Goland Sorel, Czer Lawrence S C, De Robertis Michele A, Mirocha James, Kass Robert M, Fontana Gregory P, Chang Wen, Trento Alfredo
Division of Cardiology, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA.
Ann Thorac Surg. 2007 Mar;83(3):931-7. doi: 10.1016/j.athoracsur.2006.10.047.
We aimed to determine the risk factors associated with mortality in patients with congenitally bicuspid aortic valve disease and dilation (<5 cm) of the ascending aorta after aortic valve replacement.
We reviewed 252 patients with bicuspid aortic valve undergoing aortic valve replacement at our institution from 1971 through 2000. Patients undergoing concomitant replacement of the ascending aorta were excluded.
The average patient age was 61 +/- 15 years; 66.3% were male, and 40.5% of patients had coronary artery disease. The ascending aorta was normal (<4.0 cm) in 60.3%, mildly dilated (4.0 to 4.4 cm) in 24.2%, and moderately dilated (4.5 to 4.9 cm) in 15.5% of patients. Patients with moderate aortic dilatation had significantly lower prevalence of coronary artery disease compared with patients with normal ascending aortas (20.5% and 45.4%; p = 0.006). Mean follow-up was 8.9 +/- 6.3 years. Long-term survival was significantly different across the three groups (p = 0.004). The 5-, 10-, and 15-year estimates were 78%, 59%, and 37%, respectively, in the normal aorta group; 88%, 77%, and 46%, respectively, in the mild aortic dilation group; and 92%, 83%, and 70%, respectively, in the moderate aortic dilation group. No significant difference in cardiac death was found among the groups (p = 0.08). The significant predictors of survival using the Cox regression model were coronary artery disease, age, decade of surgery, and ejection fraction. Aortic dilation was not significant after adjusting for these other variables. At follow-up, 18 patients required reoperation, 17 for aortic valve prosthesis failure and 1 for ascending aorta aneurysm.
The present study highlights the important adverse effect of concomitant coronary artery disease, advanced age, earlier decade of surgery, and reduced left ventricular ejection fraction on survival after aortic valve replacement for bicuspid aortic valve in patients with no or mild and moderate (<5 cm) dilation of the ascending aorta.
我们旨在确定先天性二叶式主动脉瓣疾病患者以及升主动脉直径扩张(<5 cm)的患者在主动脉瓣置换术后与死亡率相关的危险因素。
我们回顾了1971年至2000年在我院接受主动脉瓣置换术的252例二叶式主动脉瓣患者。排除同时进行升主动脉置换的患者。
患者平均年龄为61±15岁;66.3%为男性,40.5%的患者患有冠状动脉疾病。60.3%的患者升主动脉正常(<4.0 cm),24.2%的患者升主动脉轻度扩张(4.0至4.4 cm),15.5%的患者升主动脉中度扩张(4.5至4.9 cm)。与升主动脉正常的患者相比,主动脉中度扩张的患者冠状动脉疾病患病率显著较低(分别为20.5%和45.4%;p = 0.006)。平均随访时间为8.9±6.3年。三组患者的长期生存率有显著差异(p = 0.004)。正常主动脉组的5年、10年和15年生存率估计分别为78%、59%和37%;轻度主动脉扩张组分别为88%、77%和46%;中度主动脉扩张组分别为92%、83%和70%。各组之间的心源性死亡无显著差异(p = 0.08)。使用Cox回归模型得出的生存显著预测因素为冠状动脉疾病、年龄、手术年代和射血分数。在对这些其他变量进行校正后,主动脉扩张并不显著。随访时,18例患者需要再次手术,17例因主动脉瓣人工瓣膜功能障碍,1例因升主动脉瘤。
本研究强调了冠状动脉疾病、高龄、较早的手术年代以及左心室射血分数降低对升主动脉无扩张或轻度及中度(<5 cm)扩张的二叶式主动脉瓣患者主动脉瓣置换术后生存的重要不良影响。