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Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries

BACKGROUND AND AIMS: Conivaptan, a vasopressin receptor antagonist, is commonly used for the treatment of euvolaemic, hypervolaemic hyponatraemia. Usually, an intravenous (IV) bolus followed by infusion is administered for many days. We decided to assess the effectiveness of single dose conivaptan f...

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Autores principales: Rajan, Sunil, Srikumar, Soumya, Paul, Jerry, Kumar, Lakshmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523962/
https://www.ncbi.nlm.nih.gov/pubmed/26257414
http://dx.doi.org/10.4103/0019-5049.160943
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author Rajan, Sunil
Srikumar, Soumya
Paul, Jerry
Kumar, Lakshmi
author_facet Rajan, Sunil
Srikumar, Soumya
Paul, Jerry
Kumar, Lakshmi
author_sort Rajan, Sunil
collection PubMed
description BACKGROUND AND AIMS: Conivaptan, a vasopressin receptor antagonist, is commonly used for the treatment of euvolaemic, hypervolaemic hyponatraemia. Usually, an intravenous (IV) bolus followed by infusion is administered for many days. We decided to assess the effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients. METHODS: This was a prospective, randomised trial conducted in 40 symptomatic post-operative Intensive Care Unit (ICU) patients with a serum sodium level of ≤130 mEq/L. Group A patients received IV conivaptan 20 mg over 30 min, whereas in group B infusion of 3% hypertonic saline was started as an infusion at the rate of 20–30 ml/h. Serum sodium levels were measured at 12, 24, 48 and 72 h and the daily fluid balance was measured for 3 days. The Chi-square test, Wilcoxon signed rank test and Mann-Whitney tests were used as applicable. RESULTS: The serum sodium levels before initiating treatment were comparable between groups. However, subsequent sodium levels at 12, 24 and 48 h showed significantly high values in group A. Though at 72 h the mean sodium value was high in group A, it was not statistically significant. Group A showed a significantly high fluid loss on day 1, 2 and 3. The mean volume of hypertonic saline required in group B showed a steady decline from day 1 to 3 and only 13 patients required hypertonic saline on the 3(rd) day. CONCLUSION: Single dose conivaptan is effective in increasing serum sodium levels in post-operative ICU patients up to 72 h associated with a significant negative fluid balance.
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spelling pubmed-45239622015-08-07 Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries Rajan, Sunil Srikumar, Soumya Paul, Jerry Kumar, Lakshmi Indian J Anaesth Clinical Investigation BACKGROUND AND AIMS: Conivaptan, a vasopressin receptor antagonist, is commonly used for the treatment of euvolaemic, hypervolaemic hyponatraemia. Usually, an intravenous (IV) bolus followed by infusion is administered for many days. We decided to assess the effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients. METHODS: This was a prospective, randomised trial conducted in 40 symptomatic post-operative Intensive Care Unit (ICU) patients with a serum sodium level of ≤130 mEq/L. Group A patients received IV conivaptan 20 mg over 30 min, whereas in group B infusion of 3% hypertonic saline was started as an infusion at the rate of 20–30 ml/h. Serum sodium levels were measured at 12, 24, 48 and 72 h and the daily fluid balance was measured for 3 days. The Chi-square test, Wilcoxon signed rank test and Mann-Whitney tests were used as applicable. RESULTS: The serum sodium levels before initiating treatment were comparable between groups. However, subsequent sodium levels at 12, 24 and 48 h showed significantly high values in group A. Though at 72 h the mean sodium value was high in group A, it was not statistically significant. Group A showed a significantly high fluid loss on day 1, 2 and 3. The mean volume of hypertonic saline required in group B showed a steady decline from day 1 to 3 and only 13 patients required hypertonic saline on the 3(rd) day. CONCLUSION: Single dose conivaptan is effective in increasing serum sodium levels in post-operative ICU patients up to 72 h associated with a significant negative fluid balance. Medknow Publications & Media Pvt Ltd 2015-07 /pmc/articles/PMC4523962/ /pubmed/26257414 http://dx.doi.org/10.4103/0019-5049.160943 Text en Copyright: © Indian Journal of Anaesthesia http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigation
Rajan, Sunil
Srikumar, Soumya
Paul, Jerry
Kumar, Lakshmi
Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
title Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
title_full Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
title_fullStr Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
title_full_unstemmed Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
title_short Effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
title_sort effectiveness of single dose conivaptan for correction of hyponatraemia in post-operative patients following major head and neck surgeries
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523962/
https://www.ncbi.nlm.nih.gov/pubmed/26257414
http://dx.doi.org/10.4103/0019-5049.160943
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