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托伐普坦用于治疗抗利尿激素分泌失调综合征(SIAD)。

Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD).

作者信息

Tzoulis Ploutarchos, Kaltsas Gregory, Baldeweg Stephanie E, Bouloux Pierre-Marc, Grossman Ashley B

机构信息

Department of Metabolism & Experimental Therapeutics, Division of Medicine, UCL Medical School, University College London, Gower Street, London WC1E 6BT, UK.

First Department of Propaedeutic and Internal Medicine, Laiko University Hospital, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Ther Adv Endocrinol Metab. 2023 May 16;14:20420188231173327. doi: 10.1177/20420188231173327. eCollection 2023.

Abstract

The syndrome of inappropriate antidiuresis (SIAD), the commonest cause of hyponatraemia, is associated with significant morbidity and mortality. Tolvaptan, an oral vasopressin V2-receptor antagonist, leads through aquaresis to an increase in serum sodium concentration and is the only medication licenced in Europe for the treatment of euvolaemic hyponatraemia. Randomised controlled trials have shown that tolvaptan is highly efficacious in correcting SIAD-related hyponatraemia. Real-world data have confirmed the marked efficacy of tolvaptan, but they have also reported a high risk of overly rapid sodium increase in patients with a very low baseline serum sodium. The lower the baseline serum sodium, the higher the tolvaptan-induced correction rate occurs. Therefore, a lower starting tolvaptan dose of 7.5 mg has been evaluated in small cohort studies, demonstrating its efficacy, but it still remains unclear as to whether it can reduce the risk of overcorrection. Most international guidelines, except for the European ones, recommend tolvaptan as second-line treatment for SIAD after fluid restriction. However, the risk of unduly rapid sodium correction in combination with its high cost have limited its routine use. Prospective controlled studies are warranted to evaluate whether tolvaptan-related sodium increase can improve patient-related clinical outcomes, such as mortality and length of hospital stay in the acute setting or neurocognitive symptoms and quality of life in the chronic setting. In addition, the potential role of a low tolvaptan starting dose needs to be further explored. Until then, tolvaptan should mainly be used as second-line treatment for SIAD, especially when there is a clinical need for prompt restoration of normonatraemia. Tolvaptan should be used with specialist input according to a structured clinical pathway, including rigorous monitoring of electrolyte and fluid balance and, if needed, implementation of appropriate measures to prevent, or when necessary reverse, overly rapid hyponatraemia correction.

摘要

抗利尿激素分泌失调综合征(SIAD)是低钠血症最常见的病因,与显著的发病率和死亡率相关。托伐普坦是一种口服的血管加压素V2受体拮抗剂,通过排水作用使血清钠浓度升高,是欧洲唯一获批用于治疗等容性低钠血症的药物。随机对照试验表明,托伐普坦在纠正SIAD相关低钠血症方面非常有效。真实世界的数据证实了托伐普坦的显著疗效,但也报告了基线血清钠水平极低的患者钠水平过度快速升高的高风险。基线血清钠水平越低,托伐普坦引起的纠正率越高。因此,在小型队列研究中评估了7.5mg的较低托伐普坦起始剂量,证明了其疗效,但仍不清楚它是否能降低过度纠正的风险。除欧洲指南外,大多数国际指南推荐托伐普坦作为限液后SIAD的二线治疗药物。然而,钠纠正过快的风险及其高昂的成本限制了其常规使用。有必要进行前瞻性对照研究,以评估托伐普坦相关的钠升高是否能改善患者相关的临床结局,如急性情况下的死亡率和住院时间,或慢性情况下的神经认知症状和生活质量。此外,托伐普坦低起始剂量的潜在作用需要进一步探索。在此之前,托伐普坦应主要用作SIAD的二线治疗药物,尤其是在临床上需要迅速恢复正常血钠水平时。应根据结构化临床路径在专科医生指导下使用托伐普坦,包括严格监测电解质和液体平衡,必要时采取适当措施预防或逆转过度快速的低钠血症纠正。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9282/10192810/de6c1d5ebbf7/10.1177_20420188231173327-fig1.jpg

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