Describe the treatment.
IV immunoglobulin (IVIG)
High single-dose to reduce the risk of coronary artery aneurysms
Most effective if given within the first 10 days following disease onset
High-dose oral aspirin
IV glucocorticoids: may be considered in addition to standard treatment, esp. in cases of treatment-refractory disease, as they lower the risk of coronary involvement
What should be considered concerning Aspirin?
To avoid the risk of Reye syndrome, children should not be treated with aspirin, especially if a viral infection is suspected. Kawasaki disease is an exception to this rule.
What are complications?
Coronary artery aneurysm
The risk of aneurysms is highest during the second and third weeks following symptom onset.
Rupture or thrombosis of the aneurysm can be lethal.
Myocardial infarction
Myocarditis
Ventricular dysfunction
Most commonly occurs within the first 2 weeks of onset of Kawasaki disease
Often seen in infants with untreated Kawasaki disease
Most commonly associated with lymphocytic myocarditis
Manifests with symptoms (e.g., tachypnea or diaphoresis with feeding, exertional dyspnea) and physical examination findings of congestive heart failure (e.g., hepatomegaly, S3 gallop, rales or crackles on lung auscultation)
Increased risk of sudden death
Arrhythmias
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