Department of Thoracic and Cardiovascular Surgery, The Second of Chuanbei Clinical Medical College, Nanchong, People's Republic of China.
Ann Thorac Surg. 2009 Dec;88(6):1948-51. doi: 10.1016/j.athoracsur.2009.08.051.
Indications and outcomes of the arterial switch operation in children who are older than 1 month of age and have transposition of the great arteries plus ventricular septal defect or Taussig-Bing anomaly were studied.
Arterial switch operation was performed in 68 children between January 2000 and December 2008. Thirty infants (1 to 6 months old) had transposition of the great arteries plus ventricular septal defect or Taussig-Bing anomaly (group A), and 38 children older than 6 months of age had transposition of the great arteries plus ventricular septal defect or Taussig-Bing anomaly (group B). The preoperative pulmonary artery pressure in group B was significantly higher than that in group A (46.5 +/- 16.3 mm Hg and 31.3 +/- 8.6 mm Hg, respectively; p < 0.05). Arterial switch operation was performed under general anesthesia, hypothermia (18 degrees to 22 degrees C), and low-flow (50 mL x kg(-1) x min(-1)) extracorporeal bypass circulation. Concomitant cardiac anomalies were treated during the same surgical session.
Average extracorporeal circulation time, aortic clamping time, postoperative overall hospitalization, and intensive care unit duration were not significantly different between the two groups (p > 0.05). The operative mortality rate in group A was 10.0% (3 of 30 patients) and in group B, 7.9% (3 of 38 patients; p > 0.05). Follow-up examinations in the surviving 62 patients after a mean of 13.5 +/- 7.9 months (range, 0.5 to 56 months) showed significantly improved cardiac function without any long-term complications, and no cases of death occurred during this period.
Arterial switch operation shows satisfactory operative outcome of transposition of the great arteries plus ventricular septal defect or Taussig-Bing anomaly in children older than the age of 6 months with moderate-to-severe pulmonary hypertension.
研究了年龄大于 1 个月且患有大动脉转位伴室间隔缺损或 Taussig-Bing 畸形的儿童的动脉调转手术的适应证和结果。
2000 年 1 月至 2008 年 12 月期间,对 68 例儿童进行了动脉调转手术。30 例婴儿(1 至 6 个月)患有大动脉转位伴室间隔缺损或 Taussig-Bing 畸形(A 组),38 例年龄大于 6 个月的儿童患有大动脉转位伴室间隔缺损或 Taussig-Bing 畸形(B 组)。B 组患儿术前肺动脉压明显高于 A 组(分别为 46.5 ± 16.3mmHg 和 31.3 ± 8.6mmHg;p<0.05)。所有患儿均在全身麻醉、低温(18 至 22°C)和低流量(50ml·kg-1·min-1)体外循环下进行动脉调转手术。同期治疗合并的心脏畸形。
两组患儿体外循环时间、主动脉阻断时间、术后总住院时间和重症监护病房时间差异均无统计学意义(p>0.05)。A 组患儿手术死亡率为 10.0%(3/30 例),B 组为 7.9%(3/38 例;p>0.05)。62 例存活患儿术后平均随访 13.5 ± 7.9 个月(0.5 至 56 个月),心功能明显改善,无长期并发症,随访期间无死亡病例。
对于中重度肺动脉高压的年龄大于 6 个月的儿童,动脉调转手术治疗大动脉转位伴室间隔缺损或 Taussig-Bing 畸形可获得满意的手术效果。