Cork R C, Kramer T H, Dreischmeier B, Behr S, DiNardo J A
Department of Anesthesiology, Louisiana State University Medical Center, New Orleans 70112.
Anesth Analg. 1995 Jan;80(1):28-40. doi: 10.1097/00000539-199501000-00006.
beta-Adrenergic antagonism decreases the size of myocardial infarction and provides myocardial protection during hypothermic arrest for cardiac surgery. However, concern regarding the negative inotropic and chronotropic effects of beta-adrenergic antagonism persisting after cardiopulmonary bypass (CPB) has impeded the use of esmolol for this purpose during cardiac surgery. This is a randomized, double-blind prospective study of the effects of esmolol infused during CPB and the effects of hypothermic CPB on esmolol. Patients scheduled for CPB were randomized to receive intravenous esmolol (300.micrograms.kg-1.min-1 during CPB after a bolus of 2 mg/kg prior to CPB) or placebo. Infusion was stopped at 10 min after release of aortic cross-clamp. Hemodynamics were measured, as well as serum esmolol, catecholamines, lactate, and potassium. Postoperative variables measured included electrocardiographic changes, creatine kinase (CK)-MB fractions, post-CPB dysrhythmias and drugs, hospitalization time and cost, and mortality. Esmolol was administered to 16 patients and placebo to 14. Esmolol levels reached a high of 10.5 +/- 0.9 micrograms/mL during CPB, but decreased to 0.1 +/- 0.02 microgram/mL within 30 min after stopping infusion. Cardiac indices (cardiac index, stroke volume index, left cardiac work index, left ventricular stroke work index, right cardiac work index, and right ventricular stroke work index) were higher in the esmolol group for the first hour post-CPB (P < 0.05). Systemic arterial lactate and coronary sinus lactate were lower in the esmolol group after CPB (P < 0.05), but myocardial lactate extraction was not significantly different between groups. After CPB, hemoglobin was lower in the esmolol group (P < 0.05) due to longer CPB and aortic cross-clamp time (P < 0.05), but oxygen consumption was less than in the control group (P < 0.05). Post-CPB serum potassium was higher in the esmolol group (P < 0.05). Results are confounded by more chronically beta-adrenergically blocked patients randomized to the esmolol group (P < 0.05). Esmolol infused during CPB in this series of patients was associated with high concentrations during CPB but did not result in any adverse clinical effects after CPB.
β-肾上腺素能拮抗作用可减小心肌梗死面积,并在心脏手术低温停搏期间提供心肌保护。然而,对心肺转流(CPB)后β-肾上腺素能拮抗作用持续存在的负性肌力和负性变时作用的担忧阻碍了艾司洛尔在此类心脏手术中的应用。这是一项关于CPB期间输注艾司洛尔的效果以及低温CPB对艾司洛尔影响的随机、双盲前瞻性研究。计划进行CPB的患者被随机分为接受静脉注射艾司洛尔(CPB前先给予2mg/kg推注,然后在CPB期间以300μg·kg-1·min-1输注)或安慰剂组。在主动脉阻断钳松开后10分钟停止输注。测量血流动力学指标以及血清艾司洛尔、儿茶酚胺、乳酸和钾离子水平。测量的术后变量包括心电图变化、肌酸激酶(CK)-MB同工酶、CPB后心律失常及用药情况、住院时间和费用以及死亡率。16例患者给予艾司洛尔,14例给予安慰剂。CPB期间艾司洛尔水平最高达到10.5±0.9μg/mL,但在停止输注后30分钟内降至0.1±0.02μg/mL。CPB后第一小时,艾司洛尔组的心脏指数(心脏指数、每搏量指数、左心作功指数、左心室每搏作功指数、右心作功指数和右心室每搏作功指数)较高(P<0.05)。CPB后,艾司洛尔组的全身动脉血乳酸和冠状窦乳酸较低(P<0.05),但两组间心肌乳酸摄取无显著差异。CPB后,由于CPB和主动脉阻断时间较长(P<0.05),艾司洛尔组的血红蛋白较低(P<0.05),但氧耗低于对照组(P<0.05)。CPB后,艾司洛尔组的血清钾离子较高(P<0.05)。随机分配到艾司洛尔组的患者中,有更多长期接受β-肾上腺素能阻滞剂治疗的患者,这使结果受到混淆(P<0.05)。在这一系列患者中,CPB期间输注的艾司洛尔在CPB期间浓度较高,但CPB后未导致任何不良临床影响。