Aeba Ryo, Katogi Toshiyuki, Hashizume Kenichi, Iino Yoshimi, Koizumi Kiyoshi, Hotoda Kentaro, Inoue Shinya, Matayoshi Hideki, Yoshitake Akihiro, Yozu Ryohei
Division of Cardiovascular Surgery, Keio University, Tokyo, Japan.
Jpn J Thorac Cardiovasc Surg. 2003 Jul;51(7):302-7. doi: 10.1007/BF02719382.
Severe aortic arch obstruction including an interrupted aortic arch in congenital complex heart anomalies remains a challenge in surgical management.
Treatment and outcomes in 75 consecutive patients who underwent an aortic arch repair as the first step of the staged repair protocol between 1975 and 2000 were reviewed. Their ages at repair ranged from 1 day to 8.5 months.
Cross-sectional postoperative follow-up data were available in all the patients. The follow-up period ranged from 0 to 27.6 years (mean: 7.3 +/- 7.3 years). There were 20 postoperative hospital deaths (27%) and 7 late deaths. The Kaplan-Meier estimate of survival was 81.3% +/- 4.5% at 1 month, 68.0% +/- 5.4% at 1 year, 65.0% +/- 5.5% at 5 years, 63.1% +/- 5.7% at 10 years, 63.1% +/- 5.7% at 20 years. By Cox regression analysis, body weight of 2.5 kg or less is the only independent determinant of postoperative mortality (p = 0.04, multivariable odds ratio: 2.50, [95% confidence interval: 1.02-6.1]). The aortic arch morphology, the primary cardiac lesion, or date of operation did not reach a statistically significant level to show correlation with mortality. Reintervention to reconstruct the aortic arch was performed at 9 occasions in 8 of the 55 patients who survived the primary operation (14.5%). The Kaplan-Meier estimate of the reintervention-free rate was 91.3% +/- 4.2% at 5 years, 85.5% +/- 5.6% at 10 years, 75.6% +/- 8.2% at 20 years. Using multivariable Cox regression analysis, interrupted aortic arch (versus aortic coarctation) was the only independent predictor of a shorter time to reintervention (p = 0.001, multivariable odds ratio: 16.1, [95% confidence interval: 3.2-80.2]).
The staged repair protocol was associated with significant limitations in patient survival and with the development of recurrent aortic arch obstruction. Thus, a primary repair protocol may serve as an alternate approach, especially in patients with low weight or with an interrupted aortic arch.
在先天性复杂心脏畸形中,严重的主动脉弓梗阻,包括主动脉弓中断,仍然是外科治疗的一项挑战。
回顾了1975年至2000年间连续75例接受主动脉弓修复作为分期修复方案第一步的患者的治疗情况及预后。他们接受修复时的年龄从1天到8.5个月不等。
所有患者均有术后横断面随访数据。随访期从0至27.6年(平均:7.3±7.3年)。术后有20例医院死亡(27%)和7例晚期死亡。Kaplan-Meier生存估计值在1个月时为81.3%±4.5%,1年时为68.0%±5.4%,5年时为65.0%±5.5%,10年时为63.1%±5.7%,20年时为63.1%±5.7%。通过Cox回归分析,体重2.5kg或更低是术后死亡率的唯一独立决定因素(p = 0.04,多变量优势比:2.50,[95%置信区间:1.02 - 6.1])。主动脉弓形态、原发性心脏病变或手术日期与死亡率无统计学显著相关性。在初次手术存活的55例患者中的8例有9次进行了重建主动脉弓的再次干预(14.5%)。无再次干预率的Kaplan-Meier估计值在5年时为91.3%±4.2%,10年时为85.5%±5.6%,20年时为75.6%±8.2%。使用多变量Cox回归分析,主动脉弓中断(相对于主动脉缩窄)是再次干预时间较短的唯一独立预测因素(p = 0.001,多变量优势比:16.1,[95%置信区间:3.2 - 80.2])。
分期修复方案在患者生存方面存在显著局限性,并伴有复发性主动脉弓梗阻的发生。因此,一期修复方案可能是一种替代方法,尤其是对于体重低或主动脉弓中断的患者。