Department of Thoracic and Cardiovascular Surgery, Seoul St. Mary's Hospital, The Catholic University of Korea, Catholic Medical Center, Seoul, Republic of Korea.
Ann Thorac Surg. 2012 Jun;93(6):e159-61. doi: 10.1016/j.athoracsur.2011.12.027.
Airway compression by dilated right pulmonary artery (RPA) in infants with congenital heart disease can cause severe respiratory insufficiency and increase postoperative morbidity. Anterior aortopexy can be a good solution. However, in a case in which aortic arch repair is required, anterior aortopexy might not be effective or can be dangerous. Anterior translocation of the RPA can be a good option to avoid postoperative airway obstruction. We adopted this technique in a one-stage complete repair of distal aortopulmonary window, aortic origin of the RPA, interrupted aortic arch, and ventricular septal defect in a neonate with compression of both main bronchi. After 37 months of follow-up, no problem was encountered with her airway or RPA. We describe the technique used and the results obtained.
扩张的右肺动脉(RPA)压迫气道会导致先天性心脏病患儿出现严重呼吸功能不全,并增加术后发病率。主动脉前固定术可能是一个很好的解决方案。然而,在需要修复主动脉弓的情况下,主动脉前固定术可能无效或有危险。将 RPA 向前移位是避免术后气道阻塞的一个很好的选择。我们在一名新生儿的一期完全修复中采用了这种技术,该新生儿患有远端主肺动脉窗、RPA 起源于主动脉、主动脉弓中断和室间隔缺损,同时存在双侧主支气管受压。随访 37 个月后,她的气道或 RPA 没有出现问题。我们描述了所使用的技术和获得的结果。