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Critical Care Course of Pediatric Inflammatory Multisystem Syndrome Temporally Associated with SARS-CoV-2 and
Nicholas Richens1, Hari Krishnan Kanthimathinathan1,2, Sanket Sontakke1
1Paediatric Intensive Care Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, United Kingdom.
Insights
Children with pediatric inflammatory multisystem syndrome (PIMS) associated with COVID-19 experienced severe inflammation and cardiac issues. Critical care was brief, with improvement seen both with and without immunomodulation therapies.
Area of Science:
- Pediatric critical care medicine
- Infectious diseases
- Immunology
Background:
- A novel hyperinflammatory syndrome, pediatric inflammatory multisystem syndrome (PIMS), has been observed in children following coronavirus disease 2019 (COVID-19).
- This syndrome is temporally associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
Purpose of the Study:
- To describe the critical care course of children diagnosed with PIMS.
- To analyze the trajectory of illness before and after immunomodulatory treatments.
Main Methods:
- Analysis of 10 pediatric patients meeting the U.K. Royal College of Pediatrics and Child Health case definition for PIMS.
- Assessment of clinical data, inflammatory markers, and cardiac function during critical care admission.
- Review of treatments including inotropic/vasopressor support, intravenous immunoglobulin, and high-dose steroids.
Main Results:
- All patients tested positive for SARS-CoV-2 IgG antibodies.
- 100% required cardiovascular support (inotropic or vasopressor), though only 20% needed ventilation.
- Significantly elevated inflammatory markers (CRP, ferritin) and cardiac biomarkers (troponin-I) were noted.
- Myocardial dysfunction was present in 8/10 patients (moderate in 6, severe in 2).
- Critical care duration was brief (3-5 days) for all patients.
- Eight patients received intravenous immunoglobulin, and six received high-dose steroids.
Conclusions:
- Children with PIMS present with significant hyperinflammation and cardiac involvement requiring critical care.
- Despite severe illness, critical care stays are typically short.
- Clinical improvement and cardiovascular stability were observed irrespective of immunomodulatory treatment, suggesting a complex interplay of factors in recovery.
Abstract:
We describe the critical care course of children with a novel hyperinflammatory syndrome associated with coronavirus disease 2019 (COVID-19) pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), with focus on trajectory before and after immunomodulation. Overall, 10 patients who met the U.K. Royal College of Pediatrics and Child Health case definition during a 2-month study period were analyzed. All tested positive for SARS-CoV-2 IgG antibody. Although only 20% were ventilated, 100% required inotropic or vasopressor support. All children had significantly raised inflammatory markers with a median C-reactive protein of 248 (175-263) mg/L, ferritin of 1,561 (726-2,255) µg/L, and troponin-I of 723 (351-2,235) ng/L. Six patients had moderately impaired myocardial function and two had severe impairment. None needed extracorporeal membrane oxygenation. Despite severe illness only a brief period of critical care support of 3 to 5 days was required. Eight received at least one dose of intravenous immunoglobulin. Six received high-dose steroids. Clinical improvement including cardiovascular stability and reduction in inflammatory markers may have occurred with and without immunomodulation.
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