Gontijo Filho Bayard, Fantini Fernando Antonio, Lopes Roberto Max, Martins Cristiane Nunes, Heyden Eliana Guimarães, Vrandecic Erika Correa, Peredo Mario Osvaldo Vrandecic
Biocor Institute, MG/Brazil.
Rev Bras Cir Cardiovasc. 2007 Apr-Jun;22(2):176-83.
To analyze our experience in the surgical correction of transposition of the great arteries associated with aortic arch obstruction.
From January 1998 to December 2005 we performed 223 arterial switch operations for transposition of the great arteries; 21 (9.4%) patients had associated aortic arch obstruction. Aortic arch anatomy showed: localized aortic coarctation (n=10) and coarctation with hypoplastic aortic arch (n=6) and interrupted aortic arch (n=5). Ventricular septal defect was present in 19 (90.5%) patients. Size discrepancy between the aorta and pulmonary artery and complex coronary artery anatomy were common findings. Surgical correction was performed in either one (14) or two stages (7). Aortic arch reconstruction was achieved either by resection and extended anastomoses (13) or by relocation of the ascending aorta (8).
Hospital mortality was 23.8% (n=5); with only one death (11.1%) among the last nine patients. Reoperations in the immediate post-operative period included: bleeding (5), residual ventricular septal defect and unrecognized coarctation (1) or residual stenosis of the aortic arch (1). There were two late deaths caused by fungal infections and reoperation for severe aortic regurgitation. Three patients underwent procedures to relieve right ventricular outflow tract obstruction. Two patients have slight to moderate aortic regurgitation.
The surgical treatment of transposition of the great arteries with aortic arch obstruction is complex with high morbidity. Our present choice is one-stage treatment for all patients without using homologous or heterologous tissue for aortic arch reconstruction. We recommend resection and extended anastomoses for localized coarctation and relocation of the ascending aorta for hypoplastic or interrupted aortic arch.
分析我们在大动脉转位合并主动脉弓梗阻手术矫治方面的经验。
1998年1月至2005年12月,我们对223例大动脉转位患者进行了动脉调转手术;21例(9.4%)患者合并主动脉弓梗阻。主动脉弓解剖显示:局限性主动脉缩窄(n = 10)、主动脉缩窄合并主动脉弓发育不良(n = 6)及主动脉弓中断(n = 5)。19例(90.5%)患者存在室间隔缺损。主动脉与肺动脉大小差异及复杂冠状动脉解剖是常见表现。手术矫治分一期(14例)或二期(7例)进行。主动脉弓重建通过切除并扩大吻合(13例)或升主动脉移位(8例)完成。
住院死亡率为23.8%(n = 5);最后9例患者中仅1例死亡(11.1%)。术后早期再次手术包括:出血(5例)、残余室间隔缺损及未识别的缩窄(1例)或主动脉弓残余狭窄(1例)。有2例晚期死亡,分别因真菌感染和重度主动脉瓣反流再次手术。3例患者接受了缓解右心室流出道梗阻的手术。2例患者有轻度至中度主动脉瓣反流。
大动脉转位合并主动脉弓梗阻的手术治疗复杂且发病率高。我们目前的选择是对所有患者进行一期治疗,主动脉弓重建不使用同种或异种组织。对于局限性缩窄,我们推荐切除并扩大吻合;对于发育不良或中断的主动脉弓,推荐升主动脉移位。