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对患有主动脉弓中断和主-肺动脉窗的早产新生儿在后续进行完全矫正之前采用术中杂交手术进行分期治疗——长期随访。

Staged treatment of a premature newborn with interrupted aortic arch and aorta-pulmonary window using intraoperative hybrid procedure before subsequent total correction - Long-term follow-up.

作者信息

Weryński Piotr, Malinowska-Weryńska Agnieszka, Wójcik Agnieszka, Kołcz Jacek

机构信息

Department of Pediatric Cardiology, Medical College in Cracow, Jagiellonian University, Kraków, Poland.

出版信息

Ann Pediatr Cardiol. 2022 Mar-Apr;15(2):216-218. doi: 10.4103/apc.apc_266_20. Epub 2022 Aug 19.

Abstract

Interrupted aortic arch (IAA) associated with an aortopulmonary window (APW) is a rare cardiac malformation that needs an immediate diagnosis after birth and surgical treatment to avoid irreversible pulmonary lesions. Herein, we describe a case of successful staged treatment of premature neonate using many operative procedures. The first stage was stenting of patent ductus arteriosus with banding of pulmonary artery branches using a hybrid approach. At the age of one, he underwent total correction of malformation using Gore-Tex patch. Two procedures of implantation and redilatation of the previously implanted stents were performed in the following years. In the 8-year follow-up, the patient has been in good clinical condition, without cardiac symptoms. To the best of our knowledge, this is the first case report representing such a long-term follow-up of treatment of IAA accompanied by APW.

摘要

主动脉弓中断(IAA)合并主肺动脉窗(APW)是一种罕见的心脏畸形,出生后需要立即诊断并进行手术治疗,以避免不可逆的肺部病变。在此,我们描述了一例早产新生儿通过多次手术成功进行分期治疗的病例。第一阶段采用杂交手术,对动脉导管进行支架置入并对肺动脉分支进行束带结扎。一岁时,他使用戈尔特斯(Gore-Tex)补片进行了畸形的完全矫正。在接下来的几年里,又进行了两次先前植入支架的植入和再扩张手术。在8年的随访中,患者临床状况良好,无心脏症状。据我们所知,这是首例对伴有APW的IAA治疗进行如此长期随访的病例报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c66d/9564404/94d21931a19c/APC-15-216-g001.jpg

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