Increased blood glucose variability during therapeutic hypothermia and outcome after cardiac arrest

被引:89
作者
Cueni-Villoz, Nadine [1 ]
Devigili, Alessandro [4 ]
Delodder, Frederik [1 ]
Cianferoni, Silvia [4 ]
Feihl, Francois [3 ]
Rossetti, Andrea O. [2 ]
Eggimann, Philippe [1 ]
Vincent, Jean-Louis [4 ]
Taccone, Fabio S. [4 ]
Oddo, Mauro [1 ]
机构
[1] Univ Lausanne Hosp, CHUV, Dept Intens Care Med, Lausanne, Switzerland
[2] Univ Lausanne Hosp, CHUV, Dept Clin Neurosci, Lausanne, Switzerland
[3] Univ Lausanne Hosp, CHUV, Div Clin Pathophysiol, Lausanne, Switzerland
[4] Univ Libre Bruxelles, Erasme Univ Hosp, Dept Intens Care, Brussels, Belgium
关键词
blood glucose; blood glucose variability; cardiac arrest; hypothermia; insulin; mortality; outcome; therapeutic hypothermia; CRITICALLY-ILL PATIENTS; INTENSIVE-CARE-UNIT; EMERGENCY CARDIOVASCULAR CARE; INDUCED INSULIN-SECRETION; CRITICAL ILLNESS; COMATOSE SURVIVORS; CARDIOPULMONARY BYPASS; GLYCEMIC VARIABILITY; ENHANCES APOPTOSIS; ENDOTHELIAL-CELLS;
D O I
10.1097/CCM.0b013e31822572c9
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Objective: Hypothermia impairs blood glucose homeostasis and insulin sensitivity. However, the impact of therapeutic hypothermia on blood glucose levels and insulin requirements is unknown. We analyzed blood glucose variability during therapeutic hypothermia in patients with coma after cardiac arrest and examined its impact on outcome. Design: Prospective observational study. Setting: Two university hospital medical/surgical intensive care units. Patients: Comatose cardiac arrest patients treated with therapeutic hypothermia (33 degrees C, 24 hrs). Interventions: Insulin therapy (blood glucose target 6-8 mmol/L [110-150 mg/dL]), according to a written algorithm, with nurse-driven adjustment of insulin dose. Measurements and Main Results: Two-hundred and twenty patients (median age 61 yrs, median time to return of spontaneous circulation 20 min) were studied. Two time periods, comparable in duration, were categorized: therapeutic hypothermia (stable maintenance phase) and normothermia (after rewarming). Blood glucose variability was defined as the difference between maximum and minimum blood glucose concentration during each time period. Mean blood glucose (8.3 +/- 2.3 vs. 7.1 +/- 1.3 mmol/L), blood glucose variability (5.7 +/- 3.9 vs. 3.7 +/- 3.6 mmol/L), and insulin dose (2 +/- 2 vs. 1 +/- 1 U/h) were higher during therapeutic hypothermia compared to normothermia (all p < .001). Higher mean blood glucose (7.9 +/- 1.8 mmol/L in survivors vs. 8.7 +/- 2.6 mmol/L in nonsurvivors, p = .02) and increased blood glucose variability (4.9 +/- 3.5 vs. 6.5 +/- 4.1 mmol/L, p = .003) during therapeutic hypothermia were associated with mortality. After adjusting for time to return of spontaneous circulation, initial arrest rhythm, and cardiac arrest etiology, increased blood glucose variability during therapeutic hypothermia, but not mean blood glucose level, was an independent predictor of inhospital mortality (odds ratio for death 1.10 [confidence interval 1.02-1.19], p = .016). Conclusions: Mild therapeutic hypothermia is associated with higher blood glucose levels, increased blood glucose variability, and greater insulin requirements compared to the postrewarming normothermic phase. Increased blood glucose variability during therapeutic hypothermia is a predictor of inhospital mortality after cardiac arrest, independent of injury severity and mean blood glucose levels. (Crit Care Med 2011; 39:2225-2231)
引用
收藏
页码:2225 / 2231
页数:7
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