Department of Pediatric Cardiac Surgery, Sakakibara Heart Institute, 3-16-1 Asahi-cho, Fuchu-shi, Tokyo 183-0003, Japan.
Ann Thorac Surg. 2010 Aug;90(2):614-21. doi: 10.1016/j.athoracsur.2010.03.098.
An additional malformation of the atrioventricular valve is occasionally encountered in patients with complete atrioventricular septal defect, and this may compromise accurate correction.
We reviewed 138 patients undergoing complete repair with two-patch technique between 1992 and 2008. The mean age was 7.1 + or - 8.3 months, and the mean body weight was 5.1 + or - 2.1 kg. Preceding pulmonary arterial banding was performed in 23 patients.
The operative record delineated additional malformations of the atrioventricular valve that posed difficulty in positioning the ventricular septal patch and in accurately approximating the cleft in 45 patients. Of them, four types (n = 40) were associated with increased incidence of postoperative left valvular problems (moderate or worse regurgitation or stenosis). These included abnormalities of the papillary muscles that accompanied hypoplastic mural leaflet or incomplete opening of one commissure in (n = 15; p = 0.0054), dense insertion of the chords of the superior leaflet that obscured the right side of the ventricle septal crest in (n = 13; p = 0.0004), double orifice valve (n = 7; p = 0.0225), and severe length disparities of the cleft that resulted from either disproportional size of superior against inferior leaflets or redundant chord supporting the left extremity of one of these leaflets (n = 5; p < 0.0001). Neither greater age at operation (more than 6 months) nor preceding pulmonary arterial band reduced the incidence of left valvular problems in the malformation group.
An individualized technique is required to maintain coaptation of the atrioventricular valve, but in many cases, they are not completely correctable. Deferring complete repair by placing a pulmonary arterial band did not reduce left valvular problems.
在完全性房室间隔缺损患者中,偶尔会遇到房室瓣的额外畸形,这可能会影响准确的矫正。
我们回顾了 1992 年至 2008 年间接受双补丁技术完全修复的 138 例患者。平均年龄为 7.1±8.3 个月,平均体重为 5.1±2.1kg。23 例患者术前进行了肺动脉带环术。
手术记录描绘了房室瓣的额外畸形,这给安置室间隔补片和准确接近裂隙带来了困难,在 45 例患者中发现了这些畸形。其中,有四种类型(n=40)与术后左瓣问题(中度或更严重的反流或狭窄)发生率增加有关。这些异常包括乳头肌异常,伴有壁瓣发育不良或一个连合不完全开放(n=15;p=0.0054),上瓣的腱索密集插入,遮挡了室间隔嵴的右侧(n=13;p=0.0004),双瓣口(n=7;p=0.0225),以及由于上、下瓣不成比例的大小或支撑这些瓣叶之一的左叶的多余腱索导致的裂隙严重长度差异(n=5;p<0.0001)。手术时年龄较大(超过 6 个月)或术前肺动脉带环术并不能降低畸形组的左瓣问题发生率。
需要一种个体化的技术来维持房室瓣的对合,但在许多情况下,它们并不能完全矫正。通过放置肺动脉带环来延迟完全修复并没有减少左瓣问题。