Hypervolemic Hyponatremia (Liver).

2区 医学 Q2 Medicine Frontiers of Hormone Research Pub Date : 2019-01-01 Epub Date: 2019-01-15 DOI:10.1159/000493241
Elsa Solà, Pere Ginès
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引用次数: 5

Abstract

Hyponatremia is a frequent complication in patients with advanced cirrhosis. Patients with cirrhosis can develop two types of hyponatremia, hypovolemic or hypervolemic (dilutional) hyponatremia. Hypervolemic hyponatremia is the most common type and it develops as a consequence of an impairment in the renal capacity to eliminate solute-free water. The key mechanism leading to solute-free water retention is a non-osmotic hypersecretion of vasopressin (AVP), secondary to a reduction in effective arterial blood pressure existing in patients with advanced cirrhosis. Hypervolemic hyponatremia is associated with increased morbidity and mortality in patients with cirrhosis, and it has also been associated with increased complications after liver transplantation. Currently, the management of hypervolemic hyponatremia in cirrhosis is based on fluid restriction. Vaptans, oral selective vasopressin V2-receptor antagonists, and particularly tolvaptan, have been investigated as a pharmacological approach for the management of hypervolemic hyponatremia in cirrhosis. However, existing information on its efficacy in cirrhosis is still scarce and a recent warning has been raised about their potential role on inducing liver injury at high doses.

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高血容量性低钠血症(肝)。
低钠血症是晚期肝硬化患者的常见并发症。肝硬化患者可出现两种类型的低钠血症,低血容量性或高血容量性(稀释性)低钠血症。高血容量性低钠血症是最常见的类型,它是肾脏消除无溶质水能力受损的结果。导致无溶质水潴留的关键机制是抗利尿激素(AVP)的非渗透性高分泌,继发于晚期肝硬化患者有效动脉血压的降低。高血容量性低钠血症与肝硬化患者的发病率和死亡率增加有关,也与肝移植后并发症增加有关。目前,肝硬化高血容量性低钠血症的治疗是基于液体限制。口服选择性血管加压素v2受体拮抗剂伐伐坦,特别是托伐伐坦,已被研究作为治疗肝硬化高容性低钠血症的药理学方法。然而,关于其对肝硬化疗效的现有信息仍然很少,最近有人警告说,高剂量时它们可能会诱发肝损伤。
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来源期刊
Frontiers of Hormone Research
Frontiers of Hormone Research 医学-内分泌学与代谢
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期刊介绍: A series of integrated overviews on cutting-edge topics New sophisticated technologies and methodological approaches in diagnostics and therapeutics have led to significant improvements in identifying and characterizing an increasing number of medical conditions, which is particularly true for all aspects of endocrine and metabolic dysfunctions. Novel insights in endocrine physiology and pathophysiology allow for new perspectives in clinical management and thus lead to the development of molecular, personalized treatments. In view of this, the active interplay between basic scientists and clinicians has become fundamental, both to provide patients with the most appropriate care and to advance future research.
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