Therapies for steroid-resistant nephrotic syndrome

被引:33
|
作者
Hodson, Elisabeth M. [1 ,2 ]
Craig, Jonathan C. [1 ,2 ]
机构
[1] Childrens Hosp, Ctr Kidney Res, Westmead, NSW 2145, Australia
[2] Univ Sydney, Sch Publ Hlth, Sydney, NSW 2006, Australia
关键词
cyclophosphamide; cyclosporin; focal and segmental glomerulosclerosis; minimal change disease; randomised controlled trials;
D O I
10.1007/s00467-008-0792-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Between 10 and 20% of children with primary nephrotic syndrome are steroid-resistant (SRNS). From earlier studies in children with SRNS, we know that cyclosporin (with or without alternate-day prednisone) and cyclophosphamide (with pulse intravenous corticosteroids) result in comparable complete or partial remission rates of about 60%. An evaluation of the relative effectiveness of cyclophosphamide and cyclosporin has not been possible because of the absence of a head-to-head randomised trial. The Arbeitsgemeinschaft fur Padiatrische Nephrologie trial, published in this issue of Pediatric Nephrology, has filled this gap in our evidence base. Although there was no difference in the number of patients achieving complete remission, those patients receiving cyclosporin treatment were significantly more likely to achieve partial remission than those receiving intravenous cyclophosphamide. This result suggests that cyclosporin rather than cyclophosphamide should be used as first line therapy for children with SRNS.
引用
收藏
页码:1391 / 1394
页数:4
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