Koh Masahiro, Yagihara Toshikatsu, Uemura Hideki, Kagisaki Koji, Hagino Ikuo, Ishizaka Toru, Kitamura Soichiro
Department of Cardiovascular Surgery, National Cardiovascular Center, Osaka, Japan.
Ann Thorac Surg. 2006 May;81(5):1808-16; discussion 1816. doi: 10.1016/j.athoracsur.2005.12.008.
Biventricular repair is often difficult to accomplish in patients with right atrial isomerism because of complex anomalous structures.
Ten patients with right atrial isomerism underwent biventricular repair. Their ages ranged from 15 months to 21 years. The follow-up period ranged from 1 month to 21 years. The Fontan procedure was unsuitable in 7 patients. The atrioventricular valves were separated in 5 patients and common in 5. One patient who had severe right-sided atrioventricular valvular regurgitation required concomitant prosthetic valve replacement. Another patient with a hypoplastic intraventricular septum underwent ventricular septation. Nine patients had two balanced ventricles. A ventricular septal defect was enlarged for rerouting in 3 patients. All patients had anomalous venoatrial connections and required intra-atrial baffle rerouting. One with major aortopulmonary collateral arteries underwent staged unifocalization. Three had extracardiac conduit repair. The outcomes were compared with 97 patients who underwent the Fontan procedure.
There were 3 early deaths and 1 late death. Six survivors are in New York Heart Association functional class I or II. Two are free from medications. Two required reoperation owing to infection or prosthetic valve failure. At 1 year, cardiac index and systemic venous pressure were 3.2 +/- 0.9 L.min(-1).m(-2) and 6.6 +/- 1.6 mm Hg, respectively. There were no significant differences in survival, freedom from arrhythmia, freedom from reoperation, or exercise tolerance between biventricular repair and the Fontan procedure.
Biventricular repair provided good long-term outcomes in patients with right atrial isomerism. In selected circumstances, biventricular repair is an acceptable alternative to the Fontan procedure.
由于存在复杂的异常结构,右心房异构患者通常难以完成双心室修复。
10例右心房异构患者接受了双心室修复。他们的年龄从15个月至21岁不等。随访时间从1个月至21年不等。7例患者不适合采用Fontan手术。5例患者的房室瓣分离,5例患者的房室瓣共用。1例患有严重右侧房室瓣反流的患者需要同时进行人工瓣膜置换。另1例室间隔发育不全的患者接受了室间隔分隔术。9例患者有两个平衡的心室。3例患者扩大室间隔缺损以进行改道。所有患者均有异常的腔静脉心房连接,需要进行心房内挡板改道。1例有主要的体肺侧支动脉的患者接受了分期单灶化治疗。3例患者进行了心外管道修复。将结果与97例接受Fontan手术的患者进行比较。
有3例早期死亡和1例晚期死亡。6名幸存者的纽约心脏协会心功能分级为I级或II级。2名患者无需用药。2名患者因感染或人工瓣膜故障需要再次手术。1年时,心脏指数和体静脉压分别为3.2±0.9L·min⁻¹·m⁻²和6.6±1.6mmHg。双心室修复与Fontan手术在生存率、无心律失常、无再次手术或运动耐量方面无显著差异。
双心室修复为右心房异构患者提供了良好的长期预后。在特定情况下,双心室修复是Fontan手术的可接受替代方案。