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室间隔缺损与主动脉瓣下狭窄:41例患者分析

Ventricular septal defect and subaortic stenosis: an analysis of 41 patients.

作者信息

Vogel M, Freedom R M, Brand A, Trusler G A, Williams W G, Rowe R D

出版信息

Am J Cardiol. 1983 Dec 1;52(10):1258-63. doi: 10.1016/0002-9149(83)90583-0.

Abstract

Forty-one patients with subaortic stenosis (SAS) and ventricular septal defect (VSD) were identified from the cardiac records of the Hospital for Sick Children, Toronto, Ontario. The diagnosis of an associated SAS was made clinically in only 1 patient, who had findings of left ventricular (LV) hypertrophy with strain on the electrocardiogram. There was a delay of 3.1 years between initial presentation and detection of SAS. The SAS was not diagnosed at initial catheterization in 17 patients and was confirmed at subsequent catheter studies in 8 patients, surgery in 5 and autopsy in 4. Associated defects included coarctation of the aorta in 12 patients, mitral valve abnormalities in 4, and right-sided obstructions, including anomalous right ventricular muscle bundles in 6 patients, tetralogy in 4 and pulmonic stenosis in 1 patient. The mean gradient across the LV outflow tract was 25 mm Hg. Nineteen patients had serial catheters without intervening surgery, and the outflow gradient increased from a mean of 9 to 36 mm Hg. The mechanism of SAS consisted of fibrous diaphragm and fibromuscular obstruction in 31 cases, muscular narrowing in 4, protruding tricuspid valve leaflet in 2, hypertrophic cardiomyopathy in 2, anterolateral twist in 1 patient and redundant tissue tag in 1. Thirty-eight patients had a perimembranous VSD, 19 of whom had an associated so-called aneurysm of the membranous septum; 2 had an infundibular VSD and 1 patient had a central muscular defect. Although the SAS was located below the VSD in 30 cases, the associated heart failure and reduced cardiac output can mask the presence or severity of associated SAS.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

从安大略省多伦多市病童医院的心脏病例记录中,识别出41例患有主动脉瓣下狭窄(SAS)和室间隔缺损(VSD)的患者。仅1例患者临床上诊断出合并SAS,该患者心电图显示左心室(LV)肥厚并伴有劳损表现。从首次就诊到发现SAS有3.1年的延迟。17例患者在初次心导管检查时未诊断出SAS,8例在随后的心导管检查中得到确诊,5例在手术中确诊,4例在尸检时确诊。合并的缺陷包括12例主动脉缩窄、4例二尖瓣异常以及6例右侧梗阻,其中包括异常右心室肌束、4例法洛四联症和1例肺动脉狭窄。左心室流出道的平均压力阶差为25 mmHg。19例患者未进行手术而接受了系列心导管检查,流出道压力阶差从平均9 mmHg增加到36 mmHg。SAS的机制包括31例纤维隔膜和纤维肌性梗阻、4例肌肉狭窄、2例三尖瓣叶突出、2例肥厚型心肌病、1例患者前外侧扭曲以及1例多余组织条索。38例患者有膜周部VSD,其中19例合并所谓的膜部间隔瘤;2例有漏斗部VSD,1例患者有中央肌部缺损。尽管30例患者的SAS位于VSD下方,但合并的心力衰竭和心输出量降低可能掩盖合并SAS的存在或严重程度。(摘要截短于250字)

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