Literature DB >> 23233440

Distress in unaffected individuals who decline, delay or remain ineligible for genetic testing for hereditary diseases: a systematic review.

Louise Heiniger1, Phyllis N Butow, Melanie A Price, Margaret Charles.   

Abstract

OBJECTIVE: Reviews on the psychosocial aspects of genetic testing for hereditary diseases typically focus on outcomes for carriers and non-carriers of genetic mutations. However, the majority of unaffected individuals from high-risk families do not undergo predictive testing. The aim of this review was to examine studies on psychosocial distress in unaffected individuals who delay, decline or remain ineligible for predictive genetic testing.
METHOD: Systematic searches of Medline, CINAHL, PsychINFO, PubMed and handsearching of related articles published between 1990 and 2012 identified 23 articles reporting 17 different studies that were reviewed and subjected to quality assessment.
RESULTS: Findings suggest that definitions of delaying and declining are not always straightforward, and few studies have investigated psychological distress among individuals who remain ineligible for testing. Findings related to distress in delayers and decliners have been mixed, but there is evidence to suggest that cancer-related distress is lower in those who decline genetic counselling and testing, compared with testers, and that those who remain ineligible for testing experience more anxiety than tested individuals. Psychological, personality and family history vulnerability factors were identified for decliners and individuals who are ineligible for testing.
CONCLUSIONS: The small number of studies and methodological limitations preclude definitive conclusions. Nevertheless, subgroups of those who remain untested appear to be at increased risk for psychological morbidity. As the majority of unaffected individuals do not undergo genetic testing, further research is needed to better understand the psychological impact of being denied the option of testing, declining and delaying testing.
Copyright © 2012 John Wiley & Sons, Ltd.

Entities:  

Keywords:  anxiety; cancer; cancer-related distress; depression; genetic testing; oncology

Mesh:

Year:  2012        PMID: 23233440     DOI: 10.1002/pon.3235

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  9 in total

1.  Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.

Authors:  Anita Y Kinney; Laurie E Steffen; Barbara H Brumbach; Wendy Kohlmann; Ruofei Du; Ji-Hyun Lee; Amanda Gammon; Karin Butler; Saundra S Buys; Antoinette M Stroup; Rebecca A Campo; Kristina G Flores; Jeanne S Mandelblatt; Marc D Schwartz
Journal:  J Clin Oncol       Date:  2016-06-20       Impact factor: 44.544

Review 2.  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

3.  Facilitators and Challenges in Psychosocial Adaptation to Being at Increased Familial Risk of Breast Cancer.

Authors:  Louise Heiniger; Melanie A Price; Margaret Charles; Phyllis N Butow
Journal:  J Genet Couns       Date:  2015-03-05       Impact factor: 2.537

4.  Applying public health screening criteria: how does universal newborn screening compare to universal tumor screening for Lynch syndrome in adults with colorectal cancer?

Authors:  Deborah Cragun; Rita D DeBate; Tuya Pal
Journal:  J Genet Couns       Date:  2014-10-18       Impact factor: 2.537

5.  Postpartum women's attitudes to disclosure of adult-onset conditions in pregnancy.

Authors:  Vitalia Libman; Michal Macarov; Yechiel Friedlander; Sidra Goldman-Mellor; Salomon Israel; Drorith Hochner-Celnikier; Yishai Sompolinsky; Uri Pinchas Dior; Michael Osovsky; Lina Basel-Salmon; Arnon Wiznitzer; Yehuda Neumark; Vardiella Meiner; Ayala Frumkin; Shiri Shkedi-Rafid; Hagit Hochner
Journal:  Prenat Diagn       Date:  2022-05-04       Impact factor: 3.242

6.  Women's concerns about the emotional impact of awareness of heritable breast cancer risk and its implications for their children.

Authors:  Suzanne C O'Neill; Darren Mays; Andrea Farkas Patenaude; Judy E Garber; Tiffani A DeMarco; Beth N Peshkin; Katherine A Schneider; Kenneth P Tercyak
Journal:  J Community Genet       Date:  2014-08-07

7.  Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals.

Authors:  Shanna L Gustafson; Victoria M Raymond; Monica L Marvin; Tobias Else; Erika Koeppe; Elena M Stoffel; Jessica N Everett
Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

8.  Understanding the Needs of Young Women Regarding Breast Cancer Risk Assessment and Genetic Testing: Convergence and Divergence among Patient-Counselor Perceptions and the Promise of Peer Support.

Authors:  Chalanda Evans; Rebekah J Hamilton; Kenneth P Tercyak; Beth N Peshkin; Kantoniony Rabemananjara; Claudine Isaacs; Suzanne C O'Neill
Journal:  Healthcare (Basel)       Date:  2016-06-28

Review 9.  Family Adjustment to Hereditary Cancer Syndromes: A Systematic Review.

Authors:  Pedro Gomes; Giada Pietrabissa; Eunice R Silva; João Silva; Paula Mena Matos; Maria Emília Costa; Vanessa Bertuzzi; Eliana Silva; Maria Carolina Neves; Célia M D Sales
Journal:  Int J Environ Res Public Health       Date:  2022-01-30       Impact factor: 3.390

  9 in total

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