Ng R, Somerville J, Ross D
Eur J Cardiol. 1979 Jan;9(1):39-52.
Between 1969 and 1976, 10 severely disabled patients with Ebstein's anomaly were operated on at the National Heart Hospital using replacement of the tricuspid valve with mounted aortic homografts [9] or dura mater valve [1], plication of the atrialized right ventricle [10], and closure of an associated interatrail communication. 7 survivors have been followed up from 2 to 9 yr. 5 are asymptomatic. Symptomatic tricuspid regurgitation developed in 2 patients; from a paravalvar leak of the tricuspid homograft in one, and in the other calcification with stenosis in an irradiated homograft, 2.5 and 7.5 yr later. Permanent pacemakers were needed in 2 patients, 3 wk and 18 mth after surgery for symptomatic heart block. Despite corrective surgery for the structural abnormalities in Ebstein, late results remain influenced by disorders of rhythm and conduction disturbances, degenerative changes in the valves used for replacement and the intrinsic primary myocardial disease. Such "corrective" procedures in patients with Ebstein's anomaly can result in maintained symptomatic improvement but must be regarded as palliative surgery.
1969年至1976年间,国立心脏医院对10例患有埃布斯坦畸形的严重残疾患者进行了手术,采用带瓣主动脉同种异体移植物[9]或硬脑膜瓣膜[1]置换三尖瓣,对房化右心室进行折叠术[10],并闭合相关的房间隔交通。7名幸存者接受了2至9年的随访。5人无症状。2例患者出现有症状的三尖瓣反流;一例是由于三尖瓣同种异体移植物瓣周漏,另一例是在照射后的同种异体移植物中出现钙化并伴有狭窄,分别在术后2.5年和7.5年出现。2例患者因有症状的心脏传导阻滞在术后3周和18个月需要植入永久性起搏器。尽管对埃布斯坦畸形的结构异常进行了矫正手术,但晚期结果仍受节律紊乱、传导障碍、用于置换的瓣膜退行性改变以及原发性心肌疾病的影响。埃布斯坦畸形患者的此类“矫正”手术可使症状持续改善,但必须视为姑息性手术。