Trezzi Matteo, Cetrano Enrico, Albanese Sonia B, Borro Luca, Secinaro Aurelio, Carotti Adriano
Units of Cardiac Surgery, Department of Cardiac Surgery, Cardiology, Heart and Lung Transplantation, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Advanced Cardiothoracic Imaging Unit, Department of Imaging, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Children (Basel). 2022 Apr 5;9(4):515. doi: 10.3390/children9040515.
Pulmonary atresia with ventricular septal defect and major aortopulmonary collaterals is a complex congenital heart defect that includes a heterogeneous subgroup of patients. Variation in the sources of pulmonary blood flow contributes to the complexity of the lesion and the diversity of approaches to its management. Unifocalization and rehabilitation focus on mobilization of collateral arteries and growth of native pulmonary arteries, respectively, with the ultimate surgical goal of achieving separated systemic and pulmonary circulations with the lowest possible right ventricular pressure. Regardless of the strategy, outcomes have altered the natural history of the disease, with a complete repair rate of approximately 80% and low early and late mortality rates. Given this heterogeneity of pulmonary vasculature, a tailored approach should be adopted for each patient, using all diagnostic methods currently offered by technical developments.
肺动脉闭锁合并室间隔缺损及大量主-肺动脉侧支是一种复杂的先天性心脏缺陷,患者群体异质性高。肺血流来源的差异导致了病变的复杂性以及治疗方法的多样性。单灶化和肺血管重建分别侧重于侧支动脉的动员和固有肺动脉的生长,最终手术目标是以尽可能低的右心室压力实现体循环和肺循环分离。无论采用何种策略,治疗结果都改变了该病的自然病程,完全修复率约为80%,早期和晚期死亡率均较低。鉴于肺血管系统的这种异质性,应针对每位患者采用量身定制的方法,利用技术发展目前提供的所有诊断方法。