospitalization.
- Impaired HRQoL was more common in the COVID-19 group (60%) than the MIS-C group (14%).
- Abnormal spirometry and CPET findings were noted in both groups, with higher rates in the COVID-19 cohort; deconditioning was a frequent CPET abnormality.
Conclusions:
- Long-term respiratory sequelae and fatigue are potential outcomes of both MIS-C and severe COVID-19 in children.
- Respiratory symptoms and reduced HRQoL were more prevalent following COVID-19 compared to MIS-C.
- While COVID-19 related abnormalities often correlated with symptoms, MIS-C patients sometimes exhibited CPET changes without concurrent respiratory complaints or lung function deficits.
Background:
Although rare, COVID-19 in children may lead to hospitalization due to severe respiratory symptoms, or a hyperinflammatory state called Multisystem Inflammatory Syndrome in Children (MIS-C). This study examined respiratory morbidity in children 5 to 12 months after hospitalization for MIS-C or COVID-19.
Methods:
In this multi-center, prospective cohort study, children (0-17 years) with a history of hospitalization for MIS-C or COVID-19 in Dutch hospitals were invited for follow-up. Visits were scheduled in one of three academic hospitals, to evaluate current clinical status and health-related quality of life (HRQoL), and perform lung function tests and cardiopulmonary exercise testing (CPET).
Results:
72 children were included (43 MIS-C, 29 COVID-19), of whom 19% (5% and 41%, respectively) reported long-term respiratory symptoms including dyspnea and cough, a median of 8 months after hospitalization. Fatigue was the most common non-respiratory symptom. HRQoL was more frequently (60%) impaired in the COVID-19 group than the MIS-C group (14%). Spirometry (n = 48) and CPET (n = 40) were conducted in children aged > 4 and > 6 years, respectively. Spirometry was abnormal in 15% of the MIS-C group and 44% of COVID-19 group, CPET in 41% and 75%, respectively. Deconditioning patterns were the most common reason (30%) for abnormal CPET results.
Conclusion:
Long-term respiratory sequelae and fatigue occurred after both MIS-C and severe COVID-19, but respiratory symptoms and impaired HRQoL were more frequent after COVID-19. Lung function and CPET abnormalities in children with COVID-19 often corresponded with symptoms. Children with MIS-C often showed CPET abnormalities without respiratory complaints or lung function changes.
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