Evidence map›Paper›PMID 42439216›Full record

ArticlePediatrics international : official journal of the Japan Pediatric Society

MIS-C Overlap, Not Prior COVID-19 Itself, Drives Treatment Escalation in Kawasaki Disease: A Nationwide Cohort Study.

Min Ji Kim, Jong Seung Kim, Jee Young Hong, Jihye You

Abstract read
In one paragraph

Article in Pediatrics international : official journal of the Japan Pediatric Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Min Ji KimDepartment of Medical Informatics, Jeonbuk National University Medical School, Jeonju, Korea.ORCID https://orcid.org/0009-0008-9774-4239
Jong Seung KimDepartment of Otorhinolaryngology-Head and Neck Surgery, Jeonbuk National University Hospital, Jeonju, Korea.ORCID https://orcid.org/0000-0002-1384-6799
Jee Young HongDepartment of Preventive Medicine, College of Medicine, Jeonbuk National University, Jeonju, Korea.ORCID https://orcid.org/0000-0003-4540-0780
Jihye YouResearch Institute of Clinical Medicine of Jeonbuk National University, Jeonju, Korea.ORCID https://orcid.org/0000-0001-5172-1690

Funding

the Fund of the Biomedical Research Institute, Jeonbuk National University Hospital
6 · The paper itself

Abstract

backgroundWhether prior coronavirus disease 2019 (COVID-19) independently influences treatment response in children with Kawasaki disease (KD) is unclear, as prior reports may have been confounded by overlap with multisystem inflammatory syndrome in children (MIS-C). We investigated this in a nationwide cohort, accounting for these factors.

methodsWe conducted a retrospective cohort study using the Korean National Health Insurance Service database. Children diagnosed with KD on or after January 1, 2020 who received IVIG within 7 days were included. Prior COVID-19 was defined as documented infection within 3 months before KD diagnosis. The primary outcome was second-line treatment within 7 days after initial IVIG (composite of second IVIG or additional steroid). 1:1 propensity score matching was performed using age, sex, MIS-C status, and steroid use with initial IVIG.

resultsAmong 6572 eligible children, 512 had prior COVID-19; 431 patients were matched per group. Second-line treatment occurred in 32/431 (7.4%) versus 23/431 (5.3%) (p = 0.265). Prior COVID-19 was not independently associated with second-line treatment (adjusted HR 1.42; 95% CI 0.83-2.43). In subgroup analysis, elevated risk was confined to children with concurrent MIS-C (HR 3.01; 95% CI 1.34-6.74); prior COVID-19 without MIS-C showed no increase (HR 1.18; 95% CI 0.66-2.11). Sensitivity analyses excluding MIS-C and restricted to 2022 onward were consistent.

conclusionsPrior COVID-19 alone was not independently associated with second-line treatment once MIS-C overlap and concurrent steroid use were accounted for. The elevated treatment escalation rate appeared driven primarily by MIS-C, highlighting the importance of distinguishing MIS-C from classic KD.

Indexed as

COVID-19Immunoglobulins, IntravenousMucocutaneous Lymph Node SyndromeSystemic Inflammatory Response SyndromeChildChild, PreschoolFemaleHumansImmunologic FactorsInfantMaleRepublic of KoreaRetrospective StudiesTreatment OutcomeImmunoglobulins, IntravenousImmunologic FactorsCOVID‐19intravenous immunoglobulinsKawasaki diseasemultisystem inflammatory syndrome in childrenSARS‐CoV‐2

Identifiers

PMID42439216
PMCPMC13359311

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.