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Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit

The aim of this study was to assess the bedside brain function monitoring of color density spectral array (CDSA) for early prognostic evaluation of coma patients in pediatric intensive care unit (PICU). Forty-two consecutive pediatric coma patients were enrolled. The individual conscious state was e...

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Autores principales: Wang, Jiangtao, Hao, Xiaosheng, Zhang, Yanfeng, Liu, Guiling, Chen, Yinbo, Qu, Ge, Li, Chunnv, Liang, Jianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799503/
https://www.ncbi.nlm.nih.gov/pubmed/31593114
http://dx.doi.org/10.1097/MD.0000000000017493
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author Wang, Jiangtao
Hao, Xiaosheng
Zhang, Yanfeng
Liu, Guiling
Chen, Yinbo
Qu, Ge
Li, Chunnv
Liang, Jianmin
author_facet Wang, Jiangtao
Hao, Xiaosheng
Zhang, Yanfeng
Liu, Guiling
Chen, Yinbo
Qu, Ge
Li, Chunnv
Liang, Jianmin
author_sort Wang, Jiangtao
collection PubMed
description The aim of this study was to assess the bedside brain function monitoring of color density spectral array (CDSA) for early prognostic evaluation of coma patients in pediatric intensive care unit (PICU). Forty-two consecutive pediatric coma patients were enrolled. The individual conscious state was evaluated according to the Glasgow coma scale (GCS). CDSA parameters including CDSA pattern (CDSAP), sleep–wake cycle (SWC), sleep stage (SS), and drug-induced fast wave activity (DIFWA) were recorded. Three months later, prognosis was evaluated according to pediatric cerebral performance category (PCPC) score, based on which the patients were divided into FP-group (favorable prognosis) and PP-group (poor prognosis). The changeable type of CDSAP, appearance of SWC, SS, and DIFWA were significantly correlated with favorable prognosis. Both GCS and SWC were significantly correlated with the prognosis. However, there was substantial overlap in GCS between FP-group and PP-group. Although the absence of SWC was statistically an independent risk factor for poor prognosis but with a high false positive rate (0.143), a linear logistic regression showed the odds ratio of GCS for predicting prognosis was 0.93 (95% confidence interval: 0.48–1.80; P = .83) and that of SWC was 0.12 (95% confidence interval: 0.03–0.47; P = .03). Furthermore, the absence of SWC was correlated with poor prognosis in nonintracranial infection patients. Our study found that several CDSA factors are associated with prognosis of coma patients in PICU. SWC may be a potential indicator for evaluating the prognosis of coma patients in PICU.
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spelling pubmed-67995032019-11-18 Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit Wang, Jiangtao Hao, Xiaosheng Zhang, Yanfeng Liu, Guiling Chen, Yinbo Qu, Ge Li, Chunnv Liang, Jianmin Medicine (Baltimore) 6200 The aim of this study was to assess the bedside brain function monitoring of color density spectral array (CDSA) for early prognostic evaluation of coma patients in pediatric intensive care unit (PICU). Forty-two consecutive pediatric coma patients were enrolled. The individual conscious state was evaluated according to the Glasgow coma scale (GCS). CDSA parameters including CDSA pattern (CDSAP), sleep–wake cycle (SWC), sleep stage (SS), and drug-induced fast wave activity (DIFWA) were recorded. Three months later, prognosis was evaluated according to pediatric cerebral performance category (PCPC) score, based on which the patients were divided into FP-group (favorable prognosis) and PP-group (poor prognosis). The changeable type of CDSAP, appearance of SWC, SS, and DIFWA were significantly correlated with favorable prognosis. Both GCS and SWC were significantly correlated with the prognosis. However, there was substantial overlap in GCS between FP-group and PP-group. Although the absence of SWC was statistically an independent risk factor for poor prognosis but with a high false positive rate (0.143), a linear logistic regression showed the odds ratio of GCS for predicting prognosis was 0.93 (95% confidence interval: 0.48–1.80; P = .83) and that of SWC was 0.12 (95% confidence interval: 0.03–0.47; P = .03). Furthermore, the absence of SWC was correlated with poor prognosis in nonintracranial infection patients. Our study found that several CDSA factors are associated with prognosis of coma patients in PICU. SWC may be a potential indicator for evaluating the prognosis of coma patients in PICU. Wolters Kluwer Health 2019-10-11 /pmc/articles/PMC6799503/ /pubmed/31593114 http://dx.doi.org/10.1097/MD.0000000000017493 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 6200
Wang, Jiangtao
Hao, Xiaosheng
Zhang, Yanfeng
Liu, Guiling
Chen, Yinbo
Qu, Ge
Li, Chunnv
Liang, Jianmin
Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
title Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
title_full Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
title_fullStr Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
title_full_unstemmed Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
title_short Color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
title_sort color density spectral array for early evaluation of prognosis of patients with coma in pediatric intensive care unit
topic 6200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799503/
https://www.ncbi.nlm.nih.gov/pubmed/31593114
http://dx.doi.org/10.1097/MD.0000000000017493
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