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大动脉简单和复杂转位的动脉调转术

Arterial switch in simple and complex transposition of the great arteries.

作者信息

Idriss F S, Ilbawi M N, DeLeon S Y, Duffy C E, Muster A J, Berry T E, Paul M H

机构信息

Division of Cardiovascular-Thoracic Surgery, Children's Memorial Hospital, Chicago, IL 60614.

出版信息

J Thorac Cardiovasc Surg. 1988 Jan;95(1):29-36.

PMID:3336233
Abstract

Arterial switch for repair of transposition of the great arteries was performed on 53 patients since October 1983. These patients were divided into three groups: group I, 25 infants with an intact ventricular septum who had primary repair in the first month of life (2 to 34 days of age, mean 9.7 +/- 6.6); group II, 13 patients with an intact ventricular septum who had anatomic repair after a preliminary procedure (pulmonary artery banding in 13, shunt in 10, atrial septectomy in 1); and group III, 15 infants with transposition of the great arteries and ventricular septal defect. In group III, six patients had Taussig-Bing abnormality, nine had previous pulmonary artery banding, three had coarctation of the aorta repaired earlier in life, and four were less than 2 weeks old. Overall early mortality was 9.4% (5/53: group I 8%, group II 7.6%, group III 13.3%). Two late deaths occurred in group II 10 and 12 weeks postoperatively after infection and high fever. A third late death 18 weeks postoperatively was due to aspiration in an infant with Goldenhar's syndrome. Mortality and morbidity decreased significantly after an initial learning period (no deaths from July 1985 to March 1987 overall, and none in the last 15 infants operated on in group I). The surviving 45 patients are doing well. All have normal sinus rhythm. Two had transient asymptomatic arrhythmias. Left and right ventricular function assessed by echocardiogram and postoperative cardiac catheterization were within normal ranges in all but two patients, one with pulmonary artery stenosis and one (Taussig-Bing abnormality with two large ventricular septal defects) with severe pulmonary vascular disease (9.6 units) observed before anatomic repair. The right ventricular pressure at catheterization ranged from 27 to 42 mm Hg in 12 patients and was 55 mm Hg in two. There was no aortic stenosis. Aortic insufficiency was trivial in three patients and mild in one. We conclude that excellent results can be obtained with arterial switch for transposition of the great arteries with or without ventricular septal defect, especially in neonates.

摘要

自1983年10月以来,对53例大动脉转位患者实施了动脉调转术。这些患者被分为三组:第一组,25例室间隔完整的婴儿,于出生后第一个月(年龄2至34天,平均9.7±6.6天)接受一期修复;第二组,13例室间隔完整的患者,在先行某种手术(13例行肺动脉环扎术,10例行分流术,1例行房间隔切除术)后接受解剖修复;第三组,15例大动脉转位合并室间隔缺损的婴儿。在第三组中,6例有陶西格-宾畸形,9例曾行肺动脉环扎术,3例早年已修复主动脉缩窄,4例年龄小于2周。总体早期死亡率为9.4%(5/53:第一组8%,第二组7.6%,第三组13.3%)。第二组有2例晚期死亡,分别发生在术后10周和12周,死于感染和高热。第三例晚期死亡发生在术后18周,是一名患有Goldenhar综合征的婴儿因误吸所致。经过最初的学习期后,死亡率和发病率显著下降(1985年7月至1987年3月期间总体无死亡,第一组最后15例手术患者也无死亡)。45例存活患者情况良好。均有正常窦性心律。2例有短暂无症状性心律失常。除2例患者外,其余患者经超声心动图和术后心导管检查评估的左右心室功能均在正常范围内,1例有肺动脉狭窄,1例(陶西格-宾畸形合并两个大型室间隔缺损)在解剖修复前观察到有严重肺血管疾病(9.6单位)。心导管检查时,12例患者的右心室压力在27至42 mmHg之间,2例为55 mmHg。无主动脉狭窄。3例患者有轻微主动脉瓣关闭不全,1例为轻度。我们得出结论,无论有无室间隔缺损,大动脉转位采用动脉调转术均可取得优异效果,尤其是在新生儿中。

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