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

Author:

Tzoulis Ploutarchos1ORCID,Kaltsas Gregory2,Baldeweg Stephanie E.34,Bouloux Pierre-Marc5,Grossman Ashley B.678

Affiliation:

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

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

3. Department of Diabetes & Endocrinology, University College London Hospitals NHS Foundation Trust, London, UK

4. Division of Medicine, University College London, London, UK

5. Centre for Neuroendocrinology, University College London, London, UK

6. Green Templeton College, University of Oxford, Oxford, UK

7. Neuroendocrine Tumour Unit, Royal Free Hospital, London, UK

8. Centre for Endocrinology, Barts and the London School of Medicine, Queen Mary University of London, London, UK

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.

Publisher

SAGE Publications

Subject

Endocrinology, Diabetes and Metabolism

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