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Terlipressin and hyponatraemia: The cause or the treatment?

机译:特利加压素和低钠血症:病因或治疗?

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I read with interest the paper by Prakoso et ah on ter-lipressin in the treatment of hyponatremia in patients with advanced cirrhosis. Hyponatraemia is a clinical problem with few treatment options. The mechanism of hyponatraemia in cirrhosis is not fully understood, but the pathophysiology involves non-osmotic releases of arginine-vasopressin (AVP). Thus, central hypovolemia and decreased blood pressure with stimulation of arterial and cardiopulmonary baroreceptors are important. Any intervention that improves effective arterial blood volume can potentially improve hyponatraemia in cirrhosis. On the other hand it is noteworthy that treatment with vasopressin-2 receptor antagonists (vaptans) has not been very successful in cirrhosis, suggesting that the pathophysiology is more complex.In the retrospective study by Prakoso et ah, terlipressin (maximum dose 1 mg/4 h) was used in combination with albumin (40 g/day) at median 7 days, and the changes represent a combination of small doses of terlipressin and medium doses of albumin.
机译:我饶有兴趣地阅读了Prakoso等人关于ter-pressin在晚期肝硬化患者低钠血症治疗中的论文。低钠血症是一种临床问题,几乎没有治疗选择。肝硬化低钠血症的机制尚不完全清楚,但其病理生理学涉及精氨酸加压素(AVP)的非渗透释放。因此,在刺激动脉和心肺压力感受器方面,中枢血容量不足和血压降低很重要。任何改善有效动脉血容量的干预措施都可能改善肝硬化患者的低钠血症。另一方面,值得注意的是,血管加压素2受体拮抗剂(vaptans)的治疗在肝硬化方面还不是很成功,这表明其病理生理更为复杂.Prakoso等人的回顾性研究中,特利加压素(最大剂量为1 mg /在中位数7天将4 h)与白蛋白(40 g /天)组合使用,并且变化代表小剂量特利加压素和中剂量白蛋白的组合。

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