Takabayashi Shin, Shimpo Hideto, Kajimoto Masaki, Yokoyama Kazuto, Kado Hideaki, Mitani Yoshihide
Department of Thoracic and Cardiovascular Surgery, Mie University School of Medicine, 2-174, Edobashi, Tsu, Mie 514-8507, Japan.
Interact Cardiovasc Thorac Surg. 2005 Aug;4(4):352-5. doi: 10.1510/icvts.2004.095620. Epub 2005 May 4.
Since 2002, we have performed bilateral pulmonary artery banding for stage I palliation and maintained systemic flow by prostaglandin E1 infusion or a main pulmonary artery to the descending aorta shunt, and here report our experience. Three of the 4 patients were diagnosed with aortic atresia/mitral atresia and 1 with aortic stenosis/mitral stenosis. Balloon atrial septostomy was performed in 2 before stage I. Bilateral pulmonary artery banding (right circumference: 10 or 14, left circumference: 10.5 to 14 mm) was performed from 7 to 19 days after birth. Systemic flow was maintained by prostaglandin E1 infusion in 2 patients and a Van Praagh procedure was performed in the other 2. Balloon atrial septostomy was required in 2 patients, and an atrial septal defect enlargement was in one during the interstage before stage II palliation, which was performed at ages 3 to 9 months. Bidirectional cavopulmonary shunt with aortic arch and coronary flow reconstruction was also performed. For patients younger than 4 months, we do not require pulmonary arterioplasty in stage II. All patients are alive and well and waiting for Fontan completion. Excellent early results were obtained for this surgical strategy that avoids the stage I Norwood palliation.
自2002年以来,我们对I期姑息治疗患者实施了双侧肺动脉环扎术,并通过静脉输注前列腺素E1或主肺动脉至降主动脉分流术维持体循环血流,在此报告我们的经验。4例患者中3例诊断为主动脉闭锁/二尖瓣闭锁,1例为主动脉狭窄/二尖瓣狭窄。2例在I期手术前进行了球囊房间隔造口术。出生后7至19天进行双侧肺动脉环扎术(右侧周长:10或14,左侧周长:10.5至14毫米)。2例患者通过静脉输注前列腺素E1维持体循环血流,另外2例进行了Van Praagh手术。2例患者需要再次进行球囊房间隔造口术,1例在II期姑息治疗前的过渡期进行了房间隔缺损扩大术,II期姑息治疗于3至9个月龄时进行。还进行了双向腔肺分流术并重建主动脉弓和冠状动脉血流。对于4个月以下的患者,我们在II期不需要进行肺动脉成形术。所有患者均存活且状况良好,正在等待完成Fontan手术。对于这种避免I期诺伍德姑息治疗的手术策略,我们获得了出色的早期效果。