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Delirium in patients with acute ischemic stroke admitted to the non-intensive stroke unit: Incidence and association between clinical features and inflammatory markers
Stroke patients with development of delirium have unfavorable outcomes, higher mortality, longer hospitalizations, and a greater degree of dependence after discharge. Studies suggest that delirium is associated with abnormal immunological responses and a resultant increase in inflammatory markers. O...
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Published in: | Neurologia i neurochirurgia polska 2017-01, Vol.51 (1), p.38-44 |
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description | Stroke patients with development of delirium have unfavorable outcomes, higher mortality, longer hospitalizations, and a greater degree of dependence after discharge. Studies suggest that delirium is associated with abnormal immunological responses and a resultant increase in inflammatory markers.
Our aim was to determine whether there is an entity relationship between delirium, inflammation and acute ischemic stroke (AIS).
Sixty AIS patients admitted to the hospital were consecutively recruited. Delirium was diagnosed with the clinical assessment according to the Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria. Enzyme-linked immunosorbent assay (ELISA) was used to measure serum levels of Interleukin-1 beta (IL-1 beta), Interleukin 18 (IL-18), Tumor Necrosis Factor-alpha (TNF-alpha), Brain-Derived Neurotrophic Factor (BDNF), and Neuron Specific Enolase (NSE) at admission.
Eleven (18.3%) of 60 patients were diagnosed with delirium, and the majority (n=8, 72.7%) was the hypoactive type. Delirious and non-delirious patients had similar demographic and clinical features. Delirious patients had significantly higher lengths of hospital stay, National Institutes of Health Stroke Scale (NIHSS) at admission and discharge compared to non-delirious patients. In addition, there was no significant statistical difference between delirious and non-delirious patients with AIS in respect of levels of TNF-alpha, IL-1 beta, IL-18, BDNF and NSE. This study suggests that delirium is not scarce in patients with AIS admitted to the non-intensive stroke unit, and that delirium developing after AIS seems not to be associated with serum TNF-alpha, IL-1 beta, IL-18, BDNF and NSE but is associated with length of hospital stay and stroke severity. |
doi_str_mv | 10.1016/j.pjnns.2016.10.004 |
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Our aim was to determine whether there is an entity relationship between delirium, inflammation and acute ischemic stroke (AIS).
Sixty AIS patients admitted to the hospital were consecutively recruited. Delirium was diagnosed with the clinical assessment according to the Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria. Enzyme-linked immunosorbent assay (ELISA) was used to measure serum levels of Interleukin-1 beta (IL-1 beta), Interleukin 18 (IL-18), Tumor Necrosis Factor-alpha (TNF-alpha), Brain-Derived Neurotrophic Factor (BDNF), and Neuron Specific Enolase (NSE) at admission.
Eleven (18.3%) of 60 patients were diagnosed with delirium, and the majority (n=8, 72.7%) was the hypoactive type. Delirious and non-delirious patients had similar demographic and clinical features. Delirious patients had significantly higher lengths of hospital stay, National Institutes of Health Stroke Scale (NIHSS) at admission and discharge compared to non-delirious patients. In addition, there was no significant statistical difference between delirious and non-delirious patients with AIS in respect of levels of TNF-alpha, IL-1 beta, IL-18, BDNF and NSE. This study suggests that delirium is not scarce in patients with AIS admitted to the non-intensive stroke unit, and that delirium developing after AIS seems not to be associated with serum TNF-alpha, IL-1 beta, IL-18, BDNF and NSE but is associated with length of hospital stay and stroke severity.