Abstract
Acute Kawasaki disease (KD) is treated with high-dose intravenous immunoglobulin (IVIG), which is proven to decrease the incidence of coronary artery aneurysms from 25% to less than 5%. Aspirin is also given, although the evidence base is less secure. There is increasing evidence for steroid therapy as adjunctive primary therapy with IVIG, especially in Asian children. Approximately 10-30% of patients fail to respond to the initial IVIG and are at increased risk of coronary artery aneurysms. The optimal treatment for IVIG-nonresponsive KD remains controversial. Management options include further dose(s) of IVIG, corticosteroids, TNF-α blockade, cyclosporin A, anti-IL-1 and anti-CD20 therapy. In this article, the authors review the current evidence for treatment of acute KD and discuss options for IVIG nonresponders.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Adrenal Cortex Hormones / therapeutic use
-
Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
-
Antibodies, Monoclonal, Murine-Derived / therapeutic use
-
Aspirin / therapeutic use
-
Chemotherapy, Adjuvant
-
Coronary Aneurysm / etiology
-
Coronary Aneurysm / prevention & control
-
Cyclosporine / therapeutic use
-
Enzyme Inhibitors / therapeutic use
-
Humans
-
Immunoglobulins, Intravenous / administration & dosage
-
Immunoglobulins, Intravenous / therapeutic use*
-
Methotrexate / therapeutic use
-
Mucocutaneous Lymph Node Syndrome / complications
-
Mucocutaneous Lymph Node Syndrome / drug therapy*
-
Rituximab
-
Tumor Necrosis Factor-alpha / antagonists & inhibitors
Substances
-
Adrenal Cortex Hormones
-
Anti-Inflammatory Agents, Non-Steroidal
-
Antibodies, Monoclonal, Murine-Derived
-
Enzyme Inhibitors
-
Immunoglobulins, Intravenous
-
Tumor Necrosis Factor-alpha
-
Rituximab
-
Cyclosporine
-
Aspirin
-
Methotrexate