Literature DB >> 31909521

Clinical and genetic evaluation after sudden cardiac arrest.

Stephanie L Harris1, Steven A Lubitz1,2,3.   

Abstract

Sudden cardiac arrest (SCA) and sudden cardiac death (SCD) can be attributed to cardiac, respiratory, metabolic, and toxicologic etiologies. Most cases of SCD are caused by coronary artery disease and approximately 40% of cardiac arrests are unexplained. Inherited arrythmias and cardiomyopathies are important contributors to SCA and SCD. Identifying an inherited condition after such an event not only has important ramifications for the individual, but also for relatives who may be at risk for the familial condition. This review will provide an overview of inherited cardiovascular disorders than can predispose to SCA/SCD, review the diagnostic evaluation for an individual and/or family after an SCA/SCD, and discuss the role of genetic testing.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  arrhythmia; cardiomyopathy; gene; genetic testing; mutation; sudden cardiac arrest; sudden cardiac death

Mesh：

Year:  2020        PMID： 31909521      PMCID： PMC7008232          DOI： 10.1111/jce.14333

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN： 1045-3873


  41 in total

1.  Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

Authors:  Frank I Marcus; William J McKenna; Duane Sherrill; Cristina Basso; Barbara Bauce; David A Bluemke; Hugh Calkins; Domenico Corrado; Moniek G P J Cox; James P Daubert; Guy Fontaine; Kathleen Gear; Richard Hauer; Andrea Nava; Michael H Picard; Nikos Protonotarios; Jeffrey E Saffitz; Danita M Yoerger Sanborn; Jonathan S Steinberg; Harikrishna Tandri; Gaetano Thiene; Jeffrey A Towbin; Adalena Tsatsopoulou; Thomas Wichter; Wojciech Zareba
Journal:  Circulation       Date:  2010-02-19       Impact factor: 29.690

Review 2.  Defining and redefining the scope and goals of genetic counseling.

Authors:  Robert G Resta
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-11-15       Impact factor: 3.908

3.  Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.

Authors:  Ferhaan Ahmad; Elizabeth M McNally; Michael J Ackerman; Linda C Baty; Sharlene M Day; Iftikhar J Kullo; Peace C Madueme; Martin S Maron; Matthew W Martinez; Lisa Salberg; Matthew R Taylor; Janel E Wilcox
Journal:  Circ Genom Precis Med       Date:  2019-05-23

4.  Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.

Authors:  Chloe Reuter; Megan E Grove; Kate Orland; Katherine Spoonamore; Colleen Caleshu
Journal:  J Genet Couns       Date:  2017-12-12       Impact factor: 2.537

5.  Reduced Uptake of Family Screening in Genotype-Negative Versus Genotype-Positive Long QT Syndrome.

Authors:  Mikael Hanninen; George J Klein; Zachary Laksman; Susan S Conacher; Allan C Skanes; Raymond Yee; Lorne J Gula; Peter Leong-Sit; Jaimie Manlucu; Andrew D Krahn
Journal:  J Genet Couns       Date:  2014-10-03       Impact factor: 2.537

6.  Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.

Authors:  Laurence M Nunn; Luis R Lopes; Petros Syrris; Cian Murphy; Vincent Plagnol; Eileen Firman; Chrysoula Dalageorgou; Esther Zorio; Diana Domingo; Victoria Murday; Iain Findlay; Alexis Duncan; Gerry Carr-White; Leema Robert; Teofila Bueser; Caroline Langman; Simon P Fynn; Martin Goddard; Anne White; Henning Bundgaard; Laura Ferrero-Miliani; Nigel Wheeldon; Simon K Suvarna; Aliceson O'Beirne; Martin D Lowe; William J McKenna; Perry M Elliott; Pier D Lambiase
Journal:  Europace       Date:  2015-10-25       Impact factor: 5.214

7.  Psychological adaptation to molecular autopsy findings following sudden cardiac death in the young.

Authors:  Kezia Bates; Joanna Sweeting; Laura Yeates; Kristie McDonald; Christopher Semsarian; Jodie Ingles
Journal:  Genet Med       Date:  2018-10-16       Impact factor: 8.822

8.  The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.

Authors:  Stephanie Harris; Allison L Cirino; Christina W Carr; Hiwot M Tafessu; Siddharth Parmar; Jeffrey O Greenberg; Lara E Szent-Gyorgyi; Roya Ghazinouri; Michelle G Glowny; Kara McNeil; Efthalia F Kaynor; Catherine Neumann; Christine E Seidman; Calum A MacRae; Carolyn Y Ho; Neal K Lakdawala
Journal:  Mol Genet Genomic Med       Date:  2019-09-03       Impact factor: 2.183

9.  Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome.

Authors:  S Mohsen Hosseini; Raymond Kim; Sharmila Udupa; Gregory Costain; Rebekah Jobling; Eriskay Liston; Seema M Jamal; Marta Szybowska; Chantal F Morel; Sarah Bowdin; John Garcia; Melanie Care; Amy C Sturm; Valeria Novelli; Michael J Ackerman; James S Ware; Ray E Hershberger; Arthur A M Wilde; Michael H Gollob
Journal:  Circulation       Date:  2018-09-18       Impact factor: 29.690

10.  Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.

Authors:  Andre E Minoche; Claire Horvat; Renee Johnson; Velimir Gayevskiy; Sarah U Morton; Alexander P Drew; Kerhan Woo; Aaron L Statham; Ben Lundie; Richard D Bagnall; Jodie Ingles; Christopher Semsarian; J G Seidman; Christine E Seidman; Marcel E Dinger; Mark J Cowley; Diane Fatkin
Journal:  Genet Med       Date:  2018-07-02       Impact factor: 8.822
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  2 in total

1.  Hypoplastic Coronary Artery Disease Presenting with Ventricular Fibrillation Cardiac Arrest.

Authors:  Abra Guo; Hooman Bakhshi; James O'Hara; Leonard Genovese; Adam Fein; Alireza Maghsoudi; Chirag Sandesara
Journal:  Eur J Case Rep Intern Med       Date:  2021-08-02

Review 2.  Sudden cardiac death-update.

Authors:  P Markwerth; T Bajanowski; I Tzimas; R Dettmeyer
Journal:  Int J Legal Med       Date:  2020-12-21       Impact factor: 2.686
  2 in total

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