Cargando…

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 lice...

Descripción completa

Detalles Bibliográficos
Autores principales: Tzoulis, Ploutarchos, Kaltsas, Gregory, Baldeweg, Stephanie E., Bouloux, Pierre-Marc, Grossman, Ashley B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192810/
https://www.ncbi.nlm.nih.gov/pubmed/37214762
http://dx.doi.org/10.1177/20420188231173327
_version_ 1785043707052949504
author Tzoulis, Ploutarchos
Kaltsas, Gregory
Baldeweg, Stephanie E.
Bouloux, Pierre-Marc
Grossman, Ashley B.
author_facet Tzoulis, Ploutarchos
Kaltsas, Gregory
Baldeweg, Stephanie E.
Bouloux, Pierre-Marc
Grossman, Ashley B.
author_sort Tzoulis, Ploutarchos
collection PubMed
description 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.
format Online
Article
Text
id pubmed-10192810
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-101928102023-05-19 Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD) Tzoulis, Ploutarchos Kaltsas, Gregory Baldeweg, Stephanie E. Bouloux, Pierre-Marc Grossman, Ashley B. Ther Adv Endocrinol Metab Hyponatraemia in Clinical Practice 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. SAGE Publications 2023-05-16 /pmc/articles/PMC10192810/ /pubmed/37214762 http://dx.doi.org/10.1177/20420188231173327 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Hyponatraemia in Clinical Practice
Tzoulis, Ploutarchos
Kaltsas, Gregory
Baldeweg, Stephanie E.
Bouloux, Pierre-Marc
Grossman, Ashley B.
Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD)
title Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD)
title_full Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD)
title_fullStr Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD)
title_full_unstemmed Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD)
title_short Tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (SIAD)
title_sort tolvaptan for the treatment of the syndrome of inappropriate antidiuresis (siad)
topic Hyponatraemia in Clinical Practice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192810/
https://www.ncbi.nlm.nih.gov/pubmed/37214762
http://dx.doi.org/10.1177/20420188231173327
work_keys_str_mv AT tzoulisploutarchos tolvaptanforthetreatmentofthesyndromeofinappropriateantidiuresissiad
AT kaltsasgregory tolvaptanforthetreatmentofthesyndromeofinappropriateantidiuresissiad
AT baldewegstephaniee tolvaptanforthetreatmentofthesyndromeofinappropriateantidiuresissiad
AT boulouxpierremarc tolvaptanforthetreatmentofthesyndromeofinappropriateantidiuresissiad
AT grossmanashleyb tolvaptanforthetreatmentofthesyndromeofinappropriateantidiuresissiad