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A territory-wide study of arrhythmogenic right ventricular cardiomyopathy patients from Hong Kong
medRxiv - Cardiovascular Medicine Pub Date : 2021-11-20 , DOI: 10.1101/2021.11.17.21266304
Ishan Lakhani , Jiandong Zhou , Sharen Lee , Ka Hou Christien Lee , Keith Sai Kit Leung , Guoliang Li , Tong Liu , Ian Chi Kei Wong , Ngai Shing Mok , Chloe Mak , Wing Tak Wong , Qingpeng Zhang , Gary Tse

Background Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a hereditary disease characterized by fibrofatty infiltration of the right ventricular myocardium that predisposes affected patients to malignant ventricular arrhythmias, dual-chamber cardiac failure and sudden cardiac death (SCD). The present study aims to investigate the risk of detrimental cardiovascular events in an Asian population of ARVC/D patients, including the incidence of malignant ventricular arrhythmias, new-onset heart failure with reduced ejection fraction (HFrEF), as well as long-term mortality.
更新日期:2021-11-23
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