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A clinical perspective of sepsis-associated delirium
The term sepsis-associated encephalopathy (SAE) has been applied to animal models, postmortem studies in patients, and severe cases of sepsis. SAE is considered to include all types of brain dysfunction, including delirium, coma, seizure, and focal neurological signs. Clinical data for sepsis-associ...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804610/ https://www.ncbi.nlm.nih.gov/pubmed/27011789 http://dx.doi.org/10.1186/s40560-016-0145-4 |
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author | Tsuruta, Ryosuke Oda, Yasutaka |
author_facet | Tsuruta, Ryosuke Oda, Yasutaka |
author_sort | Tsuruta, Ryosuke |
collection | PubMed |
description | The term sepsis-associated encephalopathy (SAE) has been applied to animal models, postmortem studies in patients, and severe cases of sepsis. SAE is considered to include all types of brain dysfunction, including delirium, coma, seizure, and focal neurological signs. Clinical data for sepsis-associated delirium (SAD) have been accumulating since the establishment of definitions of coma or delirium and the introduction of validated screening tools. Some preliminary studies have examined the etiology of SAD. Neuroinflammation, abnormal cerebral perfusion, and neurotransmitter imbalances are the main mechanisms underlying the development of SAD. However, there are still no specific diagnostic blood, electrophysiological, or imaging tests or treatments specific for SAD. The duration of delirium in intensive care patients is associated with long-term functional disability and cognitive impairment, although this syndrome usually reverses after the successful treatment of sepsis. Once the respiratory and hemodynamic states are stabilized, patients with severe sepsis or septic shock should receive rehabilitation as soon as possible because early initiation of rehabilitation can reduce the duration of delirium. We expect to see further pathophysiological data and the development of novel treatments for SAD now that reliable and consistent definitions of SAD have been established. |
format | Online Article Text |
id | pubmed-4804610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48046102016-03-24 A clinical perspective of sepsis-associated delirium Tsuruta, Ryosuke Oda, Yasutaka J Intensive Care Review The term sepsis-associated encephalopathy (SAE) has been applied to animal models, postmortem studies in patients, and severe cases of sepsis. SAE is considered to include all types of brain dysfunction, including delirium, coma, seizure, and focal neurological signs. Clinical data for sepsis-associated delirium (SAD) have been accumulating since the establishment of definitions of coma or delirium and the introduction of validated screening tools. Some preliminary studies have examined the etiology of SAD. Neuroinflammation, abnormal cerebral perfusion, and neurotransmitter imbalances are the main mechanisms underlying the development of SAD. However, there are still no specific diagnostic blood, electrophysiological, or imaging tests or treatments specific for SAD. The duration of delirium in intensive care patients is associated with long-term functional disability and cognitive impairment, although this syndrome usually reverses after the successful treatment of sepsis. Once the respiratory and hemodynamic states are stabilized, patients with severe sepsis or septic shock should receive rehabilitation as soon as possible because early initiation of rehabilitation can reduce the duration of delirium. We expect to see further pathophysiological data and the development of novel treatments for SAD now that reliable and consistent definitions of SAD have been established. BioMed Central 2016-03-23 /pmc/articles/PMC4804610/ /pubmed/27011789 http://dx.doi.org/10.1186/s40560-016-0145-4 Text en © Tsuruta and Oda. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Tsuruta, Ryosuke Oda, Yasutaka A clinical perspective of sepsis-associated delirium |
title | A clinical perspective of sepsis-associated delirium |
title_full | A clinical perspective of sepsis-associated delirium |
title_fullStr | A clinical perspective of sepsis-associated delirium |
title_full_unstemmed | A clinical perspective of sepsis-associated delirium |
title_short | A clinical perspective of sepsis-associated delirium |
title_sort | clinical perspective of sepsis-associated delirium |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804610/ https://www.ncbi.nlm.nih.gov/pubmed/27011789 http://dx.doi.org/10.1186/s40560-016-0145-4 |
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