Quinonez Luis G, Dearani Joseph A, Puga Francisco J, O'Leary Patrick W, Driscoll David J, Connolly Heidi M, Danielson Gordon K
Division of Cardiovascular Surgery, Mayo Clinic and Foundation, Rochester, Minn 55905, USA.
J Thorac Cardiovasc Surg. 2007 May;133(5):1303-10. doi: 10.1016/j.jtcvs.2006.12.007. Epub 2007 Mar 26.
Repair of Ebstein anomaly and impaired right ventricular function pose challenges for the cardiac surgeon. The bidirectional cavopulmonary shunt may improve early outcomes. We reviewed our experience with the 1.5-ventricle repair in this patient population.
Between July 1999 and March 2006, 169 patients underwent operations to repair Ebstein anomaly. Fourteen patients had a bidirectional cavopulmonary shunt constructed. The median age at operation was 6 years (17 months-57.8 years). All of the patients had severe Ebstein anomaly with dilated right-sided chambers and/or right ventricular dysfunction. The mean left ventricular ejection fraction was 54.5% (range 35%-72%). Three patients were initially referred for heart transplantation, and the bidirectional cavopulmonary shunt allowed a conventional repair.
Procedures included bidirectional cavopulmonary shunting (14), tricuspid valve replacement (11), tricuspid valve repair (2), and right ventricular resection (3). Shunting was planned preoperatively in 9 patients; the indication in 5 other patients was hemodynamic instability after separation from cardiopulmonary bypass. One patient died of multiple organ failure. Median follow-up in 10 patients was 18 months (3 months-6.5 years). The preoperative left ventricular ejection fraction of less than 50% improved in 3 patients to greater than 50% postoperatively.
The 1.5-ventricle repair can be utilized in patients with severe Ebstein anomaly and impaired right ventricular function who are at high risk for surgical treatment. We believe the bidirectional cavopulmonary shunt may be considered as a planned procedure, as an intraoperative salvage maneuver, or as an alternative to cardiac transplantation in selected patients.
修复埃布斯坦畸形及改善受损的右心室功能对心脏外科医生而言颇具挑战。双向腔肺分流术可能改善早期预后。我们回顾了在这一患者群体中进行1.5心室修复术的经验。
1999年7月至2006年3月期间,169例患者接受了埃布斯坦畸形修复手术。14例患者进行了双向腔肺分流术构建。手术时的中位年龄为6岁(17个月至57.8岁)。所有患者均患有严重的埃布斯坦畸形,伴有右侧心腔扩张和/或右心室功能障碍。左心室平均射血分数为54.5%(范围35% - 72%)。3例患者最初被转诊进行心脏移植,而双向腔肺分流术使得能够进行传统修复。
手术包括双向腔肺分流术(14例)、三尖瓣置换术(11例)、三尖瓣修复术(2例)和右心室切除术(3例)。9例患者术前计划进行分流术;另外5例患者的分流指征是体外循环脱离后血流动力学不稳定。1例患者死于多器官功能衰竭。10例患者的中位随访时间为18个月(3个月至6.5年)。3例术前左心室射血分数低于50%的患者术后提高到了50%以上。
1.5心室修复术可用于手术治疗风险高的严重埃布斯坦畸形及右心室功能受损的患者。我们认为双向腔肺分流术可被视为一种计划性手术、术中挽救措施或特定患者心脏移植的替代方法。