Kostelka Martin, Walther Thomas, Geerdts Imke, Rastan Ardawan, Jacobs Stefan, Dähnert Ingo, Kiefer Herbert, Bellinghausen Wilfried, Mohr Friedrich W
Klinik für Herzchirurgie, Universität Leipzig, Herzzentrum, Leipzig, Germany.
Ann Thorac Surg. 2004 Dec;78(6):1989-93; discussion 1993. doi: 10.1016/j.athoracsur.2004.05.018.
The aim of the present study was to evaluate the current outcome and reoperation rate after applying a one-stage correction strategy for interrupted aortic arch (IAA) with ventricular septal defect (VSD) and also for aortic coarctation and hypoplastic aortic arch (CoA-HyAA) with VSD beginning September 1999.
Twenty-four consecutive patients with IAA (n = 12) or CoA-HyAA (n = 12) with VSD underwent early one-stage correction. Patients' mean age was 12 days (range, 2 to 188); mean weight was 3.6 kg (range, 2.1 to 7.3), 6 patients were less than 2.5 kg. Three IAA were type A, 5 type B1, 3 type B2, and 1 type C. Associated anomalies included a large VSD in all, left ventricular outlet tract obstruction in 5, transposition of the great arteries, aortopulmonary window, persistent truncus arteriosus, and double-outlet right ventricle in 1 patient. Selective brain perfusion through innominate artery and selective coronary perfusion through aortic root during aortic arch reconstruction was used in all patients. Mean follow-up was 2.2 +/- 0.9 years.
There was no early, no late mortality, and no postoperative neurologic complications. Mean crossclamp duration was 72 +/- 32 minutes, lowest temperature 22.8 +/- 4 degrees C and selective brain and coronary perfusion duration was 34 +/- 13 minutes. Eighteen patients required delayed sternal closure at 1.7 days postoperatively. New perioperative management reduced the overall morbidity. Four patients after IAA plus VSD repair developed aortic arch restenosis and were successfully treated by balloon dilatation. One patient with d-TGA underwent right ventricular outflow tract reconstruction of right ventricular outlet tract obstruction 7 months after the initial repair. Pressure gradients across the anastomosis at most recent follow up were less than 10 mm Hg. All patients are asymptomatic and are developing normally.
One-stage complete correction is feasible in newborns with aortic arch obstruction with VSD. Complex cardiac anatomy presents no additional risk for the procedure. The early one-stage correction yields excellent surgical results and good functional outcome.
本研究旨在评估自1999年9月起,对合并室间隔缺损(VSD)的主动脉弓中断(IAA)以及合并VSD的主动脉缩窄和主动脉弓发育不良(CoA-HyAA)应用一期矫治策略后的当前疗效及再次手术率。
24例连续的合并VSD的IAA患者(n = 12)或CoA-HyAA患者(n = 12)接受了早期一期矫治。患者平均年龄为12天(范围2至188天);平均体重为3.6千克(范围2.1至7.3千克),6例患者体重小于2.5千克。3例IAA为A型,5例为B1型,3例为B2型,1例为C型。合并的异常包括所有患者均有大型VSD,5例有左心室流出道梗阻,1例有大动脉转位、主肺动脉窗、永存动脉干和右心室双出口。所有患者在主动脉弓重建期间均采用经无名动脉选择性脑灌注和经主动脉根部选择性冠状动脉灌注。平均随访时间为2.2±0.9年。
无早期及晚期死亡病例,也无术后神经系统并发症。平均阻断时间为72±32分钟,最低体温为22.8±4℃,选择性脑灌注和冠状动脉灌注时间为34±13分钟。18例患者术后1.7天需要延迟关胸。新的围手术期管理降低了总体发病率。4例IAA加VSD修复术后患者发生主动脉弓再狭窄,经球囊扩张成功治疗。1例d-TGA患者在初次修复后7个月接受了右心室流出道梗阻的右心室流出道重建。最近一次随访时吻合口处的压力阶差小于10 mmHg。所有患者均无症状且发育正常。
对于合并VSD的主动脉弓梗阻新生儿,一期完全矫治是可行的。复杂的心脏解剖结构并未给该手术带来额外风险。早期一期矫治可产生优异的手术效果和良好的功能转归。