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The application of autologous pulmonary artery in surgical correction of complicated aortic arch anomaly

机译:自体肺动脉在复杂主动脉弓畸形手术中的应用

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Background: In the patients with longer-segment aortic arch hypoplasia or interruption with ventricular septal defect, surgery with homograft vessel or autologous pericardial patch to augment descending aortic arch will not result in adverse reactions caused by end-to-end anastomosis. In this study, we retrospectively analyzed primary experience of surgical correction of complicated aortic arch anomaly with autologous main pulmonary artery. Methods: From July 2010 to March 2016, the twenty-one cases of aortic arch complex anomalies were reconstructed with autologous main pulmonary artery. There were 5 patients with interrupted aortic arch and 16 patients with coarctation of aorta. In patients with interrupted aortic arch, anterior wall of main pulmonary artery was excised to form a conduit whose diameter varied according to the area of patient’s body surface. Both ends of the conduit were anastomosed to aortic arch and descending aorta, respectively. In other patients with coarctation of aorta, aortic arch was augmented with tailored pulmonary artery patch in oval shape. The defect of main pulmonary artery was repaired with autologous pericardial patch. Results: There was only one patient died of multiple organ failure postoperatively. The other twenty patients survived without any neurologic complications. Differences of blood pressure between upper and lower limbs were not significant in all cases. During follow-up period, the echocardiography for all patients in the third, sixth, twelfth, and twenty-fourth months showed that blood flow in the descending aortic arch was fluent and there was no obvious blood pressure gradient. Conclusions: Autologous main pulmonary artery can be used to repair complicated aortic arch anomalies completely without any anastomotic tension or bronchial obstruction postoperatively. This procedure is feasible and possesses predominant early and mid-term effects, and autologous main pulmonary artery can retain growth capacity during follow-up period. Of course, it is necessary to draw a definite conclusion of this technique during long-term follow-up period.
机译:背景:在长节段主动脉弓发育不全或室间隔缺损中断的患者中,采用同种异体血管或自体心包膜修补术以增加降主动脉弓的手术不会导致端到端吻合术引起不良反应。在这项研究中,我们回顾性分析了自体主肺动脉对复杂主动脉弓异常进行手术矫正的主要经验。方法:自2010年7月至2016年3月,采用自体主肺动脉重建21例主动脉弓复合体异常。主动脉弓中断5例,主动脉缩窄16例。在主动脉弓中断的患者中,切除主肺动脉前壁以形成导管,导管的直径根据患者的体表面积而变化。导管的两端分别吻合到主动脉弓和降主动脉。在其他主动脉缩窄的患者中,主动脉弓以椭圆形的定制肺动脉膜片增强。自体心包修补术修复了主肺动脉缺损。结果:只有1例患者死于多器官功能衰竭。其余20例患者存活,无神经系统并发症。在所有情况下上肢和下肢之间的血压差异均不显着。在随访期间,第三,第六,十二和十二个月的所有患者的超声心动图检查显示降主动脉弓内的血流通畅,并且没有明显的血压梯度。结论:自体主肺动脉可完全修复复杂的主动脉弓畸形,术后无吻合口张力或支气管阻塞。该方法是可行的,并具有主要的早期和中期效果,并且自体主肺动脉在随访期间可以保持生长能力。当然,有必要在长期随访期间得出该技术的明确结论。

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