Literature DB >> 18241075

Health-related quality of life of children with a positive carrier status for inherited cardiovascular diseases.

Ellen M A Smets1, Marinka M H Stam, Tineke M Meulenkamp, Irene M van Langen, Arthur A M Wilde, Albert Wiegman, Guido M de Wert, Aad Tibben.   

Abstract

Familial hypercholesterolemia, hypertrophic cardiomyopathy, and long QT Syndrome are genetic cardiovascular conditions which may lead to sudden cardiac death at a young age. Preventive measures include lifestyle modifications, medications, and/or cardiac devices. Hence, identification of carrier children can protect them for the potentially life threatening consequences at a young age. Yet, informing children about their genetic risk status and subjecting them to treatment may have negative consequences. This preliminary study aimed to explore (1) how the health-related quality of life of carrier children compares to the quality of life of Dutch children in general; and (2) to what extent the carrier children's quality of life and their parents' perception thereof concur. Our method involved carrier children (n = 35), aged between 8 and 18 years, and their parents (n = 37) who completed a self-report questionnaire. Children's health-related quality of life was assessed with a children and parent version of the KIDSCREEN. Dutch reference data were available from a representative national sample. Our results show no statistically significant differences in scores between carrier children and the reference group. Also, no differences were found between carrier children and their parents' ratings, with the exception of the scale "psychological well being". Parents rated their child's psychological well being significantly lower. We identified no problems with the well-being of carrier children as compared to a representative sample of peers. This may offer some initial reassurance to those who have concerns about the implications of genetically testing children for one of these cardiovascular conditions. Yet, attention to possible problems in these children remains warranted. (c) 2008 Wiley-Liss, Inc.

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Mesh:

Year:  2008        PMID: 18241075     DOI: 10.1002/ajmg.a.32218

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  17 in total

1.  Family Communication in Inherited Cardiovascular Conditions in Ireland.

Authors:  Sinead Whyte; Andrew Green; Marion McAllister; Hannah Shipman
Journal:  J Genet Couns       Date:  2016-06-08       Impact factor: 2.537

2.  Reproductive Decision Making and Genetic Predisposition to Sudden Cardiac Death.

Authors:  Dorit Barlevy; David Wasserman; Marina Stolerman; Kathleen E Erskine; Siobhan M Dolan
Journal:  AJOB Prim Res       Date:  2012-06-19

3.  Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?

Authors:  Rick D Vavolizza; Isha Kalia; Kathleen Erskine Aaron; Louise B Silverstein; Dorit Barlevy; David Wasserman; Christine Walsh; Robert W Marion; Siobhan M Dolan
Journal:  J Genet Couns       Date:  2014-11-18       Impact factor: 2.537

Review 4.  Inherited cardiac arrhythmias: diagnosis, treatment, and prevention.

Authors:  Britt-Maria Beckmann; Arne Pfeufer; Stefan Kääb
Journal:  Dtsch Arztebl Int       Date:  2011-09-16       Impact factor: 5.594

5.  Psychosocial effects in parents and children 12 years after newborn genetic screening for type 1 diabetes.

Authors:  Nicola J Kerruish; Dione M Healey; Andrew R Gray
Journal:  Eur J Hum Genet       Date:  2017-01-25       Impact factor: 4.246

6.  Parental knowledge and attitudes toward hypertrophic cardiomyopathy genetic testing.

Authors:  Sara M Fitzgerald-Butt; Lindsey Byrne; Cynthia A Gerhardt; Kathryn Vannatta; Timothy M Hoffman; Kim L McBride
Journal:  Pediatr Cardiol       Date:  2009-12-01       Impact factor: 1.655

7.  Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications.

Authors:  Elizabeth Ormondroyd; Stephanie Oates; Michael Parker; Edward Blair; Hugh Watkins
Journal:  Eur J Hum Genet       Date:  2013-05-01       Impact factor: 4.246

8.  Making the decision to participate in predictive genetic testing for arrhythmogenic right ventricular cardiomyopathy.

Authors:  April Manuel; Fern Brunger
Journal:  J Genet Couns       Date:  2014-07-01       Impact factor: 2.537

Review 9.  The psychological impact of genetic information on children: a systematic review.

Authors:  Claire E Wakefield; Lucy V Hanlon; Katherine M Tucker; Andrea F Patenaude; Christina Signorelli; Jordana K McLoone; Richard J Cohn
Journal:  Genet Med       Date:  2016-01-07       Impact factor: 8.822

10.  Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population.

Authors:  Anniken Hamang; Geir Egil Eide; Karin Nordin; Berit Rokne; Cathrine Bjorvatn; Nina Øyen
Journal:  BMC Med Genet       Date:  2010-02-17       Impact factor: 2.103

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