</description><identifier>ISSN: 0028-3843</identifier><identifier>EISSN: 1897-4260</identifier><identifier>DOI: 10.1016/j.pjnns.2016.10.004</identifier><identifier>PMID: 27816188</identifier><language>eng</language><publisher>Poland: Elsevier Urban & Partner Sp. z o.o</publisher><subject>Acute ischemic stroke ; Adult ; Aged ; Aged, 80 and over ; Biomarkers - blood ; Brain Ischemia - blood ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - blood ; Cytokine ; Cytokines ; Cytokines - blood ; Delirium ; Delirium - blood ; Female ; Humans ; Incidence ; Inflammation ; Inflammation - blood ; Interleukin-18 - blood ; Interleukin-1beta - blood ; Male ; Middle Aged ; Non-intensive care stroke unit ; Phosphopyruvate Hydratase - blood ; Stroke ; Stroke - blood ; Tumor Necrosis Factor-alpha - blood ; Tumor necrosis factor-TNF</subject><ispartof>Neurologia i neurochirurgia polska, 2017-01, Vol.51 (1), p.38-44</ispartof><rights>2016</rights><rights>Copyright © 2016. Published by Elsevier Urban & Partner Sp. z o.o.</rights><rights>2017. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-eecbbafbe3ce36f9c2832ef50a522b3fb8698957219ebe721860d9855d75f3d63</citedby><cites>FETCH-LOGICAL-c387t-eecbbafbe3ce36f9c2832ef50a522b3fb8698957219ebe721860d9855d75f3d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2464223159?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27816188$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kozak, Hasan Hüseyin</creatorcontrib><creatorcontrib>Uğuz, Faruk</creatorcontrib><creatorcontrib>Kılınç, İbrahim</creatorcontrib><creatorcontrib>Uca, Ali Ulvi</creatorcontrib><creatorcontrib>Serhat Tokgöz, Osman</creatorcontrib><creatorcontrib>Akpınar, Zehra</creatorcontrib><creatorcontrib>Özer, Nejla</creatorcontrib><title>Delirium in patients with acute ischemic stroke admitted to the non-intensive stroke unit: Incidence and association between clinical features and inflammatory markers</title><title>Neurologia i neurochirurgia polska</title><addtitle>Neurol Neurochir Pol</addtitle><description>Stroke patients with development of delirium have unfavorable outcomes, higher mortality, longer hospitalizations, and a greater degree of dependence after discharge. Studies suggest that delirium is associated with abnormal immunological responses and a resultant increase in inflammatory markers.
Our aim was to determine whether there is an entity relationship between delirium, inflammation and acute ischemic stroke (AIS).
Sixty AIS patients admitted to the hospital were consecutively recruited. Delirium was diagnosed with the clinical assessment according to the Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria. Enzyme-linked immunosorbent assay (ELISA) was used to measure serum levels of Interleukin-1 beta (IL-1 beta), Interleukin 18 (IL-18), Tumor Necrosis Factor-alpha (TNF-alpha), Brain-Derived Neurotrophic Factor (BDNF), and Neuron Specific Enolase (NSE) at admission.
Eleven (18.3%) of 60 patients were diagnosed with delirium, and the majority (n=8, 72.7%) was the hypoactive type. Delirious and non-delirious patients had similar demographic and clinical features. Delirious patients had significantly higher lengths of hospital stay, National Institutes of Health Stroke Scale (NIHSS) at admission and discharge compared to non-delirious patients. In addition, there was no significant statistical difference between delirious and non-delirious patients with AIS in respect of levels of TNF-alpha, IL-1 beta, IL-18, BDNF and NSE. This study suggests that delirium is not scarce in patients with AIS admitted to the non-intensive stroke unit, and that delirium developing after AIS seems not to be associated with serum TNF-alpha, IL-1 beta, IL-18, BDNF and NSE but is associated with length of hospital stay and stroke severity.