Literature DB >> 23026156

Communicating inherited genetic risk between parent and child: a meta-thematic synthesis.

Emma Rowland1, Alison Metcalfe.   

Abstract

OBJECTIVES: Communicating genetic risk is a distressing process for families affected by inherited genetic conditions. This systematic review identifies and explores the challenges faced by parents and their (non)affected or at risk children caused by the (non)disclosure of genetic risk information.
DESIGN: Qualitative meta-synthesis and thematic analysis. DATA SOURCES: Ovid databases; Ovid 'in progress', British Nursing Index, Embase, Medline and Psychinfo were combined with searches of EBSCOhost databases; CINAHL and ERIC and Web of science and ZETOC databases using truncations of communication, chronic illness and disease and words relating to family with specific genetic conditions; Cystic Fibrosis, Duchenne Muscular Dystrophy, Familial Adenomatous Polyposis, Hereditary Non-polyposis Colorectal Cancer, Huntington's Disease, Neurofibromatosis and Sickle Cell Anaemia. This was augmented with free Internet and hand searches and an exploration of the bibliographies of all included papers. REVIEW
METHOD: All papers were quality assessed to ascertain their research quality and methodological rigour.
RESULTS: A total of 2033 citations were retrieved. Following the removal of duplicates, irrelevant articles and the application of an inclusion criterion, 12 articles remained. A further three papers were omitted due to poor quality leaving nine papers which focussed on the disclosure of genetic information between parent and child (<18 years). Eight papers were qualitative in design and one used a mixed method approach. Thematic synthesis produced four themes that inform the structure of the paper; disclosure, emotions involved in disclosure, desired disclosure and recommendations.
CONCLUSION: Disclosure of genetic risk information within families is a highly complex and affective process often resulting in delayed disclosure. This can lead to increased family tensions generated by misunderstanding, blame and secrecy. Early, age appropriate disclosure can better prepare children for future considerations such as care planning and reproductive decision-making. It also contributes to effective coping strategies that promote enhanced adaptation and emotional well being. Early disclosure also reduces parental anxieties concerning disclosure from an unwitting source. Research shows that children and young people want their parents to engage in open and honest discussions about the genetic condition. Therefore to help facilitate effective family communication health professionals should provide family centred care and better emotional and informational support.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23026156     DOI: 10.1016/j.ijnurstu.2012.09.002

Source DB:  PubMed          Journal:  Int J Nurs Stud        ISSN: 0020-7489            Impact factor:   5.837


  25 in total

1.  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

2.  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

3.  Exploring the Discussion of Risk of Sudden Cardiac Death.

Authors:  Kristin Anne Wiley; Erin M Demo; Peggy Walker; C Osborne Shuler
Journal:  Pediatr Cardiol       Date:  2015-10-03       Impact factor: 1.655

Review 4.  Communication of cancer-related genetic and genomic information: A landscape analysis of reviews.

Authors:  Emily B Peterson; Wen-Ying Sylvia Chou; Anna Gaysynsky; Melinda Krakow; Ashley Elrick; Muin J Khoury; Kimberly A Kaphingst
Journal:  Transl Behav Med       Date:  2018-01-29       Impact factor: 3.046

5.  Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.

Authors:  Gabriel Lázaro-Muñoz; John M Conley; Arlene M Davis; Marcia Van Riper; Rebecca L Walker; Eric T Juengst
Journal:  Am J Bioeth       Date:  2015       Impact factor: 11.229

6.  The big reveal: Family disclosure patterns of BRCA genetic test results among young Black women with invasive breast cancer.

Authors:  Claire C Conley; Dana Ketcher; Maija Reblin; Monica L Kasting; Deborah Cragun; Jongphil Kim; Kimlin Tam Ashing; Cheryl L Knott; Chanita Hughes-Halbert; Tuya Pal; Susan T Vadaparampil
Journal:  J Genet Couns       Date:  2020-01-07       Impact factor: 2.537

Review 7.  Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review.

Authors:  Lisa L Shah; Sandra Daack-Hirsch
Journal:  J Genet Couns       Date:  2018-02-28       Impact factor: 2.537

8.  Toward understanding family-related characteristics of young adults with sickle-cell disease or sickle-cell trait in the USA.

Authors:  Patricia E Hershberger; Agatha M Gallo; Robert Molokie; Alexis A Thompson; Marie L Suarez; Yingwei Yao; Constance M Dallas; Diana J Wilkie
Journal:  J Clin Nurs       Date:  2016-03-11       Impact factor: 3.036

Review 9.  Retinoblastoma.

Authors:  Helen Dimaras; Timothy W Corson; David Cobrinik; Abby White; Junyang Zhao; Francis L Munier; David H Abramson; Carol L Shields; Guillermo L Chantada; Festus Njuguna; Brenda L Gallie
Journal:  Nat Rev Dis Primers       Date:  2015-08-27       Impact factor: 52.329

Review 10.  Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.

Authors:  Christopher H Wade; Beth A Tarini; Benjamin S Wilfond
Journal:  Annu Rev Genomics Hum Genet       Date:  2013-07-15       Impact factor: 8.929

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