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肺动脉瓣叶先天性缺如。

Congenital absence of pulmonary valve leaflets.

作者信息

Buendia A, Attie F, Ovseyevitz J, Zghaib A, Zamora C, Zavaleta D, Vargas-Barron J, Richheimer R

出版信息

Br Heart J. 1983 Jul;50(1):31-41. doi: 10.1136/hrt.50.1.31.

Abstract

Congenital absence of pulmonary valve leaflets is an uncommon condition usually associated with ventricular septal defect and an obstructive pulmonary valve ring. Twenty-one patients with these malformations are described. Twenty had an associated ventricular septal defect with ventriculoarterial concordance, and one also had transposition of the great arteries, ventricular septal defect, and obstructive pulmonary valve ring. The clinical features, cardiac catheterisation findings, and angiocardiographic results are presented. Twelve patients underwent cardiac surgery. Three patients died, one in the early, and the other two in the late postoperative period. The results, according to the surgical technique employed and postoperative cardiac catheterisation findings, showed that patients in whom the bioprostheses were implanted in the pulmonary position had a better late follow-up.

摘要

先天性肺动脉瓣叶缺如为一种罕见病症,通常与室间隔缺损及梗阻性肺动脉瓣环相关。本文描述了21例患有这些畸形的患者。其中20例伴有室间隔缺损且心室-动脉连接一致,1例还患有大动脉转位、室间隔缺损及梗阻性肺动脉瓣环。文中呈现了临床特征、心导管检查结果及心血管造影结果。12例患者接受了心脏手术。3例患者死亡,1例于早期死亡,另外2例于术后晚期死亡。根据所采用的手术技术及术后心导管检查结果,结果显示在肺动脉位置植入生物假体的患者后期随访情况较好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ef4/481368/a23805feb15f/brheartj00139-0042-a.jpg

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