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肺动脉吊带综合征的演变,特别提及因未治疗的气管狭窄而需要再次手术的情况。

The evolution of the pulmonary arterial sling syndrome, with particular reference to the need for reoperations because of untreated tracheal stenosis.

作者信息

Loukanov Tsvetomir S, Sebening Christian, Springer Wolfgang, Hagl Siegfried, Karck Matthias, Gorenflo Mathias

机构信息

Department of Cardiac Surgery, University of Heidelberg, Heidelberg, Germany.

出版信息

Cardiol Young. 2009 Sep;19(5):446-50. doi: 10.1017/S1047951109990576. Epub 2009 Aug 7.

Abstract

BACKGROUND

We present a group of infants and children with pulmonary arterial sling and tracheal stenosis. In some of the patients, the anomalously located pulmonary artery had previously been reimplanted, but without simultaneous repair of the trachea.

METHODS

From 1992 to 2007, we reimplanted the left pulmonary artery in 13 children with a pulmonary arterial sling. Their median age was 8 months, with a range from 1 to 72 months. We also performed tracheal resection with end-to-end anastomosis, or complex tracheal reconstructions. In 5 patients, the reoperation was indicated because of persistent tracheal stenosis not treated initially at first correction of the arterial sling. All patients presented with stridor and respiratory distress. Cardiac catheterization, bronchoscopy and multidetecting computer tomography angiography were performed in all cases prior to the operation. All operations were performed under cardiopulmonary bypass.

RESULTS

There was no operative or late mortality. The patients were extubated under bronchoscopic control. The mean period of intubation was 18 plus or minus 8 days, and the average follow-up was 8 plus or minus 4 years. The patients showed no signs of tracheal re-stenosis clinically or on bronchoscopy. The group of the patients under reoperations, however, required longer periods of intubation and hospitalization.

CONCLUSION

Our experience demonstrates that, in patients with a pulmonary arterial sling, any associated tracheal stenosis should be explored at the initial operation, since decompression of the trachea by reimplanting the anomalously located pulmonary artery fails to provide relief. The funnel trachea, if present, undergoes progressive stenosis, and will require surgical repair. The use of cardiopulmonary bypass permitted extensive mobilization of the tracheobronchial tree, and allowed us to perform a tension-free anastomotic reconstruction of the trachea.

摘要

背景

我们报告一组患有肺动脉吊带合并气管狭窄的婴幼儿。部分患者先前已对异常位置的肺动脉进行了再植术,但未同时修复气管。

方法

1992年至2007年,我们对13例患有肺动脉吊带的儿童进行了左肺动脉再植术。他们的中位年龄为8个月,年龄范围为1至72个月。我们还进行了气管切除端端吻合术或复杂的气管重建术。5例患者因在初次矫正动脉吊带时未处理的持续性气管狭窄而需要再次手术。所有患者均有喘鸣和呼吸窘迫症状。所有病例在手术前均进行了心导管检查、支气管镜检查和多层螺旋计算机断层血管造影。所有手术均在体外循环下进行。

结果

无手术或晚期死亡病例。患者在支气管镜控制下拔管。平均插管时间为18±8天,平均随访时间为8±4年。患者在临床或支气管镜检查中均未显示气管再狭窄迹象。然而,再次手术的患者组需要更长的插管和住院时间。

结论

我们的经验表明,对于患有肺动脉吊带的患者,初次手术时应探查任何相关的气管狭窄,因为通过再植异常位置的肺动脉来减轻气管压迫并不能缓解症状。漏斗状气管(如果存在)会逐渐狭窄,需要手术修复。体外循环的使用允许广泛游离气管支气管树,并使我们能够进行无张力的气管吻合重建。

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