Blood markers of oxidative stress predict weaning failure from mechanical ventilation
Patients undergoing mechanical ventilation (MV) often experience respiratory muscle dysfunction, which complicates the weaning process. There is no simple means to predict or diagnose respiratory muscle dysfunction because diagnosis depends on measurements in muscle diaphragmatic fibre. As oxidative...
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Veröffentlicht in: | Journal of cellular and molecular medicine 2015-06, Vol.19 (6), p.1253-1261 |
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creator | Verona, Cléber Hackenhaar, Fernanda S. Teixeira, Cassiano Medeiros, Tássia M. Alabarse, Paulo V. Salomon, Tiago B. Shüller, Ártur K. Maccari, Juçara G. Condessa, Robledo Leal Oliveira, Roselaine P. Rios Vieira, Silvia R. Benfato, Mara S. |
description | Patients undergoing mechanical ventilation (MV) often experience respiratory muscle dysfunction, which complicates the weaning process. There is no simple means to predict or diagnose respiratory muscle dysfunction because diagnosis depends on measurements in muscle diaphragmatic fibre. As oxidative stress is a key mechanism contributing to MV‐induced respiratory muscle dysfunction, the aim of this study was to determine if differences in blood measures of oxidative stress in patients who had success and failure in a spontaneous breathing trial (SBT) could be used to predict the outcome of MV. This was a prospective analysis of MV‐dependent patients (≥72 hrs; n = 34) undergoing a standard weaning protocol. Clinical, laboratory and oxidative stress analyses were performed. Measurements were made on blood samples taken at three time‐points: immediately before the trial, 30 min. into the trial in weaning success (WS) patients, or immediately before return to MV in weaning failure (WF) patients, and 6 hrs after the trial. We found that blood measures of oxidative stress distinguished patients who would experience WF from patients who would experience WS. Before SBT, WF patients presented higher oxidative damage in lipids and higher antioxidant levels and decreased nitric oxide concentrations. The observed differences in measures between WF and WS patients persisted throughout and after the weaning trial. In conclusion, WF may be predicted based on higher malondialdehyde, higher vitamin C and lower nitric oxide concentration in plasma. |
doi_str_mv | 10.1111/jcmm.12475 |
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There is no simple means to predict or diagnose respiratory muscle dysfunction because diagnosis depends on measurements in muscle diaphragmatic fibre. As oxidative stress is a key mechanism contributing to MV‐induced respiratory muscle dysfunction, the aim of this study was to determine if differences in blood measures of oxidative stress in patients who had success and failure in a spontaneous breathing trial (SBT) could be used to predict the outcome of MV. This was a prospective analysis of MV‐dependent patients (≥72 hrs; n = 34) undergoing a standard weaning protocol. Clinical, laboratory and oxidative stress analyses were performed. Measurements were made on blood samples taken at three time‐points: immediately before the trial, 30 min. into the trial in weaning success (WS) patients, or immediately before return to MV in weaning failure (WF) patients, and 6 hrs after the trial. We found that blood measures of oxidative stress distinguished patients who would experience WF from patients who would experience WS. Before SBT, WF patients presented higher oxidative damage in lipids and higher antioxidant levels and decreased nitric oxide concentrations. The observed differences in measures between WF and WS patients persisted throughout and after the weaning trial. In conclusion, WF may be predicted based on higher malondialdehyde, higher vitamin C and lower nitric oxide concentration in plasma.