Literature DB >> 15933464

Psychosocial aspects of risk communication and mutation testing in familial breast-ovarian cancer.

Penny Hopwood1.   

Abstract

PURPOSE OF REVIEW: As cancer genetics services develop, psychosocial research evaluating risk communication and mutation testing for familial breast-ovarian cancer has expanded rapidly. It is timely to review findings in key areas. These will inform risk counselling practice and help prepare women making risk management decisions. RECENT
FINDINGS: The psychological effect of risk communication and genetic counselling has been elucidated and women's risk perceptions explored. Knowledge of optimal risk communication strategies is lacking, but recent research shows both consistency in information giving and deficiencies in specific communication skills; the need for personally tailored risk information, which addresses counsellees' concerns, is highlighted. Outcome assessments of risk communication, such as risk perception and psychological distress, are useful but insufficient to evaluate the complex communication process, and decision making in this context is underresearched. Subsequent diffusion of risk information and interfamily communication pose difficulties for high-risk individuals. The short-term psychological consequences of predictive mutation testing are an important focus of research and are largely reassuring, but long-term outcomes are sparse.
SUMMARY: Our understanding of the psychological benefits and limitations of risk counselling and mutation testing can now inform clinical practice, but insufficient knowledge exists of long-term outcomes. Most women are unlikely to be distressed following risk communication, but some may need psychosocial support in the short term following predictive testing for BRCA1/2. Different approaches to risk communication need to be developed and evaluated in parallel with communications skills training to ensure an adequate focus on the women's agenda.

Entities:  

Mesh:

Year:  2005        PMID: 15933464     DOI: 10.1097/01.cco.0000166653.15546.06

Source DB:  PubMed          Journal:  Curr Opin Oncol        ISSN: 1040-8746            Impact factor:   3.645


  10 in total

Review 1.  Patient responses to genetic information: studies of patients with hereditary cancer syndromes identify issues for use of genetic testing in nephrology practice.

Authors:  Kimberly A Kaphingst; Colleen M McBride
Journal:  Semin Nephrol       Date:  2010-03       Impact factor: 5.299

2.  Enhanced counselling for women undergoing BRCA1/2 testing: Impact on knowledge and psychological distress-results from a randomised clinical trial.

Authors:  Pagona Roussi; Kerry Anne Sherman; Suzanne Miller; Joanne Buzaglo; Mary Daly; Alan Taylor; Eric Ross; Andrew Godwin
Journal:  Psychol Health       Date:  2010-04

3.  A family history questionnaire improves detection of women at risk for hereditary gynecologic cancer: a pilot study.

Authors:  Margot M Koeneman; Arnold-Jan Kruse; Simone J S Sep; Cynthia S Gubbels; Brigitte F M Slangen; Toon van Gorp; Alberto Lopes; Encarna Gomez-Garcia; Roy F P M Kruitwagen
Journal:  Fam Cancer       Date:  2014-09       Impact factor: 2.375

4.  Linking genetic counseling content to short-term outcomes in individuals at elevated breast cancer risk.

Authors:  Kimberly M Kelly; Lee Ellington; Nancy Schoenberg; Parul Agarwal; Thomas Jackson; Stephanie Dickinson; Jame Abraham; Electra D Paskett; Howard Leventhal; Michael Andrykowski
Journal:  J Genet Couns       Date:  2014-03-28       Impact factor: 2.537

5.  BRCA patients in Cuba, Greece and Germany: Comparative perspectives on public health, the state and the partial reproduction of 'neoliberal' subjects.

Authors:  Sahra Gibbon; Eirini Kampriani; Andrea Zur Nieden
Journal:  Biosocieties       Date:  2010-11-22

6.  The impact of breast cancer genetic risk assessment on intentions to perform cancer surveillance behaviors.

Authors:  Paul Bennett; Clare Wilkinson; Jim Turner; Gethin Griffith; Barbara France; Kate Brain; Jonathon Gray
Journal:  J Genet Couns       Date:  2007-06-05       Impact factor: 2.537

7.  Effects of a pre-visit educational website on information recall and needs fulfilment in breast cancer genetic counselling, a randomized controlled trial.

Authors:  Akke Albada; Sandra van Dulmen; Jozien M Bensing; Margreet G E M Ausems
Journal:  Breast Cancer Res       Date:  2012-03-06       Impact factor: 6.466

8.  Development and pilot testing of two decision aids for individuals considering genetic testing for cancer risk.

Authors:  Claire E Wakefield; Bettina Meiser; Judi Homewood; Michelle Peate; Judy Kirk; Beverley Warner; Elizabeth Lobb; Clara Gaff; Kathy Tucker
Journal:  J Genet Couns       Date:  2007-02-23       Impact factor: 2.717

9.  To know or not to know? Not the only question in familial breast cancer risk communication.

Authors:  C Maddock; D Schrijvers; Mrd Turco; L Marotti; R Sullivan
Journal:  Ecancermedicalscience       Date:  2011-12-13

10.  Colorectal cancer in the family: psychosocial distress and social issues in the years following genetic counselling.

Authors:  Eveline M A Bleiker; Fred H Menko; Irma Kluijt; Babs G Taal; Miranda A Gerritsma; Lidwina D V Wever; Neil K Aaronson
Journal:  Hered Cancer Clin Pract       Date:  2007-06-15       Impact factor: 2.857

  10 in total

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