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• W2773879863 abstract "Kawasaki disease (KD) is a vasculitis of unknown aetiology predominantly affecting preschool children [ [1] Kawasaki T. Kosaki F. Okawa S. Shigematsu I. Yanagawa H. A new infantile acute febrile mucocutaneous lymph node syndrome (MLNS) prevailing in Japan. Pediatrics. 1974; 54: 271-276 Crossref PubMed Google Scholar ]. With appropriate and timely treatment with intravenous immunoglobulin, the majority of patients do not develop coronary artery aneurysms, the main complication causing long-term cardiovascular morbidity and mortality [ [2] Newburger J.W. Takahashi M. Burns J.C. Kawasaki Disease. J Am Coll Cardiol. 2016; 67: 1738-1749 Crossref PubMed Scopus (322) Google Scholar ]. Notwithstanding, KD remains the leading cause of paediatric acquired heart disease in industrialised countries [ [3] Uehara R. Belay E.D. Epidemiology of Kawasaki disease in Asia, Europe, and the United States. J Epidemiol. 2012; 22: 79-85 Crossref PubMed Scopus (364) Google Scholar ]. As adults with previous KD enter middle age, an increasingly important but unresolved question is whether KD increases later cardiovascular risk. This is especially pertinent for the large group of KD patients currently considered low risk; those with normal or transiently dilated coronary arteries, or with regressed coronary artery aneurysms. Understanding the long-term risk in these patients would facilitate risk stratification for targeting ongoing management." @default.
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• W2773879863 date "2018-01-01" @default.
• W2773879863 modified "2023-09-30" @default.
• W2773879863 title "Cardiovascular Risk After Kawasaki Disease - Findings From an Australian Case-Control Study" @default.
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• W2773879863 doi "https://doi.org/10.1016/s1443-9506(17)31473-7" @default.
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