The impact of early hypoglycemia and blood glucose variability on outcome in critical illness

被引:181
作者
Bagshaw, Sean M. [1 ,2 ]
Bellomo, Rinaldo [1 ,3 ]
Jacka, Michael J. [2 ,4 ]
Egi, Moritoki [5 ]
Hart, Graeme K. [1 ,3 ]
George, Carol [6 ]
机构
[1] Monash Univ, Alfred Hosp, Dept Epidemiol & Prevent Med, Melbourne, Vic 3004, Australia
[2] Univ Alberta, Univ Alberta Hosp, Div Crit Care Med, Edmonton, AB T6G 2B7, Canada
[3] Univ Melbourne, Fac Med, Melbourne, Vic 3010, Australia
[4] Univ Alberta, Univ Alberta Hosp, Dept Anesthesiol & Pain Med, Edmonton, AB T6G 2B7, Canada
[5] Okayama Univ Hosp, Dept Anesthesiol & Resuscitol, Okayama 7008558, Japan
[6] ANZICS, Carlton, Vic 3053, Australia
关键词
INTENSIVE INSULIN THERAPY; ILL PATIENTS; NEW-ZEALAND; MORTALITY; CARE; HYPERGLYCEMIA; SEPSIS; RESUSCITATION; DEPENDENCY; GUIDELINES;
D O I
10.1186/cc7921
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction In critical illness, the association of hypoglycemia, blood glucose (BG) variability and outcome are not well understood. We describe the incidence, clinical factors and outcomes associated with an early hypoglycemia and BG variability in critically ill patients. Methods Retrospective interrogation of prospectively collected data from the Australia New Zealand Intensive Care Society Adult Patient Database on 66184 adult admissions to 24 intensive care units (ICUs) from 1 January 2000 to 31 December 2005. Primary exposure was hypoglycemia (BG < 4.5 mmol/L) and BG variability (BG < 4.5 and = 12.0 mmol/L) within 24 hours of admission. Primary outcome was all-cause mortality. Results The cumulative incidence of hypoglycemia and BG variability were 13.8% (95% confidence interval (CI) = 13.5 to 14.0; n = 9122) and 2.9% (95% CI = 2.8 to 3.0, n = 1913), respectively. Several clinical factors were associated with both hypoglycemia and BG variability including: co-morbid disease (P < 0.001), non-elective admissions (P < 0.001), higher illness severity (P < 0.001), and primary septic diagnosis (P < 0.001). Hypoglycemia was associated with greater odds of adjusted ICU (odds ratio (OR) = 1.41, 95% CI = 1.31 to 1.54) and hospital death (OR = 1.36, 95% CI = 1.27 to 1.46). Hypoglycemia severity was associated with 'dose-response' increases in mortality. BG variability was associated with greater odds of adjusted ICU (1.5, 95% CI = 1.4 to 1.6) and hospital (1.4, 95% CI = 1.3 to 1.5) mortality, when compared with either hypoglycemia only or neither. Conclusions In critically ill patients, both early hypoglycemia and early variability in BG are relatively common, and independently portend an increased risk for mortality.
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共 45 条
[1]   Glucose variability and mortality in patients with sepsis [J].
Ali, Naeem A. ;
O'Brien, James M., Jr. ;
Dungan, Kathleen ;
Phillips, Gary ;
Marsh, Clay B. ;
Lemeshow, Stanley ;
Connors, Alfred F., Jr. ;
Preiser, Jean-Charles .
CRITICAL CARE MEDICINE, 2008, 36 (08) :2316-2321
[2]   The roles of insulin and hyperglycemia in sepsis pathogenesis [J].
Andersen, SK ;
Gjedsted, J ;
Christiansen, C ;
Tonnesen, E .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 75 (03) :413-421
[3]   Intensive insulin therapy in critical illness - When is the evidence enough? [J].
Angus, DC ;
Abraham, E .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 172 (11) :1358-1359
[4]   Acute renal failure - definition, outcome measures, animal models, fluid therapy and information technology needs: the Second International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group [J].
Bellomo, R ;
Ronco, C ;
Kellum, JA ;
Mehta, RL ;
Palevsky, P .
CRITICAL CARE, 2004, 8 (04) :R204-R212
[5]   Intensive insulin therapy after severe traumatic brain injury: A randomized clinical trial [J].
Bilotta, Federico ;
Caramia, Remo ;
Cernak, Ibolja ;
Paoloni, Francesca Paola ;
Doronzio, Andrea ;
Cuzzone, Vincenzo ;
Santoro, Antonio ;
Rosa, Giovanni .
NEUROCRITICAL CARE, 2008, 9 (02) :159-166
[6]  
Bilotta Federico, 2007, J Neurosurg Anesthesiol, V19, P156, DOI 10.1097/ANA.0b013e3180338e69
[7]   Intensive insulin therapy and pentastarch resuscitation in severe sepsis [J].
Brunkhorst, Frank M. ;
Engel, Christoph ;
Bloos, Frank ;
Meier-Hellmann, Andreas ;
Ragaller, Max ;
Weiler, Norbert ;
Moerer, Onnen ;
Gruendling, Matthias ;
Oppert, Michael ;
Grond, Stefan ;
Olthoff, Derk ;
Jaschinski, Ulrich ;
John, Stefan ;
Rossaint, Rolf ;
Welte, Tobias ;
Schaefer, Martin ;
Kern, Peter ;
Kuhnt, Evelyn ;
Kiehntopf, Michael ;
Hartog, Christiane ;
Natanson, Charles ;
Loeffler, Markus ;
Reinhart, Konrad .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (02) :125-139
[8]   Surviving Sepsis Campaign guidelines for management of severe sepsis and septic shock [J].
Dellinger, RP ;
Carlet, JM ;
Masur, H ;
Gerlach, H ;
Calandra, T ;
Cohen, J ;
Gea-Banacloche, J ;
Keh, D ;
Marshall, JC ;
Parker, MM ;
Ramsay, G ;
Zimmerman, JL ;
Vincent, JL ;
Levy, MM .
CRITICAL CARE MEDICINE, 2004, 32 (03) :858-873
[9]   Current controversies around tight glucose control in critically ill patients [J].
Devos, Philippe ;
Preiser, Jean-Charles .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2007, 10 (02) :206-209
[10]  
Dossett LA, 2008, AM SURGEON, V74, P679