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Sudden cardiac death in forensic medicine - Swiss recommendations for a multidisciplinary approach.

机译:法医学中的猝死-瑞士建议采用多学科方法。

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摘要

Sudden cardiac death (SCD) is by definition unexpected and cardiac in nature. The investigation is almost invariably performed by a forensic pathologist. Under these circumstances the role of the forensic pathologist is twofold: (1.) to determine rapidly and efficiently the cause and manner of death and (2.) to initiate a multidisciplinary process in order to prevent further deaths in existing family members. If the death is determined to be due to "natural" causes the district attorney in charge often refuses further examinations. However, additional examinations, i.e. extensive histopathological investigations and/or molecular genetic analyses, are necessary in many cases to clarify the cause of death. The Swiss Society of Legal Medicine created a multidisciplinary working group together with clinical and molecular geneticists and cardiologists in the hope of harmonising the approach to investigate SCD. The aim of this paper is to close the gap between the Swiss recommendations for routine forensic post-mortem cardiac examination and clinical recommendations for genetic testing of inherited cardiac diseases; this is in order to optimise the diagnostic procedures and preventive measures for living family members. The key points of the recommendations are (1.) the forensic autopsy procedure for all SCD victims under 40 years of age, (2.) the collection and storage of adequate samples for genetic testing, (3.) communication with the families, and (4.) a multidisciplinary approach including cardiogenetic counselling.
机译:突发性心脏死亡(SCD)从定义上说是意料之外的,并且是心脏性的。该调查几乎总是由法医病理学家执行。在这种情况下,法医病理学家的作用是双重的:(1。)快速有效地确定死亡的原因和方式;(2。)启动多学科过程以防止现有家庭成员进一步死亡。如果确定死亡是由于“自然”原因造成的,负责地区的检察官通常会拒绝进一步检查。但是,在许多情况下,有必要进行额外的检查,即广泛的组织病理学检查和/或分子遗传学分析,以明确死亡原因。瑞士法律医学学会与临床和分子遗传学家以及心脏病专家一起成立了一个多学科工作组,希望能够协调研究SCD的方法。本文的目的是弥合瑞士对常规法医验尸后心脏检查的建议与对遗传性心脏病的基因检测的临床建议之间的差距;这是为了优化对在世家庭成员的诊断程序和预防措施。建议的重点是(1)对所有40岁以下的SCD受害者进行法医尸检程序;(2。)收集和存储足够的样本用于基因检测;(3。)与家人沟通;以及(4.)多学科方法,包括心源性咨询。

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