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主动脉弓中断的选择性管理策略可降低左心室流出道梗阻风险。

Selective management strategy of interrupted aortic arch mitigates left ventricular outflow tract obstruction risk.

作者信息

Alsoufi Bahaaldin, Schlosser Brian, McCracken Courtney, Sachdeva Ritu, Kogon Brian, Border William, Mahle William T, Kanter Kirk

机构信息

Division of Cardiothoracic Surgery, Department of Surgery, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, Ga.

Division of Cardiology, Department of Pediatrics, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, Ga.

出版信息

J Thorac Cardiovasc Surg. 2016 Feb;151(2):412-20. doi: 10.1016/j.jtcvs.2015.09.060. Epub 2015 Sep 28.

Abstract

BACKGROUND

Left ventricular outflow tract obstruction (LVOTO) is an important problem after interrupted aortic arch (IAA) repair, especially when early reoperation is required during infancy. Several anatomic factors have been identified that increase LVOTO risk; surgical strategies such as concomitant resection of the conal septum or left ventricular outflow tract (LVOT) bypass (single-stage Yasui operation, or staged Norwood procedure, followed by the Rastelli procedure) have been proposed for such patients.

METHODS

From 2002 to 2013, a total of 77 neonates underwent IAA repair. Based on the presence of anatomic substrate for LVOTO, patients underwent standard IAA repair and ventricular septal defect closure (n = 53; 69%), concomitant conal resection (n = 7; 9%), or LVOT bypass (n = 17; 22%, staged in 14). We analyzed anatomic details that influence procedure choice, and explored reoperation risk and survival after repair.

RESULTS

Neonates who had conal resection or LVOT bypass had significantly smaller aortic valve and subaortic areas, as well as a trend toward a higher prevalence of type B IAA, aberrant right subclavian artery, and bicuspid aortic valve. Freedom from LVOT reoperation was 96% and 80%, at 1 and 8 years, respectively, and was lower after conal resection (P = .008). Most LVOT reoperations (73%) were for discrete subaortic obstruction. Survival was 86% at 8 years, and was not related to procedure choice, whereas freedom from all-cause reoperation was 65% at 8 years, and was higher after standard repair (P = .029).

CONCLUSIONS

Compared with published reports, this selective management strategy, which is customized to the degree of aortic valve and subaortic area narrowing, has mitigated and delayed LVOTO risk. With this tailored approach, most LVOT reoperations occur after infancy and are commonly for discrete subaortic obstruction. The effect of aortic valve and LVOT narrowing on increased LVOTO risk is neutralized with LVOT bypass procedures; however, it continues to be the highest after conal resection, suggesting the superiority of LVOT bypass, compared with enlargement in neonates who are at risk of developing LVOTO.

摘要

背景

左心室流出道梗阻(LVOTO)是主动脉弓中断(IAA)修复术后的一个重要问题,尤其是在婴儿期需要早期再次手术时。已确定多种解剖因素会增加LVOTO风险;对于此类患者,已提出一些手术策略,如同时切除圆锥间隔或左心室流出道(LVOT)旁路手术(单阶段安井手术,或分期诺伍德手术,随后进行拉斯泰利手术)。

方法

2002年至2013年,共有77例新生儿接受了IAA修复术。根据是否存在LVOTO的解剖学基础,患者接受标准IAA修复和室间隔缺损闭合术(n = 53;69%)、同时进行圆锥切除(n = 7;9%)或LVOT旁路手术(n = 17;22%,14例为分期手术)。我们分析了影响手术选择的解剖学细节,并探讨了再次手术风险和修复术后的生存率。

结果

接受圆锥切除或LVOT旁路手术的新生儿,其主动脉瓣和主动脉下面积明显较小,且B型IAA、迷走右锁骨下动脉和二叶式主动脉瓣的患病率有升高趋势。LVOT再次手术的1年和8年无再手术率分别为96%和80%,圆锥切除术后较低(P = 0.008)。大多数LVOT再次手术(73%)是针对局限性主动脉下梗阻。8年生存率为86%,与手术选择无关,而8年全因再次手术的无再手术率为65%,标准修复术后较高(P = 0.029)。

结论

与已发表的报告相比,这种根据主动脉瓣和主动脉下面积狭窄程度定制的选择性管理策略,减轻并延缓了LVOTO风险。采用这种定制方法,大多数LVOT再次手术发生在婴儿期之后,且通常是针对局限性主动脉下梗阻。LVOT旁路手术可抵消主动脉瓣和LVOT狭窄对增加LVOTO风险的影响;然而,圆锥切除术后该风险仍然最高,这表明与有发生LVOTO风险的新生儿的扩大手术相比,LVOT旁路手术具有优越性。

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