McFaul R C, Davis Z, Giuliani E R, Ritter D G, Danielson G K
J Thorac Cardiovasc Surg. 1976 Dec;72(6):910-5.
At the Mayo Clinic, 13 patients with Ebstein's malformation have undergone surgical repair since 1963. Their ages ranged from 18 months to 51 years (median 13 years). Ten patients were in Functional Class III or IV. Marked cardiomegaly, cyanosis, paradoxic emboli, and dysrhythmias secondary to Wolff-Parkinson-White syndrome were indications for operation in the remaining 3 patients. A wide range of anatomic variations was encountered. All 5 patients who underwent tricuspid annuloplasty with plication of the atrialized segment of the right ventricle survived operation. Of 5 patients who underwent prosthetic valve replacement, only one survived. Other procedures included atrial septal defect closure alone in one patient, atrial septal defect closure and relief of pulmonary stenosis in one patient, and tricuspid annuloplasty alone in one patient. One patient had concomitant mapping and division of anomalous conduction pathways. Functional classification improved in 8 of 10 operative survivors. There were two late sudden deaths; both patients had had preoperative dysrhythmias. The data suggest that results are improved when the atrialized segment of the right ventricle is dealt with during repair of the tricuspid valve. A combined ventricular plication and tricuspid annuloplasty yielded better early and late results than did valve replacement.
自1963年以来,梅奥诊所已有13例埃布斯坦畸形患者接受了手术修复。他们的年龄从18个月到51岁不等(中位数为13岁)。10例患者属于心功能Ⅲ级或Ⅳ级。其余3例患者因明显的心脏扩大、发绀、反常栓塞以及 Wolff-Parkinson-White 综合征继发的心律失常而接受手术。术中发现了广泛的解剖变异。接受右心室房化段折叠三尖瓣环成形术的5例患者均存活。接受人工瓣膜置换的5例患者中,仅1例存活。其他手术包括1例单纯房间隔缺损修补术、1例房间隔缺损修补术加肺动脉狭窄解除术以及1例单纯三尖瓣环成形术。1例患者同时进行了异常传导通路标测和分离。10例手术存活者中有8例心功能分级得到改善。有2例晚期猝死;这2例患者术前均有心律失常。数据表明,在三尖瓣修复术中处理右心室房化段时,手术效果会得到改善。与瓣膜置换相比,心室折叠联合三尖瓣环成形术在早期和晚期均产生了更好的效果。