Imamura M, Drummond-Webb J J, Murphy D J, Prieto L R, Latson L A, Flamm S D, Mee R B
Department of Pediatric and Congenital Heart Surgery and Cardiology, The Cleveland Clinic Foundation, Ohio 44195-5066, USA.
Ann Thorac Surg. 2000 Jul;70(1):100-5. doi: 10.1016/s0003-4975(00)01416-8.
In patients with atrioventricular and arterioventricular discordance congenitally corrected transposition, the morphologically right ventricle may progressively deteriorate while functioning in the systemic circuit. The double switch operation has been proposed to limit this functional deterioration.
From October 1993 to August 1998, the records of 27 patients with congenitally corrected transposition were reviewed. Age at operation ranged from 3 months to 55 years. Associated defects included ventricular septal defects in 18, pulmonary atresia in 7, and pulmonary stenosis in 11 patients. Twenty-two patients had double switch operations (10 arterial switch plus Senning procedures and 12 Rastelli plus Senning procedures). Five patients were not candidates for the double switch. Before the double switch, 6 patients required pulmonary artery banding and 10 had functioning systemic to pulmonary artery or cavopulmonary shunts.
There was no early or late mortality. Two patients required pacemaker implantation, both later regained normal sinus rhythm. Tricuspid valve function improved in all patients except one. Moderate left ventricular dysfunction developed 5 months postoperatively in 1 patient.
The double switch operation can be performed in selected patients with minimal early morbidity and mortality. Longer follow-up is necessary to determine whether this complex approach is indeed warranted.
在先天性矫正型大动脉转位合并房室不一致的患者中,形态学上的右心室在体循环中发挥功能时可能会逐渐恶化。已提出双调转手术来限制这种功能恶化。
回顾了1993年10月至1998年8月期间27例先天性矫正型大动脉转位患者的记录。手术年龄从3个月至55岁不等。相关缺陷包括18例室间隔缺损、7例肺动脉闭锁和11例肺动脉狭窄。22例患者接受了双调转手术(10例动脉调转加森宁手术,12例拉斯泰利加森宁手术)。5例患者不适合进行双调转手术。在双调转手术前,6例患者需要进行肺动脉环扎术,10例患者有体肺分流或腔肺分流。
无早期或晚期死亡病例。2例患者需要植入起搏器,两者后来均恢复正常窦性心律。除1例患者外,所有患者的三尖瓣功能均有所改善。1例患者术后5个月出现中度左心室功能障碍。
双调转手术可在选定患者中进行,早期发病率和死亡率极低。需要更长时间的随访来确定这种复杂方法是否确实必要。