</description><identifier>ISSN: 1582-1838</identifier><identifier>EISSN: 1582-4934</identifier><identifier>DOI: 10.1111/jcmm.12475</identifier><identifier>PMID: 25854285</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Aged ; Aged, 80 and over ; Antioxidants ; Ascorbic acid ; Ascorbic Acid - blood ; Atrophy ; Biomarkers - blood ; Blood ; Catalase - blood ; Coma ; Data collection ; Female ; Glutathione - blood ; Glutathione Disulfide - blood ; Glutathione Peroxidase - blood ; Heart rate ; Hospitals ; Humans ; Hypoxia ; intensive care units ; Laboratories ; Lipid peroxidation ; Lipids ; Male ; Malondialdehyde ; Malondialdehyde - blood ; Mechanical ventilation ; Middle Aged ; Muscles ; Nitric oxide ; Nitric Oxide - blood ; Nitrites - blood ; Nutrition research ; Original ; Outcome Assessment (Health Care) - methods ; Oxidative Stress ; Patients ; Predictive Value of Tests ; Respiration, Artificial - methods ; Sample size ; Studies ; Superoxide Dismutase - blood ; Ventilator Weaning - methods ; Ventilators ; vitamin C ; Weaning</subject><ispartof>Journal of cellular and molecular medicine, 2015-06, Vol.19 (6), p.1253-1261</ispartof><rights>2015 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.</rights><rights>2015. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5185-f583e0a7bd0c179a534293ec47dc9ac829ab7b5139aa5a32a5805e4ae363615c3</citedby><cites>FETCH-LOGICAL-c5185-f583e0a7bd0c179a534293ec47dc9ac829ab7b5139aa5a32a5805e4ae363615c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459841/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459841/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25854285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Verona, Cléber</creatorcontrib><creatorcontrib>Hackenhaar, Fernanda S.</creatorcontrib><creatorcontrib>Teixeira, Cassiano</creatorcontrib><creatorcontrib>Medeiros, Tássia M.</creatorcontrib><creatorcontrib>Alabarse, Paulo V.</creatorcontrib><creatorcontrib>Salomon, Tiago B.</creatorcontrib><creatorcontrib>Shüller, Ártur K.</creatorcontrib><creatorcontrib>Maccari, Juçara G.</creatorcontrib><creatorcontrib>Condessa, Robledo Leal</creatorcontrib><creatorcontrib>Oliveira, Roselaine P.</creatorcontrib><creatorcontrib>Rios Vieira, Silvia R.</creatorcontrib><creatorcontrib>Benfato, Mara S.</creatorcontrib><title>Blood markers of oxidative stress predict weaning failure from mechanical ventilation</title><title>Journal of cellular and molecular medicine</title><addtitle>J Cell Mol Med</addtitle><description>Patients undergoing mechanical ventilation (MV) often experience respiratory muscle dysfunction, which complicates the weaning process. There is no simple means to predict or diagnose respiratory muscle dysfunction because diagnosis depends on measurements in muscle diaphragmatic fibre. As oxidative stress is a key mechanism contributing to MV‐induced respiratory muscle dysfunction, the aim of this study was to determine if differences in blood measures of oxidative stress in patients who had success and failure in a spontaneous breathing trial (SBT) could be used to predict the outcome of MV. This was a prospective analysis of MV‐dependent patients (≥72 hrs; n = 34) undergoing a standard weaning protocol. Clinical, laboratory and oxidative stress analyses were performed. Measurements were made on blood samples taken at three time‐points: immediately before the trial, 30 min. into the trial in weaning success (WS) patients, or immediately before return to MV in weaning failure (WF) patients, and 6 hrs after the trial. We found that blood measures of oxidative stress distinguished patients who would experience WF from patients who would experience WS. Before SBT, WF patients presented higher oxidative damage in lipids and higher antioxidant levels and decreased nitric oxide concentrations. The observed differences in measures between WF and WS patients persisted throughout and after the weaning trial. In conclusion, WF may be predicted based on higher malondialdehyde, higher vitamin C and lower nitric oxide concentration in plasma.