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新生儿重度主动脉瓣下狭窄、室间隔缺损及主动脉弓梗阻的治疗

The management of severe subaortic stenosis, ventricular septal defect, and aortic arch obstruction in the neonate.

作者信息

Bove E L, Minich L L, Pridjian A K, Lupinetti F M, Snider A R, Dick M, Beekman R H

机构信息

Department of Surgery, University of Michigan School of Medicine, Ann Arbor.

出版信息

J Thorac Cardiovasc Surg. 1993 Feb;105(2):289-95; discussion 295-6.

PMID:8429657
Abstract

Neonates with ventricular septal defect and aortic arch obstruction frequently have subaortic stenosis resulting from posterior deviation of the infundibular septum. Because the aortic anulus is often hypoplastic, making direct resection of the infundibular septum through the standard transaortic approach difficult, the optimal method of repair is uncertain. From September 1989 through November 1991, seven patients with ventricular septal defect, coarctation (n = 4), or interrupted aortic arch (n = 3) and severe subaortic stenosis underwent repair with use of a technique that included transatrial resection of the infundibular septum. Their ages ranged from 5 to 63 days (median 15 days) and weights from 1.3 to 5.4 kg (mean 3.1 kg). Only one patient was older than 1 month. The systolic and diastolic ratios of the diameter of the left ventricular outflow tract to that of the descending aorta were 0.53 +/- 0.09 mm (standard deviation) and 0.73 +/- 0.11, respectively. At operation, the posteriorly displaced infundibular septum was partially removed through a right atrial approach by resecting the superior margin of the ventricular septal defect up to the aortic anulus. The resulting enlarged ventricular septal defect was then closed with a patch to widen the subaortic area. In each patient the aortic arch was repaired by direct anastomosis. All patients survived operation; there was one late death from noncardiac causes 3 months after repair. The survivors remain well from 3 to 14 months after repair (mean 8 months). All are in sinus rhythm and none has a residual ventricular septal defect. One patient underwent successful balloon dilation of a residual aortic arch gradient late after repair. No patient has significant residual subaortic stenosis, although one has valvular aortic stenosis. This series suggests that in neonates with ventricular septal defect and severe subaortic stenosis resulting from posterior deviation of the infundibular septum, direct relief can be satisfactorily accomplished from a right atrial approach. This method provides effective widening of the left ventricular outflow tract and is superior to palliative techniques or conduit procedures.

摘要

患有室间隔缺损和主动脉弓梗阻的新生儿常因漏斗间隔向后移位而出现主动脉瓣下狭窄。由于主动脉瓣环常发育不全,使得通过标准经主动脉途径直接切除漏斗间隔变得困难,因此最佳的修复方法尚不确定。从1989年9月至1991年11月,7例患有室间隔缺损、主动脉缩窄(n = 4)或主动脉弓中断(n = 3)且伴有严重主动脉瓣下狭窄的患者接受了一种包括经心房切除漏斗间隔的技术修复。他们的年龄在5至63天之间(中位数15天),体重在1.3至5.4千克之间(平均3.1千克)。只有1例患者年龄超过1个月。左心室流出道直径与降主动脉直径的收缩期和舒张期比值分别为0.53±0.09毫米(标准差)和0.73±0.11。手术时,通过右心房途径,切除室间隔缺损的上缘直至主动脉瓣环,部分切除向后移位的漏斗间隔。然后用补片封闭由此扩大的室间隔缺损,以加宽主动脉瓣下区域。在每例患者中,主动脉弓通过直接吻合进行修复。所有患者均手术存活;1例在修复后3个月因非心脏原因晚期死亡。幸存者在修复后3至14个月(平均8个月)情况良好。所有患者均为窦性心律,且无残余室间隔缺损。1例患者在修复后晚期成功进行了球囊扩张以降低残余主动脉弓压差。尽管有1例患者存在瓣膜性主动脉狭窄,但无患者有明显的残余主动脉瓣下狭窄。该系列研究表明,对于因漏斗间隔向后移位导致室间隔缺损和严重主动脉瓣下狭窄的新生儿,经右心房途径可令人满意地直接解除梗阻。该方法可有效加宽左心室流出道,优于姑息性技术或管道手术。

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