Division of Cardiothoracic Surgery, 2345Rady Children's Hospital, San Diego, CA, USA.
Department Pediatrics, 12220University of California San Diego (UCSD) School of Medicine, San Diego, CA, USA.
World J Pediatr Congenit Heart Surg. 2021 Mar;12(2):286-290. doi: 10.1177/2150135121990387.
Van Praagh (VP) A3 variant of truncus arteriosus (or common arterial trunk) is defined by only one pulmonary artery (usually the right) originating from the common trunk, while the other lung is supplied either by collaterals or a pulmonary artery arising from the aortic arch. This report describes a staged approach to manage a VP-A3 variant truncus arteriosus with ductal origin of the left pulmonary artery (LPA), a hypoplastic right pulmonary artery, and cyanosis. Initially, the ductal portion of the proximal LPA was stented with a Resolute Onyx drug-eluting stent. The pulmonary arteries grew and at four months of age had an acceptable McGoon ratio and Nakata index. The patient then underwent repair which included unifocalization of the branch pulmonary arteries, closure of the ventricular septal defect, and placement of a right ventricle-to-pulmonary artery homograft conduit.
Van Praagh(VP)A3 型动脉干永存(或共同动脉干)的定义为仅有一条肺动脉(通常为右侧)起源于共同干,而另一侧肺由侧支循环或发自主动脉弓的肺动脉供应。本报告描述了一种分阶段的方法来管理具有左肺动脉(LPA)导管起源、右肺动脉发育不良和发绀的 VP-A3 型动脉干永存。最初,用 Resolute Onyx 药物洗脱支架对近端 LPA 的导管部分进行了支架置入。肺动脉生长,在 4 个月大时具有可接受的 McGoon 比值和 Nakata 指数。然后患者接受了修复手术,包括分支肺动脉的单一化、室间隔缺损的闭合以及右心室至肺动脉同种移植物管道的放置。