Sinha Vikash K, Ko Benjamin
Section of Nephrology, University of Chicago, Chicago, IL.
Section of Nephrology, University of Chicago, Chicago, IL.
Adv Chronic Kidney Dis. 2015 Sep;22(5):361-7. doi: 10.1053/j.ackd.2015.02.002.
Cirrhosis is characterized by systemic and splanchnic vasodilation that leads to excessive nonosmotic secretion of vasopressin (antidiuretic hormone). Hyponatremia is a common electrolyte abnormality in advanced liver disease that results from the impaired ability of the kidney to excrete solute-free water that leads to "dilutional" hyponatremia-water retention disproportionate to the retention of sodium. Hyponatremia in liver diseases carries the prognostic burden, correlates with the severity of cirrhosis, and, in recent studies, has also been implicated in the pathogenesis of hepatic encephalopathy. The current treatment options are limited to conventional therapies like fluid restriction, and the outcomes are unsatisfactory. Although currently available vasopressin (V2 receptors) antagonists have been shown to increase serum sodium concentrations and improve ascites control, their role in the treatment of hyponatremia in liver disease patients remains questionable because of adverse effect profiles, high cost, and poor data on long-term mortality benefits. More information is needed to argue the benefits vs risks of short-term use of vaptans for correction of hyponatremia especially just hours-to-days before liver transplant.
肝硬化的特征是全身和内脏血管舒张,导致血管加压素(抗利尿激素)过度非渗透性分泌。低钠血症是晚期肝病常见的电解质异常,其原因是肾脏排泄无溶质水的能力受损,导致“稀释性”低钠血症——水潴留与钠潴留不成比例。肝病中的低钠血症具有预后负担,与肝硬化的严重程度相关,并且在最近的研究中,还与肝性脑病的发病机制有关。目前的治疗选择仅限于诸如限液等传统疗法,且效果并不理想。尽管目前可用的血管加压素(V2受体)拮抗剂已被证明可提高血清钠浓度并改善腹水控制,但由于其不良反应、高成本以及关于长期死亡率益处的不良数据,它们在肝病患者低钠血症治疗中的作用仍存在疑问。需要更多信息来论证短期使用血管加压素受体拮抗剂纠正低钠血症的益处与风险,尤其是在肝移植前数小时至数天使用时。