Conte S, Lacour-Gayet F, Serraf A, Sousa-Uva M, Bruniaux J, Touchot A, Planché C
Department of Pediatric Cardiac Surgery, Marie Lannelongue Hospital, Paris Sud University, Le Plessis Robinson, France.
J Thorac Cardiovasc Surg. 1995 Apr;109(4):663-74; discussion 674-5. doi: 10.1016/S0022-5223(95)70347-0.
Between 1983 and 1994, 307 consecutive neonates underwent coarctation repair by a single surgical technique: extended end-to-end anastomosis. Mean age at operation was 13 +/- 8 days. Isolated coarctation was present in 95 patients (group 1), 102 patients had associated ventricular septal defect (group 2), and 110 patients had associated complex intracardiac lesions (group 3). Aortic arch hypoplasia was present in 81% of the patients (62% in group 1 versus 85% in group 2 and 93% in group 3: p < 0.001). In 271 patients, the aortic arch reconstruction was performed via a left thoracotomy with normothermia (100% of group 1, 95% of group 2, and 72% of group 3); in the other 36 patients, undergoing one-stage repair or palliation of the associated lesion, it was performed via a midline sternotomy during a short period of deep hypothermia and circulatory arrest (5% of group 2 and 28% of group 3). Pulmonary artery banding was performed in 94 patients. Spontaneous ventricular septal defect closure was observed in 39% of the patients of group 2 operated on via thoracotomy. Early mortality rates in groups 1 (2%) and 2 (2%) were significantly lower than in group 3 (17%) (p < 0.001). There were 29 late deaths, all related to associated cardiac lesions or their subsequent repair. The overall total mortality was 16.9%. In group 3 this rate was significantly higher in patients undergoing two-stage procedures (47%) than in those undergoing one-stage repair (23%) (p < 0.05). All but 14 survivors were followed up for a mean of 61 +/- 36 months. Actuarial survivals at 10 years were 98% in group 1, 94% in group 2, and 60% in group 3. The recoarctation rate was 9.8%, leading to 21 reoperations and three angioplasties without mortality. Patients with a more extended or severe form of aortic arch hypoplasia had a significantly higher risk of recoarctation (p < 0.001). Actuarial freedom from reoperation for recoarctation at 10 years was 93%. The findings of this study suggest that extended end-to-end anastomosis provides an adequate and safe repair of neonatal coarctation. Low recoarctation rate, owing to effective relief of the obstruction created by aortic arch hypoplasia and to complete resection of ductal tissue, freedom from major morbidity, and feasibility via both lateral and anterior approaches are the main advantages of the extended end-to-end anastomosis.(ABSTRACT TRUNCATED AT 400 WORDS)
1983年至1994年间,307例连续新生儿采用单一手术技术进行缩窄修复:扩大端端吻合术。手术时的平均年龄为13±8天。95例患者为单纯性缩窄(第1组),102例患者合并室间隔缺损(第2组),110例患者合并复杂心内病变(第3组)。81%的患者存在主动脉弓发育不全(第1组为62%,第2组为85%,第3组为93%:p<0.001)。271例患者通过左胸切口常温下进行主动脉弓重建(第1组100%,第2组95%,第3组72%);另外36例患者进行一期修复或相关病变的姑息治疗,在短时间深低温和循环停止期间通过正中胸骨切开术进行(第2组5%,第3组28%)。94例患者进行了肺动脉环扎术。通过胸切口手术的第2组患者中,39%观察到室间隔缺损自然闭合。第1组(2%)和第2组(2%)的早期死亡率显著低于第3组(17%)(p<0.001)。有29例晚期死亡,均与相关心脏病变或其后续修复有关。总死亡率为16.9%。在第3组中,接受两阶段手术的患者(47%)的这一比率显著高于接受一期修复的患者(23%)(p<0.05)。除14名幸存者外,所有患者均接受了平均61±36个月的随访。10年时的精算生存率第1组为98%,第2组为94%,第3组为60%。再缩窄率为9.8%,导致21例再次手术和3例血管成形术,无死亡。主动脉弓发育不全形式更广泛或更严重的患者再缩窄风险显著更高(p<0.001)。10年时再缩窄再次手术的精算无再手术率为93%。本研究结果表明,扩大端端吻合术为新生儿缩窄提供了充分且安全的修复。由于有效缓解了主动脉弓发育不全造成的梗阻并完全切除导管组织,再缩窄率低;无重大并发症;通过外侧和前方入路均可行,这些是扩大端端吻合术的主要优点。(摘要截断于400字)