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[肝肾综合征]

[The hepatorenal syndrome].

作者信息

Møller S, Abrahamsen J, Ring-Larsen H, Henriksen J H

机构信息

Hvidovre Hospital, klinisk fysiologisk/nuklearmedicinsk afdeling 239, København.

出版信息

Ugeskr Laeger. 1995 May 29;157(22):3185-9.

PMID:7770981
Abstract

Renal dysfunction and abnormal sodium-water handling are frequent in liver disease. The term hepatorenal syndrome (HRS) denotes a functional type of renal failure characterized by a progressive decrease in the glomerular filtration rate (GFR), greatly increased sodium retention, a high urine/plasma ratio of solutes, azotaemia, and oliguria. The main pathogenic feature is reduced renal blood flow (RBF), especially in the cortex. The kidney is morphologically intact and has been shown to rapidly regain normal function after transplantation to a recipient with a healthy liver. Three factors should be considered in the pathogenesis of HRS: 1) decreased liver function; 2) deranged haemodynamics, including abnormal blood pressure, blood volume, and blood flow distribution; and 3) deranged neuro-humoral regulation. The prognosis in HRS is very poor, and therapy for HRS has proved disappointing. However future studies should be directed towards the reduced liver function and the haemodynamic abnormalities, especially the abnormal renal vasoconstriction. Implantation of a peritoneovenous shunt, paracentesis with plasma expansion, certain "blockers", and normalization of arterial blood pressure have reversed the HRS only in the more early stages. Liver transplantation is the ultimate treatment for the HRS.

摘要

肾功能不全及钠水代谢异常在肝脏疾病中很常见。肝肾综合征(HRS)这一术语指的是一种功能性肾衰竭,其特征为肾小球滤过率(GFR)进行性下降、钠潴留显著增加、尿/血浆溶质比值升高、氮质血症及少尿。主要的致病特征是肾血流量(RBF)减少,尤其是皮质肾血流量减少。肾脏形态学上是完整的,并且已证明在移植到肝脏健康的受体后能迅速恢复正常功能。肝肾综合征的发病机制应考虑三个因素:1)肝功能下降;2)血流动力学紊乱,包括血压、血容量及血流分布异常;3)神经 - 体液调节紊乱。肝肾综合征的预后非常差,且已证明对其的治疗效果令人失望。然而,未来的研究应针对肝功能下降及血流动力学异常,尤其是肾血管异常收缩。仅在较早期阶段,植入腹腔静脉分流术、扩容性腹腔穿刺放液、某些“阻滞剂”及动脉血压正常化才可逆转肝肾综合征。肝移植是肝肾综合征的最终治疗方法。

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