Literature DB >> 15057982

Couples' experiences of predictive testing and living with the risk or reality of Huntington disease: a qualitative study.

Fiona Richards1.   

Abstract

A qualitative study, based on family systems theory, was undertaken in order to gain a better understanding of the impact of predictive testing and of living with the risk or reality of Huntington disease (HD), on couple relationships. Semi-structured interviews were conducted with 14 couples; in 9 couples the at-risk partner had undergone testing, and of these, 4 were already affected with HD. At-risk partners in the remaining five couples had not been tested. Interview transcripts were analyzed to obtain a range of themes, which reflect the salient experiences of these couples in relation to HD. Most couples reported that receiving a predictive test result had little or no adverse effect on their relationship. However for two couples who separated after the at-risk partner received a non-carrier result, emotional factors associated with years of living with the HD risk, rather than the result itself, were regarded as having caused irreparable damage to the relationship. For two couples who have remained together since the diagnosis of one partner, loyalty was identified as the main factor contributing to the continuance of the relationship. The separations of the other two couples in which one partner was diagnosed were attributed to emotional distancing, and to the obsessive behavior of the affected partner. The findings of this study highlight both the individuality and the complexity of psychological effects on the intimate relationships of couples who live with the risk or reality of HD, and provide important insights for professionals offering support to these couples. Copyright 2003 Wiley-Liss, Inc.

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Mesh:

Year:  2004        PMID: 15057982     DOI: 10.1002/ajmg.a.20583

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


  10 in total

1.  More appreciation of life or regretting the test? Experiences of living as a mutation carrier of Huntington's disease.

Authors:  Anette Hagberg; The-Hung Bui; Elisabeth Winnberg
Journal:  J Genet Couns       Date:  2010-09-28       Impact factor: 2.537

2.  What to Do with a Second Chance in Life? Long-Term Experiences of Non-carriers of Huntington's Disease.

Authors:  Elisabeth Winnberg; Ulrika Winnberg; Lilian Pohlkamp; Anette Hagberg
Journal:  J Genet Couns       Date:  2018-04-07       Impact factor: 2.537

3.  Impact of Huntington Disease Gene-Positive Status on Pre-Symptomatic Young Adults and Recommendations for Genetic Counselors.

Authors:  Ping Gong; Joanna H Fanos; Lauren Korty; Carly E Siskind; Andrea K Hanson-Kahn
Journal:  J Genet Couns       Date:  2016-04-22       Impact factor: 2.537

4.  Predictive testing and clinical trials in Huntington's disease: An ethical analysis.

Authors:  Cristina Sampaio; Jamie Levey; Robert Klitzman
Journal:  Mov Disord       Date:  2017-12-04       Impact factor: 10.338

5.  Couples' attributions for work function changes in prodromal Huntington disease.

Authors:  Nancy R Downing; Janet K Williams; Jane S Paulsen
Journal:  J Genet Couns       Date:  2010-03-23       Impact factor: 2.537

6.  An exploration of the experience of Huntington's disease in family dyads: an interpretative phenomenological analysis.

Authors:  Caroline Maxted; Jane Simpson; Stephen Weatherhead
Journal:  J Genet Couns       Date:  2013-11-10       Impact factor: 2.537

7.  How do partners find out about the risk of Huntington's disease in couple relationships?

Authors:  Karen Forrest Keenan; Sheila A Simpson; Zosia Miedzybrodzka; David A Alexander; June Semper
Journal:  J Genet Couns       Date:  2013-01-09       Impact factor: 2.537

8.  Impact of Huntington's across the entire disease spectrum: the phases and stages of disease from the patient perspective.

Authors:  A K Ho; M B Hocaoglu
Journal:  Clin Genet       Date:  2011-08-04       Impact factor: 4.438

9.  Decision-making about reproductive choices among individuals at-risk for Huntington's disease.

Authors:  Robert Klitzman; Deborah Thorne; Jennifer Williamson; Wendy Chung; Karen Marder
Journal:  J Genet Couns       Date:  2007-06       Impact factor: 2.717

10.  Families Affected by Huntington's Disease Report Difficulties in Communication, Emotional Involvement, and Problem Solving.

Authors:  Celine M H Jona; Izelle Labuschagne; Emily-Clare Mercieca; Fiona Fisher; Cathy Gluyas; Julie C Stout; Sophie C Andrews
Journal:  J Huntingtons Dis       Date:  2017
  10 in total

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