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Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Recent advances in the treatment of Kawasaki disease
Ken-Pen Weng1, Shan-F Ou, Chu-Chuan Lin
1Department of Pediatrics, Kaohsiung Veterans General Hospital, Kaohsiung, and National Yang-Ming University School of Medicine, Taipei, Taiwan, ROC.
Insights
Kawasaki disease (KD) is a childhood vasculitis. Current treatments like IVIG and aspirin may not prevent coronary artery lesions (CALs) in all children, necessitating further research into optimal management strategies.
Area of Science:
- Pediatric Rheumatology
- Cardiovascular Research
- Immunology
Background:
- Kawasaki disease (KD) is a leading cause of acquired heart disease in children.
- Coronary artery lesions (CALs) are a significant complication, affecting 15-25% of untreated patients.
- Intravenous immunoglobulin (IVIG) is standard therapy, but 8-38% of patients are unresponsive.
Purpose of the Study:
- To review current therapeutic strategies for Kawasaki disease.
- To evaluate the efficacy of existing treatments in preventing CALs.
- To identify areas for future research in KD management.
Main Methods:
- Literature review of Kawasaki disease treatment protocols.
- Analysis of data on the effectiveness of IVIG and aspirin in preventing CALs.
- Discussion of alternative and emerging therapies.
Main Results:
- High-dose IVIG is the gold standard but has limitations in unresponsive patients.
- Aspirin, in conjunction with IVIG, showed no evidence of efficacy in preventing CALs.
- The role of steroids and other immunosuppressants like infliximab requires further investigation.
Conclusions:
- Optimal management of KD, especially for IVIG-resistant cases, remains to be defined.
- Early intervention to manage chronic inflammation is crucial due to early subclinical atherosclerosis.
- Multicenter studies are needed to establish definitive treatment guidelines for Kawasaki disease.
Abstract:
Kawasaki disease (KD) is acute systemic vasculitis that occurs mainly in infants and children under 5 years of age. The etiology of KD remains unknown. KD is liable to be complicated by coronary artery lesions (CALs), which develop in approximately 15-25% of untreated KD children and in approximately 5% of KD children after intravenous immunoglobulin (IVIG) therapy. A single high dose of IVIG (2 g/kg) is the gold standard therapy in the acute stage of KD. However, approximately 8--38% of children are unresponsive to initial IVIG treatment and at increased risk for CAL development. Anti-inflammatory high doses of aspirin are recommended in conjunction with IVIG, but our study demonstrated that there is no evidence of efficacy in preventing CAL development. The usefulness of steroids in initial therapy for KD or treatment of IVIG-resistant patients is not well established. Other immunosuppressive therapies, including infliximab, have been used in the treatment of refractory KD, but merit additional investigation. Subclinical atherosclerosis may develop early in KD patients, which makes early initiation of therapy to improve chronic inflammation an important issue. Future multicenter studies may help to define the optimal management of KD patients.
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