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致心律失常性心肌病:诊断、进展、危险分层及儿科人群——我们目前的状况如何?

Arrhythmogenic Cardiomyopathy: Diagnosis, Evolution, Risk Stratification and Pediatric Population-Where Are We?

作者信息

Cicenia Marianna, Drago Fabrizio

机构信息

Pediatric Cardiology and Arrhythmia/Syncope Complex Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.

出版信息

J Cardiovasc Dev Dis. 2022 Mar 27;9(4):98. doi: 10.3390/jcdd9040098.

DOI:10.3390/jcdd9040098
PMID:35448074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9024428/
Abstract

Arrhythmogenic cardiomyopathy (ACM) is a cardiomyopathy characterized by the occurrence of a high risk of life-threatening ventricular arrhythmias and sudden cardiac death even at presentation. Diagnosis, evolution and outcomes in adults have been extensively reported, but little data in pediatric population are available. Risk stratification in this particular setting is still a matter of debate and new risk factors are needed in a model of an ever more "individualized medicine".

摘要

致心律失常性心肌病(ACM)是一种心肌病,其特征是即使在发病时也存在发生危及生命的室性心律失常和心源性猝死的高风险。关于成人ACM的诊断、病情演变及预后已有大量报道,但儿科人群的数据却很少。在这种特殊情况下的风险分层仍是一个有争议的问题,在日益“个体化医疗”的模式下,还需要新的风险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abb/9024428/9bb770bc35c6/jcdd-09-00098-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abb/9024428/9bb770bc35c6/jcdd-09-00098-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9abb/9024428/9bb770bc35c6/jcdd-09-00098-g001.jpg

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