Najm H K, Van Arsdell G S, Watzka S, Hornberger L, Coles J G, Williams W G
Division of Cardiovascular Surgery, Department of Surgery, Hospital for Sick Children and the Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
J Thorac Cardiovasc Surg. 1998 Dec;116(6):905-13. doi: 10.1016/S0022-5223(98)70040-6.
The objective was to explore the best management algorithm for atrioventricular septal defect in conjunction with tetralogy of Fallot.
We reviewed the cases of 38 children referred to our division (March 1981-August 1997) who had atrioventricular septal defect associated with tetralogy of Fallot; 32 (84%) had Down syndrome. Twenty-one received initial palliation with a systemic-to-pulmonary artery shunt; of these, 2 (9.5%) died before complete repair. Thirty-one children underwent complete repair; 14 of these (45%) had undergone initial palliation (mean age at shunt 20 +/- 24 months). Right ventricular outflow obstruction was relieved by a transannular patch in 22 (71%); 14 (64% of 22) had a monocuspid valve inserted. Four required an infundibular patch.
Two children (6.4%) died early after repair; 1 had undergone previous palliation. Patients with palliation underwent repair at an older age (78 vs 36 months), required longer ventilatory support (8 vs 4 days) and inotropic support (8 vs 4 days), and had longer intensive care stays (11 vs 6 days) and hospital stays (24 vs 15 days). Eleven children (35%) underwent reoperation, 7 (58%) for right ventricular outflow reconstruction and pulmonary arterioplasty. Reoperation was more frequent in the palliation group than in the primary operation group (64% vs 12%). The single late death was related to a reoperation in the palliation group.
Atrioventricular septal defect with tetralogy of Fallot can be repaired with a low mortality rate. Initial palliation with a shunt resulted in a more complex postoperative course and a higher reoperative rate. Primary repair is superior to initial palliation with later repair.
探讨房室间隔缺损合并法洛四联症的最佳治疗方案。
我们回顾了1981年3月至1997年8月转诊至我科的38例患有房室间隔缺损合并法洛四联症的儿童病例;其中32例(84%)患有唐氏综合征。21例最初接受了体肺分流姑息治疗;其中2例(9.5%)在完全修复前死亡。31例儿童接受了完全修复;其中14例(45%)曾接受过初始姑息治疗(分流时平均年龄为20±24个月)。22例(71%)通过跨环补片解除右心室流出道梗阻;其中14例(22例中的64%)植入了单叶瓣膜。4例需要漏斗部补片。
2例儿童(6.4%)在修复后早期死亡;1例曾接受过姑息治疗。接受姑息治疗的患者修复时年龄较大(78个月对36个月),需要更长时间的通气支持(8天对4天)和正性肌力支持(8天对4天),重症监护停留时间更长(11天对6天)和住院时间更长(24天对15天)。11例儿童(35%)接受了再次手术,7例(58%)进行右心室流出道重建和肺动脉成形术。再次手术在姑息治疗组比初次手术组更频繁(64%对12%)。唯一的晚期死亡与姑息治疗组的再次手术有关。
房室间隔缺损合并法洛四联症可以低死亡率进行修复。分流初始姑息治疗导致术后病程更复杂且再次手术率更高。一期修复优于初始姑息治疗后二期修复。