Literature DB >> 26433939

Exploring the Discussion of Risk of Sudden Cardiac Death.

Kristin Anne Wiley1, Erin M Demo2, Peggy Walker3, C Osborne Shuler4.   

Abstract

Sudden arrhythmic death syndrome (SADS), where death is secondary to cardiac arrhythmia, is associated with several cardiac ion channelopathies, including long QT syndrome and Brugada syndrome, as well as cardiomyopathies such as hypertrophic cardiomyopathy and dilated cardiomyopathy. Many of these conditions often present in childhood or adolescence. This study investigates how diagnoses of cardiac diseases associated with SADS are communicated within families. A questionnaire was distributed through cardiac disease-focused support groups and organizations. Data from 114 parents who have a child with a SADS condition were used for analysis. Based on the responses, parents explained the risk of SADS in a straightforward manner and related the risk to the importance of compliance with the prescribed treatment. Participants also found it difficult to determine and enforce lifestyle modifications, manage individuals' emotional reactions, convey the seriousness of the information without scaring their children, and discuss the risk of SADS during these conversations. Concerns regarding disease progression, length and quality of life, and treatment failures were also expressed. Healthcare providers, the Internet, other affected people, visual aids, and personal experience were all reported to be helpful for facilitating these discussions. Services and resources requested by participants included children's support groups, a counselor or psychologist, and child-oriented materials. Increased understanding of how families discuss children's diagnosis of SADS conditions will equip healthcare providers with the information to address parental concerns and help facilitate meaningful and informative discussions within families.

Entities:  

Keywords:  Communication; Family; Genetics; LQTS; Risk; SADS

Mesh:

Year:  2015        PMID: 26433939     DOI: 10.1007/s00246-015-1272-8

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  13 in total

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Authors:  Michael J Ackerman; Silvia G Priori; Stephan Willems; Charles Berul; Ramon Brugada; Hugh Calkins; A John Camm; Patrick T Ellinor; Michael Gollob; Robert Hamilton; Ray E Hershberger; Daniel P Judge; Hervè Le Marec; William J McKenna; Eric Schulze-Bahr; Chris Semsarian; Jeffrey A Towbin; Hugh Watkins; Arthur Wilde; Christian Wolpert; Douglas P Zipes
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2.  Communicating inherited genetic risk between parent and child: a meta-thematic synthesis.

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Journal:  Int J Nurs Stud       Date:  2012-09-29       Impact factor: 5.837

3.  Adolescents with implantable cardioverter defibrillators: a patient and parent perspective.

Authors:  Belinda Rahman; Ivan Macciocca; Margaret Sahhar; Suleman Kamberi; Vanessa Connell; Rony E Duncan
Journal:  Pacing Clin Electrophysiol       Date:  2011-10-03       Impact factor: 1.976

4.  When I go in to wake them ... I wonder: parental perceptions about congenital long QT syndrome.

Authors:  Monica M Farnsworth; Diane Fosyth; Carla Haglund; Michael J Ackerman
Journal:  J Am Acad Nurse Pract       Date:  2006-06

5.  Experiences of genetic risk: disclosure and the gendering of responsibility.

Authors:  L d'Agincourt-Canning
Journal:  Bioethics       Date:  2001-06       Impact factor: 1.898

6.  Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.

Authors:  Carlo Napolitano; Raffaella Bloise; Nicola Monteforte; Silvia G Priori
Journal:  Circulation       Date:  2012-04-24       Impact factor: 29.690

7.  Family-based cardiac screening in relatives of victims of sudden arrhythmic death syndrome.

Authors:  Catherine McGorrian; Orla Constant; Nicola Harper; Catherine O'Donnell; Mary Codd; Edward Keelan; Andrew Green; James O'Neill; Joseph Galvin; Niall G Mahon
Journal:  Europace       Date:  2013-02-03       Impact factor: 5.214

8.  Genetic risk communication: experiences of adolescent girls and young women from families with fragile X syndrome.

Authors:  Allyn McConkie-Rosell; Elizabeth Melvin Heise; Gail A Spiridigliozzi
Journal:  J Genet Couns       Date:  2009-03-11       Impact factor: 2.537

9.  Living with long QT syndrome: a qualitative study of coping with increased risk of sudden cardiac death.

Authors:  Janice Andersen; Nina Øyen; Cathrine Bjorvatn; Eva Gjengedal
Journal:  J Genet Couns       Date:  2008-08-22       Impact factor: 2.537

Review 10.  The investigation of sudden arrhythmic death syndrome (SADS)-the current approach to family screening and the future role of genomics and stem cell technology.

Authors:  Vishal Vyas; Pier D Lambiase
Journal:  Front Physiol       Date:  2013-09-12       Impact factor: 4.566

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  2 in total

1.  Experience of Asian males communicating cardiac genetic risk within the family.

Authors:  Sylvia Kam; Yasmin Bylstra; Laura Forrest; Ivan Macciocca; Roger Foo
Journal:  J Community Genet       Date:  2018-01-08

2.  Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction.

Authors:  Maria Pia Leone; Pietro Palumbo; Johan Saenen; Sandra Mastroianno; Stefano Castellana; Cesare Amico; Tommaso Mazza; Domenico Rosario Potenza; Antonio Petracca; Marco Castori; Massimo Carella; Giuseppe Di Stolfo
Journal:  Front Cardiovasc Med       Date:  2021-05-20
  2 in total

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