Hemolytic uremic syndrome; pathogenesis, treatments and outcome

被引:92
作者
Siegler, R [1 ]
Oakes, R [1 ]
机构
[1] Univ Utah, Sch Med, Dept Pediat, Div Nephrol, Salt Lake City, UT 84132 USA
关键词
ACE inhibitors; complement system; factor H; hemolytic uremic syndrome (HUS); shiga toxin;
D O I
10.1097/01.mop.0000152997.66070.e9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose of review The hemolytic uremic syndrome (HUS) is the most common cause of acute renal failure in infants and young children, and is a substantial cause of-acute mortality and chronic morbidity, It is therefore relevant and appropriate that pediatricians remain familiar with the various subsets of the disease including its classification, management, and outcome. Recent findings This review will focus on recent information relative to epidemiology, pathogenesis, treatment, and outcome. It will include some of the newer associations between HUS and a variety of infections, including, but not limited to E coli O157:H7 (Shiga toxin-mediated) HUS, as well as the ever-increasing,number of associations between HUS and a variety of drugs. It will review some of the newer therapies for, the more common subsets, but will acknowledge that choosing evidence-based therapies is often limited by our incomplete understanding of the various pathogenic cascades, and that with the possible exception of Shiga toxin-mediated HUS(D+HUS), long-term outcome information is often limited by small numbers and limited follow-up. Summary This review should provide a framework for making the proper diaghosis,implementing appropriate treatment, and advising the family about anticipated outcome.
引用
收藏
页码:200 / 204
页数:5
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