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婴儿期孤立性继发孔房间隔缺损的矫治

Correction of isolated secundum atrial septal defect in infancy.

作者信息

Bull C, Deanfield J, de Leval M, Stark J, Taylor J F, Macartney F J

出版信息

Arch Dis Child. 1981 Oct;56(10):784-6. doi: 10.1136/adc.56.10.784.

Abstract

Although it is a common congenital cardiac lesion, secundum atrial septal defect (ASD) rarely presents in infancy. Its natural history in the first two decades of life is generally benign. Reports of symptomatic ASD in early childhood stress the place of conservative management, and recommend that the operation should be deferred until school age. Few accounts of the indications for surgery in infancy exist. We present our experience of 6 patients who failed to respond adequately to conservative treatment and required operation for intractable heart failure due to isolated secundum ASD in the first year of life. As their presentation and physical signs were not typical of ASD seen in later childhood, they presented problems both of diagnosis and management.

摘要

尽管继发孔型房间隔缺损(ASD)是一种常见的先天性心脏病变,但在婴儿期很少出现。其在生命最初二十年的自然病程通常是良性的。关于幼儿期有症状ASD的报道强调了保守治疗的地位,并建议手术应推迟到学龄期。关于婴儿期手术指征的报道很少。我们介绍了6例患者的经验,这些患者对保守治疗反应不佳,因孤立性继发孔型ASD在出生后第一年出现难治性心力衰竭而需要手术。由于他们的临床表现和体征并非儿童后期所见ASD的典型表现,因此在诊断和治疗方面都存在问题。

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