Literature DB >> 21503823

Parents' communication with siblings of children affected by an inherited genetic condition.

Gillian Plumridge1, Alison Metcalfe, Jane Coad, Paramjit Gill.   

Abstract

The objective of this study was to explore parents' communication about risk with siblings of children affected by an inherited genetic condition, and to ascertain what level of support, if any, is required from health professionals. Semi-structured interviews were conducted with affected and unaffected children and their parents. Families were affected by one of six genetic conditions representing different patterns of inheritance and variations in age of onset, life expectancy and impact on families. Interviews were analysed using constructivist grounded theory and informed by models which focused on three different aspects of family communication. Interviews with 33 families showed that siblings' information and support needs go largely unrecognized by health professionals and sometimes by parents. Some siblings were actively informed about the genetic condition by parents, others were left to find out and assimilate information by themselves. Siblings were given information about the current symptoms and management of the genetic condition but were less likely to know about its hereditary nature and their own potential risk. When siblings were fully informed about the condition and included in family discussion, they had a better understanding of their role within their family, and family relationships were reported to be more harmonious. The information and support needs of siblings can be overlooked. Parents with the responsibility for caring for a child affected by a genetic condition may require support from health professionals to understand and respond to their unaffected children's need for more information about the genetic condition and its implications for the children's own future health and reproductive decision-making.

Entities:  

Mesh:

Year:  2011        PMID: 21503823     DOI: 10.1007/s10897-011-9361-1

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


  25 in total

1.  Experiences of college-age youths in families with a recessive genetic condition.

Authors:  Marcia J Hern; Theresa A Beery; Detrice G Barry
Journal:  J Fam Nurs       Date:  2006-05       Impact factor: 3.818

2.  Experiences of siblings of patients with Fanconi anemia.

Authors:  Sadie P Hutson; Blanche P Alter
Journal:  Pediatr Blood Cancer       Date:  2007-01       Impact factor: 3.167

3.  Sibling self-report, parental proxies, and quality of life: the importance of multiple informants for siblings of a critically ill child.

Authors:  B A Houtzager; M A Grootenhuis; H N Caron; B F Last
Journal:  Pediatr Hematol Oncol       Date:  2005 Jan-Feb       Impact factor: 1.969

4.  Family communication about genetic risk information: particular issues for Duchenne muscular dystrophy.

Authors:  Gillian Plumridge; Alison Metcalfe; Jane Coad; Paramjit Gill
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

Review 5.  Adaptation to living with a genetic condition or risk: a mini-review.

Authors:  B B Biesecker; L Erby
Journal:  Clin Genet       Date:  2008-09-24       Impact factor: 4.438

6.  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

7.  Parent interview findings regarding the impact of cystic fibrosis on families.

Authors:  S Phillips; W E Bohannon; W F Gayton; S B Friedman
Journal:  J Dev Behav Pediatr       Date:  1985-06       Impact factor: 2.225

Review 8.  Involving children and young people in the development of art-based research tools.

Authors:  Jane Coad; Gill Plumridge; Alison Metcalfe
Journal:  Nurse Res       Date:  2009

9.  Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research.

Authors:  Alison Metcalfe; Jane Coad; Gill M Plumridge; Paramjit Gill; Peter Farndon
Journal:  Eur J Hum Genet       Date:  2008-04-23       Impact factor: 4.246

10.  Psychologic adjustment of the family with a member who has cystic fibrosis.

Authors:  L Cowen; J Mok; M Corey; H MacMillan; R Simmons; H Levison
Journal:  Pediatrics       Date:  1986-05       Impact factor: 7.124

View more
  11 in total

1.  Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.

Authors:  Dana Faux; Kelly Schoch; Sonja Eubanks; Stephen R Hooper; Vandana Shashi
Journal:  J Genet Couns       Date:  2012-08-31       Impact factor: 2.537

2.  Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family.

Authors:  Brenna Hayes; Susan Hassed; Jae Lindsay Chaloner; Christopher E Aston; Carrie Guy
Journal:  J Genet Couns       Date:  2015-10-19       Impact factor: 2.537

3.  The impact of participation in genetic research for families with cleft lip with and without cleft palate: a qualitative study.

Authors:  Lynley J Donoghue; Margaret A Sahhar; Ravi Savarirayan; Supriya Raj; Nicky M Kilpatrick; Laura E Forrest
Journal:  J Community Genet       Date:  2014-02-06

4.  Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families.

Authors:  Peter James B Abad; Cora A Anonuevo; Sandra Daack-Hirsch; Lorna R Abad; Carmencita D Padilla; Mercy Y Laurino
Journal:  J Genet Couns       Date:  2016-11-10       Impact factor: 2.537

5.  Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome.

Authors:  Rebecca Okashah; Kelly Schoch; Stephen R Hooper; Vandana Shashi; Nancy Callanan
Journal:  J Genet Couns       Date:  2014-12-27       Impact factor: 2.537

6.  Parents' perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS).

Authors:  Courtney B Cook; Caitlin Slomp; Jehannine Austin
Journal:  J Community Genet       Date:  2021-11-16

7.  A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders.

Authors:  J Goodwin; K Schoch; V Shashi; S R Hooper; O Morad; M Zalevsky; D Gothelf; L E Campbell
Journal:  J Intellect Disabil Res       Date:  2014-07-25

8.  Talking with Children About Adult-Onset Hereditary Cancer Risk: A Developmental Approach for Parents.

Authors:  Allison Werner-Lin; Shana L Merrill; Amanda C Brandt; Rachel E Barnett; Ellen T Matloff
Journal:  J Genet Couns       Date:  2018-01-30       Impact factor: 2.537

9.  Whether, when, and how to communicate genetic risk to minors: 'I wanted more information but I think they were scared I couldn't handle it'.

Authors:  Kelsey Stuttgen; Allison McCague; Juli Bollinger; Rachel Dvoskin; Debra Mathews
Journal:  J Genet Couns       Date:  2020-07-23       Impact factor: 2.537

10.  Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals.

Authors:  Sandi Dheensa; Anneke Lucassen; Angela Fenwick
Journal:  J Genet Couns       Date:  2017-11-01       Impact factor: 2.537

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.