Low brain tissue oxygenation contributes to the development of delirium in critically ill patients: A prospective observational study
Abstract Purpose To test the hypothesis that poor brain tissue oxygenation (BtO2 ) during the first 24 h of critical illness correlates with the proportion of time spent delirious. We also sought to define the physiological determinants of BtO2. Materials and methods Adult patients admitted to the I...
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creator | Wood, Michael D., BA Maslove, David M., MSc, MD Muscedere, John G., MD Day, Andrew G., MSc Gordon Boyd, J., MD, PhD |
description | Abstract Purpose To test the hypothesis that poor brain tissue oxygenation (BtO2 ) during the first 24 h of critical illness correlates with the proportion of time spent delirious. We also sought to define the physiological determinants of BtO2. Materials and methods Adult patients admitted to the ICU within the previous 24 h were considered eligible for enrollment if they required mechanical ventilation, and/or vasopressor support. BtO2 was measured using near-infrared spectroscopy, for 24 h after enrollment. Hourly vital signs and clinically ordered arterial and central venous blood gases were collected throughout BtO2 monitoring. Patients were screened daily for delirium with the confusion assessment method for the intensive care unit (CAM-ICU). Results BtO2 and the proportion of time spent delirious did not result in significant correlation (p = 0.168). However, critically ill patients who spent the majority of their ICU stay delirious had significantly lower mean BtO2 compared to non-delirious patients, (p = 0.017). BtO2 correlated positively with central venous pO2 (p = 0.00003) and hemoglobin concentration (p = 0.001). Logistic regression indicated that lower BtO2 , higher narcotic doses and a history of alcohol abuse were independent risk factors for delirium. Conclusions Poor cerebral oxygenation during the first 24 hours of critical illness contributes to the development of delirium. Trial registration This trial is registered on clinicaltrials.gov (Identifier: NCT02344043), retrospectively registered January 8, 2015. |
doi_str_mv | 10.1016/j.jcrc.2017.06.009 |
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We also sought to define the physiological determinants of BtO2. Materials and methods Adult patients admitted to the ICU within the previous 24 h were considered eligible for enrollment if they required mechanical ventilation, and/or vasopressor support. BtO2 was measured using near-infrared spectroscopy, for 24 h after enrollment. Hourly vital signs and clinically ordered arterial and central venous blood gases were collected throughout BtO2 monitoring. Patients were screened daily for delirium with the confusion assessment method for the intensive care unit (CAM-ICU). Results BtO2 and the proportion of time spent delirious did not result in significant correlation (p = 0.168). However, critically ill patients who spent the majority of their ICU stay delirious had significantly lower mean BtO2 compared to non-delirious patients, (p = 0.017). BtO2 correlated positively with central venous pO2 (p = 0.00003) and hemoglobin concentration (p = 0.001). Logistic regression indicated that lower BtO2 , higher narcotic doses and a history of alcohol abuse were independent risk factors for delirium. Conclusions Poor cerebral oxygenation during the first 24 hours of critical illness contributes to the development of delirium. Trial registration This trial is registered on clinicaltrials.gov (Identifier: NCT02344043), retrospectively registered January 8, 2015.</description><identifier>ISSN: 0883-9441</identifier><identifier>EISSN: 1557-8615</identifier><identifier>DOI: 10.1016/j.jcrc.2017.06.009</identifier><identifier>PMID: 28668768</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Alcohol abuse ; Anesthesia ; Brain - metabolism ; Brain tissue oxygenation ; CAM-ICU ; Cerebral perfusion ; Coma ; Critical Care ; Critical Illness ; Delirium ; Delirium - diagnosis ; Delirium - metabolism ; Feasibility studies ; Female ; Humans ; Hypotheses ; Illnesses ; Intensive care ; Intensive Care Units ; Logistic Models ; Male ; Middle Aged ; Near-infrared spectroscopy ; Observational studies ; Oxygen Consumption ; Patients ; Physiology ; Predictive Value of Tests ; Prospective Studies ; Risk Factors ; Sepsis ; Spectroscopy, Near-Infrared - methods ; Spectrum analysis ; Ventilators</subject><ispartof>Journal of critical care, 2017-10, Vol.41, p.289-295</ispartof><rights>2017 The Authors</rights><rights>Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Oct 1, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-d791823c52c4c8593a29632309f93222688bdbaf7601ad9b48e9dedb6d8032903</citedby><cites>FETCH-LOGICAL-c483t-d791823c52c4c8593a29632309f93222688bdbaf7601ad9b48e9dedb6d8032903</cites><orcidid>0000-0002-0765-7158</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1952585229?