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The Trilogy of SARS-CoV-2 in Pediatrics (Part 2): Multisystem Inflammatory Syndrome in Children
Insights
Multisystem Inflammatory Syndrome in Children (MIS-C) is a new illness with varied severity, often causing fever and GI issues. Current treatments for MIS-C are based on Kawasaki disease experience, lacking specific trials.
Area of Science:
- Pediatric critical care medicine
- Pediatric rheumatology
- Infectious diseases
Background:
- Multisystem Inflammatory Syndrome in Children (MIS-C) emerged in 2020.
- It shares features with hyperinflammatory syndromes like Kawasaki disease and macrophage activation syndrome.
- Clinical presentation ranges from mild febrile illness to critical shock.
Purpose of the Study:
- To provide a comprehensive review of published data on MIS-C evaluation and management.
- To focus on pharmacotherapy treatment considerations for MIS-C.
- To address the lack of controlled trials for MIS-C treatment.
Main Methods:
- Systematic review of published literature on MIS-C.
- Analysis of clinical manifestations, diagnostic criteria, and treatment strategies.
- Synthesis of data from case reports, case series, and observational studies.
Main Results:
- Common symptoms include persistent fever and gastrointestinal issues.
- Cardiac involvement, such as ventricular dysfunction and coronary aneurysms, is a significant concern.
- Current treatment relies on immunomodulatory agents, often extrapolated from Kawasaki disease protocols.
Conclusions:
- MIS-C requires prompt recognition and multidisciplinary management.
- Pharmacotherapy for MIS-C is largely empirical, necessitating further research.
- Evidence-based guidelines for MIS-C treatment are needed.
Abstract:
Multisystem Inflammatory Syndrome in Children (MIS-C) was first recognized as a novel illness in 2020 with manifestations similar to other hyperinflammatory syndromes, such as Kawasaki disease or macrophage activation syndrome. Severity varies from a self-limited febrile illness to shock requiring inotropes and mechanical ventilation. Gastrointestinal symptoms and persistent fevers are the most common clinical symptoms, with the addition of cardiac manifestations inclusive of ventricular dysfunction and coronary artery aneurysms. With no controlled trials or comparative effectiveness studies evaluating treatment of MIS-C to date, current treatment with immunomodulatory agents has mainly been derived from previous experience treating Kawasaki disease. This article provides a comprehensive review summarizing published data for the evaluation and management of MIS-C, with a focus on pharmacotherapy treatment considerations.
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