Backer C L, Mavroudis C, Zias E A, Amin Z, Weigel T J
Children's Memorial Hospital, and Department of Surgery, Northwestern University Medical School, Chicago, Illinois 60614, USA.
Ann Thorac Surg. 1998 Oct;66(4):1365-70; discussion 1370-1. doi: 10.1016/s0003-4975(98)00671-7.
Our surgical strategy for infant coarctation changed from subclavian flap aortoplasty to resection with extended end-to-end anastomosis in 1991. The purpose of this review was to evaluate the results of that strategy.
From 1991 through 1997, 55 infants underwent repair of coarctation of the aorta using resection with extended end-to-end anastomosis. Isolated coarctation of the aorta was present in 26 patients, 20 patients had a ventricular septal defect, and 9 patients had other associated intracardiac lesions. Mean age at surgery was 0.20+/-0.24 years (median, 21 days). In 34 patients (62%), arch reconstruction was performed through a left thoracotomy. Twenty patients (36%) had median sternotomy with simultaneous repair of coarctation of the aorta and intracardiac repair of associated lesions. One patient had recoarctation repair through a median sternotomy. All coarctation and ductal tissue was resected and the anastomosis was constructed starting opposite the left carotid artery with running polypropylene suture.
There was one early death 26 days after coarctation of the aorta and ventricular septal defect repair in a child on extracorporeal membrane oxygenation for meconium aspiration and 2 late deaths owing to pneumonia and pulmonary hypertension (1) and interventricular hemorrhage (1). There were no instances of paraplegia. Follow-up in survivors ranges from 10 to 76 months (mean, 39.8+/-17.2 months). Recoarctation has developed in 2 patients, who have had successful balloon dilation 6 and 14 months after the operation. This yields a low recoarctation rate of 3.6%.
Resection with extended end-to-end anastomosis yields a low mortality and particularly a low recoarctation rate and is our procedure of choice for infants with coarctation of the aorta.
1991年,我们针对婴儿主动脉缩窄的手术策略从锁骨下动脉瓣主动脉成形术转变为切除并进行扩大端端吻合术。本综述的目的是评估该策略的效果。
1991年至1997年期间,55例婴儿接受了主动脉缩窄修复术,采用切除并扩大端端吻合术。26例患者为单纯主动脉缩窄,20例患者合并室间隔缺损,9例患者合并其他心脏内相关病变。手术时的平均年龄为0.20±0.24岁(中位数为21天)。34例患者(62%)通过左胸切口进行主动脉弓重建。20例患者(36%)采用正中胸骨切开术,同时修复主动脉缩窄并进行心脏内相关病变的修复。1例患者通过正中胸骨切开术进行再狭窄修复。所有缩窄段和导管组织均被切除,吻合口从左颈动脉相对处开始,采用聚丙烯连续缝合。
1例因胎粪吸入接受体外膜肺氧合治疗的儿童在主动脉缩窄和室间隔缺损修复术后26天早期死亡,2例因肺炎和肺动脉高压(1例)以及脑室内出血(1例)晚期死亡。无截瘫病例。存活患者的随访时间为10至76个月(平均39.8±17.2个月)。2例患者出现再狭窄,分别在术后6个月和14个月成功进行了球囊扩张。再狭窄率低至3.6%。
切除并扩大端端吻合术死亡率低,尤其是再狭窄率低,是我们治疗婴儿主动脉缩窄的首选术式。