Volume 41, Issue 3 pp. 87-93

The diagnosis and management of Kawasaki disease

J Royle

J Royle

Department of General Medicine, Royal Children's Hospital, Melbourne

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D Burgner

D Burgner

School of Paediatrics and Child Health, University of Western Australia, and Princess Margaret Hospital, Perth, Western Australia

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N Curtis

N Curtis

Department of Paediatrics, University of Melbourne, and Paediatric Infectious Diseases Unit, Department of General Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia

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First published: 17 March 2005
Citations: 35
Dr Nigel Curtis, Head of Paediatric Infectious Diseases Unit, Department of General Medicine, Royal Children's Hospital, Parkville, Vic. 3052, Australia. Fax: +61 3 9345 6667; email: [email protected]

Abstract

Abstract: Kawasaki disease (KD) is a systemic vasculitis of childhood with a predilection for the coronary arteries. It is the predominant cause of paediatric acquired heart disease in developed countries. The aetiology of KD remains unknown and consequently there is no diagnostic test. The diagnosis is made using a constellation of clinical criteria that in isolation have poor sensitivity and specificity. Early treatment prevents overt coronary artery damage in the majority of children. The long-term effects of childhood KD on later cardiovascular health remain unknown. A recent study showed that treatment of KD in Australia is suboptimal, with late diagnosis occurring in approximately half of the cases and an unacceptably high incidence of acute cardiac involvement. These guidelines highlight the difficulties in the diagnosis of KD and offer some clues that may assist early recognition of this important paediatric disease. They also detail current treatment recommendations and the evidence on which they are based. Increased awareness of the epidemiology and spectrum of the clinical presentation of KD is essential for early recognition and optimal management.

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