Pediatric Heart Center Giessen, Justus-Liebig-University, Giessen, Germany.
Pediatric Heart Center Giessen, Justus-Liebig-University, Giessen, Germany.
J Thorac Cardiovasc Surg. 2016 Apr;151(4):1112-21, 1123.e1-5. doi: 10.1016/j.jtcvs.2015.10.066. Epub 2015 Oct 27.
This retrospective study presents our operative results, mortality, and morbidity with regard to pulmonary artery growth and reinterventions on the pulmonary artery and aortic arch, including key features of our institutional standards for the 3-stage hybrid palliation of patients with hypoplastic left heart syndrome.
Between June 1998 and February 2015, 182 patients with hypoplastic left heart structures underwent the Giessen hybrid stage I procedure. Among these, 126 patients with hypoplastic left heart syndrome who received a univentricular palliation or heart transplantation were included in the main analysis. Median age and body weight of patients at hybrid stage I were 6 days (0-237) and 3.2 kg (1.2-7), respectively. Comprehensive stage II operation was performed at 4.5 months (2.9-39.5), and Fontan completion was established at 33.7 months (21.1-108.2). Operative and interstage mortality, morbidity, growth and reinterventions on the pulmonary arteries, and long-term operative results of the aortic arch reconstruction were assessed.
Median follow-up time after Giessen hybrid stage I palliation was 4.6 years (0-16.8). Operative mortality at hybrid stage I, comprehensive stage II, and Fontan completion was 2.5%, 4.9%, and 0%, respectively. Cumulative interstage mortality was 14.2%. At 10 years, the probability of survival is 77.8%. Body weight (<2.5 kg) and aortic atresia had no significant impact on survival. McGoon ratio did not differ at comprehensive stage II and Fontan completion (P = .991). Freedom from pulmonary artery intervention was estimated to be 32.2% at 10 years. Aortic arch reinterventions were needed in 16.7% of patients; 2 reoperations on the aortic arch were necessary.
In view of the early results and long-term outcome, the hybrid approach has become an alternative to the conventional strategy to treat neonates with hypoplastic left heart syndrome and variants. Further refinements are warranted to decrease patient morbidity.
本回顾性研究介绍了我们在肺动脉生长方面的手术结果、死亡率和发病率,以及我们为左心发育不全综合征患者实施三阶段杂交姑息治疗的机构标准的关键特征。
1998 年 6 月至 2015 年 2 月期间,182 例左心结构发育不全的患者接受了吉森杂交一期手术。其中,126 例接受单心室姑息治疗或心脏移植的左心发育不全综合征患者纳入主要分析。一期杂交手术时患者的中位年龄和体重分别为 6 天(0-237)和 3.2kg(1.2-7)。综合二期手术在 4.5 个月(2.9-39.5)进行,Fontan 手术在 33.7 个月(21.1-108.2)进行。评估了手术和分期死亡率、发病率、肺动脉生长和再干预以及主动脉弓重建的长期手术结果。
吉森杂交一期姑息手术后的中位随访时间为 4.6 年(0-16.8)。一期杂交、综合二期和 Fontan 完成手术的死亡率分别为 2.5%、4.9%和 0%。累计分期死亡率为 14.2%。10 年时的生存率为 77.8%。体重(<2.5kg)和主动脉闭锁对生存率无显著影响。综合二期和 Fontan 完成时的 McGoon 比值无差异(P=0.991)。10 年时,免于肺动脉干预的概率估计为 32.2%。需要再次干预主动脉弓的患者占 16.7%,有 2 例患者需要再次行主动脉弓手术。
鉴于早期结果和长期预后,杂交方法已成为治疗新生儿左心发育不全综合征及其变异的一种替代传统策略。需要进一步改进以降低患者的发病率。