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婴儿期发现的继发孔型房间隔缺损。

Secundum atrial septal defect encountered in infancy.

作者信息

Spangler J G, Feldt R H, Danielson G K

出版信息

J Thorac Cardiovasc Surg. 1976 Mar;71(3):398-401.

PMID:1249972
Abstract

From 1953 to 1972, approximately 170 patients less than 16 years old were seen at the Mayo Clinic for isolated secundum atrial septal defect. Thirteen of these patients were initially seen when they were less than 2 years old. Eleven of the patients had symptoms, and one of these died. Four patients failed to respond to medical management and underwent successful repair of their defects before they were 2 years old. Infants with isolated secundum atrial septal defect and significant symptoms are at an increased risk of death. Consideration should be given to early surgical closure of the defect in those infants who do not respond promptly and completely to medical therapy. Surgical repair in infancy can be accomplished with minimal risk and excellent early and long-term clinical results.

摘要

1953年至1972年期间,梅奥诊所接待了约170名16岁以下的单纯继发孔型房间隔缺损患者。其中13名患者初诊时年龄小于2岁。11名患者有症状,其中1名死亡。4名患者药物治疗无效,在2岁前成功接受了缺损修复。患有单纯继发孔型房间隔缺损且有明显症状的婴儿死亡风险增加。对于那些对药物治疗没有迅速且完全反应的婴儿,应考虑早期手术关闭缺损。婴儿期进行手术修复风险极小,早期和长期临床效果都很好。

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