» Articles » PMID: 18596625

Glucose Variability and Mortality in Patients with Sepsis

Overview
Journal Crit Care Med
Date 2008 Jul 4
PMID 18596625
Citations 153
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Treatment and prevention of hyperglycemia has been advocated for subjects with sepsis. Glucose variability, rather than the glucose level, has also been shown to be an important factor associated with in-hospital mortality, in general, critically ill patients. Our objective was to determine the association between glucose variability and hospital mortality in septic patients and the expression of glucose variability that best reflects this risk.

Design: Retrospective, single-center cohort study.

Setting: Academic, tertiary care hospital.

Patients: Adult subjects hospitalized for >1 day, with a diagnosis of sepsis were included.

Interventions: None.

Measurements: Glucose variability was calculated for all subjects as the average and standard deviation of glucose, the mean amplitude of glycemic excursions, and the glycemic lability index. Hospital mortality was the primary outcome variable. Logistic regression was used to determine the odds of hospital death in relation to measures of glucose variability after adjustment for important covariates.

Main Results: Of the methods used to measure glucose variability, the glycemic lability index had the best discrimination for mortality (area under the curve = 0.67, p < 0.001). After adjustment for confounders, including the number of organ failures and the occurrence of hypoglycemia, there was a significant interaction between glycemic lability index and average glucose level, and the odds of hospital mortality. Higher glycemic lability index was not independently associated with mortality among subjects with average glucose levels above the median for the cohort. However, subjects with increased glycemic lability index, but lower average glucose values had almost five-fold increased odds of hospital mortality (odds ratio = 4.73, 95% confidence interval = 2.6-8.7) compared with those with lower glycemic lability index.

Conclusions: Glucose variability is independently associated with hospital mortality in septic patients. Strategies to reduce glucose variability should be studied to determine whether they improve the outcomes of septic patients.

Citing Articles

Association between various blood glucose variability-related indicators during early ICU admission and 28-day mortality in non-diabetic patients with sepsis.

Zhou J, Chen Z, Huang H, Ou C, Li X Diabetol Metab Syndr. 2025; 17(1):22.

PMID: 39828689 PMC: 11744847. DOI: 10.1186/s13098-025-01580-4.


Association of Glycemic Variability with Outcomes in Non-diabetic Sepsis Patients: A Prospective Observational Study.

Prakash P, Sethi P, Vikram N, Khan M, Gupta Y, Jadon R Indian J Crit Care Med. 2025; 29(1):27-35.

PMID: 39802255 PMC: 11719557. DOI: 10.5005/jp-journals-10071-24873.


"When the Going Gets Tough": Novel Roles for TRPV4 in Stiffness-induced Phagolysosome Maturation.

Estrada-Bernal A, Sharma L, Shah F Am J Respir Cell Mol Biol. 2024; 70(6):431-432.

PMID: 38502902 PMC: 11160420. DOI: 10.1165/rcmb.2024-0070ED.


Association between glycemic variability and short-term mortality in patients with acute kidney injury: a retrospective cohort study of the MIMIC-IV database.

Guo Y, Qiu Y, Xue T, Zhou Y, Yan P, Liu S Sci Rep. 2024; 14(1):5945.

PMID: 38467770 PMC: 10928232. DOI: 10.1038/s41598-024-56564-7.


Prevalence and outcomes of chronic comorbid conditions in patients with sepsis in Korea: a nationwide cohort study from 2011 to 2016.

Kang C, Choi S, Jang E, Joo S, Jeong J, Oh S BMC Infect Dis. 2024; 24(1):184.

PMID: 38347513 PMC: 10860243. DOI: 10.1186/s12879-024-09081-x.


References
1.
Rusavy Z, Sramek V, Lacigova S, Novak I, Tesinsky P, Macdonald I . Influence of insulin on glucose metabolism and energy expenditure in septic patients. Crit Care. 2004; 8(4):R213-20. PMC: 522837. DOI: 10.1186/cc2868. View

2.
Chiasson J, Josse R, Gomis R, Hanefeld M, Karasik A, Laakso M . Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance: the STOP-NIDDM trial. JAMA. 2003; 290(4):486-94. DOI: 10.1001/jama.290.4.486. View

3.
Weiser M, Cabanillas M, Konopleva M, Thomas D, Pierce S, Escalante C . Relation between the duration of remission and hyperglycemia during induction chemotherapy for acute lymphocytic leukemia with a hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone/methotrexate-cytarabine regimen. Cancer. 2004; 100(6):1179-85. DOI: 10.1002/cncr.20071. View

4.
Angus D, Lidicker J, Clermont G, Carcillo J, Pinsky M . Epidemiology of severe sepsis in the United States: analysis of incidence, outcome, and associated costs of care. Crit Care Med. 2001; 29(7):1303-10. DOI: 10.1097/00003246-200107000-00002. View

5.
Pinto D, Skolnick A, Kirtane A, Murphy S, Barron H, Giugliano R . U-shaped relationship of blood glucose with adverse outcomes among patients with ST-segment elevation myocardial infarction. J Am Coll Cardiol. 2005; 46(1):178-80. DOI: 10.1016/j.jacc.2005.03.052. View