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28668768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wood, Michael D., BA</creatorcontrib><creatorcontrib>Maslove, David M., MSc, MD</creatorcontrib><creatorcontrib>Muscedere, John G., MD</creatorcontrib><creatorcontrib>Day, Andrew G., MSc</creatorcontrib><creatorcontrib>Gordon Boyd, J., MD, PhD</creatorcontrib><creatorcontrib>Canadian Critical Care Trials Group</creatorcontrib><creatorcontrib>The Cerebral Oxygenation and Neurological Outcomes Following Critical Illness (CONFOCAL) Research Group</creatorcontrib><creatorcontrib>Cerebral Oxygenation and Neurological Outcomes Following Critical Illness (CONFOCAL) Research Group</creatorcontrib><title>Low brain tissue oxygenation contributes to the development of delirium in critically ill patients: A prospective observational study</title><title>Journal of critical care</title><addtitle>J Crit Care</addtitle><description>Abstract Purpose To test the hypothesis that poor brain tissue oxygenation (BtO2 ) during the first 24 h of critical illness correlates with the proportion of time spent delirious. We also sought to define the physiological determinants of BtO2. Materials and methods Adult patients admitted to the ICU within the previous 24 h were considered eligible for enrollment if they required mechanical ventilation, and/or vasopressor support. BtO2 was measured using near-infrared spectroscopy, for 24 h after enrollment. Hourly vital signs and clinically ordered arterial and central venous blood gases were collected throughout BtO2 monitoring. Patients were screened daily for delirium with the confusion assessment method for the intensive care unit (CAM-ICU). Results BtO2 and the proportion of time spent delirious did not result in significant correlation (p = 0.168). However, critically ill patients who spent the majority of their ICU stay delirious had significantly lower mean BtO2 compared to non-delirious patients, (p = 0.017). BtO2 correlated positively with central venous pO2 (p = 0.00003) and hemoglobin concentration (p = 0.001). Logistic regression indicated that lower BtO2 , higher narcotic doses and a history of alcohol abuse were independent risk factors for delirium. Conclusions Poor cerebral oxygenation during the first 24 hours of critical illness contributes to the development of delirium. Trial registration This trial is registered on clinicaltrials.gov (Identifier: NCT02344043), retrospectively registered January 8, 2015.</description><subject>Aged</subject><subject>Alcohol abuse</subject><subject>Anesthesia</subject><subject>Brain - metabolism</subject><subject>Brain tissue oxygenation</subject><subject>CAM-ICU</subject><subject>Cerebral perfusion</subject><subject>Coma</subject><subject>Critical Care</subject><subject>Critical Illness</subject><subject>Delirium</subject><subject>Delirium - diagnosis</subject><subject>Delirium - metabolism</subject><subject>Feasibility studies</subject><subject>Female</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Illnesses</subject><subject>Intensive care</subject><subject>Intensive Care Units</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Near-infrared spectroscopy</subject><subject>Observational studies</subject><subject>Oxygen Consumption</subject><subject>Patients</subject><subject>Physiology</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Sepsis</subject><subject>Spectroscopy, Near-Infrared - methods</subject><subject>Spectrum analysis</subject><subject>Ventilators</subject><issn>0883-9441</issn><issn>1557-8615</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9ks-KFDEQxhtR3NnVF_AgAS9eZsyfTjoRWVgWV4UBD-o5pJMaTZvujEl6dB7A9zbtrAp78BQCv_qq6vuqaZ4QvCGYiBfDZrDJbigm3QaLDcbqXrMinHdrKQi_36ywlGyt2pacNec5D7iCjPGHzRmVQshOyFXzcxu_oz4ZP6Hic54BxR_HzzCZ4uOEbJxK8v1cIKMSUfkCyMEBQtyPMBUUd_UbfPLziKqATb54a0I4Ih8C2leNSuWX6ArtU8x7sMUfaoM-Qzr8bmACymV2x0fNg50JGR7fvhfNp5vXH6_frrfv37y7vtqubStZWbtOEUmZ5dS2VnLFDFWCUYbVTjFKqZCyd73ZdQIT41TfSlAOXC-cxIwqzC6a5yfdOs-3GXLRo88WQjATxDlroqp9XLVkQZ_dQYc4pzrxQnHKJadUVYqeKFsXzAl2ep_8aNJRE6yXkPSgl5D0EpLGQteQatHTW-m5H8H9LfmTSgVenQCoXhw8JJ1ttdKC86maqF30_9e_vFNug5-WZL7CEfK_PXSmGusPy5ksV1KvA3NBKfsFgSG5tQ</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Wood, Michael D., BA</creator><creator>Maslove, David M., MSc, MD</creator><creator>Muscedere, John G., MD</creator><creator>Day, Andrew G., MSc</creator><creator>Gordon Boyd, J., MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0765-7158</orcidid></search><sort><creationdate>20171001</creationdate><title>Low brain tissue oxygenation contributes to the development of delirium in critically ill patients: A prospective observational study</title><author>Wood, Michael D., BA ; Maslove, David M., MSc, MD ; Muscedere, John G., MD ; Day, Andrew G., MSc ; Gordon Boyd, J., MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-d791823c52c4c8593a29632309f93222688bdbaf7601ad9b48e9dedb6d8032903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Alcohol abuse</topic><topic>Anesthesia</topic><topic>Brain - metabolism</topic><topic>Brain