Sudden Cardiac Arrest
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Last Posted: May 21, 2023
- Rare Genetic Variants Associated With Sudden Cardiac Arrest in the Young: A Prospective, Population-Based Study.
Lauri Holmstrom et al. Circ Genom Precis Med 2023 5 e004105 - Management of Inherited Arrhythmia Syndromes: A HiRO Consensus Handbook on Process of Care.
Mikyla L Janzen et al. CJC Open 2023 5(4) 268-284 - Machine learning of electrophysiological signals for the prediction of ventricular arrhythmias: systematic review and examination of heterogeneity between studies.
Maarten Z H Kolk et al. EBioMedicine 2023 89104462 - Phenotypes of Overdiagnosed Long QT Syndrome.
Sahej Bains et al. Journal of the American College of Cardiology 2023 81(5) 477-486 - Genetic characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry.
Girolami Francesca et al. Frontiers in cardiovascular medicine 2023 91080608 - Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Hoorntje Edgar T et al. Circulation. Genomic and precision medicine 2022 e003672 - Genetic variants in Colombian patients with inherited cardiac conditions.
Rucinski Cynthia et al. Molecular genetics & genomic medicine 2022 e2046 - Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics.
Nafissi Navid A et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003675 - Out-of-hospital pediatric sudden cardiac arrest and inherited arrhythmia syndromes in Hungary.
Környei László et al. Orvosi hetilap 2022 163(12) 473-477 - User interface approaches implemented with automated patient deterioration surveillance tools: protocol for a scoping review.
Wan Yik-Ki Jacob et al. BMJ open 2022 12(1) e055525 - Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death.
Neves Raquel et al. Circulation. Genomic and precision medicine 2021 CIRCGEN121003497 - Sudden Death in the Young: Information for the Primary Care Provider.
Erickson Christopher C et al. Pediatrics 2021 - 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.
Stiles Martin K et al. Journal of arrhythmia 2021 37(3) 481-534 - Non-Ischemic Sudden Cardiac Arrest: Role of 12 Lead Holter, Family Screening and Genetic Testing.
Blich Miry et al. Pacing and clinical electrophysiology : PACE 2021 - Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death.
Scrocco Chiara et al. Nature reviews. Cardiology 2021 - Health data research on sudden cardiac arrest: perspectives of survivors and their next-of-kin.
Bak Marieke A R et al. BMC medical ethics 2021 Jan 22(1) 7 - The End Unexplained Cardiac Death (EndUCD) Registry for Young Australian Sudden Cardiac Arrest.
Paratz Elizabeth D et al. Heart, lung & circulation 2020 Nov - "Concealed cardiomyopathy" as a cause of previously unexplained sudden cardiac arrest.
Isbister Julia C et al. International journal of cardiology 2020 Sep - A Population-Based Registry of Patients With Inherited Cardiac Conditions and Resuscitated Cardiac Arrest.
Rucinski Cynthia et al. Journal of the American College of Cardiology 2020 Jun 75(21) 2698-2707 - Clinical and Genetic Evaluation After Sudden Cardiac Arrest.
Harris Stephanie L et al. Journal of cardiovascular electrophysiology 2020 Jan
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About HLBS-PopOmics
HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Site Citation:
Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2023
- Page last updated:May 31, 2023
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