Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, Australia Sydney Medical School, University of Sydney, Sydney, Australia Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, Australia Sydney Medical School, University of Sydney, Sydney, Australia Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia.
Eur Heart J. 2015 Jun 1;36(21):1290-6. doi: 10.1093/eurheartj/ehv063. Epub 2015 Mar 11.
The sudden death of a young, apparently fit and healthy person is amongst the most challenging scenarios in clinical medicine. Sudden cardiac death (SCD) is a devastating and tragic outcome of a number of underlying cardiovascular diseases. While coronary artery disease and acute myocardial infarction are the most common causes of SCD in older populations, genetic (inherited) cardiac disorders comprise a substantial proportion of SCD cases aged 40 years and less. This includes the primary arrhythmogenic disorders such as long QT syndromes and inherited cardiomyopathies, namely hypertrophic cardiomyopathy. In up to 30% of young SCD, no cause of death is identified at postmortem, so-called autopsy-negative or sudden arrhythmic death syndrome (SADS). Management of families following SCD begins with a concerted effort to identify the cause of death in the decedent, based on either premorbid clinical details or the pathological findings at postmortem. Where no cause of death is identified, genetic testing of deoxyribonucleic acid extracted from postmortem blood (the molecular autopsy) may identify a cause of death in up to 30% of SADS cases. Irrespective of the genetic testing considerations, all families in which a sudden unexplained death has occurred require targeted and standardized clinical testing in an attempt to identify relatives who may be at-risk of having the same inherited heart disease and therefore also predisposed to an increased risk of SCD. Optimal care of SCD families therefore requires dedicated and appropriately trained staff in the setting of a specialized multidisciplinary cardiac genetic clinic.
年轻、看似健康的人突然死亡是临床医学中最具挑战性的情况之一。心源性猝死(SCD)是多种潜在心血管疾病的灾难性和悲剧性结局。虽然冠状动脉疾病和急性心肌梗死是老年人群中 SCD 的最常见原因,但遗传性(遗传)心脏病构成了 40 岁及以下 SCD 病例的很大一部分。这包括原发性心律失常性疾病,如长 QT 综合征和遗传性心肌病,即肥厚型心肌病。在多达 30%的年轻 SCD 中,死后无法确定死因,所谓的尸检阴性或心律失常性猝死综合征(SADS)。SCD 后对家庭的管理始于根据生前临床详细信息或死后病理学发现,共同努力确定死者的死因。如果无法确定死因,则可以对死后血液中提取的脱氧核糖核酸(分子尸检)进行基因检测,在多达 30%的 SADS 病例中可以确定死因。无论遗传检测如何考虑,所有发生突然不明原因死亡的家庭都需要进行有针对性和标准化的临床检测,以试图识别可能存在相同遗传性心脏病风险的亲属,因此也容易发生 SCD 的风险增加。因此,SCD 家庭的最佳护理需要在专门的多学科心脏遗传诊所中配备专门和适当培训的工作人员。