Reddy V M, Rajasinghe H A, Teitel D F, Haas G S, Hanley F L
Division of Cardiothoracic Surgery, University of California San Francisco, USA.
J Thorac Cardiovasc Surg. 1996 Jan;111(1):158-65; discussion 165-7. doi: 10.1016/S0022-5223(96)70412-9.
For patients with complex left ventricular outflow tract obstruction, including hypoplastic aortic anulus with or without severe diffuse subaortic stenosis, various aortoventriculoplasty procedures (e.g., Konno procedure and its modifications; extended aortic allograft root replacement) are important management options. In younger patients, however, reoperation for valve replacement is inevitably required, and anticoagulation issues pose additional problems. The pulmonary autograft provides a promising option for aortic valve replacement as part of the aortoventriculoplasty procedure in children. Long-term follow up shows that the pulmonary autograft functions well as the systemic arterial (neoaortic) valve and that valve growth occurs.
Between July 1993 and May 1995, 11 patients 4 days to 17 years old (median 12 months) underwent aortoventriculoplasty with pulmonary autograft (Ross-Konno procedure). The diagnoses were aortic stenosis with or without subaortic stenosis (n = 8), Shone complex (n = 2), and interrupted aortic arch with subaortic stenosis (n = 1). On average, 1.9 previous interventions had been performed per patient, including a previous Konno procedure in one patient. The aortic root was replaced with a pulmonary autograft valve. The left ventricular outflow tract was enlarged with a Dacron polyester fabric patch in two patients, with an allograft aortic patch in two patients and a right ventricular infundibular free wall muscular extension harvested in continuity with the autograft in seven patients.
Intraoperative transesophageal echocardiographic assessment revealed mild aortic insufficiency in one patient. One patient had a residual left ventricular outflow tract gradient of 15 mm Hg. Significant complications were cardiac tamponade from bleeding (n = 1) and complete heart block necessitating a permanent pacemaker (n = 1). Follow-up ranged from 2 weeks to 16 months. To date, there have been no late deaths or reoperations. Follow-up echocardiography revealed mild autograft insufficiency in one patient and a 16 mm Hg residual left ventricular outflow tract gradient in one patient.
Initial experience suggests that aortoventriculoplasty with the pulmonary autograft is an excellent alternative for young patients with complex left ventricular outflow tract obstruction. Because the pulmonary autograft has been shown to grow after implantation, reoperation on the left ventricular outflow tract is likely to be avoided.
对于患有复杂左心室流出道梗阻的患者,包括伴有或不伴有严重弥漫性主动脉瓣下狭窄的主动脉瓣环发育不全,各种主动脉心室成形术(例如,Konno手术及其改良术式;扩大的主动脉同种异体移植根部置换术)是重要的治疗选择。然而,对于较年轻的患者,不可避免地需要再次进行瓣膜置换手术,并且抗凝问题带来了额外的难题。自体肺动脉瓣移植为儿童主动脉瓣置换作为主动脉心室成形术的一部分提供了一个有前景的选择。长期随访表明,自体肺动脉瓣作为体循环动脉(新主动脉)瓣功能良好,并且瓣膜会生长。
在1993年7月至1995年5月期间,11例年龄在4天至17岁(中位数为12个月)的患者接受了自体肺动脉瓣主动脉心室成形术(Ross-Konno手术)。诊断包括伴有或不伴有主动脉瓣下狭窄的主动脉狭窄(n = 8)、Shone综合征(n = 2)以及伴有主动脉瓣下狭窄的主动脉弓中断(n = 1)。每位患者平均先前接受过1.9次干预措施,其中1例患者先前接受过Konno手术。用自体肺动脉瓣置换主动脉根部。2例患者用涤纶补片扩大左心室流出道,2例患者用同种异体主动脉补片,7例患者在切取自体肺动脉瓣时连续切取右心室漏斗部游离壁肌肉进行延伸以扩大左心室流出道。
术中经食管超声心动图评估显示1例患者有轻度主动脉瓣关闭不全。1例患者左心室流出道残余压差为15 mmHg。严重并发症包括出血导致的心包填塞(n = 1)和需要永久起搏器的完全性心脏传导阻滞(n = 1)。随访时间为2周至16个月。迄今为止,尚无晚期死亡或再次手术情况。随访超声心动图显示1例患者有轻度自体肺动脉瓣关闭不全,1例患者左心室流出道残余压差为16 mmHg。
初步经验表明,自体肺动脉瓣主动脉心室成形术是患有复杂左心室流出道梗阻的年轻患者的一种极佳替代方案。由于已证明自体肺动脉瓣在植入后会生长,因此可能避免对左心室流出道进行再次手术。