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先天性心脏病中的心房大折返

Atrial macroreentry in congenital heart disease.

作者信息

Twomey Darragh J, Sanders Prashanthan, Roberts-Thomson Kurt C

机构信息

Centre for Heart Rhythm Disorders, Level 5, McEwin Building, Royal Adelaide Hospital, North Terrace, Adelaide, SA 5000, Australia.

出版信息

Curr Cardiol Rev. 2015;11(2):141-8. doi: 10.2174/1573403x10666141013122231.

Abstract

Macroreentrant atrial tachycardia is a common complication following surgery for congenital heart disease (CHD), and is often highly symptomatic with potentially significant hamodynamic consequences. Medical management is often unsuccessful, requiring the use of invasive procedures. Cavotricuspid isthmus dependent flutter is the most common circuit but atypical circuits also exist, involving sites of surgical intervention or areas of scar related to abnormal hemodynamics. Ablation can be technically challenging, due to complex anatomy, and difficulty with catheter stability. A thorough assessment of the patients status and pre-catheter ablation planning is critical to successfully managing these patients.

摘要

大折返性房性心动过速是先天性心脏病(CHD)手术后常见的并发症,通常症状严重,可能产生显著的血流动力学后果。药物治疗往往不成功,需要采用侵入性操作。三尖瓣峡部依赖性房扑是最常见的折返环路,但也存在非典型环路,涉及手术干预部位或与异常血流动力学相关的瘢痕区域。由于解剖结构复杂以及导管稳定性困难,消融在技术上具有挑战性。对患者状况进行全面评估并在导管消融术前进行规划对于成功治疗这些患者至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/4356721/1e0150e97301/CCR-11-141_F1.jpg

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