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肝肾综合征及其治疗新进展。

Hepatorenal syndrome and novel advances in its management.

机构信息

Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Milano, Italy.

出版信息

Kidney Blood Press Res. 2013;37(6):588-601. doi: 10.1159/000355739. Epub 2013 Dec 5.

Abstract

Hepatorenal syndrome is a complication of end stage liver disease. It is a unique form of functional renal failure related to kidney vasoconstriction in the absence of underlying kidney pathology. Hepatorenal syndrome is classified into 2 types: type-1 HRS shows a rapid and progressive decline in renal function with a very poor prognosis (median survival of about 2 weeks); type-2 HRS has a more stable kidney failure, with a median survival of 6 months; its main clinical manifestation is refractory ascites. The most appropriate therapy for HRS is liver transplantation but only a minority of HRS patients undergo the procedure due to the high mortality; survival among liver transplant recipients is lower in HRS than among their counterparts without HRS. A large body of evidence, based on observational studies and randomized controlled trials, has been accumulated in the last decade showing that terlipressin represents a milestone in the management of HRS. According to our meta-analysis of randomized trials comparing terlipressin vs. placebo (five trials, n=243 patients), the pooled rate of patients who reversed HRS by terlipressin was 8.09 (95% CI, 3.52; 18.59) (P<0.001). Among vasoconstrictors, terlipressin (a V1 vasopressin agonist) is the most widely used; however, noradrenaline is another good choice. Vasoconstrictor drugs alone or with albumin reduce mortality compared with no intervention or albumin (RR of mortality, 0.82; 95% Confidence Intervals, 0.70; 0.96) (P<0.01). Two series of patients with HRS recurrence after the first treatment have recently shown that long-term therapy with terlipressin and albumin is beneficial as a bridge to liver transplant. Nevertheless, recovery of renal function can be achieved in less than 50% of patients with HRS after terlipressin use and the recovery of renal function may also be partial in patients who are defined full responders. Renal replacement therapy should not be considered a first-line therapy for HRS Clinical trials are under way in order to assess efficacy and safety of novel therapeutic agents for the treatment of type-1 and type-2 HRS.

摘要

肝肾综合征是终末期肝病的并发症。它是一种独特的功能性肾功能衰竭形式,与肾脏血管收缩有关,而无潜在的肾脏病理学。肝肾综合征分为 2 型:1 型 HRS 表现为肾功能迅速进行性下降,预后极差(中位生存期约 2 周);2 型 HRS 肾功能衰竭较稳定,中位生存期 6 个月;其主要临床表现为难治性腹水。HRS 最适宜的治疗方法是肝移植,但由于死亡率高,只有少数 HRS 患者接受该手术;肝移植受者的存活率低于无 HRS 的受者。过去十年中,基于观察性研究和随机对照试验积累了大量证据,表明特利加压素在 HRS 治疗中具有里程碑意义。根据我们对特利加压素与安慰剂比较的随机试验的荟萃分析(五项试验,共 243 例患者),特利加压素逆转 HRS 的患者比例为 8.09(95%CI,3.52;18.59)(P<0.001)。在血管收缩剂中,特利加压素(一种 V1 血管加压素激动剂)应用最广泛;然而,去甲肾上腺素也是另一个不错的选择。血管收缩剂单独或与白蛋白使用可降低死亡率,与无干预或白蛋白相比(死亡率的 RR,0.82;95%置信区间,0.70;0.96)(P<0.01)。最近有两项 HRS 首次治疗后复发患者的系列研究表明,特利加压素和白蛋白的长期治疗作为肝移植的桥梁是有益的。然而,在使用特利加压素后,不到 50%的 HRS 患者可以恢复肾功能,而在被定义为完全反应者的患者中,肾功能的恢复也可能是部分的。肾功能衰竭患者不应考虑肾替代治疗作为 HRS 的一线治疗。目前正在进行临床试验,以评估新型治疗药物治疗 1 型和 2 型 HRS 的疗效和安全性。

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