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Factors Associated with COVID-19 Infection Related Multisystem Inflammatory Syndrome in Children: A Multicenter
Buddhaporn Prasertsakul1,2, Phanthila Sitthikarnkha3, Chetta Ngamjarus4
1Department of Pediatrics, Chum Phae Hospital, Khon Kaen 40130, Thailand.
Antiviral therapy during COVID-19 infection significantly reduced the risk of developing Multisystem Inflammatory Syndrome in Children (MIS-C). This finding offers crucial insights for managing pediatric post-COVID conditions.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Public Health
Background:
- The COVID-19 pandemic led to an increased incidence of Multisystem Inflammatory Syndrome in Children (MIS-C).
- Factors linking COVID-19 infection to MIS-C in children remain incompletely understood.
- This study addresses the need for clarity on MIS-C development post-COVID-19.
Purpose of the Study:
- To investigate factors associated with MIS-C in children following COVID-19 infection.
- To identify potential protective or risk factors for MIS-C development.
- To inform clinical management and public health strategies for pediatric COVID-19 complications.
Main Methods:
- A multicenter-matched case-control study was conducted in Thailand.
- Included were pediatric patients (under 21) diagnosed with MIS-C (cases) and COVID-19 survivors without MIS-C (controls).
- Conditional logistic regression analyzed associations between factors and MIS-C, with a 1:2 case-to-control ratio matched for age and gender.
Main Results:
- Antiviral therapy during COVID-19 infection was associated with a significantly reduced risk of MIS-C (adjusted odds ratio: 0.06).
- No association was found between COVID-19 vaccination status and MIS-C development.
- Nutritional status did not show a significant link to MIS-C incidence in this cohort.
Conclusions:
- Antiviral treatment during acute COVID-19 infection appears to be a protective factor against MIS-C in children.
- Further research is warranted to explore the mechanisms behind this protective effect.
- Findings suggest a potential therapeutic strategy to mitigate MIS-C risk.
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