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Pediatric infection with the Omicron variant increases the risks of febrile seizures among COVID-19 infected children. | LitMetric

Background: The Omicron variant of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is less likely to cause severe disease in children than the other variants but has become an increasing cause of febrile seizures (FS) among children. In this case-control study, we aimed to examine the risk factors associated with FS in children infected with the COVID-19 Omicron variant and related treatment modalities.

Methods: This retrospective case-control study includes 113 subjects infected with the COVID-19 Omicron variant, grouped into 45 cases (those with FS) and 68 controls (those without FS). Data on clinical features, laboratory parameters, and treatment modalities were collected and analyzed.

Results: Approximately 5.74% of COVID-19 infected children developed COVID-19-associated FS. Children with COVID-19 and high body temperatures [RR 1.474; (95% CI: 1.196-1.818),  < 0.001], previous history of FS [RR 1.421; (95% CI: 1.088-1.855),  = 0.010], high procalcitonin levels [RR 1.140; (95% CI: 1.043-1.246),  = 0.048] and high neutrophil counts [RR 1.015; (95% CI: 1.000-1.029),  = 0.048] were more likely to experience FS than the controls. In contrast, children with COVID-19 and low eosinophil counts, low hemoglobin levels, and cough had a lower risk of developing FS [RR 0.494; (95% CI: 0.311-0.783),  = 0.003], [RR 0.979; (95% CI: 0.959-0.999),  = 0.044]; and [RR 0.473 (95% CI 0.252-0.890),  = 0.020]; respectively. Children with FS received more anti-flu medications than those without.

Conclusion: A significant increase in FS was observed in children with Omicron SARS-CoV-2 infection. A higher body temperature, a history of FS, a higher procalcitonin level, and a high neutrophil count were all associated with an increased risk of FS in children with COVID-19. The risk of developing FS was lower in children with COVID-19 and low eosinophil counts and hemoglobin levels than in those without.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469930PMC
http://dx.doi.org/10.3389/fped.2023.1226403DOI Listing

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