Arakelyan Valery, Spiridonov Alexey, Bockeria Leo
Department of Vascular Surgery, Bakoulev Scientific Center of Cardiovascular Surgery, 135 Roublevskoe shosse, 121552 Moscow, Russian Federation.
Eur J Cardiothorac Surg. 2005 May;27(5):815-20. doi: 10.1016/j.ejcts.2005.01.059.
Operation for aortic recoarctation and/or residual hypoplastic arch represents a surgical challenge because of surrounding scar tissue in the coarctation area, hazard of spinal cord ischemia due to aortic cross-clamping, laceration of the recurrent nerve, and the choice of the best approach. We demonstrate the results of 52 operations of an extra anatomically bypass technique via right thoracotomy approach without establishment of cardiopulmonary bypass.
Since 1987, 52 patients underwent extra anatomically positioned ascending-descending bypass grafting. Indication was aortic recoarctation with concomitant hypoplastic aortic arch (45 patients), atypical coarctation of aortic arch (2 patients), congenital anomalies of aortic arch (2 patients) and concomitant aortic coarctation and associated cardiac problems that required surgical repair (2 patient), infected stent-graft of descending aorta (1 patient). Mean age was 19.3 years. Systolic pressure gradients at rest ranged from 35 to 90mmHg; upper extremity hypertension was present in all patients. Operative technique consisted of performing aorta ascending-descending bypass graft size 16 or 18mm in diameter, via right thoracotomy (in 51 patient) or sternotomy (in 1 patient).
The mortality rate was 1.9% (1/52). Five patients returned to the operating room (in 3-5 days after operation) for a lymphorrhea complication. An arterial pressure gradient in the limbs was totally corrected. During a follow-up period of actually 79+/-54 months, no adverse event was noticed and antihypertensive medication was stopped in all patients.
Ascending-to-descending aortic bypass via right thoracotomy is a safe and effective method for management complex (re-) coarctation and hypoplastic aortic arch.
主动脉再缩窄和/或残余主动脉弓发育不全的手术是一项具有挑战性的外科手术,这是因为缩窄区域周围存在瘢痕组织、主动脉交叉钳夹导致脊髓缺血的风险、喉返神经撕裂以及最佳手术入路的选择。我们展示了52例通过右胸壁切开入路采用非解剖学旁路技术进行手术的结果,术中未建立体外循环。
自1987年以来,52例患者接受了非解剖学位置的升主动脉-降主动脉旁路移植术。手术指征为主动脉再缩窄合并主动脉弓发育不全(45例患者)、主动脉弓非典型缩窄(2例患者)、主动脉弓先天性异常(2例患者)以及合并主动脉缩窄和需要手术修复的相关心脏问题(2例患者)、降主动脉感染性支架移植物(1例患者)。平均年龄为19.3岁。静息时收缩压梯度为35至90mmHg;所有患者均存在上肢高血压。手术技术包括通过右胸壁切开(51例患者)或胸骨切开(1例患者)进行直径为16或18mm的升主动脉-降主动脉旁路移植。
死亡率为1.9%(1/52)。5例患者(术后3至5天)因淋巴漏并发症返回手术室。肢体动脉压梯度完全纠正。在实际79±54个月的随访期内,未观察到不良事件,所有患者均停用了抗高血压药物。
通过右胸壁切开进行升主动脉-降主动脉旁路移植术是治疗复杂(再)缩窄和主动脉弓发育不全的一种安全有效的方法。