Kieffer E, Bahnini A, Koskas F
Department of Vascular Surgery, Pitié-Salpêtrière University Hospital, Paris, France.
J Vasc Surg. 1994 Jan;19(1):100-9; discussion 110-1. doi: 10.1016/s0741-5214(94)70125-3.
Because of the scarcity of large series in the literature, our experience with surgery for aberrant subclavian arteries (aSA) in adults was reviewed.
During the last 16 years we have surgically treated 33 adult patients with aSA. Twenty-eight patients had a left-sided aortic arch with a right aSA whereas five had a right-sided aortic arch with a left aSA. Eleven patients (group 1) had dysphagia caused by esophageal compression by a nonaneurysmal aSA; five patients (group 2) had ischemic symptoms caused by occlusive disease of a nonaneurysmal aSA; 10 patients (group 3) had aneurysms of the aSA with or without symptoms caused by esophageal compression or arterial thromboembolism; and seven patients (group 4) had an aSA arising from a diseased (usually aneurysmal) thoracic aorta. In all cases the divided aSA was revascularized, most often by direct transposition into the ipsilateral common carotid artery. Nine of the 16 patients in groups 1 and 2 underwent operation with a cervical approach alone. In the remaining seven, the cervical approach was combined with a median sternotomy (six cases) or a left thoracotomy (one case). In the 17 patients in groups 3 and 4, either a cervical approach (two cases), a median sternotomy (four cases), or a two-staged approach combining a supraclavicular incision on the side of the aSA with a posterolateral thoracotomy on the side of the aortic arch (11 cases) was used. Aortic cross-clamping was required in 12 of these patients to perform the transaortic closure of the origin of the aSA with patch angioplasty (three cases), or prosthetic replacement of the descending thoracic aorta (nine cases). Cardiopulmonary bypass was used in six patients (including three with hypothermic circulatory arrest).
Four patients, all in groups 3 and 4, died after operation: two of multiorgan failure, one of heart failure, and one of esophageal rupture. Satisfactory clinical and anatomic results were obtained in the remaining 29 patients.
The surgical approach to aSA must be flexible and adapted to the anatomic conditions found. We recommend routine reconstruction of the aSA to avoid ischemic complications in the vertebrobasilar territory or upper extremity. Provision should be made for cardiopulmonary bypass in patients with aneurysm of aSA or associated aortic aneurysm.
鉴于文献中大宗病例报道稀缺,我们回顾了成人异常锁骨下动脉(aSA)的手术治疗经验。
在过去16年里,我们对33例成年aSA患者进行了手术治疗。28例患者为左侧主动脉弓伴右侧aSA,5例为右侧主动脉弓伴左侧aSA。11例患者(第1组)因非动脉瘤性aSA压迫食管导致吞咽困难;5例患者(第2组)因非动脉瘤性aSA闭塞性疾病出现缺血症状;10例患者(第3组)aSA有动脉瘤,伴有或不伴有食管压迫或动脉血栓栓塞引起的症状;7例患者(第4组)aSA起源于病变(通常为动脉瘤性)胸主动脉。在所有病例中,离断的aSA均进行了血运重建,最常用的方法是直接转位至同侧颈总动脉。第1组和第2组的16例患者中有9例仅采用颈部入路进行手术。其余7例患者中,颈部入路联合正中胸骨切开术(6例)或左胸切开术(1例)。第3组和第4组的17例患者中,采用了颈部入路(2例)、正中胸骨切开术(4例)或两阶段入路,即aSA侧锁骨上切口联合主动脉弓侧后外侧胸切开术(11例)。其中12例患者需要进行主动脉交叉阻断,以通过补片血管成形术(3例)经主动脉关闭aSA起始部,或进行胸降主动脉人工血管置换(9例)。6例患者使用了体外循环(包括3例低温循环停搏)。
4例患者术后死亡,均在第3组和第4组:2例死于多器官功能衰竭,1例死于心力衰竭,1例死于食管破裂。其余29例患者获得了满意的临床和解剖学结果。
aSA的手术入路必须灵活,应根据实际解剖情况进行调整。我们建议常规重建aSA,以避免椎基底动脉区域或上肢出现缺血性并发症。对于aSA动脉瘤或合并主动脉瘤的患者,应做好体外循环准备。