Abstract
Intravenous methylprednisolone pulse (IVMP) therapy is administered to children with severe illnesses, such as Kawasaki disease (KD), collagen disease, and kidney disease, because of its powerful, rapid, and probably nongenomic immunosuppressive action. In a randomized controlled trial, IVMP plus initial intravenous immunoglobulin (IVIG) therapy did not decrease the incidence of coronary artery lesions (CAL) in KD patients as compared with IVIG plus placebo. Predicted nonresponders to IVIG treated with initial IVIG plus IVMP had earlier defervescence and lower incidence of CAL than did those treated with IVIG alone. Some studies showed that IVMP was effective for fast defervescence and prevention of CAL in nonresponders to initial or additional IVIG. The adverse effects of IVMP for KD patients include sinus bradycardia, hypertension, hyperglycemia, and hypothermia, but these effects were usually transient and not serious. Present evidence indicates that IVMP should be given as initial therapy for predicted IVIG nonresponders and as rescue therapy for confirmed nonresponders to initial or additional IVIG.
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Miura, M. (2017). Methylprednisolone Pulse Therapy for Nonresponders to Immunoglobulin Therapy. In: Saji, B., Newburger, J., Burns, J., Takahashi, M. (eds) Kawasaki Disease. Springer, Tokyo. https://doi.org/10.1007/978-4-431-56039-5_18
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DOI: https://doi.org/10.1007/978-4-431-56039-5_18
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