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首页> 外文期刊>The Canadian journal of cardiology >Assessment of Genetic Causes of Cardiac Arrest
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Assessment of Genetic Causes of Cardiac Arrest

机译:心脏骤停的遗传原因评估

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Unexplained cardiac arrest is defined as a cardiac arrest in the absence of coronary artery disease and overt structural heart disease, present in 5%-10% of cardiac arrest survivors. A genetic contribution to cardiac arrest is more common in this population, most commonly attributed to an inherited ion channel abnormality leading to familial syncope and sudden death. The common causes are Long QT and Brugada syndrome, catecholaminergic ventricular tachycardia, idiopathic ventricular fibrillation, and early repolarization syndrome. Latent structural causes include inherited cardiomyopathy such as arrhythmogenic right ventricular cardiomyopathy. We review these causes in detail and a structured approach to the investigation of these patients, which provides a diagnosis in approximately half of these patients. This allows for the initiation of disease-specific treatments and enables family screening. ? 2013 Canadian Cardiovascular Society.
机译:无法解释的心脏骤停被定义为在无冠心病和明显的结构性心脏病的情况下发生的心脏骤停,在5%-10%的心脏骤停幸存者中存在。对心脏骤停的遗传贡献在该人群中更为常见,最常见的原因是遗传性离子通道异常导致家族性晕厥和猝死。常见原因是Long QT和Brugada综合征,儿茶酚胺能性室性心动过速,特发性室颤和早期复极化综合征。潜在的结构性病因包括遗传性心肌病,例如心律失常性右室心肌病。我们详细审查了这些原因,并以结构化的方式对这些患者进行了调查,这为大约一半的患者提供了诊断。这允许启动疾病特异性治疗并进行家庭筛查。 ? 2013加拿大心血管学会。

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