Kitchiner D, Jackson M, Malaiya N, Walsh K, Peart I, Arnold R, Smith A
Cardiac Unit, Royal Liverpool Children's NHS Trust.
Br Heart J. 1994 Sep;72(3):251-60. doi: 10.1136/hrt.72.3.251.
To compare the incidence and prognosis of subaortic stenosis associated with a ventricular septal defect and to define the morphological basis of subaortic stenosis.
Presentation and follow up data on 202 patients with subaortic stenosis seen at the Royal Liverpool Children's Hospital between 1 January 1960 and 31 December 1991 were reviewed. Survivors were traced to assess their current clinical state. Necropsy specimens of 291 patients with lesions associated with subaortic stenosis were also examined.
In the clinical study; 65 (32.1%) of the 202 patients with subaortic stenosis had a ventricular septal defect (excluding an atrioventricular septal defect). 32 of these patients had a short segment (fibromuscular) subaortic stenosis. 33 had subaortic stenosis produced by deviation of muscular components of the outflow tracts. In 17 patients (51.5%) this was caused by posterior deviation or extension of structures into the left ventricular outflow tract, resulting in obstruction above the ventricular septal defect. In the other 16 patients (48.5%) there was over-riding of the aorta with concordant ventriculoarterial connections, (without compromise to right ventricular outflow) producing subaortic stenosis below the ventricular septal defect. Additional fibrous obstruction occurred in 39% of the patients with deviated structures. The age at presentation was lower (P < 0.01) in patients with deviated structures (median (range) 0.4 (0 to 9.2) months) than in those with short segment obstruction (median (range) 4.2 (0 to 84.9) months). The incidence of aortic arch obstruction was higher (P < 0.002) in patients with deviated structures than in those with short segment obstruction (38%). In the morphological study 35 pathological specimens showed obstructive muscular structures in the left ventricular outflow tract either above or below the ventricular septal defect. 16 had either posterior deviation of the outlet septum or extension of the right ventriculoinfundibular fold, or both of these together into the left ventricle. 19 had anterior deviation of the outlet septum into the right ventricle with overriding of the aorta (without compromise to right ventricular outflow). The earliest age at which additional fibrous obstruction was seen was 9 months. The aortic valve circumference was small in 18% of specimens.
The median (range) duration of follow up in survivors from the clinical study was 6.6 (1 to 25.7) years. 16 patients with deviated musculature (49%) and 16 with short segment fibromuscular stenosis (50%) underwent operation for subaortic stenosis. Patients with deviated structures were younger at operation than those with short segment stenosis (P < 0.005). Patients with posterior deviation or extension of structures into the left ventricular outflow tract underwent operation for subaortic stenosis more frequently (P < 0.05) than those with anterior deviation of the outlet septum and aortic override. The ventricular septal defect required surgical closure more frequently (P < 0.005) in patients with deviation (93.9%) than in those with short segment obstruction (21.9%). There was no significant difference in the mortality between patients with deviation (27%) and those with short segment obstruction (12%).
32% of patients in the clinical study with subaortic stenosis had a ventricular septal defect. Only 51% of these had obstructive and deviated muscular structures in the left ventricular outflow tract. These patients had a significantly higher incidence of aortic arch obstruction and required surgery for subaortic stenosis at a younger age than those with short segment obstruction. The ventricular septal defect also required surgical closure more frequently in those patients with deviation. The morphological study defined the two sites of obstruction. The presence or absence and type of deviation should be clearly defined in all patients with a ventricular septal defect,
比较室间隔缺损合并主动脉瓣下狭窄的发病率及预后,并明确主动脉瓣下狭窄的形态学基础。
回顾了1960年1月1日至1991年12月31日在皇家利物浦儿童医院就诊的202例主动脉瓣下狭窄患者的临床表现及随访数据。对存活者进行追踪以评估其目前的临床状况。还检查了291例与主动脉瓣下狭窄相关病变患者的尸检标本。
在临床研究中;202例主动脉瓣下狭窄患者中有65例(32.1%)合并室间隔缺损(不包括房室间隔缺损)。其中32例患者为短段(纤维肌性)主动脉瓣下狭窄。33例患者的主动脉瓣下狭窄是由流出道肌肉成分移位所致。在17例患者(51.5%)中,这是由于结构向后移位或延伸至左心室流出道,导致室间隔缺损上方梗阻。在另外16例患者(48.5%)中,主动脉骑跨且心室动脉连接一致(不影响右心室流出道),导致室间隔缺损下方的主动脉瓣下狭窄。39%结构移位的患者出现了额外的纤维性梗阻。结构移位的患者发病年龄更低(P<0.01)(中位数(范围)0.4(0至9.2)个月),低于短段梗阻患者(中位数(范围)4.2(0至84.9)个月)。结构移位患者的主动脉弓梗阻发生率高于短段梗阻患者(P<0.002)(38%)。在形态学研究中,35个病理标本显示左心室流出道在室间隔缺损上方或下方存在梗阻性肌肉结构。16例存在出口间隔向后移位或右心室漏斗褶延伸,或两者同时存在并延伸至左心室。19例存在出口间隔向前移位至右心室且主动脉骑跨(不影响右心室流出道)。最早在9个月时发现额外的纤维性梗阻。18%的标本中主动脉瓣环周长较小。
临床研究中存活者的随访时间中位数(范围)为6.6(1至25.7)年。16例肌肉结构移位患者(49%)和16例短段纤维肌性狭窄患者(50%)接受了主动脉瓣下狭窄手术。结构移位的患者手术时年龄比短段狭窄患者小(P<0.005)。结构向后移位或延伸至左心室流出道的患者比出口间隔向前移位且主动脉骑跨的患者更频繁地接受主动脉瓣下狭窄手术(P<0.05)。结构移位的患者中室间隔缺损更频繁地需要手术闭合(P<0.005)(93.9%),高于短段梗阻患者(21.9%)。结构移位患者(27%)和短段梗阻患者(12%)的死亡率无显著差异。
临床研究中32%的主动脉瓣下狭窄患者合并室间隔缺损。其中只有51%的患者左心室流出道存在梗阻性和移位的肌肉结构。这些患者的主动脉弓梗阻发生率显著更高,且比短段梗阻患者更年轻就需要接受主动脉瓣下狭窄手术。室间隔缺损在结构移位的患者中也更频繁地需要手术闭合。形态学研究明确了两个梗阻部位。所有室间隔缺损患者都应明确是否存在移位及其类型。