医学
Brugada综合征
心脏病学
内科学
表型
遗传学
基因
生物
作者
Martin Martinek,Helmut Pürerfellner
标识
DOI:10.1111/j.1540-8159.2010.02715.x
摘要
This case study shows a young male presenting a mixture of two disease entities: (1) Brugada syndrome with a nearly-normal baseline electrocardiogram and positive Ajmaline drug challenge as well as (2) idiopathic ventricular fibrillation including extremely short-coupled monomorphic ventricular premature beats (VPB) triggering ventricular fibrillation (coupling interval 318 ± 21 ms). In this phenotypic patient group—more suggestive of idiopathic ventricular fibrillation due to the ultra-short coupling interval of the VPBs—drug treatment with a class IA agent such as Quinidine might be an important option to implantable cardioverter-defibrillator and ablation therapy. (PACE 2010; 33:e84–e87)
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