McElhinney D B, Reddy V M, Silverman N H, Hanley F L
Division of Cardiothoracic Surgery, University of California, San Francisco, USA.
J Thorac Cardiovasc Surg. 1997 Nov;114(5):718-25; discussion 725-6. doi: 10.1016/S0022-5223(97)70075-8.
A modified Damus-Kaye-Stansel procedure is one of several options for palliation of single ventricle with subaortic obstruction, but results in neonates have been disappointing. In the presence of arch obstruction, this procedure is typically performed with circulatory arrest, which may contribute to neurologic insult.
Since 1990, a modified Damus-Kaye-Stansel procedure has been performed in 14 neonates and seven infants with single ventricle and subaortic stenosis, including 15 with arch obstruction. Diagnoses were double-inlet left ventricle (n = 12), tricuspid atresia (n = 2), and other forms of hypoplastic ventricle with subaortic obstruction (n = 7). Three patients underwent concurrent bidirectional Glenn shunt. In the most recent seven patients with arch obstruction, arch repair was achieved with an end-to-side anastomosis of the descending aorta to the ascending aorta with continuous upper body perfusion.
One early death occurred among the 14 neonates (7%) and three among the infants, for an early mortality of 19%. At a median follow-up of 33 months, there were no late deaths or neurologic complications. Nine patients underwent subsequent bidirectional Glenn anastomosis, including three who had Fontan completion and one who later underwent conversion to a partial biventricular repair. One patient required a transplant for cardiomyopathy of unknown etiology. The remaining 12 patients are considered good candidates for Fontan completion. No patient has recurrent arch obstruction. Four patients have mild (n = 1) or trivial (n = 3) semilunar valvular regurgitation.
The modified Damus-Kaye-Stansel procedure is an effective primary palliation for single ventricle and subaortic stenosis, with or without arch obstruction. Results are especially encouraging in neonates. Arch repair can be achieved without circulatory arrest to the brain.
改良的达姆斯-凯-斯坦塞尔手术是缓解伴有主动脉下梗阻的单心室的几种选择之一,但新生儿的手术结果一直令人失望。在存在主动脉弓梗阻的情况下,该手术通常在循环骤停下进行,这可能会导致神经损伤。
自1990年以来,对14例新生儿和7例患有单心室和主动脉下狭窄的婴儿实施了改良的达姆斯-凯-斯坦塞尔手术,其中15例伴有主动脉弓梗阻。诊断包括双入口左心室(n = 12)、三尖瓣闭锁(n = 2)以及其他形式的伴有主动脉下梗阻的发育不全心室(n = 7)。3例患者同时进行了双向格林分流术。在最近的7例伴有主动脉弓梗阻的患者中,通过降主动脉与升主动脉的端侧吻合并持续进行上身灌注实现了主动脉弓修复。
14例新生儿中有1例早期死亡(7%),婴儿中有3例,早期死亡率为19%。中位随访33个月时,无晚期死亡或神经并发症。9例患者随后进行了双向格林吻合术,其中3例完成了Fontan手术,1例后来转为部分双心室修复。1例患者因不明原因的心肌病需要进行移植。其余12例患者被认为是完成Fontan手术的良好候选者。无患者出现复发性主动脉弓梗阻。4例患者有轻度(n = 1)或轻微(n = 3)半月瓣反流。
改良的达姆斯-凯-斯坦塞尔手术是治疗伴有或不伴有主动脉弓梗阻的单心室和主动脉下狭窄的一种有效的一期姑息治疗方法。结果在新生儿中尤其令人鼓舞。可以在不导致脑部循环骤停的情况下实现主动脉弓修复。