Glycemic lability index and mortality in critically ill patients—A multicenter cohort study

Background Emerging evidence indicates a relationship between glycemic variability during intensive care unit (ICU) admission and death. We assessed whether mean glucose, hypoglycemia occurrence, or premorbid glycemic control modified this relationship. Methods In this retrospective, multicenter coh...

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Veröffentlicht in:Acta anaesthesiologica Scandinavica 2021-10, Vol.65 (9), p.1267-1275
Hauptverfasser: Hanna, Michel, Balintescu, Anca, Glassford, Neil, Lipcsey, Miklos, Eastwood, Glenn, Oldner, Anders, Bellomo, Rinaldo, Mårtensson, Johan
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container_end_page 1275
container_issue 9
container_start_page 1267
container_title Acta anaesthesiologica Scandinavica
container_volume 65
creator Hanna, Michel
Balintescu, Anca
Glassford, Neil
Lipcsey, Miklos
Eastwood, Glenn
Oldner, Anders
Bellomo, Rinaldo
Mårtensson, Johan
description Background Emerging evidence indicates a relationship between glycemic variability during intensive care unit (ICU) admission and death. We assessed whether mean glucose, hypoglycemia occurrence, or premorbid glycemic control modified this relationship. Methods In this retrospective, multicenter cohort study, we included adult patients admitted to five ICUs in Australia and Sweden with available preadmission glycated hemoglobin A1c (HbA1c) and three or more glucose readings. We calculated the glycemic lability index (GLI), a measure of glycemic variability, and the time‐weighted average blood glucose (TWA‐BG) from all glucose readings. We used logistic regression analysis with adjustment for hypoglycemia and admission characteristics to assess the independent association of GLI (above vs. below cohort median) and TWA‐BG (above vs. below cohort median) with hospital mortality. Results Among 2305 patients, 859 (37%) had diabetes, median GLI was 40 [mmol/L]2/h/week, median TWA‐BG was 8.2 mmol/L, 171 (7%) developed hypoglycemia, and 371 (16%) died. The adjusted odds ratio for death was 1.61 (95% CI, 1.19‐2.15; P = .002) for GLI above versus below median and 1.06 (95% CI, 0.80‐1.41; P = .67) for TWA‐BG above versus below median. The relationship between GLI and mortality was not modified by TWA‐BG (P [interaction] = 0.66), a history of diabetes (P [interaction] = 0.89) or by HbA1c ≥52 mmol/mol (vs.
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We assessed whether mean glucose, hypoglycemia occurrence, or premorbid glycemic control modified this relationship. Methods In this retrospective, multicenter cohort study, we included adult patients admitted to five ICUs in Australia and Sweden with available preadmission glycated hemoglobin A1c (HbA1c) and three or more glucose readings. We calculated the glycemic lability index (GLI), a measure of glycemic variability, and the time‐weighted average blood glucose (TWA‐BG) from all glucose readings. We used logistic regression analysis with adjustment for hypoglycemia and admission characteristics to assess the independent association of GLI (above vs. below cohort median) and TWA‐BG (above vs. below cohort median) with hospital mortality. Results Among 2305 patients, 859 (37%) had diabetes, median GLI was 40 [mmol/L]2/h/week, median TWA‐BG was 8.2 mmol/L, 171 (7%) developed hypoglycemia, and 371 (16%) died. The adjusted odds ratio for death was 1.61 (95% CI, 1.19‐2.15; P = .002) for GLI above versus below median and 1.06 (95% CI, 0.80‐1.41; P = .67) for TWA‐BG above versus below median. The relationship between GLI and mortality was not modified by TWA‐BG (P [interaction] = 0.66), a history of diabetes (P [interaction] = 0.89) or by HbA1c ≥52 mmol/mol (vs. &lt;52 mmol/mol) (P [interaction] = 0.29). Conclusion In adult patients admitted to an ICU in Sweden and Australia, a high GLI was associated with increased hospital mortality irrespective of the level of mean glycemia, hypoglycemia occurrence, or premorbid glycemic control. These findings support the assessment of interventions to reduce glycemic variability during critical illness.