Weintraub R G, Brawn W J, Venables A W, Mee R B
Department of Cardiology, Royal Children's Hospital, Melbourne, Australia.
J Thorac Cardiovasc Surg. 1990 Feb;99(2):320-6.
Before January 1987, 62 infants underwent two-patch repair of complete (51) or intermediate (11) atrioventricular septal defect at the Royal Children's Hospital, Melbourne. Median age at repair was 4.3 months and median weight was 4.4 kg. Early deaths (3%) were confined to two infants with preoperative respiratory tract infections; a further two patients died during follow-up (late mortality rate 3%). Reoperation for severe postoperative mitral regurgitation was necessary in 10 infants (16%), two of whom subsequently required mitral valve replacement with a prosthesis. Preoperative atrioventricular valve regurgitation was assessed retrospectively in 49 patients from angiography or Doppler echocardiography and was found to be absent or mild in 33 (68%), moderate in 9 (18%), and severe in 7 (14%). At the time of latest review (at a mean of 2.4 years after repair), judged from a combination of clinical and echocardiographic criteria, mitral regurgitation was absent or mild in 49 (84%) of the 58 survivors; none of them had symptomatic regurgitation or were requiring continuing medical treatment. Analysis of sequential atrioventricular valve function in 46 of the 49 patients in whom objective preoperative data were available showed no relationship between the degree of preoperative and postoperative atrioventricular valve regurgitation. Infants without Down's syndrome, however, had a significantly higher reoperation rate for severe postoperative mitral valve regurgitation (50%) than those with Down's syndrome (10%) (p = 0.007). Complete atrioventricular septal defect can be repaired in early infancy with a low mortality rate and good intermediate term results.
1987年1月以前,墨尔本皇家儿童医院对62例婴儿进行了完全性(51例)或中间型(11例)房室间隔缺损的双片修补术。修补时的中位年龄为4.3个月,中位体重为4.4千克。早期死亡(3%)仅限于2例术前有呼吸道感染的婴儿;另有2例患者在随访期间死亡(晚期死亡率3%)。10例婴儿(16%)因严重的术后二尖瓣反流需要再次手术,其中2例随后需要用人工瓣膜置换二尖瓣。对49例患者的术前房室瓣反流情况进行了回顾性评估,通过血管造影或多普勒超声心动图检查发现,33例(68%)无反流或轻度反流,9例(18%)中度反流,7例(14%)重度反流。在最近一次复查时(修补术后平均2.4年),根据临床和超声心动图标准综合判断,58例存活者中有49例(84%)无二尖瓣反流或轻度反流;他们中没有人有症状性反流或需要持续药物治疗。对49例有术前客观数据的患者中的46例进行的序贯房室瓣功能分析显示,术前和术后房室瓣反流程度之间没有关系。然而,没有唐氏综合征的婴儿因严重的术后二尖瓣反流进行再次手术的比例(50%)明显高于患有唐氏综合征的婴儿(10%)(p = 0.007)。完全性房室间隔缺损在婴儿早期即可修补,死亡率低,中期效果良好。