Uno Yoshimasa, Masuoka Ayumu, Hotoda Kentarou, Katogi Toshiyuki, Suzuki Takaaki
1 Department of Pediatric Cardiovascular Surgery, International Medical Center, Saitama Medical University, Saitama, Japan.
World J Pediatr Congenit Heart Surg. 2017 May;8(3):332-336. doi: 10.1177/2150135117690125.
Open heart surgery for interrupted aortic arch in the neonatal period is still a high-risk procedure related in part to patient factors such as low birth weight, other morphologic anomalies, and, especially, small aortic valve size. Recently, we performed hybrid palliation with bilateral pulmonary artery banding and ductal stenting as the first-stage palliation for such cases. In this study, the outcomes of this procedure were examined.
Six cases of interrupted aortic arch with a small aortic valve underwent the hybrid procedure in the neonatal period in our institute from 2010 to 2015 (mean age: 6.8 days, mean body weight: 3.2 kg, mean z score of the aortic valve annulus: -8.3). Their postoperative clinical courses and results of the second-stage surgery were evaluated.
No mortality or severe morbidity was seen in association with initial hybrid palliation. Five of six patients were discharged from the hospital; the one exception had a significant urinary tract anomaly. None needed an additional catheter intervention or surgical procedure postoperatively. All surviving patients underwent second-stage surgery; three had biventricular repair by the conventional method or Damus-Kaye-Stansel anastomosis with the Rastelli procedure and the other three proceeded toward staged Fontan reconstruction. Growth of the aortic valve was seen in four patients, and increased indexed left ventricle volume was recognized in one after the palliation.
Hybrid palliation could be useful not only to avoid high-risk neonatal surgery but also to allow for eventual selection of the second-stage surgery based on the observations of potential interval development of left ventricular structures.
新生儿期主动脉弓中断的心脏直视手术仍然是一种高风险手术,部分原因与患者因素有关,如低出生体重、其他形态学异常,尤其是主动脉瓣尺寸小。最近,我们对这类病例采用双侧肺动脉环扎和导管支架置入术进行了杂交姑息治疗作为一期姑息治疗。在本研究中,对该手术的结果进行了检查。
2010年至2015年期间,我院6例主动脉瓣小的主动脉弓中断患儿在新生儿期接受了杂交手术(平均年龄:6.8天,平均体重:3.2kg,主动脉瓣环平均z值:-8.3)。评估了他们的术后临床病程和二期手术结果。
初始杂交姑息治疗未出现死亡或严重并发症。6例患者中有5例出院;唯一例外的患者有严重的泌尿系统异常。术后均无需额外的导管介入或手术。所有存活患者均接受了二期手术;3例采用传统方法或Damus-Kaye-Stansel吻合术联合Rastelli手术进行双心室修复,另外3例进行分期Fontan重建。4例患者的主动脉瓣出现生长,1例患者在姑息治疗后左心室指数容积增加。
杂交姑息治疗不仅有助于避免高风险的新生儿手术,还能根据左心室结构潜在的间隔期发育情况最终选择二期手术。