Williams William G, McCrindle Brian W, Ashburn David A, Jonas Richard A, Mavroudis Constantine, Blackstone Eugene H
Congenital Heart Surgeons Society Data Center, 555 University Avenue, Toronto, ON, Canada M5G 1X8.
Eur J Cardiothorac Surg. 2003 Jul;24(1):1-9; discussion 9-10. doi: 10.1016/s1010-7940(03)00264-1.
Between 1985 and 1989, the surgical management of neonates with complete transposition (TGA) underwent a transition from atrial to arterial repair. We sought to examine the intermediate outcomes and their associated risk factors in neonates repaired during the era of transition.
Twenty-four institutions entered 829 neonates age less than 15 days in a prospective study. Diagnosis was simple TGA (n=631), TGA with ventricular septal defect (VSD) (n=167), TGA with VSD and pulmonary stenosis (TGA/VSD/PS) (n=30), or TGA with PS (n=1). Repair was by arterial switch (n=516), atrial repair (Senning=175, Mustard=110) or Rastelli (n=28). Time-related events were analysed by parametric hazard function modeling and incremental risk factors for mortality, re-intervention, and late functional assessment were sought.
Survival estimates at 6 months, 5, 10, and 15 years are 85, 83, 83, and 81%, respectively. The hazard function for death after repair has two phases: an early rapidly declining phase and an ongoing constant one. Constant phase mortality is less likely after the arterial switch operation and in children with simple TGA. During follow up, at least one re-intervention was required in 167 children (pacemaker, n=35; percutaneous intervention, n=32; baffle re-intervention, n=27; re-operation, n=125). Freedom from re-intervention at 6 months, 5, 10 and 15 years is 93, 82, 77, and 76%, respectively. Of survivors, 87% have been followed up to the last 3 years, including an assessment of functional ability of 562 children (83%). Functional class 15 years after repair is class I in 76%, II in 22%, III in 2%. The proportion in functional class I decreased over time. Psychosocial deficits, especially learning disorders are prevalent.
Survival 15 years after TGA repair is good with most children functioning well, and results are best after an arterial switch operation. There is an ongoing risk of death that is less after the arterial switch operation. With the exception of Rastelli patients, the likelihood of survivors needing re-intervention after 5 years is low. There is need for improved neurodevelopmental outcomes.
在1985年至1989年间,完全性大动脉转位(TGA)新生儿的手术治疗从心房修复过渡到动脉修复。我们试图研究过渡时期接受修复的新生儿的中期结局及其相关危险因素。
24家机构纳入了829名年龄小于15天的新生儿进行前瞻性研究。诊断为单纯性TGA(n = 631)、合并室间隔缺损(VSD)的TGA(n = 167)、合并VSD和肺动脉狭窄的TGA(TGA/VSD/PS,n = 30)或合并肺动脉狭窄的TGA(n = 1)。修复方式为动脉调转术(n = 516)、心房修复术(森宁术 = 175例,马斯塔德术 = 110例)或罗斯蒂利术(n = 28)。通过参数风险函数建模分析与时间相关的事件,并寻找死亡率、再次干预和晚期功能评估的增量危险因素。
6个月、5年、10年和15年的生存估计分别为85%、83%、83%和81%。修复后死亡的风险函数有两个阶段:早期快速下降阶段和持续稳定阶段。动脉调转术后和单纯性TGA患儿在稳定阶段的死亡率较低。在随访期间,167名儿童(起搏器植入,n = 35;经皮介入,n = 32;挡板再次干预,n = 27;再次手术,n = 125)至少需要进行一次再次干预。6个月、5年、10年和15年无再次干预的比例分别为93%、82%、77%和76%。在幸存者中,87%在过去3年接受了随访,其中包括对562名儿童(83%)的功能能力评估。修复后15年功能分级为I级的占76%,II级的占22%,III级的占2%。I级功能分级的比例随时间下降。心理社会缺陷,尤其是学习障碍很普遍。
TGA修复术后15年生存率良好,大多数儿童功能良好,动脉调转术后效果最佳。存在持续的死亡风险,动脉调转术后风险较低。除罗斯蒂利手术患者外,幸存者5年后需要再次干预的可能性较低。需要改善神经发育结局。