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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Veröffentlicht in:Journal of critical care 2017-10, Vol.41, p.289-295
Hauptverfasser: Wood, Michael D., BA, Maslove, David M., MSc, MD, Muscedere, John G., MD, Day, Andrew G., MSc, Gordon Boyd, J., MD, PhD
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container_issue
container_start_page 289
container_title Journal of critical care
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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 ; 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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.</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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