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儿童原发性房间隔缺损:早期结果、危险因素及再次手术的无复发生存率

Primum atrial septal defect in children: early results, risk factors, and freedom from reoperation.

作者信息

Najm H K, Williams W G, Chuaratanaphong S, Watzka S B, Coles J G, Freedom R M

机构信息

Department of Surgery, The Hospital of Sick Children, University of Toronto, Faculty of Medicine, Ontario, Canada.

出版信息

Ann Thorac Surg. 1998 Sep;66(3):829-35. doi: 10.1016/s0003-4975(98)00607-9.

Abstract

BACKGROUND

Repair of primum atrial septal defect in children usually is associated with a low operative mortality, except for a subgroup of children with congestive heart failure. To determine the early mortality and incidence of reoperation in children with primum atrial septal defect, we analyzed retrospectively the results of patients who underwent repair of this defect.

METHODS

Between July 1982 and December 1996, 180 children underwent repair of primum atrial septal defect. The mean age at repair was 4.6 years (median, 3.6 years; range, 1 month to 16.4 years); of the 180 children, 23 were infants less than 1 year of age. Absent or mild symptoms were present in 145 (80%), whereas 34 (20%) of children presented with severe symptoms or congestive heart failure.

RESULTS

Early mortality occurred in 3 (1.6%); 2 were less than 1 year of age. Follow-up ranged from 2 months to 14.5 years (mean, 6 +/- 4.2 years). Actuarial survival is 98% at 10 years with no late deaths. Age less than 1 year is a predictor of death. During follow-up, 17 (9%) of the 180 patients underwent reoperation, 5 of whom were in the infant group. Five underwent reoperation for subaortic obstruction, and 12 for left atrioventricular valve regurgitation of whom 11 were repaired; and 1 required valve replacement. Age and preoperative moderate-to-severe left atrioventricular valve regurgitation were predictors of reoperation.

CONCLUSIONS

Results of the repair of primum atrial septal defect during childhood are favorable. Infants have a higher risk for death and reoperation. Left atrioventricular valve insufficiency and subaortic stenosis are important late complications and can be repaired safely at reoperation.

摘要

背景

儿童原发孔型房间隔缺损修补术的手术死亡率通常较低,但患有充血性心力衰竭的儿童亚组除外。为了确定原发孔型房间隔缺损患儿的早期死亡率和再次手术发生率,我们回顾性分析了接受该缺损修补术患者的结果。

方法

1982年7月至1996年12月期间,180例儿童接受了原发孔型房间隔缺损修补术。修补时的平均年龄为4.6岁(中位数为3.6岁;范围为1个月至16.4岁);180例儿童中,23例为1岁以下婴儿。145例(80%)症状轻微或无症状,而34例(20%)儿童有严重症状或充血性心力衰竭。

结果

3例(1.6%)发生早期死亡;2例年龄小于1岁。随访时间为2个月至14.5年(平均6±4.2年)。10年时的精算生存率为98%,无晚期死亡。年龄小于1岁是死亡的预测因素。随访期间,180例患者中有17例(9%)接受了再次手术,其中5例在婴儿组。5例因主动脉下梗阻接受再次手术,12例因左房室瓣反流接受再次手术,其中11例修补成功;1例需要瓣膜置换。年龄和术前中重度左房室瓣反流是再次手术的预测因素。

结论

儿童期原发孔型房间隔缺损修补术的结果良好。婴儿死亡和再次手术的风险较高。左房室瓣关闭不全和主动脉下狭窄是重要的晚期并发症,再次手术时可安全修复。

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