Intravenous glucose intake independently related to intensive care unit and hospital mortality: an argument for glucose toxicity in critically ill patients

被引:47
作者
van der Voort, PHJ
Feenstra, RA
Bakker, AJ
de Heide, L
Boerma, EC
van der Horst, ICC
机构
[1] Med Ctr Leeuwarden, Dept Intens Care, NL-8901 BR Leeuwarden, Netherlands
[2] Med Ctr Leeuwarden, Dept Clin Chem, NL-8901 BR Leeuwarden, Netherlands
[3] Med Ctr Leeuwarden, Dept Internal Med, NL-8901 BR Leeuwarden, Netherlands
[4] Univ Groningen, Med Ctr, Dept Cardiol, NL-9700 AB Groningen, Netherlands
关键词
D O I
10.1111/j.1365-2265.2006.02437.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective It is assumed that the toxic effects of glucose play a role in the outcome of critically ill patients. We studied the impact of the amount of infused glucose as a determinant of mortality. Design A retrospective cohort study design was used as blood glucose levels in critically ill patients are nowadays tightly controlled. Patiens Long-stay critically ill patients (7-30 days). Measurements The association between the mean amount of glucose infusion and both intensive care unit (ICU) and hospital mortality was determined. We corrected for the mean glucose serum concentration, the mean dosage of insulin and for severity of illness, using the acute physiology and chronic health evaluation (APACHE II) score. Results Of the 2042 admitted patients, 273 met the inclusion criteria. The mean length of stay was 14.4 days [interquartile range (IQR) 9-18]. Hospital mortality was significantly lower for patients with a mean glucose level below 8 mmol/l (30/79; 38%) compared to patients with a level above 8 mmol/l (104/194; 54%, P = 0.023). Logistic stepwise multivariate regression analysis for both ICU and hospital mortality as dependent variables showed that APACHE II score and the mean daily amount of infused glucose were associated with mortality. Conclusions In long-stay ICU patients without blood glucose level control, the ICU and hospital mortality was independently related to the mean amount of infused glucose. In addition, mortality in patients with a mean glucose level above 8.0 mmol/l was higher. Both these determinants of mortality can exert their effects by insulin-independent uptake of glucose with subsequent toxic intracellular effects.
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页码:141 / 145
页数:5
相关论文
共 17 条
[1]   Increased glycolytic substrate protection improves ischemic cardiac dysfunction and reduces injury [J].
Apstein, CS .
AMERICAN HEART JOURNAL, 2000, 139 (02) :S107-S114
[2]   SHORT-TERM HYPERGLYCEMIA DEPRESSES IMMUNITY THROUGH NONENZYMATIC GLYCOSYLATION OF CIRCULATING IMMUNOGLOBULIN [J].
BLACK, CT ;
HENNESSEY, PJ ;
ANDRASSY, RJ .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1990, 30 (07) :830-833
[3]   Inflammatory cytokine concentrations are acutely increased by hyperglycemia in humans - Role of oxidative stress [J].
Esposito, K ;
Nappo, F ;
Marfella, R ;
Giugliano, G ;
Giugliano, F ;
Ciotola, M ;
Quagliaro, L ;
Ceriello, A ;
Giugliano, D .
CIRCULATION, 2002, 106 (16) :2067-2072
[4]   Glucose control and mortality in critically ill patients [J].
Finney, SJ ;
Zekveld, C ;
Elia, A ;
Evans, TW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (15) :2041-2047
[5]  
Khaodhiar L, 1999, Curr Opin Clin Nutr Metab Care, V2, P79, DOI 10.1097/00075197-199901000-00013
[6]   Association between hyperglycemia and increased hospital mortality in a heterogeneous population of critically ill patients [J].
Krinsley, JS .
MAYO CLINIC PROCEEDINGS, 2003, 78 (12) :1471-1478
[7]   Stress-induced hyperglycemia [J].
McCowen, KC ;
Malhotra, A ;
Bistrian, BR .
CRITICAL CARE CLINICS, 2001, 17 (01) :107-+
[8]   Contribution of circulating lipids to the improved outcome of critical illness by glycemic control with intensive insulin therapy [J].
Mesotten, D ;
Swinnen, JV ;
Vanderhoydonc, F ;
Wouters, PJ ;
Van den Berghe, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (01) :219-226
[9]   Alterations in fuel metabolism in critical illness: hyperglycaemia [J].
Mizock, BA .
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 15 (04) :533-551
[10]   Maximal parenteral glucose oxidation in hypermetabolic young children: A stable isotope study [J].
Sheridan, RL ;
Yu, YM ;
Prelack, K ;
Young, VR ;
Burke, JF ;
Tompkins, RG .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1998, 22 (04) :212-216