Ullmann Michael V, Born Sabine, Sebening Christian, Gorenflo Matthias, Ulmer Herbert E, Hagl Siegfried
Department of Cardiac Surgery, University of Heidelberg, Heidelberg, Germany.
Ann Thorac Surg. 2004 Sep;78(3):918-24; discussion 924-5. doi: 10.1016/j.athoracsur.2004.02.134.
We report results of a technique of Ebstein's anomaly repair by creating a predominantly monocuspid valve with simultaneous ventricularization of the atrialized right ventricular (aRV) chamber.
Between March 1993 and April 2003, Ebstein's anomaly repair by valvuloplasty with combined ventricularization was performed in 23 patients aged 13.6 (4.1-52.6) years presenting with tricuspid valve regurgitation (TVR) (I degrees, n = 1; II degrees, n = 3; III degrees, n = 13; IV degrees, n = 6). Valvuloplasty consisted of creating a predominantly monocuspid valve at the level of the anatomical atrioventricular junction resulting in a ventricularization of the atrialized chamber. Postoperatively all survivors were examined regularly with an actual prospective evaluation.
One early death (4.4%) occurred and was caused by right heart failure. Follow-up was 4.6 (0.5-10.9) years. Important recurrent atrioventricular valve regurgitation caused by rupture of fixation sutures occurred in 3 patients (13%), necessitating reintervention at 3 (0.03-4) months (revalvuloplasty, n = 2; TV replacement, n = 1). One patient presenting with hypoplastic right ventricle with consecutive right heart failure underwent creation of a total cavopulmonary connection at 10 months. At present all patients are doing well. Actual echocardiographic examination revealed significant improvement of right atrioventricular valve regurgitation (p < 0.0001) and favorable restoration of RV geometry and function.
This technique of Ebstein's anomaly repair with ventricularization of the atrialized chamber provides excellent results regarding right atrioventricular valve function and leads to a favorable restoration of RV geometry and function.
我们报告了一种通过创建主要为单尖瓣并同时使房化右心室(aRV)腔心室化来修复埃布斯坦畸形的技术的结果。
1993年3月至2003年4月期间,对23例年龄为13.6(4.1 - 52.6)岁、患有三尖瓣反流(TVR)(I度,n = 1;II度,n = 3;III度,n = 13;IV度,n = 6)的患者进行了瓣膜成形术联合心室化修复埃布斯坦畸形。瓣膜成形术包括在解剖房室交界处创建一个主要为单尖瓣,从而使房化腔心室化。术后所有幸存者均接受定期实际前瞻性评估。
发生1例早期死亡(4.4%),原因是右心衰竭。随访时间为4.6(0.5 - 10.9)年。3例患者(13%)出现因固定缝线断裂导致的重要复发性房室瓣反流,需要在3(0.03 - 4)个月时再次干预(再次瓣膜成形术,n = 2;TV置换,n = 1)。1例右心室发育不全并伴有连续性右心衰竭的患者在10个月时进行了全腔静脉 - 肺动脉连接术。目前所有患者情况良好。实际超声心动图检查显示右房室瓣反流有显著改善(p < 0.0001),且右心室几何形状和功能得到良好恢复。
这种使房化腔心室化的埃布斯坦畸形修复技术在右房室瓣功能方面提供了优异的结果,并导致右心室几何形状和功能的良好恢复。