Coefficient of glucose variation is independently associated with mortality in critically ill patients receiving intravenous insulin

• Published in: Critical care (London, England) Vol. 18; no. 2; p. R86
• Main Authors: Lanspa, Michael J, Dickerson, Justin, Morris, Alan H, Orme, James F, Holmen, John, Hirshberg, Eliotte L
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 30.04.2014; BioMed Central
• Subjects: Aged; Blood Glucose - drug effects; Blood Glucose - metabolism; Care and treatment; Cohort Studies; Comorbidity; Critical Illness - mortality; Critical Illness - therapy; Development and progression; Diabetics; Female; Hospital patients; Humans; Infusions, Intravenous; Insulin; Insulin - administration & dosage; Male; Medical research; Medicine, Experimental; Middle Aged; Mortality - trends; Patient outcomes; Physiological aspects; Retrospective Studies
• ISSN: 1364-8535; 1466-609X; 1364-8535
• DOI: 10.1186/cc13851

Both patient- and context-specific factors may explain the conflicting evidence regarding glucose control in critically ill patients. Blood glucose variability appears to correlate with mortality, but this variability may be an indicator of disease severity, rather than an independent predictor of mortality. We assessed blood glucose coefficient of variation as an independent predictor of mortality in the critically ill. We used eProtocol-Insulin, an electronic protocol for managing intravenous insulin with explicit rules, high clinician compliance, and reproducibility. We studied critically ill patients from eight hospitals, excluding patients with diabetic ketoacidosis and patients supported with eProtocol-insulin for < 24 hours or with < 10 glucose measurements. Our primary clinical outcome was 30-day all-cause mortality. We performed multivariable logistic regression, with covariates of age, gender, glucose coefficient of variation (standard deviation/mean), Charlson comorbidity score, acute physiology score, presence of diabetes, and occurrence of hypoglycemia < 60 mg/dL. We studied 6101 critically ill adults. Coefficient of variation was independently associated with 30-day mortality (odds ratio 1.23 for every 10% increase, P < 0.001), even after adjustment for hypoglycemia, age, disease severity, and comorbidities. The association was higher in non-diabetics (OR = 1.37, P < 0.001) than in diabetics (OR 1.15, P = 0.001). Blood glucose variability is associated with mortality and is independent of hypoglycemia, disease severity, and comorbidities. Future studies should evaluate blood glucose variability.