Mehta Rajendra H, Hafley Gail E, Gibson C Michael, Harrington Robert A, Peterson Eric D, Mack Michael J, Kouchoukos Nicholas T, Califf Robert M, Ferguson T Bruce, Alexander John H
Duke Clinical Research Institute and Duke University Medical Center, Durham, NC 27715, USA.
J Thorac Cardiovasc Surg. 2008 Nov;136(5):1149-55. doi: 10.1016/j.jtcvs.2008.02.085. Epub 2008 Aug 27.
Limited information exists on the impact of preoperative renal dysfunction on internal thoracic artery and saphenous vein graft failure and 2-year clinical outcomes in patients undergoing coronary artery bypass surgery.
We studied the impact of preoperative renal dysfunction (creatinine clearance < 60 mL/min) on 1-year internal thoracic artery and saphenous vein graft failure (defined as > or = 75% angiographic stenosis) and 2-year clinical events (death; death or myocardial infarction; and death, myocardial infarction, or revascularization) in 3014 patients undergoing coronary artery bypass surgery enrolled in the Project of Ex-vivo Vein Graft Engineering via Transfection-IV study.
Of 2973 patients (98.6%) with preoperative measurement of renal function, 440 (14.8%) had renal dysfunction. Most baseline comorbidities were higher in these patients. Two-year clinical events were higher in patients with preoperative renal dysfunction (adjusted death, myocardial infarction, or revascularization, hazard ratio 1.21, 95% confidence interval 0.97-1.50; adjusted death or myocardial infarction, hazard ratio 1.35, 95% confidence interval 1.05-1.74; adjusted death, hazard ratio 1.47, 95% confidence interval 0.98-2.21). However, saphenous vein graft (odds ratio 1.02, 95% confidence interval 0.79-1.33) and internal thoracic artery (odds ratio 0.76, 95% confidence interval 0.40-1.44) failure were similar in the 2 groups.
Although the risk of adverse clinical events is higher in patients with preoperative renal dysfunction, that of internal thoracic artery and saphenous vein graft failure is not. This suggests that factors other than graft failure account for the worse clinical outcomes in this high-risk cohort. Further studies are needed to identify other mechanisms of these worse outcomes so that appropriate measures can be developed to improve long-term outcomes in patients with renal dysfunction undergoing coronary artery bypass surgery.
关于术前肾功能不全对冠状动脉搭桥手术患者胸廓内动脉和大隐静脉移植血管失败及2年临床结局的影响,目前相关信息有限。
我们在“通过转染进行体外静脉移植血管工程 - IV研究项目”中,研究了术前肾功能不全(肌酐清除率<60 mL/分钟)对3014例接受冠状动脉搭桥手术患者1年胸廓内动脉和大隐静脉移植血管失败(定义为血管造影狭窄≥75%)及2年临床事件(死亡;死亡或心肌梗死;死亡、心肌梗死或血运重建)的影响。
在2973例(98.6%)术前进行肾功能测定的患者中,440例(14.8%)存在肾功能不全。这些患者的大多数基线合并症情况更为严重。术前肾功能不全患者的2年临床事件发生率更高(校正后死亡、心肌梗死或血运重建,风险比1.21,95%置信区间0.97 - 1.50;校正后死亡或心肌梗死,风险比1.35,95%置信区间1.05 - 1.74;校正后死亡,风险比1.47,95%置信区间0.98 - 2.21)。然而,两组的大隐静脉移植血管(比值比1.02,95%置信区间0.79 - 1.33)和胸廓内动脉(比值比0.76,95%置信区间0.40 - 1.44)失败情况相似。
虽然术前肾功能不全患者发生不良临床事件的风险更高,但胸廓内动脉和大隐静脉移植血管失败的风险并非如此。这表明,除移植血管失败外的其他因素导致了这一高危队列中更差的临床结局。需要进一步研究以确定这些更差结局的其他机制,从而制定适当措施来改善接受冠状动脉搭桥手术的肾功能不全患者的长期结局。