E R de Vivie, P G Björnstad, H Rastan, A J Beuren, J Koncz
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引用次数: 0
摘要
瓣上主动脉瓣狭窄是一种结合典型面部特征、智力低下和肺外周动脉狭窄的综合征,或者是一种孤立的先天性心脏缺陷。137例患者经导管插管和心血管造影确诊;由于疾病的严重程度,35名儿童和10名成人患者被认为是矫正手术的候选人。年龄从3岁到32岁不等。死亡7例(15.5%)。12例患儿术后5年、6年+/- 4年、1年进行再导管置入术。左心室压力从184,1 +/- 28,4降至155,5 +/- 32,1 mm Hg,左心室与主动脉之间的压力梯度从101,2 +/- 19,7降至29,1 +/- 23,1 mm Hg,术后值在0 ~ 80 mm Hg之间变化。
[Hemodynamic results of surgery for congenital supravalvular aortic stenoses (author's transl)].
Supravalvular aortic stenosis is either a syndrome combined with typical face characteristics mental retardation and peripheral pulmonary artery stenosis or it occurs as an isolated congenital heart defect. The diagnosis was confirmed in 137 patients by means of catheterization and angiocardiography; 35 pediatric and 10 adult patients were considered to be candidates for corrective surgery because of the severity of their disease. Age varied from 3 to 32 years. 7 patients (15,5%) died. Recatheterization was performed in 12 children 5,6 +/- 4,1 years after surgery. Left ventricular pressures were decreased from 184,1 +/- 28,4 to 155,5 +/- 32,1 mm Hg, and the pressure gradients between left ventricle and the aorta fell from 101,2 +/- 19,7 to 29,1 +/- 23,1 mm Hg. The postoperative values varied between 0 and 80 mm Hg. Operative results are discussed in relation to the anatomical type malformation and the operative technique.