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我的做法:用于“揭示”和治疗先天性心脏病中先天性门体静脉连接的新技术。

How I do it: Novel technique to "Unmask" and treat congenital portosystemic venous connections in congenital heart disease.

作者信息

Batlivala Sarosh P, McGovern Eiméar, Goldstein Bryan H

机构信息

Department of Pediatrics, The Heart Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Department of Pediatrics, University of Kentucky Health Care and Kentucky Children's Hospital, Lexington, KY, USA.

出版信息

Ann Pediatr Cardiol. 2022 Jul-Aug;15(4):394-398. doi: 10.4103/apc.apc_34_22. Epub 2023 Jan 6.

Abstract

Congenital portosystemic venous connections are rare vascular anomalies that connect the portal and systemic venous circulations. These vascular lesions can lead to complex and varied physiologic manifestations in single-ventricle patients as they progress through the various stages of palliation in the Fontan pathway. Specifically, these connections may be unmasked after a superior cavopulmonary anastomosis operation, but then "re-masked" after Fontan completion. We describe the complex physiology with an illustrative case report and present a novel method to unmask these pathologic connections after Fontan completion to facilitate transcatheter occlusion and resolve downstream symptoms.

摘要

先天性门体静脉连接是一种罕见的血管异常,它连接门静脉和体静脉循环。这些血管病变在单心室患者沿着Fontan路径进行各个阶段的姑息治疗过程中,会导致复杂多样的生理表现。具体而言,这些连接可能在进行上腔静脉-肺动脉吻合术后显现出来,但在Fontan手术完成后又会“重新隐匿”。我们通过一个病例报告来说明这种复杂的生理情况,并提出一种新方法,在Fontan手术完成后揭示这些病理性连接,以便于经导管封堵并解决下游症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3710/10015395/4b6a5becfed2/APC-15-394-g001.jpg

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