Initial intravenous gammaglobulin treatment failure in Kawasaki disease

被引:221
作者
Wallace, CA
French, JW
Kahn, SJ
Sherry, DD
机构
[1] Childrens Hosp & Reg Med Ctr, Seattle, WA 98105 USA
[2] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
关键词
corticosteroids; vasculitis; Kawasaki disease; heart disease; gammaglobulin therapy; cyclophosphamide;
D O I
10.1542/peds.105.6.e78
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives. To determine initial intravenous gammaglobulin (IVIG) treatment failures in Kawasaki disease (KD) and to report the outcome of retreatment and our use of pulse intravenous (IV) methylprednisolone and cyclophosphamide in patients with persistent KD. Study Design. Retrospective analysis of the treatment and response of children with KD over 3 years. Results. Fifty (77%) of 65 patients completely responded to a single treatment with IVIG (2 g/kg). Fifteen patients (23%) required retreatment; 10 patients fully responded but 5 had persistent disease (3 developed coronary aneurysms and 4 developed coronary artery thrombosis). Four of these 5 patients with persistent disease were treated with pulse IV methylprednisolone and 2 were also treated with IV cyclophosphamide. There was no progression of coronary aneurysms and no deaths. No initial patient characteristics predicted IVIG treatment failure or the development of coronary aneurysms. Conclusion. Nearly 23% of patients with KD may require retreatment and 8% may develop coronary aneurysm. Additional antiinflammatory therapy, such as IV methylprednisolone and IV cyclophosphamide, may be helpful in treating persistent KD.
引用
收藏
页码:art. no. / e78
页数:4
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