Department of Pediatric Cardiac Surgery, University Paris Descartes and Necker Sick Children Hospital, Paris, France.
Eur J Cardiothorac Surg. 2012 Feb;41(2):248-55. doi: 10.1016/j.ejcts.2011.03.063. Epub 2011 Dec 12.
Long-term evaluation of the impact of bicuspid pulmonary valve on neoaortic valve regurgitation and aortic root dilatation (ARD) after arterial switch operation (ASO) for transposition of the great arteries (TGA).
Between January 1987 and March 2010, 980 neonates underwent ASO for TGA. A total of 40 patients (4.0%) had a pulmonary bicuspid valve with no significant left ventricular outflow tract obstruction. In this group, 11 patients (28%) had associated ventricular septal defect, three hypoplastic aortic arch, and three had a right ventricular hypoplasia. No pulmonary valvuloplasty was attempted. Mean follow-up was 7.7 ± 5.5 years. Echocardiography evaluations of neoaortic valve function and morphology and aortic root dimensions were performed.
There were two hospital deaths (5%) related to hypoplastic right ventricle and left ventricular dysfunction, and no late death yielding an actuarial survival to 95% SD at 1, 5, and 10 years. At last follow-up, five patients (12%) had mild-to-moderate aortic regurgitation (AR). None had aortic valve stenosis. ARD was noted in 28% of the patients (Z-score up to +3). One patient needed a Bentall procedure for significant AR and severe dilatation of the ascending aorta at 11 years of age. As many as four patients underwent reoperation (10%) for stenosis of the left coronary artery. Freedom from reoperation was 95% SD, 88% SD, and 75% SD at 1,5, and 10 years, respectively.
ASO is a safe option for TGA associated with a well-functioning bicuspid pulmonary valve with low morbidity and mortality. Prevalence of AR was not particularly high. Even though ARD was frequent, neoaortic bicuspid valve did not represent a high risk for aortic reoperation. Long-term individual follow-up is mandatory to observe the potential risk of root dilatation and AR.
长期评估二叶式肺动脉瓣对大动脉转位(TGA)患者动脉调转术后新发主动脉瓣反流(AR)和升主动脉扩张(ARD)的影响。
1987 年 1 月至 2010 年 3 月期间,共有 980 例新生儿接受了 TGA 的动脉调转术。共有 40 例(4.0%)患者存在二叶式肺动脉瓣,且无明显左心室流出道梗阻。在这组患者中,11 例(28%)合并室间隔缺损,3 例合并主动脉弓发育不良,3 例合并右心室发育不良。未行肺动脉瓣成形术。平均随访时间为 7.7±5.5 年。对新发主动脉瓣功能和形态以及主动脉根部大小进行超声心动图评估。
2 例(5%)患儿因右心室发育不良和左心室功能障碍导致院内死亡,无晚期死亡,1、5、10 年的生存率估计值分别为 95%±标准差。最后一次随访时,5 例(12%)患者存在轻至中度 AR。无一例患者存在主动脉瓣狭窄。28%的患者出现了 ARD(Z 值高达+3)。1 例患者在 11 岁时因严重 AR 和升主动脉严重扩张而接受了 Bentall 手术。多达 4 例患者(10%)因左冠状动脉狭窄而接受了再次手术。1、5、10 年的无再次手术生存率分别为 95%±标准差、88%±标准差和 75%±标准差。
对于 TGA 患者,动脉调转术是一种安全的选择,合并功能良好的二叶式肺动脉瓣时,其发病率和死亡率均较低。AR 的发生率并不特别高。尽管 ARD 较为常见,但新发的二叶式主动脉瓣并不会对主动脉再次手术造成较高风险。需要进行个体化的长期随访,以观察根部扩张和 AR 的潜在风险。