Literature DB >> 27193897

Why Do Parents Want to Know their Child's Carrier Status? A Qualitative Study.

Danya F Vears1,2,3,4, Clare Delany5,6, John Massie7,5,8,9, Lynn Gillam10,5.   

Abstract

When a child is identified with a genetic condition, some parents want to know the carrier status of their other children. There has been little exploration of why parents want this information. To address this question, semi-structured interviews were conducted with parents of 32 children with cystic fibrosis, haemophilia, and Duchenne muscular dystrophy who wanted to know the carrier status of their other children. Data was analyzed using inductive content analysis. Parents expressed a range of reasons for desiring their child's carrier status, which fell into two broad categories: 1) benefit for the parents and 2) perceived benefit to the child. Parents discussed the desire for certainty and peace of mind derived from having knowledge of their child's status. The most commonly expressed reason for wanting to know their child's carrier status was in order to communicate the information to their child to provide them with the ability to make informed reproductive decisions. These reasons suggest parents are seeking their children's carrier information both as a coping strategy and to communicate carrier information as part of their role as a parent. This has important implications for genetic counseling practice, especially as international guidelines generally recommend against carrier testing in children.

Entities:  

Keywords:  Carrier testing; Children; Communication; Coping; Genetic testing; Information-seeking; Parenting

Mesh:

Year:  2016        PMID: 27193897     DOI: 10.1007/s10897-016-9964-7

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  41 in total

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Authors:  I Matsuda; N Niikawa; K Sato; K Suzumori; Y Fukushima; N Fujiki; I Kanazawa; Y Nakamura; S Yonemoto; Y Nakagome
Journal:  J Hum Genet       Date:  2001       Impact factor: 3.172

Review 2.  Inappropriate genetic testing of children.

Authors:  A Fryer
Journal:  Arch Dis Child       Date:  2000-10       Impact factor: 3.791

3.  Personal experiences of cystic fibrosis (CF) carrier couples prospectively identified in CF families.

Authors:  Lidewij Henneman; Loes Kooij; Katelijne Bouman; Leo P ten Kate
Journal:  Am J Med Genet       Date:  2002-07-15

4.  Coming full circle: a reciprocal-engagement model of genetic counseling practice.

Authors:  Patricia McCarthy Veach; Dianne M Bartels; Bonnie S Leroy
Journal:  J Genet Couns       Date:  2007-10-13       Impact factor: 2.537

5.  Monitoring: a dual-function coping style.

Authors:  Shoshana Shiloh; Michal Orgler-Shoob
Journal:  J Pers       Date:  2006-04

6.  Parents' difficulties and information needs in coping with acute illness in preschool children: a qualitative study.

Authors:  J Kai
Journal:  BMJ       Date:  1996-10-19

7.  Coping with a child with disabilities from the parents' perspective: the function of information.

Authors:  H Pain
Journal:  Child Care Health Dev       Date:  1999-07       Impact factor: 2.508

8.  The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

Authors:  A Clarke
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

9.  Attitudes towards and beliefs about genetic testing in the haemophilia community: a qualitative study.

Authors:  S Thomas; D Herbert; A Street; C Barnes; J Boal; P Komesaroff
Journal:  Haemophilia       Date:  2007-09       Impact factor: 4.287

10.  Technical report: Ethical and policy issues in genetic testing and screening of children.

Authors:  Lainie Friedman Ross; Laine Friedman Ross; Howard M Saal; Karen L David; Rebecca R Anderson
Journal:  Genet Med       Date:  2013-02-21       Impact factor: 8.822

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  6 in total

1.  "They Just Want to Know" - Genetic Health Professionals' Beliefs About Why Parents Want to Know their Child's Carrier Status.

Authors:  Danya F Vears; Clare Delany; John Massie; Lynn Gillam
Journal:  J Genet Couns       Date:  2017-02-04       Impact factor: 2.537

2.  "It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.

Authors:  Charlotte von der Lippe; Jan C Frich; Anna Harris; Kari Nyheim Solbrække
Journal:  J Genet Couns       Date:  2017-05-26       Impact factor: 2.537

3.  Predictive Psychiatric Genetic Testing in Minors: An Exploration of the Non-Medical Benefits.

Authors:  Arianna Manzini; Danya F Vears
Journal:  J Bioeth Inq       Date:  2017-12-11       Impact factor: 1.352

4.  Experiences of Women Who Have Had Carrier Testing for Duchenne Muscular Dystrophy and Becker Muscular Dystrophy During Adolescence.

Authors:  Harry G Fraser; Rebecca Z Redmond; Diana F Scotcher
Journal:  J Genet Couns       Date:  2018-07-04       Impact factor: 2.537

5.  When to break the news and whose responsibility is it? A cross-sectional qualitative study of health professionals' views regarding disclosure of BRCA genetic cancer risk.

Authors:  Alison Luk Young; Phyllis N Butow; Katherine M Tucker; Claire E Wakefield; Emma Healey; Rachel Williams
Journal:  BMJ Open       Date:  2020-02-25       Impact factor: 2.692

6.  Challenges and knowledge gaps facing hemophilia carriers today: Perspectives from patients and health care providers.

Authors:  Megan Chaigneau; Monique Botros; Julie Grabell; Wilma Hopman; Paula James
Journal:  Res Pract Thromb Haemost       Date:  2022-09-20
  6 in total

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