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Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis

This study investigates the prognostic value of immune cell subsets in assessing the risk of death in patients with sepsis. This retrospective study collected 169 patients from March 2020 to February 2021 at our hospital. Baseline data were collected from patients. The absolute values (Abs) and perc...

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Autores principales: Zhang, Ying, Wang, Jia, Hu, Le, Xuan, Jingchao, Qu, Yifan, Li, Yixuan, Ye, Xinghua, Yang, Long, Yang, Jun, Zhang, Xiangqun, Wang, Junyu, Wei, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586162/
https://www.ncbi.nlm.nih.gov/pubmed/34755551
http://dx.doi.org/10.1177/10760296211059498
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author Zhang, Ying
Wang, Jia
Hu, Le
Xuan, Jingchao
Qu, Yifan
Li, Yixuan
Ye, Xinghua
Yang, Long
Yang, Jun
Zhang, Xiangqun
Wang, Junyu
Wei, Bing
author_facet Zhang, Ying
Wang, Jia
Hu, Le
Xuan, Jingchao
Qu, Yifan
Li, Yixuan
Ye, Xinghua
Yang, Long
Yang, Jun
Zhang, Xiangqun
Wang, Junyu
Wei, Bing
author_sort Zhang, Ying
collection PubMed
description This study investigates the prognostic value of immune cell subsets in assessing the risk of death in patients with sepsis. This retrospective study collected 169 patients from March 2020 to February 2021 at our hospital. Baseline data were collected from patients. The absolute values (Abs) and percentages (%) of immune cell subsets for lymphocytes, T cells, CD4+ cells, CD8+, B cells, NK cells, and NKT cells were measured using flow Cytometry. Among the included patients, 43 patients were in the nonsurvivor group and 126 patients were in the survivor group. The age of patients in the nonsurvivor survivor was higher than that of survivor group patients (P = .020). SOFA, APACHE II, C-reactive protein, and procalcitonin were higher in the nonsurvivor group than in the survivor group (all P values < .05). Multivariate regression analysis showed that lymphocytes (%) and SOFA were independent risk factors affecting patients’ prognosis. Lymphocytes (%) have the highest area under the receiver operating characteristic (ROC) curve (0.812). The model area under the ROC curve for immune cell subsets was 0.800, with a sensitivity of 72.09%, and specificity of 79.27% (z = 7.796, P <  .001). Analysis of patient prognosis by immune cell subsets diagnostic showed statistically significant differences in the grouping of cut-off values for all 5 indicators (all P < .05). The lymphocytes (%) and SOFA score are independent risk factors affecting the prognosis of patients. A moderate predictive power for mortality in sepsis patients by immune cell subsets model.
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spelling pubmed-85861622021-11-13 Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis Zhang, Ying Wang, Jia Hu, Le Xuan, Jingchao Qu, Yifan Li, Yixuan Ye, Xinghua Yang, Long Yang, Jun Zhang, Xiangqun Wang, Junyu Wei, Bing Clin Appl Thromb Hemost Original Manuscript This study investigates the prognostic value of immune cell subsets in assessing the risk of death in patients with sepsis. This retrospective study collected 169 patients from March 2020 to February 2021 at our hospital. Baseline data were collected from patients. The absolute values (Abs) and percentages (%) of immune cell subsets for lymphocytes, T cells, CD4+ cells, CD8+, B cells, NK cells, and NKT cells were measured using flow Cytometry. Among the included patients, 43 patients were in the nonsurvivor group and 126 patients were in the survivor group. The age of patients in the nonsurvivor survivor was higher than that of survivor group patients (P = .020). SOFA, APACHE II, C-reactive protein, and procalcitonin were higher in the nonsurvivor group than in the survivor group (all P values < .05). Multivariate regression analysis showed that lymphocytes (%) and SOFA were independent risk factors affecting patients’ prognosis. Lymphocytes (%) have the highest area under the receiver operating characteristic (ROC) curve (0.812). The model area under the ROC curve for immune cell subsets was 0.800, with a sensitivity of 72.09%, and specificity of 79.27% (z = 7.796, P <  .001). Analysis of patient prognosis by immune cell subsets diagnostic showed statistically significant differences in the grouping of cut-off values for all 5 indicators (all P < .05). The lymphocytes (%) and SOFA score are independent risk factors affecting the prognosis of patients. A moderate predictive power for mortality in sepsis patients by immune cell subsets model. SAGE Publications 2021-11-10 /pmc/articles/PMC8586162/ /pubmed/34755551 http://dx.doi.org/10.1177/10760296211059498 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Manuscript
Zhang, Ying
Wang, Jia
Hu, Le
Xuan, Jingchao
Qu, Yifan
Li, Yixuan
Ye, Xinghua
Yang, Long
Yang, Jun
Zhang, Xiangqun
Wang, Junyu
Wei, Bing
Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis
title Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis
title_full Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis
title_fullStr Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis
title_full_unstemmed Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis
title_short Predictive Value of Immune Cell Subsets for Mortality Risk in Patients With Sepsis
title_sort predictive value of immune cell subsets for mortality risk in patients with sepsis
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586162/
https://www.ncbi.nlm.nih.gov/pubmed/34755551
http://dx.doi.org/10.1177/10760296211059498
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