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Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure

BACKGROUND: Coma’s are a major cause of clinical deterioration or death. Identification of risks that predispose to coma are important in managing patients; however, the risk factors for nosocomial nontraumatic coma (NNC) are not well known. Our aim was to investigate the risk factors in patients wi...

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Autores principales: Zhou, Ye-Ting, Wang, Shao-Dan, Wang, Guang-Sheng, Chen, Xiao-Dong, Tong, Dao-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045239/
https://www.ncbi.nlm.nih.gov/pubmed/27713634
http://dx.doi.org/10.2147/JMDH.S113682
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author Zhou, Ye-Ting
Wang, Shao-Dan
Wang, Guang-Sheng
Chen, Xiao-Dong
Tong, Dao-Ming
author_facet Zhou, Ye-Ting
Wang, Shao-Dan
Wang, Guang-Sheng
Chen, Xiao-Dong
Tong, Dao-Ming
author_sort Zhou, Ye-Ting
collection PubMed
description BACKGROUND: Coma’s are a major cause of clinical deterioration or death. Identification of risks that predispose to coma are important in managing patients; however, the risk factors for nosocomial nontraumatic coma (NNC) are not well known. Our aim was to investigate the risk factors in patients with NNC. METHODS: A retrospective case–control design was used to compare patients with NNC and a control group of patients without coma in a population-based cohort of 263 participants from the neurological intensive care unit in Shuyang County People’s Hospital of Northern China. Coma was diagnosed by a Glasgow Coma Scale score ≤8. Adjusted odds ratios for patients with NNC were derived from multivariate logistic regression analyses. RESULTS: A total of 96 subjects had NNC. The prevalence of NNC was 36.5% among the subjects. Among these, 82% had acute cerebrovascular etiology. Most of the NNC usually occurred at day 3 after admission to the neurological intensive care unit. Patients with NNC had higher hospital mortality rates (67.7% vs 3%, P<0.0001) and were more likely to have a central herniation (47.9% vs 0%, P<0.001) or uncal herniation (11.5% vs 0%, P<0.001) than those without NNC. Multiple logistic regression showed that systemic inflammatory response syndrome-positive sepsis (odds ratio =4, 95% confidence interval =1.875−8.567, P<0.001) and acute respiratory failure (odds ratio =3.275, 95% confidence interval =1.014−10.573, P<0.05) were the factors independently associated with a higher risk of NNC. CONCLUSION: Systemic inflammatory response syndrome-positive sepsis and acute respiratory failure are independently associated with an increased risk of NNC. This information may be important for patients with NNC.
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spelling pubmed-50452392016-10-06 Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure Zhou, Ye-Ting Wang, Shao-Dan Wang, Guang-Sheng Chen, Xiao-Dong Tong, Dao-Ming J Multidiscip Healthc Original Research BACKGROUND: Coma’s are a major cause of clinical deterioration or death. Identification of risks that predispose to coma are important in managing patients; however, the risk factors for nosocomial nontraumatic coma (NNC) are not well known. Our aim was to investigate the risk factors in patients with NNC. METHODS: A retrospective case–control design was used to compare patients with NNC and a control group of patients without coma in a population-based cohort of 263 participants from the neurological intensive care unit in Shuyang County People’s Hospital of Northern China. Coma was diagnosed by a Glasgow Coma Scale score ≤8. Adjusted odds ratios for patients with NNC were derived from multivariate logistic regression analyses. RESULTS: A total of 96 subjects had NNC. The prevalence of NNC was 36.5% among the subjects. Among these, 82% had acute cerebrovascular etiology. Most of the NNC usually occurred at day 3 after admission to the neurological intensive care unit. Patients with NNC had higher hospital mortality rates (67.7% vs 3%, P<0.0001) and were more likely to have a central herniation (47.9% vs 0%, P<0.001) or uncal herniation (11.5% vs 0%, P<0.001) than those without NNC. Multiple logistic regression showed that systemic inflammatory response syndrome-positive sepsis (odds ratio =4, 95% confidence interval =1.875−8.567, P<0.001) and acute respiratory failure (odds ratio =3.275, 95% confidence interval =1.014−10.573, P<0.05) were the factors independently associated with a higher risk of NNC. CONCLUSION: Systemic inflammatory response syndrome-positive sepsis and acute respiratory failure are independently associated with an increased risk of NNC. This information may be important for patients with NNC. Dove Medical Press 2016-09-26 /pmc/articles/PMC5045239/ /pubmed/27713634 http://dx.doi.org/10.2147/JMDH.S113682 Text en © 2016 Zhou et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zhou, Ye-Ting
Wang, Shao-Dan
Wang, Guang-Sheng
Chen, Xiao-Dong
Tong, Dao-Ming
Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
title Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
title_full Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
title_fullStr Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
title_full_unstemmed Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
title_short Risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
title_sort risk factors for nosocomial nontraumatic coma: sepsis and respiratory failure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045239/
https://www.ncbi.nlm.nih.gov/pubmed/27713634
http://dx.doi.org/10.2147/JMDH.S113682
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