Davies Ryan R, Kaple Ryan K, Mandapati Divakar, Gallo Amy, Botta Donald M, Elefteriades John A, Coady Michael A
Section of Cardiothoracic Surgery, Yale University School of Medicine, New Haven, Connecticut, USA.
Ann Thorac Surg. 2007 Apr;83(4):1338-44. doi: 10.1016/j.athoracsur.2006.10.074.
Patients with bicuspid aortic valve (BAV) are at risk for valvular disease and ascending aortic aneurysms and dissections. Although others have investigated the need for concomitant repair, the natural history of aortic disease has not been addressed.
A review of our institutional clinical database identified 514 patients (326 male, 188 female) with unrepaired ascending aortic aneurysms followed from 1985 to 2005. Seventy patients (13.4%) diagnosed with BAV form group A; the remaining 445 patients form group B. Growth rates and risk factors for complications were assessed.
Patients in group A had a lower incidence of hypertension (p = 0.0185), carotid artery disease, and stroke (p = 0.0184), and presented at an earlier age (49.0 versus 64.2 years, p < 0.0001). Group A also had a higher rate of aortic growth (0.19 versus 0.13 cm/year, p = 0.0102). The incidence of rupture and dissection were similar. Overall survival was better among patients with BAV (p < 0.0001). Among patients with BAV, those with aortic stenosis had a higher risk of rupture, dissection, or death before operative repair than did those with normally functioning valves (odds ratio 10.475, 95% confidence interval: 1.153 to 95.155).
Aortic stenosis presents a significant added risk for patients with aneurysmal disease in the face of BAV. Despite faster rates of growth, however, patients with BAV have similar rates of aortic rupture, dissection, and death and improved long-term survival. Contributing to this finding may be the lower incidence of comorbidities, the younger age at presentation, and the more attentive follow-up with earlier operative repair.
二叶式主动脉瓣(BAV)患者有发生瓣膜疾病以及升主动脉瘤和夹层的风险。尽管其他人已经研究了同期修复的必要性,但主动脉疾病的自然病史尚未得到探讨。
对我们机构的临床数据库进行回顾,确定了1985年至2005年期间随访的514例未修复的升主动脉瘤患者(男性326例,女性188例)。70例(13.4%)被诊断为BAV的患者组成A组;其余445例患者组成B组。评估了生长率和并发症的危险因素。
A组患者高血压(p = 0.0185)、颈动脉疾病和中风的发生率较低(p = 0.0184),且发病年龄较早(49.0岁对64.2岁,p < 0.0001)。A组主动脉生长率也更高(0.19对0.13 cm/年,p = 0.0102)。破裂和夹层的发生率相似。BAV患者的总体生存率更好(p < 0.0001)。在BAV患者中,与瓣膜功能正常的患者相比,主动脉狭窄患者在手术修复前发生破裂、夹层或死亡的风险更高(优势比10.475,95%置信区间:1.153至95.155)。
面对BAV,主动脉狭窄给动脉瘤疾病患者带来了显著的额外风险。然而,尽管BAV患者的生长速度更快,但主动脉破裂、夹层和死亡的发生率相似,且长期生存率有所提高。这一发现可能归因于合并症发生率较低、发病年龄较轻以及因早期手术修复而进行的更密切随访。