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Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization

BACKGROUND: There was considerable debate regarding the effect of mean blood glucose (MBG) and glycemic variability (GV) on the mortality of septic patients. This retrospective cohort study aimed to assess the association between MBG and GV with ICU mortality of sepsis patients and to explore the op...

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Autores principales: Lu, Zongqing, Tao, Gan, Sun, Xiaoyu, Zhang, Yijun, Jiang, Mengke, Liu, Yu, Ling, Meng, Zhang, Jin, Xiao, Wenyan, Hua, Tianfeng, Zhu, Huaqing, Yang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099235/
https://www.ncbi.nlm.nih.gov/pubmed/35570924
http://dx.doi.org/10.3389/fpubh.2022.857368
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author Lu, Zongqing
Tao, Gan
Sun, Xiaoyu
Zhang, Yijun
Jiang, Mengke
Liu, Yu
Ling, Meng
Zhang, Jin
Xiao, Wenyan
Hua, Tianfeng
Zhu, Huaqing
Yang, Min
author_facet Lu, Zongqing
Tao, Gan
Sun, Xiaoyu
Zhang, Yijun
Jiang, Mengke
Liu, Yu
Ling, Meng
Zhang, Jin
Xiao, Wenyan
Hua, Tianfeng
Zhu, Huaqing
Yang, Min
author_sort Lu, Zongqing
collection PubMed
description BACKGROUND: There was considerable debate regarding the effect of mean blood glucose (MBG) and glycemic variability (GV) on the mortality of septic patients. This retrospective cohort study aimed to assess the association between MBG and GV with ICU mortality of sepsis patients and to explore the optimal MBG range. METHODS: Sepsis patients were enrolled from the Medical Information Mart for Intensive Care IV database (MIMIC-IV). MBG and glycemic coefficient of variation (Glu(CV)) were, respectively, calculated to represent the overall glycemic status and GV during ICU stay. The associations between MBG, Glu(CV), and ICU mortality of the septic patients were assessed by using multivariate logistic regression in different subgroups and the severity of sepsis. Restricted cubic splines evaluated the optimal MBG target. RESULTS: A total of 7,104 adult sepsis patients were included. The multivariate logistic regression results showed that increased MBG and Glu(CV) were significantly correlated with ICU mortality. The adjusted odds ratios were 1.14 (95% CI 1.09–1.20) and 1.05 (95% CI 1.00–1.12). However, there was no association between hyperglycemia and ICU mortality among diabetes, liver disease, immunosuppression, and hypoglycemia patients. And the impact of high Glu(CV) on ICU mortality was not observed in those with diabetes, immunosuppression, liver disease, and non-septic shock. The ICU mortality risk of severe hyperglycemia (≧200 mg/dl) and high Glu(CV) (>31.429%), respectively, elevated 2.30, 3.15, 3.06, and 2.37, 2.79, 3.14-folds in mild (SOFA ≦ 3), middle (SOFA 3–7), and severe group (SOFA ≧ 7). The MBG level was associated with the lowest risk of ICU mortality and hypoglycemia between 120 and 140 mg/dl in the subgroup without diabetes. For the diabetic subset, the incidence of hypoglycemia was significantly reduced when the MBG was 140–190 mg/dl, but a glycemic control target effectively reducing ICU mortality was not observed. CONCLUSION: MBG and Glu(CV) during the ICU stay were associated with all-cause ICU mortality in sepsis patients; however, their harms are not apparent in some particular subgroups. The impact of hyperglycemia and high GV on death increased with the severity of sepsis. The risk of ICU mortality and hypoglycemia in those with no pre-existing diabetes was lower when maintaining the MBG in the range of 120–140 mg/dl.
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spelling pubmed-90992352022-05-14 Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization Lu, Zongqing Tao, Gan Sun, Xiaoyu Zhang, Yijun Jiang, Mengke Liu, Yu Ling, Meng Zhang, Jin Xiao, Wenyan Hua, Tianfeng Zhu, Huaqing Yang, Min Front Public Health Public Health BACKGROUND: There was considerable debate regarding the effect of mean blood glucose (MBG) and glycemic variability (GV) on the mortality of septic patients. This retrospective cohort study aimed to assess the association between MBG and GV with ICU mortality of sepsis patients and to explore the optimal MBG range. METHODS: Sepsis patients were enrolled from the Medical Information Mart for Intensive Care IV database (MIMIC-IV). MBG and glycemic coefficient of variation (Glu(CV)) were, respectively, calculated to represent the overall glycemic status and GV during ICU stay. The associations between MBG, Glu(CV), and ICU mortality of the septic patients were assessed by using multivariate logistic regression in different subgroups and the severity of sepsis. Restricted cubic splines evaluated the optimal MBG target. RESULTS: A total of 7,104 adult sepsis patients were included. The multivariate logistic regression results showed that increased MBG and Glu(CV) were significantly correlated with ICU mortality. The adjusted odds ratios were 1.14 (95% CI 1.09–1.20) and 1.05 (95% CI 1.00–1.12). However, there was no association between hyperglycemia and ICU mortality among diabetes, liver disease, immunosuppression, and hypoglycemia patients. And the impact of high Glu(CV) on ICU mortality was not observed in those with diabetes, immunosuppression, liver disease, and non-septic shock. The ICU mortality risk of severe hyperglycemia (≧200 mg/dl) and high Glu(CV) (>31.429%), respectively, elevated 2.30, 3.15, 3.06, and 2.37, 2.79, 3.14-folds in mild (SOFA ≦ 3), middle (SOFA 3–7), and severe group (SOFA ≧ 7). The MBG level was associated with the lowest risk of ICU mortality and hypoglycemia between 120 and 140 mg/dl in the subgroup without diabetes. For the diabetic subset, the incidence of hypoglycemia was significantly reduced when the MBG was 140–190 mg/dl, but a glycemic control target effectively reducing ICU mortality was not observed. CONCLUSION: MBG and Glu(CV) during the ICU stay were associated with all-cause ICU mortality in sepsis patients; however, their harms are not apparent in some particular subgroups. The impact of hyperglycemia and high GV on death increased with the severity of sepsis. The risk of ICU mortality and hypoglycemia in those with no pre-existing diabetes was lower when maintaining the MBG in the range of 120–140 mg/dl. Frontiers Media S.A. 2022-04-29 /pmc/articles/PMC9099235/ /pubmed/35570924 http://dx.doi.org/10.3389/fpubh.2022.857368 Text en Copyright © 2022 Lu, Tao, Sun, Zhang, Jiang, Liu, Ling, Zhang, Xiao, Hua, Zhu and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Lu, Zongqing
Tao, Gan
Sun, Xiaoyu
Zhang, Yijun
Jiang, Mengke
Liu, Yu
Ling, Meng
Zhang, Jin
Xiao, Wenyan
Hua, Tianfeng
Zhu, Huaqing
Yang, Min
Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization
title Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization
title_full Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization
title_fullStr Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization
title_full_unstemmed Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization
title_short Association of Blood Glucose Level and Glycemic Variability With Mortality in Sepsis Patients During ICU Hospitalization
title_sort association of blood glucose level and glycemic variability with mortality in sepsis patients during icu hospitalization
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099235/
https://www.ncbi.nlm.nih.gov/pubmed/35570924
http://dx.doi.org/10.3389/fpubh.2022.857368
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