Tchervenkov C I, Tahta S A, Jutras L, Béland M J
Divisions of Cardiovascular Surgery and Cardiology, The Montreal Children's Hospital, McGill University, Montreal, Quebec, Canada.
J Thorac Cardiovasc Surg. 1998 Dec;116(6):897-904. doi: 10.1016/S0022-5223(98)70039-X.
Intracardiac malformations associated with coarctation and aortic arch hypoplasia have traditionally been repaired in 2 stages, with a high mortality rate. We review our experience with single-stage biventricular repair of intracardiac defects associated with aortic arch hypoplasia by means of pulmonary homograft patch aortoplasty.
Between October 1988 and October 1997, 39 of 40 consecutive patients underwent single-stage biventricular repair for aortic arch obstruction and associated intracardiac defects. The median age at operation was 17 days and the mean weight was 3.71 +/- 1.09 kg. Nineteen patients had either dextrotransposition of the great arteries or the Taussig-Bing anomaly. Sixteen patients had multiple left-sided obstructive lesions (2 cases of critical aortic stenosis, 3 of subaortic stenosis and ventricular septal defect, and 11 of hypoplastic left heart complex). One patient had an associated complete atrioventricular septal defect. Four patients had only an associated ventricular septal defect. Through a median sternotomy, the hypoplastic aortic arch was enlarged with a pulmonary homograft patch in 36 patients. In 4 patients an extended end-to-end anastomosis was performed.
There were 2 early deaths (5%) and 2 late deaths (5%). One late death was not cardiac related. The mean follow-up time was 36 months (range 1 month-9 years). The recoarctation rate after pulmonary homograft patch aortoplasty was 8. 3%, but after exclusion of those patients with associated left-sided obstructive lesions this decreased to 0%. No aneurysm formation in the aorta has occurred. The actuarial survival at 8 years is 89% +/- 10%.
Single-stage biventricular repair of aortic arch obstruction and associated intracardiac defects can achieve excellent survival. We recommend pulmonary homograft patch aortoplasty because it achieves complete relief of anatomic afterload with a tension-free anastomosis and low incidence of recoarctation.
与缩窄和主动脉弓发育不全相关的心内畸形传统上采用两阶段修复,死亡率较高。我们回顾了通过同种异体肺动脉补片主动脉成形术对与主动脉弓发育不全相关的心内缺损进行单阶段双心室修复的经验。
1988年10月至1997年10月,连续40例患者中的39例接受了针对主动脉弓梗阻及相关心内缺损的单阶段双心室修复。手术时的中位年龄为17天,平均体重为3.71±1.09千克。19例患者患有大动脉右位转位或陶西格-宾氏畸形。16例患者有多个左侧梗阻性病变(2例为严重主动脉狭窄,3例为主动脉下狭窄合并室间隔缺损,11例为左心发育不全综合征)。1例患者合并完全性房室间隔缺损。4例患者仅合并室间隔缺损。通过正中胸骨切开术,36例患者用同种异体肺动脉补片扩大发育不全的主动脉弓。4例患者进行了扩大的端端吻合术。
有2例早期死亡(5%)和2例晚期死亡(5%)。1例晚期死亡与心脏无关。平均随访时间为36个月(范围1个月至9年)。同种异体肺动脉补片主动脉成形术后再缩窄率为8.3%,但排除合并左侧梗阻性病变的患者后,该率降至0%。主动脉未发生动脉瘤形成。8年时的预期生存率为89%±10%。
对主动脉弓梗阻及相关心内缺损进行单阶段双心室修复可实现良好的生存率。我们推荐同种异体肺动脉补片主动脉成形术,因为它能通过无张力吻合完全解除解剖学后负荷,且再缩窄发生率低。