Perioperative glucose infusion and the catabolic response to surgery: The effect of epidural block

被引:51
作者
Lattermann, R
Carli, F
Wykes, L
Schricker, T
机构
[1] McGill Univ, Sch Dietet & Human Nutr, Montreal, PQ, Canada
[2] McGill Univ, Dept Anesthesia, Montreal, PQ, Canada
关键词
D O I
10.1097/00000539-200302000-00047
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Although the nitrogen-sparing properties of epidural block and IV glucose on the days after surgical trauma have been well established, their metabolic effects during the acute phase of the stress response remain unclear. Therefore, in this study we investigated the effect of epidural block on glucose and protein kinetics during and immediately after surgery in patients receiving IV glucose at 2 mg . kg(1)(-) . min(-1). Sixteen patients undergoing colorectal surgery received either general anesthesia with epidural block with bupivacaine (EDA; n = 8) or general anesthesia alone (control; n = 8). Glucose and protein kinetics were determined during and 2 h after the operation by stable isotope tracers [6,62 H-2(2)]glucose and L-[1-C-13]leucine. Plasma concentrations of glucose, insulin, cortisol, and glucagon were also determined. Epidural block attenuated the perioperative increase in plasma glucose concentration (P < 0.05). The rate of appearance of glucose (R-a glucose) and endogenous glucose production (EGP) were slower in the EDA group than in control subjects during (R-a glucose, EDA 13.2 +/- 1.0 versus control 15.3 +/- 1.8 mu mol . kg(-1) . min(-1); P < 0.05; EGP, EDA 1.2 +/- 1.2 versus control 3.8 +/- 1.7 mumol . kg(-1) . min(-1); P < 0.05) and after the operation (P > 0.05). Whereas protein breakdown and amino acid oxidation decreased in both groups (P < 0.05), whole-body protein synthesis remained unchanged. Insulin levels increased with both anesthetic techniques (P < 0.05). Intraoperative plasma concentrations of cortisol and glucagon were smaller in the EDA group (P < 0.05). The intraoperative suppression of EGP by exogenous glucose was more pronounced in the presence of epidural block. However, epidural block failed to exert a protein-sparing effect during the acute phase of the stress response in patients receiving IV glucose.
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收藏
页码:555 / 562
页数:8
相关论文
共 25 条
[1]
NUTRITION FOR THE PATIENT WITH RESPIRATORY-FAILURE - GLUCOSE VS FAT [J].
ASKANAZI, J ;
NORDENSTROM, J ;
ROSENBAUM, SH ;
ELWYN, DH ;
HYMAN, AI ;
CARPENTIER, YA ;
KINNEY, JM .
ANESTHESIOLOGY, 1981, 54 (05) :373-377
[2]
EFFECT OF GENERAL-ANESTHESIA ON WHOLE-BODY PROTEIN-TURNOVER IN PATIENTS UNDERGOING ELECTIVE SURGERY [J].
CARLI, F ;
RAMACHANDRA, V ;
GANDY, J ;
MERRITT, H ;
FORD, GC ;
READ, M ;
HALLIDAY, D .
BRITISH JOURNAL OF ANAESTHESIA, 1990, 65 (03) :373-379
[3]
A nitrogen-free hypocaloric diet and recombinant human growth hormone stimulate postoperative protein synthesis: Fasted and fed leucine kinetics in the surgical patient [J].
Carli, F ;
Webster, JD ;
Halliday, D .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (07) :796-800
[4]
Quantifying gluconeogenesis during fasting [J].
Chandramouli, V ;
Ekberg, K ;
Schumann, WC ;
Kalhan, SC ;
Wahren, J ;
Landau, BR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (06) :E1209-E1215
[5]
SIGNIFICANCE OF ALTERED GLUCONEOGENESIS IN SURGICAL CATABOLISM [J].
GUMP, FE ;
LONG, CL ;
GEIGER, JW ;
KINNEY, JM .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1975, 15 (08) :704-713
[6]
Kehlet H, 1998, NEURAL BLOCKADE CLIN, P129
[7]
Immunologic effects of acute hyperglycemia in nondiabetic rats [J].
Kwoun, MO ;
Ling, PR ;
Lydon, E ;
Imrich, A ;
Qu, ZS ;
Palombo, J ;
Bistrian, BR .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1997, 21 (02) :91-95
[8]
Epidural blockade modifies perioperative glucose production without affecting protein catabolism [J].
Lattermann, R ;
Carli, F ;
Wykes, L ;
Schricker, T .
ANESTHESIOLOGY, 2002, 97 (02) :374-381
[9]
Lattermann R, 2001, ANESTH ANALG, V93, P121
[10]
THE EXCHANGE OF BLOOD-BORNE AMINO-ACIDS IN THE LEG DURING ABDOMINAL SURGICAL TRAUMA - EFFECTS OF GLUCOSE-INFUSION [J].
LUND, J ;
STJERNSTROM, H ;
BERGHOLM, U ;
JORFELDT, L ;
VINNARS, E ;
WIKLUND, L .
CLINICAL SCIENCE, 1986, 71 (05) :487-496