Corno Antonio F, Findley Tina O, Salazar Jorge D
Pediatric and Congenital Cardiac Surgery, Children's Heart Institute, Department of Pediatrics, Memorial Hermann Children's Hospital, McGovern Medical School at the University of Texas Health Science Center in Houston, Houston, TX, USA.
Division of Neonatal-Perinatal Medicine, Department of Pediatrics, Memorial Hermann Children's Hospital, McGovern Medical School at the University of Texas Health Science Center in Houston, Houston, TX, USA.
Transl Pediatr. 2023 Feb 28;12(2):221-244. doi: 10.21037/tp-22-573. Epub 2023 Feb 7.
Key medical and surgical advances have been made in the longitudinal management of patients with "functionally" single ventricle physiology, with the principles of Fontan circulation applied to other complex congenital heart defects. The purpose of this article is to review all of the innovations, starting from fetal life, that led to a change of strategy for single ventricle.
Our literature review included all full articles published in English language on the Cochrane, MedLine, and Embase with references to "single ventricle" and "univentricular hearts", including the initial history of the treatments for this congenital heart defects as well as the innovations reported within the last decades.
All innovations introduced have been analyzed, including: (I) fetal diagnosis and interventions, in particular to prevent or reduce brain damages; (II) neonatal care; (III) post-natal diagnosis; (IV) interventional cardiology procedures; (V) surgical procedures, including neonatal palliations, hybrid procedures, bidirectional Glenn and variations, Fontan completion, biventricular repair; (VI) peri-operative management; (VII) Fontan failure, with Fontan take-down and conversion, and mechanical circulatory support; (VIII) transplantation, including heart, heart and lung, heart and liver; (IX) exercise; (X) pregnancy; (XI) adolescents and adults without Fontan completion; (XII) future studies, including experimental studies on animals, computational studies, genetics, stem cells and bioengineering.
These last 40 years have certainly changed the course of natural history for children born with any form of "functionally" single ventricle, thanks to the improvement in diagnostic and treatment techniques, and particularly to the increased knowledge of the morphology and function of these complex hearts, from fetal to adult life. There is still much left unexplored and room for improvement, and all efforts should be concentrated in collaborations among different institutions and specialties, focused on the same matter.
在“功能性”单心室生理患者的纵向管理方面已取得关键的医学和外科进展,Fontan循环原则也应用于其他复杂先天性心脏缺陷。本文旨在回顾从胎儿期开始的所有创新,这些创新导致了单心室治疗策略的改变。
我们的文献综述包括在Cochrane、MedLine和Embase上发表的所有英文全文文章,这些文章提及“单心室”和“单心室心脏”,包括这种先天性心脏缺陷治疗的初始历史以及过去几十年报道的创新。
已对引入的所有创新进行了分析,包括:(I)胎儿诊断与干预,特别是预防或减少脑损伤;(II)新生儿护理;(III)产后诊断;(IV)介入性心脏病学程序;(V)外科手术,包括新生儿姑息手术、杂交手术、双向格林分流术及其变体、Fontan手术完成、双心室修复;(VI)围手术期管理;(VII)Fontan手术失败,包括Fontan手术拆除与转换以及机械循环支持;(VIII)移植,包括心脏、心肺、心肝移植;(IX)运动;(X)妊娠;(XI)未完成Fontan手术的青少年和成年人;(XII)未来研究,包括动物实验研究、计算研究、遗传学、干细胞和生物工程。
在过去40年里,得益于诊断和治疗技术的进步,尤其是对这些复杂心脏从胎儿期到成年期形态和功能认识的增加,无疑改变了任何形式“功能性”单心室患儿的自然病程。仍有许多未被探索的领域和改进空间,所有努力都应集中在不同机构和专业之间的合作上,专注于同一问题。