Evidence map›Paper›PMID 41557166›Full record

ArticleClinical rheumatology2026

Kawasaki disease in adolescents: age-specific clinical features and factors associated with outcomes.

Hee Joung Choi, So Hyeon Gwon, Nak-Hoon Son, Gi Beom Kim

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Article in Clinical rheumatology, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hee Joung ChoiDepartment of Pediatrics, Keimyung University Dongsan Hospital, Keimyung University School of Medicine, 1035 Dalgubeol-Daero, Dalseo-Gu, Daegu, 42601, Republic of Korea. joung-756@hanmail.net.ORCID http://orcid.org/0000-0002-7119-4194
So Hyeon GwonDepartment of Statistics, College of Natural Science, Keimyung University, Daegu, Republic of Korea.ORCID http://orcid.org/0009-0000-6591-8291
Nak-Hoon SonDepartment of Statistics, College of Natural Science, Keimyung University, Daegu, Republic of Korea.ORCID http://orcid.org/0000-0002-6192-8852
Gi Beom KimDepartment of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-7880-280X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn adolescents, Kawasaki disease (KD) often manifests with non-specific clinical symptoms, which delays diagnosis and treatment and consequently increases the risk of coronary artery lesions (CALs). This study investigated the clinical characteristics of KD across age groups, focusing on adolescents, and identified age-specific factors associated with treatment resistance and CALs.

methodsA retrospective analysis was conducted using nationwide survey data compiled in South Korea from 2009 to 2017.

resultsA total of 34,408 patients with KD were stratified into four age groups at the time of diagnosis: < 1 year (7425; 21.6%), 1-4 years (22,629; 65.8%), 5-9 years (4089; 11.9%), and ≥ 10 years (265; 0.8%). Compared to younger age groups, the ≥ 10-year age group had a greater proportion of males, longer total and pre-admission fever duration, a greater likelihood of incomplete KD with fewer typical symptoms, more cervical lymphadenopathy, and less erythema at the Bacillus Calmette-Guérin inoculation site. Although some differences were not statistically significant, this group had higher rates of unresponsiveness to first and second intravenous immunoglobulin (IVIG) treatments and second-line steroid use, and more coronary dilatation and aneurysms, but no differences in coronary stenosis, occlusion, or mortality. In adolescents, IVIG unresponsiveness was only associated with prolonged fever, and CALs was associated with recurrent KD, prolonged fever, lower total protein levels, and fewer acute-phase extremity changes.

conclusionsAdolescents with KD exhibit distinct clinical features, characteristic age-specific risk factors, and a higher risk of CALs, highlighting the need for age-specific management strategies. Key Points • KD in adolescence is rare, accounting for approximately 0.8% of all cases. • Adolescents with KD exhibited longer fever duration, more incomplete KD presentation, higher rates of unresponsiveness to IVIG, and a greater incidence of CALs. • Prolonged fever and recurrent KD were associated with treatment resistance and CALs in adolescent KD.

Indexed as

Immunoglobulins, IntravenousMucocutaneous Lymph Node SyndromeAdolescentAge FactorsChildChild, PreschoolCoronary AneurysmCoronary Artery DiseaseFemaleHumansInfantMaleRepublic of KoreaRetrospective StudiesRisk FactorsTreatment OutcomeImmunoglobulins, IntravenousAdolescentsCoronary artery lesionKawasaki diseaseOutcomePediatric

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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.