Vouhé P R, Macé L, Vernant F, Jayais P, Pouard P, Mauriat P, Leca F, Neveux J Y
Department of Cardiac Surgery, Laënnec Hospital, Paris, France.
Eur J Cardiothorac Surg. 1990;4(7):365-70. doi: 10.1016/1010-7940(90)90044-z.
The optimal surgical management (primary or staged repair) of interrupted aortic arch (IAA) with ventricular septal defect (VSD) remains to be determined. A consecutive series of 14 neonates, aged 3-18 days (mean: 10 +/- 6 days) underwent primary complete repair. Mean weight was 3.3 +/- 0.4 kg. Eleven patients had IAA type B, 2 had type A and 1 had type C. Six infants had the Di George syndrome. Preoperative management (mean: 5 +/- 4 days) included prostaglandin E1 (14/14), intubation and ventilation (13/14), and inotropic support (11/14). Surgery was performed under deep hypothermia and circulatory arrest and involved resection of all ductal tissue, direct end-to-side aortic arch anastomosis and patch closure of the VSD. There were 2 early deaths (14%, 70% CL: 5%-31%): low cardiac output (1), residual VSD (1). Four patients (33%, 70% CL: 13%-52%) underwent reoperation for recurrent aortic obstruction (3 patients, 1 death) or left ventricular outflow tract obstruction (LVOTO) (1 patient). The results improved with time: no death and no recurrent aortic obstruction in the last 8 patients. At last follow-up (11 patient, mean follow-up = 24 +/- 9 months), all patients were free of cardiac symptoms; none had persistent aortic obstruction; 4 had LVOTO (gradient greater than 20 mm Hg) and 1 (with the Di George syndrome) had severe mental disorders. Primary complete repair provides satisfactory results in most infants born with IAA and VSD. An adequate direct aortic arch anastomosis should entail a low risk of recurrent obstruction. LVOTO develops in many cases and may require further surgery.
主动脉弓中断(IAA)合并室间隔缺损(VSD)的最佳手术管理方式(一期修复或分期修复)仍有待确定。连续14例年龄在3 - 18天(平均:10±6天)的新生儿接受了一期完全修复。平均体重为3.3±0.4千克。11例患者为B型IAA,2例为A型,1例为C型。6例婴儿患有Di George综合征。术前管理(平均:5±4天)包括使用前列腺素E1(14/14)、插管和通气(13/14)以及使用正性肌力药物支持(11/14)。手术在深低温和循环停止下进行,包括切除所有导管组织、直接端端主动脉弓吻合以及VSD的补片修补。有2例早期死亡(14%,95%置信区间:5% - 31%):低心排血量(1例)、残余VSD(1例)。4例患者(33%,95%置信区间:13% - 52%)因复发性主动脉梗阻(3例,1例死亡)或左心室流出道梗阻(LVOTO)(1例)接受了再次手术。随着时间推移结果有所改善:最后8例患者无死亡且无复发性主动脉梗阻。在最后一次随访时(11例患者,平均随访时间 = 24±9个月),所有患者均无心脏症状;无人有持续性主动脉梗阻;4例有LVOTO(压差大于20 mmHg),1例(患有Di George综合征)有严重精神障碍。一期完全修复在大多数患有IAA和VSD的婴儿中可提供满意的结果。充分的直接主动脉弓吻合应使复发性梗阻风险较低。许多病例会发生LVOTO,可能需要进一步手术。