Tchervenkov C I, Tahta S A, Jutras L C, Béland M J
Division of Cardiovascular Surgery, The Montreal Children's Hospital, McGill University, Quebec, Canada.
Ann Thorac Surg. 1998 Oct;66(4):1350-7. doi: 10.1016/s0003-4975(98)00803-0.
Multiple obstructions in the left heart-aorta complex have been associated with poor survival. No consensus exists as to whether these patients will have a favorable outcome with biventricular repair where most advocate a univentricular approach.
Since late 1988, all 11 neonates seen with hypoplastic left heart complex, which includes aortic arch obstruction, underwent biventricular repair. All patients had antegrade aortic flow and no intrinsic aortic or mitral stenosis. Elimination of the extracardiac afterload was achieved by extensive ascending aorta and aortic arch reconstruction with a pulmonary homograft patch. All intracardiac shunts were eliminated to fully preload the left heart. The median age at first operation was 7 days and the mean weight, 3.59+/-0.49 kg. The echocardiographic variables used to evaluate the left heart-aorta complex were reviewed, and the preoperative and postoperative measurements were compared.
There were two early deaths. Four patients had six reoperations for left ventricular outflow tract obstruction, 2 of whom have required prosthetic valve replacement (1, aortic and mitral; 1, aortic), and 2 patients had three reoperations for recurrent coarctation. There was one late death at 3 years from pulmonary hypertension. Mean follow-up was 44+/-35 months. The 8 current survivors are all in New York Heart Association class I or II. The actuarial survival rate at 8 years is 63%, and the freedom from reoperation at 3 years is 25%.
We have successfully achieved biventricular repair in most of the patients with hypoplastic left heart complex, a subset of patients with hypoplastic left heart syndrome. Some growth of the left ventricular structures was already observed at the time of hospital discharge. However, reoperation, particularly for left ventricular outflow tract obstruction, appears likely. Increasing experience will more accurately define predictive criteria for the feasibility of biventricular repair.
左心-主动脉复合体的多处梗阻与生存率低相关。对于这些患者采用双心室修复是否会有良好预后尚无共识,大多数人主张采用单心室修复方法。
自1988年末起,所有11例患有左心发育不全综合征(包括主动脉弓梗阻)的新生儿均接受了双心室修复。所有患者均有顺行性主动脉血流,且无先天性主动脉或二尖瓣狭窄。通过使用肺动脉同种异体移植补片进行广泛的升主动脉和主动脉弓重建来消除心外后负荷。消除所有心内分流以充分预充左心。首次手术时的中位年龄为7天,平均体重为3.59±0.49千克。回顾了用于评估左心-主动脉复合体的超声心动图变量,并比较了术前和术后测量值。
有2例早期死亡。4例患者因左心室流出道梗阻接受了6次再次手术,其中2例需要进行人工瓣膜置换(1例为主动脉瓣和二尖瓣置换;1例为主动脉瓣置换),2例患者因复发性缩窄接受了3次再次手术。有1例患者在3岁时因肺动脉高压晚期死亡。平均随访时间为44±35个月。目前的8名幸存者均为纽约心脏协会心功能I级或II级。8年时的精算生存率为63%,3年时无需再次手术的比例为25%。
我们已成功地为大多数左心发育不全综合征患者(左心发育不全复合体患者的一个子集)实施了双心室修复。出院时已观察到左心室结构有一定生长。然而,再次手术似乎难以避免,尤其是针对左心室流出道梗阻。经验的增加将更准确地界定双心室修复可行性的预测标准。