Glucocorticoid effects on the inflammatory and clinical responses to cardiac surgery

被引:82
作者
Fillinger, MP
Rassias, AJ
Guyre, PM
Sanders, JH
Beach, M
Pahl, J
Watson, RB
Whalen, PK
Yeo, KTJ
Yeager, MP
机构
[1] Dartmouth Hitchcock Med Ctr, Dept Anesthesiol, Lebanon, NH 03756 USA
[2] Dartmouth Hitchcock Med Ctr, Dept Surg, Lebanon, NH 03756 USA
[3] Dartmouth Hitchcock Med Ctr, Dept Physiol, Lebanon, NH 03756 USA
[4] Dartmouth Hitchcock Med Ctr, Dept Pathol, Lebanon, NH 03756 USA
[5] Dartmouth Coll Sch Med, Hanover, NH USA
关键词
steroid; glucocorticoid; methylprednisolone; cardiac surgery; inflammation; cytokine; interleukin-6; interleukin-10; etomidate;
D O I
10.1053/jcan.2002.31057
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Objective: To measure the effects of glucocorticoids on the systemic inflammatory response and clinical recovery after cardiac surgery. Design: Randomized, prospective, double-blind, placebocontrolled clinical trial with concurrent comparison groups. Setting: University medical center. Participants: Patients scheduled for elective coronary artery bypass graft surgery using normothermic cardiopulmonary bypass (CPB) and a standardized anesthetic. Interventions: Participants randomly received either methylprednisolone, 15 mg/kg intravenously 1 hour before surgery and 0.3 mg/kg intravenously every 6 hours x 4 doses, or placebo. Comparison groups included cardiac surgical patients who received etomidate to lower endogenous cortisol during surgery and healthy volunteers who received methylprednisolone only. Measurements and Main Results: Patients who received methylprednisolone had a significant reduction in circulating interleukin (IL)-6 at 60 minutes after CPB (p < 0.05) and on the morning of the 1st (p < 0.01) and 3rd (p < 0.05) postoperative days and a significant increase in circulating IL-10 at 60 minutes after CPB (p < 0.01) compared with the placebo group. Etomidate, given to lower cortisol during surgery, was associated with significantly decreased IL-6 and IL-10 responses to surgery compared with the placebo group, whereas methylprednisolone alone, given to healthy nonsurgical volunteers, had no effect on these cytokines. After adjusting for age, there were no significant differences in postoperative length of hospital stay between the methylprednisolone-treated (4.6 days) and placebo (6.1 days) groups or in the duration of mechanical ventilation (9.9 hours and 15.6 hours). No patient treated with methylprednisolone had nausea and vomiting on the 1st postoperative day compared with 33% of placebo-treated patients (p = 0.02). Glucose was significantly higher after methylprednisolone treatment at 1 hour after CPB (276 mg/dL v 210 mg/dL; p = 0.001) and at 2 hours (289 mg/dL v 213 mg/dL; p = 0.009) and 8 hours (247 mg/dL v 196 mg/dL; p = 0.02) after surgery. There were no differences in pain scores and no significant intergroup differences in lung peak expiratory flow rate or alveolar-arterial oxygen gradients after surgery. Conclusion: This study shows significant effects of gluc icoids on the production of IL-6 and IL-10 in response to cardiac surgery but only minor effects on clinical recovery. Copyright 2002, Elsevier Science (USA). All rights reserved.
引用
收藏
页码:163 / 169
页数:7
相关论文
共 33 条
[1]
Boyle EM, 1997, ANN THORAC SURG, V63, P277
[2]
Calvano SE, 1996, ARCH SURG-CHICAGO, V131, P434
[3]
Pulmonary effects of methylprednisolone in patients undergoing coronary artery bypass grafting and early tracheal extubation [J].
Chaney, MA ;
Nikolov, MP .
ANESTHESIA AND ANALGESIA, 1998, 87 (01) :27-33
[4]
EFFECT OF ANESTHESIA ON THE CYTOKINE RESPONSES TO ABDOMINAL-SURGERY [J].
CROZIER, TA ;
MULLER, JE ;
QUITTKAT, D ;
SYDOW, M ;
WUTTKE, W ;
KETTLER, D .
BRITISH JOURNAL OF ANAESTHESIA, 1994, 72 (03) :280-285
[5]
Increase in plasma interleukin-10 following hydrocortisone injection [J].
Dandona, P ;
Aljada, A ;
Garg, R ;
Mohanty, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (03) :1141-1144
[6]
DIETZMAN RH, 1975, J THORAC CARDIOV SUR, V69, P870
[7]
INFLUENCE OF STEROIDS ON COMPLEMENT AND CYTOKINE GENERATION AFTER CARDIOPULMONARY BYPASS [J].
ENGELMAN, RM ;
ROUSOU, JA ;
FLACK, JE ;
DEATON, DW ;
KALFIN, R ;
DAS, D .
ANNALS OF THORACIC SURGERY, 1995, 60 (03) :801-804
[8]
The systemic inflammatory response to cardiopulmonary bypass: Pathophysiological, therapeutic, and pharmacological considerations [J].
Hall, RI ;
Smith, MS ;
Rocker, G .
ANESTHESIA AND ANALGESIA, 1997, 85 (04) :766-782
[9]
CYTOKINE INDUCTION DURING CARDIAC-SURGERY - ANALYSIS OF TNF-ALPHA EXPRESSION PRECARDIOPULMONARY AND POSTCARDIOPULMONARY BYPASS [J].
HATTLER, BG ;
ZEEVI, A ;
ODDIS, CV ;
FINKEL, MS .
JOURNAL OF CARDIAC SURGERY, 1995, 10 (04) :418-422
[10]
APROTININ AND METHYLPREDNISOLONE EQUALLY BLUNT CARDIOPULMONARY BYPASS-INDUCED INFLAMMATION IN HUMANS [J].
HILL, GE ;
ALONSO, A ;
SPURZEM, JR ;
STAMMERS, AH ;
ROBBINS, RA .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1995, 110 (06) :1658-1662