</description><subject>Acute ischemic stroke</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers - blood</subject><subject>Brain Ischemia - blood</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - blood</subject><subject>Cytokine</subject><subject>Cytokines</subject><subject>Cytokines - blood</subject><subject>Delirium</subject><subject>Delirium - blood</subject><subject>Female</subject><subject>Humans</subject><subject>Incidence</subject><subject>Inflammation</subject><subject>Inflammation - blood</subject><subject>Interleukin-18 - blood</subject><subject>Interleukin-1beta - blood</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Non-intensive care stroke unit</subject><subject>Phosphopyruvate Hydratase - blood</subject><subject>Stroke</subject><subject>Stroke - blood</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><subject>Tumor necrosis factor-TNF</subject><issn>0028-3843</issn><issn>1897-4260</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kctuFDEQRS0EIkPgC5CQJTZsevCjH24kFlF4JFIkNrC23Ha1pibd9mC7E-WL8pu4MwkLFqxKLp1bVb6XkLecbTnj7cf99rD3Pm1FeZTOlrH6Gdlw1XdVLVr2nGwYE6qSqpYn5FVK-wI0DWMvyYnoFG-5Uhty_wUmjLjMFD09mIzgc6K3mHfU2CUDxWR3MKOlKcdwDdS4GXMGR3OgeQfUB1-hz-AT3sATtHjMn-ilt-jA2yLyjpqUgsWyIXg6QL4F8NRO6NGaiY5g8hIhPZDox8nMs8kh3tHZxGuI6TV5MZopwZvHekp-ffv68_yiuvrx_fL87KqyUnW5ArDDYMYBpAXZjr0VSgoYG2YaIQY5DqrtVd90gvcwQCmqZa5XTeO6ZpSulafkw3HuIYbfC6Ss5-IATJPxEJakuZIdk5zJFX3_D7oPS_TlOi3qthZC8qYvlDxSNoaUIoz6ELF86k5zptcc9V4_5KjXHNdmiamo3j3OXoYZ3F_NU3AF-HwEoJhxgxB1srh67TCCzdoF_O-CPxOks9M</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Kozak, Hasan Hüseyin</creator><creator>Uğuz, Faruk</creator><creator>Kılınç, İbrahim</creator><creator>Uca, Ali Ulvi</creator><creator>Serhat Tokgöz, Osman</creator><creator>Akpınar, Zehra</creator><creator>Özer, Nejla</creator><general>Elsevier Urban & Partner Sp. z o.o</general><general>Wydawnictwo Via Medica</general><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>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201701</creationdate><title>Delirium in patients with acute ischemic stroke admitted to the non-intensive stroke unit: Incidence and association between clinical features and inflammatory markers</title><author>Kozak, Hasan Hüseyin ; 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Studies suggest that delirium is associated with abnormal immunological responses and a resultant increase in inflammatory markers.
Our aim was to determine whether there is an entity relationship between delirium, inflammation and acute ischemic stroke (AIS).
Sixty AIS patients admitted to the hospital were consecutively recruited. Delirium was diagnosed with the clinical assessment according to the Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria. Enzyme-linked immunosorbent assay (ELISA) was used to measure serum levels of Interleukin-1 beta (IL-1 beta), Interleukin 18 (IL-18), Tumor Necrosis Factor-alpha (TNF-alpha), Brain-Derived Neurotrophic Factor (BDNF), and Neuron Specific Enolase (NSE) at admission.
Eleven (18.3%) of 60 patients were diagnosed with delirium, and the majority (n=8, 72.7%) was the hypoactive type. Delirious and non-delirious patients had similar demographic and clinical features. Delirious patients had significantly higher lengths of hospital stay, National Institutes of Health Stroke Scale (NIHSS) at admission and discharge compared to non-delirious patients. In addition, there was no significant statistical difference between delirious and non-delirious patients with AIS in respect of levels of TNF-alpha, IL-1 beta, IL-18, BDNF and NSE. This study suggests that delirium is not scarce in patients with AIS admitted to the non-intensive stroke unit, and that delirium developing after AIS seems not to be associated with serum TNF-alpha, IL-1 beta, IL-18, BDNF and NSE but is associated with length of hospital stay and stroke severity.</abstract><cop>Poland</cop><pub>Elsevier Urban & Partner Sp. z o.o</pub><pmid>27816188</pmid><doi>10.1016/j.pjnns.2016.10.004</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute ischemic stroke Adult Aged Aged, 80 and over Biomarkers - blood Brain Ischemia - blood Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - blood Cytokine Cytokines Cytokines - blood Delirium Delirium - blood Female Humans Incidence Inflammation Inflammation - blood Interleukin-18 - blood Interleukin-1beta - blood Male Middle Aged Non-intensive care stroke unit Phosphopyruvate Hydratase - blood Stroke Stroke - blood Tumor Necrosis Factor-alpha - blood Tumor necrosis factor-TNF |
title | Delirium in patients with acute ischemic stroke admitted to the non-intensive stroke unit: Incidence and association between clinical features and inflammatory markers |
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