托伐普坦治疗不适当抗利尿综合征(SIAD)。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ploutarchos Tzoulis, Gregory Kaltsas, Stephanie E Baldeweg, Pierre-Marc Bouloux, Ashley B Grossman
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引用次数: 0

摘要

不适当抗利尿综合征(SIAD)是低钠血症的最常见原因,与显著的发病率和死亡率相关。Tolvaptan是一种口服抗利尿激素v2受体拮抗剂,可导致血钠浓度升高,是欧洲唯一获批用于治疗低血容量性低钠血症的药物。随机对照试验表明,托伐普坦在纠正siad相关的低钠血症方面非常有效。真实世界的数据已经证实了托伐普坦的显著疗效,但他们也报道了基线血清钠含量非常低的患者钠含量过快增加的高风险。基线血清钠越低,托伐普坦诱导的纠正率越高。因此,在小型队列研究中评估了较低的起始剂量为7.5 mg的托伐普坦,证明了它的有效性,但它是否能降低矫枉过正的风险仍不清楚。除欧洲指南外,大多数国际指南推荐托伐普坦作为SIAD输液限制后的二线治疗。然而,钠校正过快的风险以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钠的增加是否可以改善患者相关的临床结果,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,低托伐普坦起始剂量的潜在作用需要进一步探讨。在此之前,托伐普坦应主要用作SIAD的二线治疗,特别是当临床需要迅速恢复正常血症时。托伐普坦应根据结构化的临床途径与专家意见一起使用,包括严格监测电解质和液体平衡,并在必要时采取适当措施防止或在必要时逆转过快的低钠血症纠正。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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CiteScore
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