Lima Brian, Williams Judson B, Bhattacharya S Dave, Shah Asad A, Andersen Nicholas, Wang Andrew, Harrison J Kevin, Hughes G Chad
Division of Thoracic and Cardiovascular Surgery, Department of Surgery, Duke University Medical Center, Durham, NC, USA.
J Heart Valve Dis. 2011 Jul;20(4):387-95.
Bicuspid aortic valve (BAV) disease is associated with an aortopathy resulting in aneurysmal dilatation spanning the root, ascending, and arch segments. To date, no large series of proximal aortic replacement in this population has been reported. The study aim was to report contemporary surgical outcomes for proximal aortic replacement in BAV disease, and to examine the relationships between valve morphology, valve pathophysiology, and pathology of the thoracic aorta.
Between September 2005 and December 2009, a total of 100 consecutive patients (mean age 54 +/- 13 years; range: 29-80 years) with BAV and proximal aortic enlargement underwent aortic replacement at a single referral institution. Of these patients, 16% had undergone prior aortic valve replacement (AVR). The aortic repair was individually tailored to treat the aortic valve and thoracic aortic pathology, and included supracoronary ascending aortic (AA) replacement (n = 17), AVR with separate supracoronary AA replacement (n = 39), aortic root replacement (n = 42), and valve-sparing root replacement (n = 2). Concomitant arch replacement was performed in 82 patients (80 hemi-arch, two full arch). Other concomitant cardiac procedures were performed in 28 patients.
The 30-day/in-hospital rates of death and stroke were both 1%. The predominant aortic valve pathophysiology was aortic stenosis (AS; 33%), aortic insufficiency (AI; 29%), mixed AS/AI (17%), normally functioning BAV (17%), and unknown (4%). Valve morphology included Sievers Type I, R/L (75%), Type I, R/N (9%), Type I, L/N (2%), Type 0 (7%), and Type II (7%). BAV patients with predominantly AI had more frequent root dilatation (62%) than those with either AS (30%) or normal valve function (35%). Based on BAV morphology, there were no significant differences in maximal thoracic aortic diameters between groups. At a mean follow up of 16 months, there were no late deaths or valve-related complications.
Proximal aortic replacement in patients with BAV can be performed with low rates of mortality and morbidity. The pathologic anatomy of the thoracic aorta was not predicted by the aortic valve morphology, although dilation of the aortic root was most common in BAV patients with a predominant AI pathophysiology. These findings convey the safety and feasibility of treating concomitant aortopathy, including arch replacement as needed, and may help tailor the specific operation needed to the patient's pathology.
二叶式主动脉瓣(BAV)疾病与一种主动脉病变相关,可导致主动脉根部、升主动脉和主动脉弓节段的动脉瘤样扩张。迄今为止,尚未有关于该人群近端主动脉置换的大型系列报道。本研究的目的是报告BAV疾病近端主动脉置换的当代手术结果,并探讨瓣膜形态、瓣膜病理生理学与胸主动脉病理之间的关系。
2005年9月至2009年12月期间,共有100例连续的BAV合并近端主动脉扩张患者(平均年龄54±13岁;范围:29 - 80岁)在一家转诊机构接受了主动脉置换术。其中,16%的患者曾接受过主动脉瓣置换术(AVR)。主动脉修复根据主动脉瓣和胸主动脉病变进行个体化定制,包括冠状动脉上升主动脉(AA)置换(n = 17)、AVR联合冠状动脉上AA置换(n = 39)、主动脉根部置换(n = 42)以及保留瓣膜的根部置换(n = 2)。82例患者(80例半弓置换,2例全弓置换)进行了同期主动脉弓置换。28例患者进行了其他同期心脏手术。
30天/住院期间的死亡率和卒中率均为1%。主要的主动脉瓣病理生理学表现为主动脉瓣狭窄(AS;33%)、主动脉瓣关闭不全(AI;29%)、混合性AS/AI(17%)、功能正常的BAV(17%)以及情况不明(4%)。瓣膜形态包括Sievers I型,R/L(75%)、I型,R/N(9%)、I型,L/N(2%)、0型(7%)和II型(7%)。以AI为主的BAV患者根部扩张(62%)比以AS为主(30%)或瓣膜功能正常(35%)的患者更常见。基于BAV形态,各组之间胸主动脉最大直径无显著差异。平均随访16个月时,无晚期死亡或瓣膜相关并发症。
BAV患者进行近端主动脉置换术的死亡率和发病率较低。尽管在以AI为主的病理生理学表现的BAV患者中主动脉根部扩张最为常见,但主动脉瓣形态并不能预测胸主动脉的病理解剖结构。这些发现表明治疗合并的主动脉病变(包括根据需要进行主动脉弓置换)具有安全性和可行性,并且可能有助于根据患者的病理情况定制所需的具体手术方式。