Onset of pulmonary stenosis after arterial switch operation for transposition of great arteries with intact ventricular septum.

E M Delmo Walter, O Miera, B Nasseri, M Huebler, V Alexi-Meskishvili, F Berger, R Hetzer
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Abstract

Introduction: Pulmonary stenosis remains the most frequent complication and cause of reintervention after the arterial switch operation for transposition of the great arteries We investigated the onset, incidence, and outcome of pulmonary stenosis after arterial switch operation in neonates with transposition of the great arteries and intact ventricular septum.

Methods: Arterial switch operation using Lecompte maneuver was performed in 222 neonates with transposition of great arteries and intact ventricular septum. Complete medical records with serial echocardiograms were available for 174 (73%) patients and were reviewed for incidence of postoperative pulmonary stenosis defined as a thickened and doming pulmonary valve and/or a pressure gradient of >25 mmHg.

Results: During a mean follow-up of 14.4 ± 0.54 years, 31 children developed pulmonary stenosis. Onset of significant stenosis occurred as early as 30 days and as late as 10 years after arterial switch operation. Uncomplicated interventional balloon/stent angioplasty was performed in 11 patients with supravalvular stenosis (mean pressure gradients of 65 mmHg). Severe restenosis occurred in these patients post-angioplasty (range 2-7 years). In other 10 patientseither patch enlargement of the area involved or angioplasty were performed. Freedom from intervention was 68.6±8.7% at 1 year and 42.8.1±9.5% at 15 years and onwards.

Conclusion: Over time, pulmonary stenosis developed after arterial switch operation. Balloon angioplasty for supravalvular pulmonary stenosis could be the initial treatment of choice owing to the high success rate. Surgical intervention is offered to those with pulmonary valve stenosis having pressure gradients of >50 mmHg, and for re-stenosis after intervention/stent implantation.

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完全性室间隔完全性大动脉转位手术后肺动脉狭窄的发生。
前言:肺动脉狭窄仍然是大动脉转位手术后最常见的并发症和再干预的原因。我们研究了大动脉转位和室间隔完整的新生儿动脉转位手术后肺动脉狭窄的发病、发病率和结局。方法:对222例大动脉转位、室间隔完整的新生儿采用leomte手法行动脉切换术。174例(73%)患者有完整的连续超声心动图病历,并回顾了术后肺动脉狭窄的发生率,肺动脉狭窄定义为肺动脉瓣增厚和圆顶和/或压力梯度>25 mmHg。结果:平均随访14.4±0.54年,31例患儿发生肺狭窄。明显狭窄最早发生在动脉转换手术后30天,最晚10年。对11例瓣上狭窄患者(平均压力梯度为65 mmHg)行无并发症介入球囊/支架血管成形术。这些患者在血管成形术后(2-7年)发生严重的再狭窄。在其他10例患者中,进行了斑块扩大或血管成形术。干预自由度1年为68.6±8.7%,15年及以后为42.8.1±9.5%。结论:随着时间的推移,肺动脉开关术后出现肺动脉狭窄。由于成功率高,球囊血管成形术可作为瓣上肺动脉狭窄的首选治疗方法。对于压力梯度> 50mmhg的肺动脉瓣狭窄,以及介入治疗/支架植入后再次狭窄的患者,可进行手术干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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