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antioxidants</subject><subject>Ascorbic acid</subject><subject>Ascorbic Acid - blood</subject><subject>Atrophy</subject><subject>Biomarkers - blood</subject><subject>Blood</subject><subject>Catalase - blood</subject><subject>Coma</subject><subject>Data collection</subject><subject>Female</subject><subject>Glutathione - blood</subject><subject>Glutathione Disulfide - blood</subject><subject>Glutathione Peroxidase - blood</subject><subject>Heart rate</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>intensive care units</subject><subject>Laboratories</subject><subject>Lipid peroxidation</subject><subject>Lipids</subject><subject>Male</subject><subject>Malondialdehyde</subject><subject>Malondialdehyde - blood</subject><subject>Mechanical ventilation</subject><subject>Middle Aged</subject><subject>Muscles</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - blood</subject><subject>Nitrites - blood</subject><subject>Nutrition research</subject><subject>Original</subject><subject>Outcome Assessment (Health Care) - methods</subject><subject>Oxidative Stress</subject><subject>Patients</subject><subject>Predictive Value of Tests</subject><subject>Respiration, Artificial - methods</subject><subject>Sample size</subject><subject>Studies</subject><subject>Superoxide Dismutase - blood</subject><subject>Ventilator Weaning - methods</subject><subject>Ventilators</subject><subject>vitamin C</subject><subject>Weaning</subject><issn>1582-1838</issn><issn>1582-4934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kUtPGzEUha2qVaHQDT8AWeqmqhTqZ8beVGqjPgViU9bWjecOOHjGwZ4J5d_XNCmCLurNtezvHp2jQ8gRZye8nvcr3_cnXKhGPyP7XBsxU1aq57s7N9LskVelrBiTcy7tS7IntNFKGL1PLj7FlFraQ77GXGjqaPoVWhjDBmkZM5ZC1xnb4Ed6izCE4ZJ2EOKUkXY59bRHf1WfPUS6wWEMsa6m4ZC86CAWfL2bB-Tiy-efi2-z0_Ov3xcfT2dec6NnnTYSGTTLlnneWNBSCSvRq6b1FrwRFpbNUlfPABqkAG2YRgUo5zWJ9vKAfNjqrqdlj62vDjJEt86hBrpzCYJ7-jOEK3eZNk4pbY3iVeDtTiCnmwnL6PpQPMYIA6apOD43utGy-qrom3_QVZryUOM5ISzjorHMVurdlvI5lZKxezDDmbtvy9235f60VeHjx_Yf0L_1VIBvgdsQ8e4_Uu7H4uxsK_ob2WmhDg</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Verona, Cléber</creator><creator>Hackenhaar, Fernanda S.</creator><creator>Teixeira, Cassiano</creator><creator>Medeiros, Tássia M.</creator><creator>Alabarse, Paulo V.</creator><creator>Salomon, Tiago B.</creator><creator>Shüller, Ártur K.</creator><creator>Maccari, Juçara G.</creator><creator>Condessa, Robledo Leal</creator><creator>Oliveira, Roselaine P.</creator><creator>Rios Vieira, Silvia R.</creator><creator>Benfato, Mara S.</creator><general>John Wiley & Sons, Inc</general><general>BlackWell Publishing Ltd</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201506</creationdate><title>Blood markers of oxidative stress predict weaning failure from mechanical ventilation</title><author>Verona, Cléber ; Hackenhaar, Fernanda S. ; Teixeira, Cassiano ; Medeiros, Tássia M. ; Alabarse, Paulo V. ; Salomon, Tiago B. ; Shüller, Ártur K. ; Maccari, Juçara G. ; Condessa, Robledo Leal ; Oliveira, Roselaine P. ; Rios Vieira, Silvia R. ; Benfato, Mara S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5185-f583e0a7bd0c179a534293ec47dc9ac829ab7b5139aa5a32a5805e4ae363615c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antioxidants</topic><topic>Ascorbic acid</topic><topic>Ascorbic Acid - blood</topic><topic>Atrophy</topic><topic>Biomarkers - blood</topic><topic>Blood</topic><topic>Catalase - blood</topic><topic>Coma</topic><topic>Data collection</topic><topic>Female</topic><topic>Glutathione - blood</topic><topic>Glutathione Disulfide - blood</topic><topic>Glutathione Peroxidase - blood</topic><topic>Heart rate</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>intensive care units</topic><topic>Laboratories</topic><topic>Lipid peroxidation</topic><topic>Lipids</topic><topic>Male</topic><topic>Malondialdehyde</topic><topic>Malondialdehyde - blood</topic><topic>Mechanical ventilation</topic><topic>Middle Aged</topic><topic>Muscles</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - blood</topic><topic>Nitrites - blood</topic><topic>Nutrition research</topic><topic>Original</topic><topic>Outcome Assessment (Health Care) - methods</topic><topic>Oxidative Stress</topic><topic>Patients</topic><topic>Predictive Value of Tests</topic><topic>Respiration, Artificial - methods</topic><topic>Sample size</topic><topic>Studies</topic><topic>Superoxide Dismutase - blood</topic><topic>Ventilator Weaning - methods</topic><topic>Ventilators</topic><topic>vitamin C</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Verona, Cléber</creatorcontrib><creatorcontrib>Hackenhaar, Fernanda S.