</description><identifier>ISSN: 0001-5172</identifier><identifier>ISSN: 1399-6576</identifier><identifier>EISSN: 1399-6576</identifier><identifier>DOI: 10.1111/aas.13843</identifier><identifier>PMID: 33964015</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Blood glucose ; Cohort analysis ; critical care ; Diabetes ; Diabetes mellitus ; Glucose ; glycemic variability ; Hemoglobin ; hyperglycemia ; Hypoglycemia ; Lability ; Mean ; Medicin och hälsovetenskap ; Mortality ; Patients ; Regression analysis</subject><ispartof>Acta anaesthesiologica Scandinavica, 2021-10, Vol.65 (9), p.1267-1275</ispartof><rights>2021 The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley &amp; Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation.</rights><rights>2021. 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We assessed whether mean glucose, hypoglycemia occurrence, or premorbid glycemic control modified this relationship. Methods In this retrospective, multicenter cohort study, we included adult patients admitted to five ICUs in Australia and Sweden with available preadmission glycated hemoglobin A1c (HbA1c) and three or more glucose readings. We calculated the glycemic lability index (GLI), a measure of glycemic variability, and the time‐weighted average blood glucose (TWA‐BG) from all glucose readings. We used logistic regression analysis with adjustment for hypoglycemia and admission characteristics to assess the independent association of GLI (above vs. below cohort median) and TWA‐BG (above vs. below cohort median) with hospital mortality. Results Among 2305 patients, 859 (37%) had diabetes, median GLI was 40 [mmol/L]2/h/week, median TWA‐BG was 8.2 mmol/L, 171 (7%) developed hypoglycemia, and 371 (16%) died. The adjusted odds ratio for death was 1.61 (95% CI, 1.19‐2.15; P = .002) for GLI above versus below median and 1.06 (95% CI, 0.80‐1.41; P = .67) for TWA‐BG above versus below median. The relationship between GLI and mortality was not modified by TWA‐BG (P [interaction] = 0.66), a history of diabetes (P [interaction] = 0.89) or by HbA1c ≥52 mmol/mol (vs. &lt;52 mmol/mol) (P [interaction] = 0.29). Conclusion In adult patients admitted to an ICU in Sweden and Australia, a high GLI was associated with increased hospital mortality irrespective of the level of mean glycemia, hypoglycemia occurrence, or premorbid glycemic control. 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We assessed whether mean glucose, hypoglycemia occurrence, or premorbid glycemic control modified this relationship. Methods In this retrospective, multicenter cohort study, we included adult patients admitted to five ICUs in Australia and Sweden with available preadmission glycated hemoglobin A1c (HbA1c) and three or more glucose readings. We calculated the glycemic lability index (GLI), a measure of glycemic variability, and the time‐weighted average blood glucose (TWA‐BG) from all glucose readings. We used logistic regression analysis with adjustment for hypoglycemia and admission characteristics to assess the independent association of GLI (above vs. below cohort median) and TWA‐BG (above vs. below cohort median) with hospital mortality. Results Among 2305 patients, 859 (37%) had diabetes, median GLI was 40 [mmol/L]2/h/week, median TWA‐BG was 8.2 mmol/L, 171 (7%) developed hypoglycemia, and 371 (16%) died. The adjusted odds ratio for death was 1.61 (95% CI, 1.19‐2.15; P = .002) for GLI above versus below median and 1.06 (95% CI, 0.80‐1.41; P = .67) for TWA‐BG above versus below median. The relationship between GLI and mortality was not modified by TWA‐BG (P [interaction] = 0.66), a history of diabetes (P [interaction] = 0.89) or by HbA1c ≥52 mmol/mol (vs. &lt;52 mmol/mol) (P [interaction] = 0.29). Conclusion In adult patients admitted to an ICU in Sweden and Australia, a high GLI was associated with increased hospital mortality irrespective of the level of mean glycemia, hypoglycemia occurrence, or premorbid glycemic control. These findings support the assessment of interventions to reduce glycemic variability during critical illness.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33964015</pmid><doi>10.1111/aas.13843</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1976-4129</orcidid><orcidid>https://orcid.org/0000-0001-8739-7896</orcidid><oa>free_for_read</oa></addata></record>
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subjects Blood glucose
Cohort analysis
critical care
Diabetes
Diabetes mellitus
Glucose
glycemic variability
Hemoglobin
hyperglycemia
Hypoglycemia
Lability
Mean
Medicin och hälsovetenskap
Mortality
Patients
Regression analysis
title Glycemic lability index and mortality in critically ill patients—A multicenter cohort study
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