Management Options for Congenitally Corrected Transposition: Which, When, and for Whom?

Jacob R Miller, Vinod Sebastian, Pirooz Eghtesady
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Abstract

Management strategies for congenitally corrected transposition of the great arteries (ccTGA) historically consisted of a physiologic repair, resulting in the morphologic right ventricle (mRV) supporting systemic circulation. This strategy persisted despite the development of heart failure by middle age because of the reasonable short-term outcomes, and the natural history of some patients with favorable anatomy (felt to demonstrate the mRV's ability to function in the long-term), and due to the less-than-optimal outcomes associated with anatomical repair. As outcomes with anatomical repair improved, and the long-term risk of systemic mRV dysfunction became apparent, more have begun to realize its advantages. In addition to the decision on whether or not to pursue anatomical repair, and the optimal timing, studies demonstrating the nuance to morphologic left ventricle retraining have demonstrated its feasibility. Further considerations in ccTGA have begun to be better understood, including: the management of a poorly functioning mRV, systemic tricuspid valve regurgitation, the utility of morphologic left ventricle outflow tract obstruction (native or surgically created) and pacing strategies. While some considerations are apparent: biventricular pacing is superior to univentricular, tricuspid regurgitation must be managed early with either progression towards anatomical repair (pulmonary artery banding if needed for retraining) or tricuspid replacement (not repair) based on the patient's age; others remain to be completely elucidated. Overall, the heterogeneity of ccTGA, as well as the unique presentation with each patient regarding ventricular and valvular function and center-to-center variability in management strategies has made the interpretation of published data difficult. That said, more recent long-term outcomes favor anatomical repair in most situations.

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先天性纠正移位的管理选择:哪种,何时,为谁?
先天性大动脉转位(ccTGA)的治疗策略历来包括生理性修复,导致形态右心室(mRV)支持体循环。尽管中年心力衰竭的发展,由于合理的短期结果,以及一些具有良好解剖结构的患者的自然史(感觉证明mRV的长期功能),并且由于与解剖修复相关的不太理想的结果,这种策略仍然存在。随着解剖修复效果的改善,以及mRV功能障碍的长期风险变得明显,越来越多的人开始意识到它的优势。除了决定是否进行解剖修复和最佳时机外,研究表明形态学左心室再训练的细微差别也证明了其可行性。ccTGA的进一步考虑已经开始被更好地理解,包括:功能不佳的mRV的处理,系统性三尖瓣反流,形态学左心室流出道阻塞(原生或手术造成)的应用和起搏策略。虽然有一些考虑是显而易见的:双心室起搏优于单心室起搏,但三尖瓣反流必须及早处理,根据患者的年龄进行解剖修复(如果需要再训练,可以进行肺动脉绑扎)或三尖瓣置换(不修复);其他的仍有待完全阐明。总的来说,ccTGA的异质性,以及每个患者关于心室和瓣膜功能的独特表现,以及管理策略的中心到中心变异性,使得对已发表数据的解释变得困难。也就是说,在大多数情况下,最近的长期结果倾向于解剖修复。
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CiteScore
3.80
自引率
0.00%
发文量
7
期刊介绍: The Pediatric Cardiac Surgery Annual is a companion to Seminars in Thoracic and Cardiovascular Surgery . Together with the Seminars, the Annual provides complete coverage of the specialty by focusing on important developments in pediatric cardiac surgery. Each annual volume has an expert guest editor who invites prominent surgeons to review the areas of greatest change in pediatric cardiac surgery during the year. Topics include 1) Complete Atrioventricular Canal; 2) New Concepts of Cardiac Anatomy and Function -- The Helical Heart; 3) Valve Reconstruction (Replacement) in Congenital Heart Disease; 4) Evolving Developments in Congenital Heart Surgery.
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