</creatorcontrib><creatorcontrib>Teixeira, Cassiano</creatorcontrib><creatorcontrib>Medeiros, Tássia M.</creatorcontrib><creatorcontrib>Alabarse, Paulo V.</creatorcontrib><creatorcontrib>Salomon, Tiago B.</creatorcontrib><creatorcontrib>Shüller, Ártur K.</creatorcontrib><creatorcontrib>Maccari, Juçara G.</creatorcontrib><creatorcontrib>Condessa, Robledo Leal</creatorcontrib><creatorcontrib>Oliveira, Roselaine P.</creatorcontrib><creatorcontrib>Rios Vieira, Silvia R.</creatorcontrib><creatorcontrib>Benfato, Mara S.</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cellular and molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Verona, Cléber</au><au>Hackenhaar, Fernanda S.</au><au>Teixeira, Cassiano</au><au>Medeiros, Tássia M.</au><au>Alabarse, Paulo V.</au><au>Salomon, Tiago B.</au><au>Shüller, Ártur K.</au><au>Maccari, Juçara G.</au><au>Condessa, Robledo Leal</au><au>Oliveira, Roselaine P.</au><au>Rios Vieira, Silvia R.</au><au>Benfato, Mara S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood markers of oxidative stress predict weaning failure from mechanical ventilation</atitle><jtitle>Journal of cellular and molecular medicine</jtitle><addtitle>J Cell Mol Med</addtitle><date>2015-06</date><risdate>2015</risdate><volume>19</volume><issue>6</issue><spage>1253</spage><epage>1261</epage><pages>1253-1261</pages><issn>1582-1838</issn><eissn>1582-4934</eissn><abstract>Patients undergoing mechanical ventilation (MV) often experience respiratory muscle dysfunction, which complicates the weaning process. There is no simple means to predict or diagnose respiratory muscle dysfunction because diagnosis depends on measurements in muscle diaphragmatic fibre. As oxidative stress is a key mechanism contributing to MV‐induced respiratory muscle dysfunction, the aim of this study was to determine if differences in blood measures of oxidative stress in patients who had success and failure in a spontaneous breathing trial (SBT) could be used to predict the outcome of MV. This was a prospective analysis of MV‐dependent patients (≥72 hrs; n = 34) undergoing a standard weaning protocol. Clinical, laboratory and oxidative stress analyses were performed. Measurements were made on blood samples taken at three time‐points: immediately before the trial, 30 min. into the trial in weaning success (WS) patients, or immediately before return to MV in weaning failure (WF) patients, and 6 hrs after the trial. We found that blood measures of oxidative stress distinguished patients who would experience WF from patients who would experience WS. Before SBT, WF patients presented higher oxidative damage in lipids and higher antioxidant levels and decreased nitric oxide concentrations. The observed differences in measures between WF and WS patients persisted throughout and after the weaning trial. In conclusion, WF may be predicted based on higher malondialdehyde, higher vitamin C and lower nitric oxide concentration in plasma.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>25854285</pmid><doi>10.1111/jcmm.12475</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Antioxidants Ascorbic acid Ascorbic Acid - blood Atrophy Biomarkers - blood Blood Catalase - blood Coma Data collection Female Glutathione - blood Glutathione Disulfide - blood Glutathione Peroxidase - blood Heart rate Hospitals Humans Hypoxia intensive care units Laboratories Lipid peroxidation Lipids Male Malondialdehyde Malondialdehyde - blood Mechanical ventilation Middle Aged Muscles Nitric oxide Nitric Oxide - blood Nitrites - blood Nutrition research Original Outcome Assessment (Health Care) - methods Oxidative Stress Patients Predictive Value of Tests Respiration, Artificial - methods Sample size Studies Superoxide Dismutase - blood Ventilator Weaning - methods Ventilators vitamin C Weaning |
title | Blood markers of oxidative stress predict weaning failure from mechanical ventilation |
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