European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

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European Soc Human Genetics , European Council Legal Med , European Soc Cardiology Working , European Reference Network Rare , Assoc European Cardiovasc , Fellmann , F , van El , C G & Sajantila , A 2019 , ' European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death ' , European Journal of Human Genetics , vol. 27 , no. 12 , pp. 1763-1773 . https://doi.org/10.1038/s41431-019-0445-y

Title: European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
Author: European Soc Human Genetics; European Council Legal Med; European Soc Cardiology Working; European Reference Network Rare; Assoc European Cardiovasc; Fellmann, Florence; van El, Carla G.; Sajantila, Antti
Contributor: University of Helsinki, Department of Forensic Medicine
Date: 2019-12
Language: eng
Number of pages: 11
Belongs to series: European Journal of Human Genetics
ISSN: 1018-4813
URI: http://hdl.handle.net/10138/308174
Abstract: Sudden cardiac death (SCD) accounts for 10-20% of total mortality, i.e., one in five individuals will eventually die suddenly. Given the substantial genetic component of SCD in younger cases, postmortem genetic testing may be particularly useful in elucidating etiological factors in the cause of death in this subset. The identification of genes responsible for inherited cardiac diseases have led to the organization of cardiogenetic consultations in many countries worldwide. Expert recommendations are available, emphasizing the importance of genetic testing and appropriate information provision of affected individuals, as well as their relatives. However, the context of postmortem genetic testing raises some particular ethical, legal, and practical (including economic or financial) challenges. The Public and Professional Policy Committee of the European Society of Human Genetics (ESHG), together with international experts, developed recommendations on management of SCD after a workshop sponsored by the Brocher Foundation and ESHG in November 2016. These recommendations have been endorsed by the ESHG Board, the European Council of Legal Medicine, the European Society of Cardiology working group on myocardial and pericardial diseases, the ERN GUARD-HEART, and the Association for European Cardiovascular Pathology. They emphasize the importance of increasing the proportion of both medical and medicolegal autopsies and educating the professionals. Multidisciplinary collaboration is of utmost importance. Public funding should be allocated to reach these goals and allow public health evaluation.
Subject: EXPERT CONSENSUS STATEMENT
MOLECULAR AUTOPSY
DIAGNOSTIC YIELD
YOUNG
ASSOCIATION
GUIDELINES
HARMONIZATION
PREVENTION
NATIONWIDE
VARIANTS
3111 Biomedicine
1184 Genetics, developmental biology, physiology
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