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室间隔缺损和主动脉瓣反流。

Ventricular septal defect and aortic regurgitation.

作者信息

Hallidie-Smith K A, Olsen E G, Oakley C M, Goodwin J F, Cleland W P

出版信息

Thorax. 1969 May;24(3):257-75. doi: 10.1136/thx.24.3.257.

Abstract

We have reviewed our experience of 29 patients with the association of ventricular septal defect and aortic regurgitation, 27 of whom have been treated surgically. Our present approach to the surgical management is outlined and the embryology and pathological anatomy are reviewed. The most common cause of aortic regurgitation was a prolapsed aortic valve cusp, which occurred in 19 patients. Aneurysmal dilatation of an aortic sinus accounted for the regurgitation in three patients, and two patients had both abnormalities. In two patients no cause for the aortic regurgitation was found. Those patients with aortic cusp prolapse commonly had large ventricular septal defects, of which nearly a third were supracristal. Because of cusp prolapse into the ventricular septal defect, and sometimes into the right ventricular outflow tract, the findings at cardiac catheterization often suggested erroneously that the ventricular septal defect was small and that infundibular obstruction was present. Characteristic angiographic features have been demonstrated, in particular the deformed and prolapsed aortic cusp. The various techniques of surgical correction which were used are described, the majority of patients having had a patch closure of the ventricular septal defect and repair of the aortic valve. Some residual aortic regurgitation was usual, but it was improved or minimized in 18 of the 23 survivors, and the more recent results have been particularly encouraging. Closure of the ventricular septal defect alone relieved heart failure in a 3-year-old child. There were four operative deaths (15% mortality) in patients with severe aortic regurgitation, three of whom were in heart failure before operation. The medical course was commonly of slowly increasing severity of the aortic regurgitation with progression to heart failure. However, the individual course was unpredictable and three children developed heart failure within a year of the onset of their aortic regurgitation. Infective endocarditis occurred in a quarter of the patients and usually followed the development of the aortic regurgitation. Despite the difficulties of surgical management it is felt that the unpredictable prognosis, high operative risk once cardiac failure has supervened, and the hazard of infective endocarditis make early operation desirable.

摘要

我们回顾了29例室间隔缺损合并主动脉瓣关闭不全患者的治疗经验,其中27例接受了手术治疗。本文概述了我们目前的手术治疗方法,并回顾了胚胎学和病理解剖学。主动脉瓣关闭不全最常见的原因是主动脉瓣叶脱垂,19例患者出现这种情况。主动脉窦瘤样扩张导致3例患者出现反流,2例患者同时存在这两种异常。2例患者未发现主动脉瓣关闭不全的病因。那些主动脉瓣叶脱垂的患者通常有较大的室间隔缺损,其中近三分之一为嵴上型。由于瓣叶脱垂至室间隔缺损,有时进入右心室流出道,心导管检查结果常错误地提示室间隔缺损较小且存在漏斗部梗阻。已证实存在特征性血管造影表现,尤其是变形和脱垂的主动脉瓣叶。描述了所采用的各种手术矫正技术,大多数患者接受了室间隔缺损补片修补和主动脉瓣修复。通常会有一些残余的主动脉瓣反流,但23例幸存者中有18例的反流得到改善或降至最低,最近的结果尤其令人鼓舞。仅室间隔缺损的闭合就使一名3岁儿童的心衰得到缓解。重度主动脉瓣关闭不全患者中有4例手术死亡(死亡率15%),其中3例术前即有心衰。病程通常是主动脉瓣关闭不全的严重程度缓慢增加并进展至心衰。然而,个体病程不可预测,3名儿童在主动脉瓣关闭不全发病后一年内出现心衰。四分之一的患者发生感染性心内膜炎,通常在主动脉瓣关闭不全出现后发生。尽管手术治疗存在困难,但考虑到预后不可预测、一旦发生心衰手术风险高以及感染性心内膜炎的风险,早期手术是可取的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a4d/471965/c058b0ff5e60/thorax00105-0008-a.jpg

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