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肺动脉瓣缺如综合征。采用肺动脉成形术进行手术矫正。

Absent pulmonary valve syndrome. Surgical correction with pulmonary arterioplasty.

作者信息

Rao P S, Lawrie G M

出版信息

Br Heart J. 1983 Dec;50(6):586-9. doi: 10.1136/hrt.50.6.586.

Abstract

A 13 month old child with classic features of absent pulmonary valve with tetralogy of Fallot underwent successful surgical repair by closure of the ventricular septal defect, relief of the right ventricular outflow tract obstruction, and partial resection and plastic repair of the aneurysmally dilated pulmonary arteries. Cardiac catheterisation data and clinical follow up for more than 18 months after the operation indicated excellent results. It is suggested that plastic repair of the aneurysmally dilated pulmonary arteries along with closure of the ventricular septal defect and relief of the right ventricular outflow tract obstruction should be performed early, perhaps between 1 and 2 years of age.

摘要

一名患有法洛四联症且具有肺动脉瓣缺如典型特征的13个月大儿童,通过闭合室间隔缺损、解除右心室流出道梗阻以及对瘤样扩张的肺动脉进行部分切除和整形修复,成功接受了手术治疗。术后心脏导管检查数据及超过18个月的临床随访显示效果极佳。建议在1至2岁之间尽早对瘤样扩张的肺动脉进行整形修复,同时闭合室间隔缺损并解除右心室流出道梗阻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/115b/481464/241c90ff33ab/brheartj00144-0089-a.jpg

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