Division of Pediatric Cardiac Surgery, University Paris Descartes and Necker Sick Children Hospital, Paris, France.
Division of Cardiac Surgery, Montreal Heart Institute, University of Montreal School of Medicine, Montreal, QC, Canada.
Eur J Cardiothorac Surg. 2018 Sep 1;54(3):532-538. doi: 10.1093/ejcts/ezy116.
The physiological repair of the congenitally corrected transposition of the great arteries (ccTGA) has been associated with a long-term risk of the right ventricular dysfunction and tricuspid valve regurgitation. On the other side, the anatomical repair with the restoration of the left ventricle in a systemic position has been hypothesized to improve long-term outcomes. The aim of this study was to determine the results of the anatomical repair.
Between 1990 and 2015, 39 patients underwent an anatomical repair of a ccTGA. The median age was 7 years (range from 8 days to 42.8 years). Eighteen (46%) patients had a double switch. Of these, 21 (54%) patients had an atrial switch with a Rastelli technique (n = 16, 41%), with a réparation à l'étage ventriculaire (REV) procedure (n = 4, 10%) or a truncal rotation (n = 1, 3%). The follow-up was 100% complete at 2 years with a median follow-up of 3.17 years (range 0-26 years).
The early mortality was 10% (n = 4) and the late mortality was 20% (n = 8). The long-term survival was 77 ± 10% at 10 years for the double switch group and 62 ± 11% at 10 years for the Rastelli group (P = 0.25). Eight (20%) patients required reintervention. Freedom from reoperation at 10 years was 82 ± 11% in the double switch group and 88 ± 11% in the Rastelli group. At the last follow-up, 23 (82%) patients were in New York Heart Association (NYHA) functional class I and 2 (7%) patients in NYHA class II.
The anatomical repair of the ccTGA is associated with significant early mortality and morbidity. However, the long-term functional status is satisfactory. The anatomical repair of the ccTGA should be reserved for a carefully selected group of patients.
先天性矫正型大动脉转位(ccTGA)的生理修复与右心室功能障碍和三尖瓣反流的长期风险相关。另一方面,假设通过将左心室恢复到系统位置进行解剖修复可以改善长期结果。本研究的目的是确定解剖修复的结果。
1990 年至 2015 年间,39 例 ccTGA 患者接受了解剖修复。中位年龄为 7 岁(范围为 8 天至 42.8 岁)。18 例(46%)患者接受了双开关手术。其中,18 例(54%)患者接受了心房切换术,采用 Rastelli 技术(n=16,41%),采用 réparation à l'étage ventriculaire(REV)手术(n=4,10%)或干旋转(n=1,3%)。2 年时随访率为 100%,中位随访时间为 3.17 年(范围 0-26 年)。
早期死亡率为 10%(n=4),晚期死亡率为 20%(n=8)。双切换组的 10 年生存率为 77±10%,Rastelli 组为 62±11%(P=0.25)。8 例(20%)患者需要再次干预。双切换组 10 年无再手术率为 82±11%,Rastelli 组为 88±11%。在最后一次随访时,23 例(82%)患者纽约心脏协会(NYHA)心功能分级为 I 级,2 例(7%)患者为 II 级。
ccTGA 的解剖修复与显著的早期死亡率和发病率相关。然而,长期的功能状态是令人满意的。ccTGA 的解剖修复应保留给一组经过精心挑选的患者。