tissue oxygenation</topic><topic>CAM-ICU</topic><topic>Cerebral perfusion</topic><topic>Coma</topic><topic>Critical Care</topic><topic>Critical Illness</topic><topic>Delirium</topic><topic>Delirium - diagnosis</topic><topic>Delirium - metabolism</topic><topic>Feasibility studies</topic><topic>Female</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Illnesses</topic><topic>Intensive care</topic><topic>Intensive Care Units</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Near-infrared spectroscopy</topic><topic>Observational studies</topic><topic>Oxygen Consumption</topic><topic>Patients</topic><topic>Physiology</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Sepsis</topic><topic>Spectroscopy, Near-Infrared - methods</topic><topic>Spectrum analysis</topic><topic>Ventilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wood, Michael D., BA</creatorcontrib><creatorcontrib>Maslove, David M., MSc, MD</creatorcontrib><creatorcontrib>Muscedere, John G., MD</creatorcontrib><creatorcontrib>Day, Andrew G., MSc</creatorcontrib><creatorcontrib>Gordon Boyd, J., MD, PhD</creatorcontrib><creatorcontrib>Canadian Critical Care Trials Group</creatorcontrib><creatorcontrib>The Cerebral Oxygenation and Neurological Outcomes Following Critical Illness (CONFOCAL) Research Group</creatorcontrib><creatorcontrib>Cerebral Oxygenation and Neurological Outcomes Following Critical Illness (CONFOCAL) Research Group</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</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>MEDLINE - Academic</collection><jtitle>Journal of critical care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wood, Michael D., BA</au><au>Maslove, David M., MSc, MD</au><au>Muscedere, John G., MD</au><au>Day, Andrew G., MSc</au><au>Gordon Boyd, J., MD, PhD</au><aucorp>Canadian Critical Care Trials Group</aucorp><aucorp>The Cerebral Oxygenation and Neurological Outcomes Following Critical Illness (CONFOCAL) Research Group</aucorp><aucorp>Cerebral Oxygenation and Neurological Outcomes Following Critical Illness (CONFOCAL) Research Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low brain tissue oxygenation contributes to the development of delirium in critically ill patients: A prospective observational study</atitle><jtitle>Journal of critical care</jtitle><addtitle>J Crit Care</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>41</volume><spage>289</spage><epage>295</epage><pages>289-295</pages><issn>0883-9441</issn><eissn>1557-8615</eissn><abstract>Abstract Purpose To test the hypothesis that poor brain tissue oxygenation (BtO2 ) during the first 24 h of critical illness correlates with the proportion of time spent delirious. We also sought to define the physiological determinants of BtO2. Materials and methods Adult patients admitted to the ICU within the previous 24 h were considered eligible for enrollment if they required mechanical ventilation, and/or vasopressor support. BtO2 was measured using near-infrared spectroscopy, for 24 h after enrollment. Hourly vital signs and clinically ordered arterial and central venous blood gases were collected throughout BtO2 monitoring. Patients were screened daily for delirium with the confusion assessment method for the intensive care unit (CAM-ICU). Results BtO2 and the proportion of time spent delirious did not result in significant correlation (p = 0.168). However, critically ill patients who spent the majority of their ICU stay delirious had significantly lower mean BtO2 compared to non-delirious patients, (p = 0.017). BtO2 correlated positively with central venous pO2 (p = 0.00003) and hemoglobin concentration (p = 0.001). Logistic regression indicated that lower BtO2 , higher narcotic doses and a history of alcohol abuse were independent risk factors for delirium. Conclusions Poor cerebral oxygenation during the first 24 hours of critical illness contributes to the development of delirium. Trial registration This trial is registered on clinicaltrials.gov (Identifier: NCT02344043), retrospectively registered January 8, 2015.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28668768</pmid><doi>10.1016/j.jcrc.2017.06.009</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0765-7158</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Alcohol abuse Anesthesia Brain - metabolism Brain tissue oxygenation CAM-ICU Cerebral perfusion Coma Critical Care Critical Illness Delirium Delirium - diagnosis Delirium - metabolism Feasibility studies Female Humans Hypotheses Illnesses Intensive care Intensive Care Units Logistic Models Male Middle Aged Near-infrared spectroscopy Observational studies Oxygen Consumption Patients Physiology Predictive Value of Tests Prospective Studies Risk Factors Sepsis Spectroscopy, Near-Infrared - methods Spectrum analysis Ventilators |
title | Low brain tissue oxygenation contributes to the development of delirium in critically ill patients: A prospective observational study |
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