Suppr超能文献

首例成功缓解Fontan术后合并肺动脉起源异常左冠状动脉的左心发育不全综合征患者的报道。

First report of successfully palliating a hypoplastic left heart syndrome patient with anomalous left coronary artery from the pulmonary artery beyond Fontan.

作者信息

Riggs Kyle W, Price Nina M, Szugye Nicholas, Goldstein Bryan H, Morales David L S

机构信息

Cincinnati Children's Hospital Medical Center, Heart Institute, Cincinnati, OH, USA.

出版信息

Ann Pediatr Cardiol. 2019 Sep-Dec;12(3):318-320. doi: 10.4103/apc.APC_152_18.

Abstract

We report a case of hypoplastic left heart syndrome with an anomalous left coronary artery from the pulmonary artery (ALCAPA) identified intraoperatively during the Stage-II palliation. Due to recurring ventricular fibrillation on sternotomy, a hybrid Stage-I palliation was performed. During comprehensive Stage-II, the ALCAPA was reimplanted in the neoaorta and measures, including a nontraditional Damus connection/arch reconstruction and classic bilateral Glenn procedures, were taken to avoid compression of the coronary artery. After a successful Fontan procedure, he continues to do well at 5 years old, becoming the first patient reported in the literature to survive all the three stages of single-ventricle palliation.

摘要

我们报告了一例左心发育不全综合征病例,该病例在二期姑息治疗术中发现存在源自肺动脉的异常左冠状动脉(ALCAPA)。由于胸骨切开时反复出现心室颤动,遂进行了一期杂交姑息治疗。在全面的二期治疗中,将ALCAPA重新植入新主动脉,并采取了包括非传统Damus连接/主动脉弓重建和经典双侧格林手术在内的措施,以避免冠状动脉受压。在成功完成Fontan手术之后,他在5岁时情况持续良好,成为文献报道中首例成功度过单心室姑息治疗所有三个阶段的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6c5/6716304/5233d58c1ef3/APC-12-318-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验