Sokos George G, Bolukoglu Hakki, German Judy, Hentosz Teresa, Magovern George J, Maher Thomas D, Dean David A, Bailey Stephen H, Marrone Gary, Benckart Daniel H, Elahi Dariush, Shannon Richard P
Department of Medicine, Allegheny General Hospital, Pittsburgh, Pennsylvania, USA.
Am J Cardiol. 2007 Sep 1;100(5):824-9. doi: 10.1016/j.amjcard.2007.05.022. Epub 2007 Jun 14.
Increasing evidence suggests that tight glycemic control improves clinical outcomes after coronary artery bypass grafting (CABG). However, the risk for hypoglycemia with insulin often results in less aggressive glycemic control. Glucagon-like peptide-1 (GLP-1) is a naturally occurring peptide whose insulinotropic effects are predicated on the glucose concentration, minimizing the risk for hypoglycemia. This study was conducted to examine whether perioperative treatment with GLP-1 would affect glycemic control and improve hemodynamic recovery after CABG. Twenty patients with coronary heart disease and preserved left ventricular function who were scheduled to undergo CABG were randomized to receive standard therapy at the discretion of the surgeon or treatment with GLP-1 (1.5 pmol/kg/min) as a continuous infusion beginning 12 hours before CABG and continuing for 48 hours. Perioperative hemodynamics, the left ventricular ejection fraction, plasma glucose, and requirements for insulin drips and inotropic support were monitored. There were no differences between groups in the preoperative, postoperative, or 7-day left ventricular ejection fraction (GLP-1 61 +/- 4%, control 59 +/- 3%) or cardiac index at 18 hours (GLP-1 3.0 +/- 0.2 L/min/m(2), control 3.3 +/- 0.4 L/min/m(2)). However, the control group required greater use of inotropic and vasoactive infusions during the 48 hours after the operation to achieve the same hemodynamic result. There were also more frequent arrhythmias requiring antiarrhythmic agents in the control group. GLP-1 resulted in better glycemic control in the pre- and perioperative periods (GLP-1 95 +/- 3 mg/dl, control 140 +/- 10 mg/dl, p </=0.02), with 45% less insulin requirements to achieve the same glycemic control in the postoperative period (GLP-1 139 +/- 4 mg/dl, control 140 +/- 3 mg/dl). In conclusion, the perioperative use of GLP-1 achieves better glycemic control and comparable hemodynamic recovery without the requirements for high-dose insulin or inotropes.
越来越多的证据表明,严格的血糖控制可改善冠状动脉旁路移植术(CABG)后的临床结局。然而,胰岛素所致的低血糖风险常常导致血糖控制不够积极。胰高血糖素样肽-1(GLP-1)是一种天然存在的肽,其促胰岛素作用取决于葡萄糖浓度,可将低血糖风险降至最低。本研究旨在探讨围手术期应用GLP-1是否会影响血糖控制并改善CABG后的血流动力学恢复。20例计划接受CABG且左心室功能正常的冠心病患者被随机分组,一组由外科医生酌情给予标准治疗,另一组在CABG前12小时开始持续输注GLP-1(1.5 pmol/kg/min)并持续48小时。监测围手术期血流动力学、左心室射血分数、血糖以及胰岛素滴注和血管活性药物支持的需求。术前、术后或术后7天的左心室射血分数(GLP-1组61±4%,对照组59±3%)或术后18小时的心指数(GLP-1组3.0±0.2 L/min/m²,对照组3.3±0.4 L/min/m²)在两组间无差异。然而,对照组在术后48小时需要更多地使用血管活性药物输注以达到相同的血流动力学结果。对照组中需要抗心律失常药物治疗的心律失常也更频繁。GLP-1在术前和围手术期能更好地控制血糖(GLP-1组95±3 mg/dl,对照组140±10 mg/dl,p≤0.02),术后达到相同血糖控制所需的胰岛素量减少45%(GLP-1组139±4 mg/dl,对照组140±3 mg/dl)。总之,围手术期应用GLP-1可实现更好的血糖控制和相当的血流动力学恢复,且无需大剂量胰岛素或血管活性药物。