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Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis
BACKGROUND: High glycemic variability (GV) is common in critically ill patients; however, the prevalence and mortality association with early GV in patients with sepsis remains unclear. METHODS: This retrospective cohort study was conducted in a medical intensive care unit (ICU) in central Taiwan. P...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007493/ https://www.ncbi.nlm.nih.gov/pubmed/32034567 http://dx.doi.org/10.1186/s13613-020-0635-3 |
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author | Chao, Wen-Cheng Tseng, Chien-Hua Wu, Chieh-Liang Shih, Sou-Jen Yi, Chi-Yuan Chan, Ming-Cheng |
author_facet | Chao, Wen-Cheng Tseng, Chien-Hua Wu, Chieh-Liang Shih, Sou-Jen Yi, Chi-Yuan Chan, Ming-Cheng |
author_sort | Chao, Wen-Cheng |
collection | PubMed |
description | BACKGROUND: High glycemic variability (GV) is common in critically ill patients; however, the prevalence and mortality association with early GV in patients with sepsis remains unclear. METHODS: This retrospective cohort study was conducted in a medical intensive care unit (ICU) in central Taiwan. Patients in the ICU with sepsis between January 2014 and December 2015 were included for analysis. All of these patients received protocol-based management, including blood sugar monitoring every 2 h for the first 24 h of ICU admission. Mean amplitude of glycemic excursions (MAGE) and coefficient of variation (CoV) were used to assess GV. RESULTS: A total of 452 patients (mean age 71.4 ± 14.7 years; 76.7% men) were enrolled for analysis. They were divided into high GV (43.4%, 196/452) and low GV (56.6%, 256/512) groups using MAGE 65 mg/dL as the cut-off point. Patients with high GV tended to have higher HbA1c (6.7 ± 1.8% vs. 5.9 ± 0.9%, p < 0.01) and were more likely to have diabetes mellitus (DM) (50.0% vs. 23.4%, p < 0.01) compared with those in the low GV group. Kaplan–Meier analysis showed that a high GV was associated with increased 30-day mortality (log-rank test, p = 0.018). The association remained strong in the non-DM (log-rank test, p = 0.035), but not in the DM (log-rank test, p = 0.254) group. Multivariate Cox proportional hazard regression analysis identified that high APACHE II score (adjusted hazard ratio (aHR) 1.045, 95% confidence interval (CI) 1.013–1.078), high serum lactate level at 0 h (aHR 1.009, 95% CI 1.003–1.014), having chronic airway disease (aHR 0.478, 95% CI 0.302–0.756), high mean day 1 glucose (aHR 1.008, 95% CI 1.000–1.016), and high MAGE (aHR 1.607, 95% CI 1.008–2.563) were independently associated with increased 30-day mortality. The association with 30-day mortality remained consistent when using CoV to assess GV. CONCLUSIONS: We found that approximately 40% of the septic patients had a high early GV, defined as MAGE > 65 mg/dL. Higher GV within 24 h of ICU admission was independently associated with increased 30-day mortality. These findings highlight the need to monitor GV in septic patients early during an ICU admission. |
format | Online Article Text |
id | pubmed-7007493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-70074932020-02-24 Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis Chao, Wen-Cheng Tseng, Chien-Hua Wu, Chieh-Liang Shih, Sou-Jen Yi, Chi-Yuan Chan, Ming-Cheng Ann Intensive Care Research BACKGROUND: High glycemic variability (GV) is common in critically ill patients; however, the prevalence and mortality association with early GV in patients with sepsis remains unclear. METHODS: This retrospective cohort study was conducted in a medical intensive care unit (ICU) in central Taiwan. Patients in the ICU with sepsis between January 2014 and December 2015 were included for analysis. All of these patients received protocol-based management, including blood sugar monitoring every 2 h for the first 24 h of ICU admission. Mean amplitude of glycemic excursions (MAGE) and coefficient of variation (CoV) were used to assess GV. RESULTS: A total of 452 patients (mean age 71.4 ± 14.7 years; 76.7% men) were enrolled for analysis. They were divided into high GV (43.4%, 196/452) and low GV (56.6%, 256/512) groups using MAGE 65 mg/dL as the cut-off point. Patients with high GV tended to have higher HbA1c (6.7 ± 1.8% vs. 5.9 ± 0.9%, p < 0.01) and were more likely to have diabetes mellitus (DM) (50.0% vs. 23.4%, p < 0.01) compared with those in the low GV group. Kaplan–Meier analysis showed that a high GV was associated with increased 30-day mortality (log-rank test, p = 0.018). The association remained strong in the non-DM (log-rank test, p = 0.035), but not in the DM (log-rank test, p = 0.254) group. Multivariate Cox proportional hazard regression analysis identified that high APACHE II score (adjusted hazard ratio (aHR) 1.045, 95% confidence interval (CI) 1.013–1.078), high serum lactate level at 0 h (aHR 1.009, 95% CI 1.003–1.014), having chronic airway disease (aHR 0.478, 95% CI 0.302–0.756), high mean day 1 glucose (aHR 1.008, 95% CI 1.000–1.016), and high MAGE (aHR 1.607, 95% CI 1.008–2.563) were independently associated with increased 30-day mortality. The association with 30-day mortality remained consistent when using CoV to assess GV. CONCLUSIONS: We found that approximately 40% of the septic patients had a high early GV, defined as MAGE > 65 mg/dL. Higher GV within 24 h of ICU admission was independently associated with increased 30-day mortality. These findings highlight the need to monitor GV in septic patients early during an ICU admission. Springer International Publishing 2020-02-07 /pmc/articles/PMC7007493/ /pubmed/32034567 http://dx.doi.org/10.1186/s13613-020-0635-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Chao, Wen-Cheng Tseng, Chien-Hua Wu, Chieh-Liang Shih, Sou-Jen Yi, Chi-Yuan Chan, Ming-Cheng Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis |
title | Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis |
title_full | Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis |
title_fullStr | Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis |
title_full_unstemmed | Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis |
title_short | Higher glycemic variability within the first day of ICU admission is associated with increased 30-day mortality in ICU patients with sepsis |
title_sort | higher glycemic variability within the first day of icu admission is associated with increased 30-day mortality in icu patients with sepsis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007493/ https://www.ncbi.nlm.nih.gov/pubmed/32034567 http://dx.doi.org/10.1186/s13613-020-0635-3 |
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