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Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide
BACKGROUND: Hyponatremia in the setting of cirrhosis is a common electrolyte disorder with few therapeutic options. The free water retention is due to non-osmotic vasopressin secretion resulting from the cirrhosis-associated splanchnic vasodilatation. Therefore, vasoconstrictive therapy may correct...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348528/ https://www.ncbi.nlm.nih.gov/pubmed/28352627 http://dx.doi.org/10.3389/fmed.2017.00017 |
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author | Patel, Sharad Nguyen, Dai-Scott Rastogi, Anjay Nguyen, Minh-Kevin Nguyen, Minhtri K. |
author_facet | Patel, Sharad Nguyen, Dai-Scott Rastogi, Anjay Nguyen, Minh-Kevin Nguyen, Minhtri K. |
author_sort | Patel, Sharad |
collection | PubMed |
description | BACKGROUND: Hyponatremia in the setting of cirrhosis is a common electrolyte disorder with few therapeutic options. The free water retention is due to non-osmotic vasopressin secretion resulting from the cirrhosis-associated splanchnic vasodilatation. Therefore, vasoconstrictive therapy may correct this electrolyte abnormality. The aim of this study was to assess the efficacy of midodrine and octreotide as a therapeutic approach to increasing urinary electrolyte-free water clearance (EFWC) in the correction of cirrhosis-associated hyponatremia. METHODS: This observational study consisted of 10 patients with cirrhosis-associated hyponatremia. Hypovolemia was ruled out as the cause of the hyponatremia with a 48-h albumin challenge (25 g IV q6 h). Patients whose hyponatremia failed to improve with albumin challenge were started on midodrine and octreotide at 10 mg po tid and 100 μg sq tid, respectively, with rapid up-titration as tolerated to respective maximal doses of 15 mg tid and 200 μg tid within the first 24 h. We assessed urinary EFWC and serum sodium concentration before and 72 h after treatment. RESULTS: Pretreatment serum sodium levels ranged from 119 to 133 mmol/L. The mean pretreatment serum sodium concentration ± SEM was 124 mmol/L ± 1.6 vs 130 mmol/L ± 1.5 posttreatment (p = 0.00001). The mean pretreatment urinary EFWC ± SEM was 0.33 L ± 0.07 vs 0.82 L ± 0.11 posttreatment (p = 0.0003). CONCLUSION: Our data show a statistically significant increase in serum sodium concentration and urinary EFWC with the use of midodrine and octreotide in the treatment of cirrhosis-associated hyponatremia. |
format | Online Article Text |
id | pubmed-5348528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53485282017-03-28 Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide Patel, Sharad Nguyen, Dai-Scott Rastogi, Anjay Nguyen, Minh-Kevin Nguyen, Minhtri K. Front Med (Lausanne) Medicine BACKGROUND: Hyponatremia in the setting of cirrhosis is a common electrolyte disorder with few therapeutic options. The free water retention is due to non-osmotic vasopressin secretion resulting from the cirrhosis-associated splanchnic vasodilatation. Therefore, vasoconstrictive therapy may correct this electrolyte abnormality. The aim of this study was to assess the efficacy of midodrine and octreotide as a therapeutic approach to increasing urinary electrolyte-free water clearance (EFWC) in the correction of cirrhosis-associated hyponatremia. METHODS: This observational study consisted of 10 patients with cirrhosis-associated hyponatremia. Hypovolemia was ruled out as the cause of the hyponatremia with a 48-h albumin challenge (25 g IV q6 h). Patients whose hyponatremia failed to improve with albumin challenge were started on midodrine and octreotide at 10 mg po tid and 100 μg sq tid, respectively, with rapid up-titration as tolerated to respective maximal doses of 15 mg tid and 200 μg tid within the first 24 h. We assessed urinary EFWC and serum sodium concentration before and 72 h after treatment. RESULTS: Pretreatment serum sodium levels ranged from 119 to 133 mmol/L. The mean pretreatment serum sodium concentration ± SEM was 124 mmol/L ± 1.6 vs 130 mmol/L ± 1.5 posttreatment (p = 0.00001). The mean pretreatment urinary EFWC ± SEM was 0.33 L ± 0.07 vs 0.82 L ± 0.11 posttreatment (p = 0.0003). CONCLUSION: Our data show a statistically significant increase in serum sodium concentration and urinary EFWC with the use of midodrine and octreotide in the treatment of cirrhosis-associated hyponatremia. Frontiers Media S.A. 2017-03-14 /pmc/articles/PMC5348528/ /pubmed/28352627 http://dx.doi.org/10.3389/fmed.2017.00017 Text en Copyright © 2017 Patel, Nguyen, Rastogi, Nguyen and Nguyen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Patel, Sharad Nguyen, Dai-Scott Rastogi, Anjay Nguyen, Minh-Kevin Nguyen, Minhtri K. Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide |
title | Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide |
title_full | Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide |
title_fullStr | Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide |
title_full_unstemmed | Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide |
title_short | Treatment of Cirrhosis-Associated Hyponatremia with Midodrine and Octreotide |
title_sort | treatment of cirrhosis-associated hyponatremia with midodrine and octreotide |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348528/ https://www.ncbi.nlm.nih.gov/pubmed/28352627 http://dx.doi.org/10.3389/fmed.2017.00017 |
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