A randomized, blinded trial of the antioxidant pegorgotein: No reduction in neuropsychological deficits, inotropic drug support, or myocardial ischemia after coronary artery bypass surgery

被引:15
作者
Butterworth, J
Legault, C
Stump, DA
Coker, L
Hammon, JW
Troost, BT
Royster, RL
Prough, DS
机构
[1] Wake Forest Univ, Sch Med, Dept Anesthesiol, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Sch Med, Dept Cardiothorac Surg, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Sch Med, Dept Neurol, Winston Salem, NC 27157 USA
[4] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27157 USA
[5] Univ Texas, Med Branch, Dept Anesthesiol, Galveston, TX 77550 USA
关键词
coronary artery bypass grafting; outcomes; ischemia-reperfusion injury; superoxide dismutase;
D O I
10.1016/S1053-0770(99)90121-0
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Objective: To determine whether patients receiving pegorgotein preoperatively would be less likely than patients receiving placebo to demonstrate postoperative cerebral or myocardial dysfunction and thus would be less likely to (1) demonstrate a decline in neuropsychologic testing after cardiopulmonary bypass, (2) receive inotropic drug support, or (3) demonstrate electrocardiographic signs of ischemia or infarction. Design: Prospective, randomized, blinded clinical trial. Setting: University teaching hospital and clinics. Participants: Sixty-seven patients with normal left ventricular function undergoing elective, primary coronary artery bypass surgery. Interventions:Six to 18 hours before aortic crossclamping, patients received a single dose of placebo (n = 22); pegorgotein, 2,000 IU/kg intravenously (n = 23); or pegorgotein, 5,000 IU/kg intravenously (n = 22). Measurements and Main Results; Patients in the three groups were similar; the mean ages were 65, 66, and 67 years, and there were seven, eight, and seven women in the placebo; pegorgotein, 2,000 IU/kg; and pegorgotein, 5,000 IU/kg groups. Fifty-one of 67 patients demonstrated neuro-psychologic deficit 5 to 7 days postoperatively (n = 17, 19, and 15 for placebo, 2,000 IU/kg, and 5,000 IU/kg; p = NS). Median duration of cardiopulmonary bypass was longer in patients with two or more deficits at 4 to 6 weeks than in those with fewer than two deficits (121 v 98 minutes; p = 0.04). No patient demonstrated a perioperative stroke. Twenty-seven patients required inotropic drug support after cardiopulmonary bypass (n = 8, 11, and 8 for placebo, 2,000 IU/kg, and 5,000 IU/kg; p = NS). Inotropic drug support was associated with history of angina (p = 0.01) and increasing weight (p = 0.03). Nine patients demonstrated early postoperative ischemia or infarction (n = 1, 7, and 1 for placebo, 2,000 IU/kg, and 5.000 IU/kg; p = 0.07). Conclusions: This study showed no positive influence of pegorgotein on the incidence of any of the findings and showed a trend toward an increased incidence of myocardial ischemia or infarction. Copyright (C) 1999 by W.B. Saunders Company.
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收藏
页码:690 / 694
页数:5
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