Hepatorenal syndrome

被引:13
作者
Guevara, M [1 ]
Rodés, J [1 ]
机构
[1] Univ Barcelona, Liver Unit, Hosp Clin, Inst Invest Biomed August Pi i Sunyer, Barcelona 08032, Spain
关键词
hepatorerial syndromes; ascites; renal failures; cirrhosis; vasoconstrictors;
D O I
10.1016/j.biocel.2004.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatorenal syndrome (HRS) is a major complication of patients with cirrhosis, with the annual incidence in patients with ascites being approximately 8% [Bataller, Gines, Guevara, & Arroyo, 1997: Semin Liv Dis 17, 233]. This syndrome develops in the latest phase of the disease and there is now evidence that it is an important determinant of patient survival. Many aspects of HRS are, however, still poorly understood. There are two types of HRS: type I or progressive HRS which is associated with a very poor prognosis (median survival rate lower than 2 weeks), and Type 2 HRS which is characterized by a steady impairment in circulatory and renal function. The pathogenesis of HRS is a deterioration in effective arterial blood volume due to splanchnic arterial vasodilation and a reduction in venous return and cardiac output. It is therefore not surprising that the syndrome can be reversed by the simultaneous intravenous administration of albumin and arterial vasoconstrictors. Intrarenal mechanisms are also important and require prolonged improvement in circulatory function to be deactivated. Long-term administration of intravenous albumin and vasoconstrictors or the correction of portal hypertension with a transjugular intrahepatic portacaval shunt are effective in the treatment of HRS. They also appear to improve survival and may serve as a bridge to liver transplantation, which is the treatment of choice in these patients. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 26
页数:5
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