한빛사논문
Ji-Man Kang a,b*, Minsun Kang c*, Young-Eun Kim d, Yoonkyung Choi d, Soo Jeong An e, Jaehyun Seong f, Min Jin Go f, Kyungmin Huh g, Jaehun Jung c,h*
aDepartment of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, South Korea
bInstitute for Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, South Korea
cArtificial Intelligence and Big-Data Convergence Center, Gil Medical Center, Gachon University College of Medicine, Incheon, South Korea
dDepartment of Bigdata Strategy, National Health Insurance Service, Wonju, South Korea
eDepartment of Big Data Management, National Health Insurance Service, Wonju, South Korea
fDivision of Clinical Research, Center for Emerging Virus Research, National Institute of Infectious Disease, National Institute of Health, Osong, South Korea
gDivision of Infectious Diseases, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea
hDepartment of Preventive Medicine, Gachon University College of Medicine, Incheon, South Korea
⁎Ji-Man Kang, Minsun Kang and Jaehun Jung contributed equally to this work.
Corresponding author: Kyungmin Huh, MD, Jaehun Jung, MD, PhD
Abstract
Objectives: The risk of severe COVID-19 in children with a solid organ transplant (SOT) is not well established. We compare the relative risk of severe COVID-19 infection between pediatric SOT and non-SOT children.
Methods: The newly constructed K-COV-N cohort (Korea Disease Control and Prevention Agency-COVID-19-National Health Insurance Service) was used. Children with COVID-19 (<18 years old) who underwent SOT between January 2008-January 2022 were included. Non-SOT children with COVID-19 were selected in a ratio of 1:4 using propensity score matching. Three definitions of severe COVID-19 were established based on their requirement of respiratory support: Severe I (requiring respiratory support above a high-flow nasal cannula or prolonged hospitalization ≥6 days), Severe II (requiring any oxygen supplement), and Severe III (requiring any oxygen supplement or prolonged hospitalization ≥6 days).
Results: Among 2,957,323 children with COVID-19, 206 pediatric SOTRs were identified and included in the analysis along with 803 matched non-SOT children. Most infections (96.6%) occurred during the Omicron period; no cases of mortality were reported. Pediatric SOTR had a 3.6-fold (95% CI=1.1-11.7, P=0.03) higher risk of Severe I, and a 4.9-fold (95% CI=1.6-15.0, P=0.006) higher risk of Severe III than non-SOT children. No cases of Severe II occurred in the non-SOT children. Although not statistically significant, no severe COVID-19 cases were reported in the vaccinated SOT group (0.0% vs 5.7%, P=0.09 in Severe III).
Conclusions: Pediatric SOTRs have a significantly higher risk of severe COVID-19 than non-SOT children. Our findings support the need for tailored strategies for these high-risk children.
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