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121例先天性矫正型大动脉转位患者的预后

Outcome of 121 patients with congenitally corrected transposition of the great arteries.

作者信息

Rutledge J M, Nihill M R, Fraser C D, Smith O'Brian E, McMahon C J, Bezold L I

机构信息

Department of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Pediatr Cardiol. 2002 Mar-Apr;23(2):137-45. doi: 10.1007/s00246-001-0037-8. Epub 2002 Feb 19.

Abstract

Congenitally corrected transposition of the great arteries (ccTGA) is a rare disorder with reduced survival that is influenced by the presence of associated anomalies, tricuspid regurgitation (TR), and right ventricular (RV) function. The double switch procedure has been proposed as an aggressive surgical approach in selected patients. We sought to review our experience with conventional repair to determine if a change in surgical strategy was warranted. Clinical records of 121 patients with ccTGA and two adequate-sized ventricles were retrospectively reviewed. Median length of follow-up was 9.3 years; 5-, 10-, and 20-year survival rates were 92%, 91%, and 75%, respectively. Surgery was performed in 86 patients, including conventional biventricular repair in 47 patients. Risk factors for mortality by univariate analysis included age at biventricular repair (p = 0.04), complete atrioventricular (AV) canal defect (p = 0.02), dextrocardia (p = 0.05), moderate or severe TR (p = 0.05), and poor RV function (p = 0.001). By multivariate analysis, complete AV canal defect (p = 0.006) and poor RV function (p = 0.002) remained significant as risk factors for mortality. Risk factors for the development of significant TR included conventional biventricular repair (p = 0.03) and complete AV block (p = 0.04). Risk factors for progressive RV dysfunction included conventional biventricular repair (p = 0.02), complete AV block (p = 0.001), and moderate or severe TR (p < 0.001). This is the largest nonselected cohort of patients with ccTGA followed at a single center. Our results confirm that significant TR and poor RV function are risk factors for poor outcome and provide convincing evidence that patients undergoing conventional biventricular repair are at higher risk for deterioration of tricuspid valve and right ventricular function compared to palliated or unoperated patients. We support a move toward an alternative surgical approach (double switch procedure) in carefully selected patients.

摘要

先天性矫正型大动脉转位(ccTGA)是一种罕见疾病,其生存率降低,受相关异常、三尖瓣反流(TR)及右心室(RV)功能的影响。双调转手术已被提议作为特定患者的一种积极手术方法。我们试图回顾我们在传统修复方面的经验,以确定是否有必要改变手术策略。对121例ccTGA且有两个大小合适心室的患者的临床记录进行了回顾性分析。中位随访时间为9.3年;5年、10年和20年生存率分别为92%、91%和75%。86例患者接受了手术,其中47例患者接受了传统双心室修复。单因素分析显示,死亡的危险因素包括双心室修复时的年龄(p = 0.04)、完全性房室通道缺损(p = 0.02)、右位心(p = 0.05)、中度或重度TR(p = 0.05)以及右心室功能差(p = 0.001)。多因素分析显示,完全性房室通道缺损(p = 0.006)和右心室功能差(p = 0.002)仍是死亡的危险因素。发生严重TR的危险因素包括传统双心室修复(p = 0.03)和完全性房室传导阻滞(p = 0.04)。右心室功能进行性恶化的危险因素包括传统双心室修复(p = 0.02)、完全性房室传导阻滞(p = 0.001)以及中度或重度TR(p < 0.001)。这是在单一中心随访的最大一组未经选择的ccTGA患者队列。我们的结果证实,严重TR和右心室功能差是预后不良的危险因素,并提供了令人信服的证据,表明与姑息治疗或未手术的患者相比,接受传统双心室修复的患者三尖瓣和右心室功能恶化的风险更高。我们支持在精心挑选的患者中采用替代手术方法(双调转手术)。

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