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主动脉弓中断修复术:不使用补片的主动脉弓推进术可减少主动脉弓再次干预。

Interrupted aortic arch repair: aortic arch advancement without a patch minimizes arch reinterventions.

作者信息

Morales David L S, Scully Peter T, Braud Brandi E, Booth Justin H, Graves Daniel E, Heinle Jeffrey S, McKenzie E Dean, Fraser Charles D

机构信息

Division of Congenital Heart Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Ann Thorac Surg. 2006 Nov;82(5):1577-83; discussion 1583-4. doi: 10.1016/j.athoracsur.2006.05.105.

Abstract

BACKGROUND

Surgical repair of interrupted aortic arch (IAA) remains challenging and is associated with significant mortality and incidence of late arch obstruction, as recently reported by the Congenital Heart Surgeons' Society (CHSS). In particular, the CHSS reported that any technique other than direct anastomosis with patch augmentation is a risk factor for arch reintervention. The experience at Texas Children's Hospital with IAA repair using an aortic arch advancement technique without a patch was examined.

METHODS

Between July 1995 and December 2005, 60 patients underwent IAA repair using aortic arch advancement without a patch. Selective cerebral perfusion was used in 25 patients (42%). Cox proportional hazards models were used to analyze 20 variables to determine risk factors for death, arch reintervention, and left ventricular outflow tract (LVOT) reintervention.

RESULTS

Median age was 8 days (range, 2 to 271 days) and weight was 3.0 kg (range, 1.7 to 6.1 kg). IAA types were A in 18 (30%) and B in 42 (70%). Associated anomalies were multiple congenital anomalies in 30 (50%) patients, DiGeorge syndrome in 21 (35%), LVOT obstruction in 26 (43%), a single ventricle in 11 (18%), and truncus arteriosus in 6 (10%). Mean follow-up was 3.0 +/- 2.6 years. Five-year freedom from aortic arch reintervention was 100%. Survival at 30 days, 1 year, and 5 years was 93%, 78%, and 76%, respectively. Since July 2000, two of 32 patients have died for an overall survival of 94%. Risk factors for death are older age, multiple congenital anomalies, DiGeorge syndrome, and bicuspid aortic valve. Selective cerebral perfusion was an independent protective variable for survival. Survival for an IAA patient with a ventricular septal defect and no complicating cardiac anomalies was 100%.

CONCLUSIONS

Aortic arch advancement without a patch can be applied to IAA patients, with the expectation of a minimal need for arch reintervention. This technique affords an excellent survival, to which selective cerebral perfusion may be a contributing factor.

摘要

背景

如先天性心脏病外科医生协会(CHSS)最近所报道的,主动脉弓中断(IAA)的手术修复仍然具有挑战性,并且与显著的死亡率和晚期主动脉弓梗阻发生率相关。特别是,CHSS报告称,除了带补片扩大的直接吻合术之外的任何技术都是主动脉弓再次干预的危险因素。我们研究了德克萨斯儿童医院使用无补片的主动脉弓推进技术修复IAA的经验。

方法

在1995年7月至2005年12月期间,60例患者接受了无补片的主动脉弓推进技术修复IAA。25例患者(42%)采用了选择性脑灌注。使用Cox比例风险模型分析20个变量,以确定死亡、主动脉弓再次干预和左心室流出道(LVOT)再次干预的危险因素。

结果

中位年龄为8天(范围为2至271天),体重为3.0千克(范围为1.7至6.1千克)。IAA类型中,A型18例(30%),B型42例(70%)。相关异常情况为:30例(50%)患者有多种先天性异常,21例(35%)患有DiGeorge综合征,26例(43%)存在LVOT梗阻,11例(18%)为单心室,6例(10%)为动脉干。平均随访时间为3.0±2.6年。主动脉弓无再次干预的5年自由度为100%。30天、1年和5年的生存率分别为93%、78%和76%。自2000年7月以来,32例患者中有2例死亡,总体生存率为94%。死亡的危险因素包括年龄较大、多种先天性异常、DiGeorge综合征和二叶式主动脉瓣。选择性脑灌注是生存方面的一个独立保护变量。患有室间隔缺损且无复杂心脏异常的IAA患者的生存率为100%。

结论

无补片的主动脉弓推进技术可应用于IAA患者,预期主动脉弓再次干预的需求最小。这项技术具有出色的生存率,选择性脑灌注可能是一个促成因素。

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