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Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial
BACKGROUND AND AIMS: Vasopressin (VP) in sepsis apart from vasoconstrictive effect may have some immunomodulatory effects. The aim of this study was to evaluate the effect of VP on different aspect of sepsis by measuring of sepsis biomarkers. MATERIALS AND METHODS: In this trial, a total number of 4...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613609/ https://www.ncbi.nlm.nih.gov/pubmed/28970657 http://dx.doi.org/10.4103/ijccm.IJCCM_258_17 |
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author | Barzegar, Elchin Nouri, Masoumeh Mousavi, Sarah Ahmadi, Arezoo Mojtahedzadeh, Mojtaba |
author_facet | Barzegar, Elchin Nouri, Masoumeh Mousavi, Sarah Ahmadi, Arezoo Mojtahedzadeh, Mojtaba |
author_sort | Barzegar, Elchin |
collection | PubMed |
description | BACKGROUND AND AIMS: Vasopressin (VP) in sepsis apart from vasoconstrictive effect may have some immunomodulatory effects. The aim of this study was to evaluate the effect of VP on different aspect of sepsis by measuring of sepsis biomarkers. MATERIALS AND METHODS: In this trial, a total number of 42 septic shock patients were included. The first group received norepinephrine (NE) infusion to reach the target mean arterial pressure (MAP) of ≥ 65 mm Hg and the second group received arginine vasopressin (AVP) infusion in addition to NE. Serum lactate, C-reactive protein (CRP), interleukin-6 (IL-6), IL-10, pentraxin 3 (PTX3), angiopoietin 1 and 2 (Ang 1 and 2) levels were assessed. RESULTS: Level of IL-6 and IL-10 decreased, but there was no significant difference between the two groups after 48 h. CRP and PTX3 levels were not also significantly different between groups. Although Angs were not statistically different, there was a trend toward higher Ang-1 in and lower Ang 2 in AVP group after 24 and 48 h. In addition, lactate level did not differ between NE and AVP groups. There was no interaction between VP and hydrocortisone use on IL-6, IL-10, and PTX3, but a significant statistical interaction on Ang 1 and Ang 2 were observed. CONCLUSIONS: Although analysis of sepsis biomarkers showed no significant difference between two groups, no immunomodulatory effect for VP alone, subgroup analysis of hydrocortisone used in this study showed that the combination of glucocorticoids and AVP had a significant effect on Angs level which eventually causes less endothelial permeability and higher MAP in this group of patients. |
format | Online Article Text |
id | pubmed-5613609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56136092017-10-02 Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial Barzegar, Elchin Nouri, Masoumeh Mousavi, Sarah Ahmadi, Arezoo Mojtahedzadeh, Mojtaba Indian J Crit Care Med Research Article BACKGROUND AND AIMS: Vasopressin (VP) in sepsis apart from vasoconstrictive effect may have some immunomodulatory effects. The aim of this study was to evaluate the effect of VP on different aspect of sepsis by measuring of sepsis biomarkers. MATERIALS AND METHODS: In this trial, a total number of 42 septic shock patients were included. The first group received norepinephrine (NE) infusion to reach the target mean arterial pressure (MAP) of ≥ 65 mm Hg and the second group received arginine vasopressin (AVP) infusion in addition to NE. Serum lactate, C-reactive protein (CRP), interleukin-6 (IL-6), IL-10, pentraxin 3 (PTX3), angiopoietin 1 and 2 (Ang 1 and 2) levels were assessed. RESULTS: Level of IL-6 and IL-10 decreased, but there was no significant difference between the two groups after 48 h. CRP and PTX3 levels were not also significantly different between groups. Although Angs were not statistically different, there was a trend toward higher Ang-1 in and lower Ang 2 in AVP group after 24 and 48 h. In addition, lactate level did not differ between NE and AVP groups. There was no interaction between VP and hydrocortisone use on IL-6, IL-10, and PTX3, but a significant statistical interaction on Ang 1 and Ang 2 were observed. CONCLUSIONS: Although analysis of sepsis biomarkers showed no significant difference between two groups, no immunomodulatory effect for VP alone, subgroup analysis of hydrocortisone used in this study showed that the combination of glucocorticoids and AVP had a significant effect on Angs level which eventually causes less endothelial permeability and higher MAP in this group of patients. Medknow Publications & Media Pvt Ltd 2017-09 /pmc/articles/PMC5613609/ /pubmed/28970657 http://dx.doi.org/10.4103/ijccm.IJCCM_258_17 Text en Copyright: © 2017 Indian Journal of Critical Care Medicine 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Barzegar, Elchin Nouri, Masoumeh Mousavi, Sarah Ahmadi, Arezoo Mojtahedzadeh, Mojtaba Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial |
title | Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial |
title_full | Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial |
title_fullStr | Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial |
title_full_unstemmed | Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial |
title_short | Vasopressin in Septic Shock; Assessment of Sepsis Biomarkers: A Randomized, Controlled Trial |
title_sort | vasopressin in septic shock; assessment of sepsis biomarkers: a randomized, controlled trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613609/ https://www.ncbi.nlm.nih.gov/pubmed/28970657 http://dx.doi.org/10.4103/ijccm.IJCCM_258_17 |
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