DeLeon S Y, Ilbawi M N, Tubeszewski K, Wilson W R, Idriss F S
Division of Pediatric Cardiac Surgery, Children's Memorial Hospital, Northwestern University Medical School, Chicago, Illinois.
Ann Thorac Surg. 1991 Sep;52(3):680-7. doi: 10.1016/0003-4975(91)90977-x.
Seven of 119 patients undergoing anatomical correction for transposition of the great arteries and Taussig-Bing anomalies without pulmonary stenosis had the Damus-Stansel-Kaye procedure and the rest, the arterial switch. The age of the patients having the Damus-Stansel-Kaye procedure ranged from 0.5 year to 5 years (mean age, 2.2 +/- 1 years). Four patients had transposition, 2 had Taussig-Bing anomaly, and 1 had corrected transposition. Indications for the Damus-Stansel-Kaye procedure were side-by-side great arteries associated with difficult coronary anatomy (5 patients), single coronary system (1 patient), and subaortic stenosis (1). A graft between the ascending and descending aorta for interrupted aortic arch made mobilization and posterior displacement of the ascending aorta for the arterial switch difficult. Subaortic stenosis (1 patient), subpulmonary ventricular septal defect (2 patients), and restrictive ventricular septal defect (4) precluded the Rastelli procedure. In 6 patients, the main pulmonary artery was transected at the band, a proximal main pulmonary artery to aorta anastomosis was complemented with a synthetic patch, and a right ventricle to distal main pulmonary artery valved conduit was inserted. Four patients had closure of the aortic outflow. Two patients had postoperative bleeding and 2, heart block. The only patient who did not have transection of the main pulmonary artery, an omission that led to an obstructed conduit at the distal anastomosis, died late. Two patients subsequently needed aortic outflow closure for critical aortic insufficiency. The Damus-Stansel-Kaye procedure has a definite role and can be safely performed in patients with transposition of the great arteries and Taussig-Bing anomalies.(ABSTRACT TRUNCATED AT 250 WORDS)
119例接受大动脉转位和无肺动脉狭窄的陶西格-宾(Taussig-Bing)畸形解剖矫治的患者中,7例行达穆斯-斯坦塞尔-凯伊(Damus-Stansel-Kaye)手术,其余行动脉调转术。行达穆斯-斯坦塞尔-凯伊手术的患者年龄为0.5岁至5岁(平均年龄2.2±1岁)。4例为大动脉转位,2例为陶西格-宾畸形,1例为矫正型大动脉转位。达穆斯-斯坦塞尔-凯伊手术的指征为并列大动脉伴冠状动脉解剖困难(5例)、单一冠状动脉系统(1例)和主动脉瓣下狭窄(1例)。升主动脉和降主动脉之间用于治疗主动脉弓中断的移植物使得为动脉调转术而进行升主动脉的游离和向后移位变得困难。主动脉瓣下狭窄(1例)、肺动脉瓣下室间隔缺损(2例)和限制性室间隔缺损(4例)排除了使用罗斯蒂利(Rastelli)手术。6例患者中,主肺动脉在束带处横断,近端主肺动脉至主动脉吻合口用合成补片修补,并插入右心室至远端主肺动脉带瓣管道。4例患者关闭了主动脉流出道。2例患者术后出血,2例发生心脏传导阻滞。唯一未横断主肺动脉的患者因这一疏忽导致远端吻合口处管道梗阻,术后死亡。2例患者随后因严重主动脉瓣关闭不全需要关闭主动脉流出道。达穆斯-斯坦塞尔-凯伊手术有明确的作用,可安全地应用于大动脉转位和陶西格-宾畸形患者。(摘要截取自250字)