Literature DB >> 22777929

Genetic counseling does not fulfill the counselees' need for certainty in hereditary breast/ovarian cancer families: an explorative assessment.

Joël Vos1, Fred H Menko, Jan C Oosterwijk, Christi J van Asperen, Anne M Stiggelbout, Aad Tibben.   

Abstract

BACKGROUND: Many cancer-patients undergo DNA testing in the BRCA1/2 genes to receive information about the likelihood that cancer is heritable. Previous nonsystematic studies suggested that DNA testing often does not fulfill the counselees' needs for certainty. We explored the balance between the counselees' need for certainty and perceived certainty (NfC-PC, i.e., level of fulfillment of NfC) regarding the specific domains of DNA test result, heredity and cancer. We also examined relationships of NfC-PC with coping styles and distress.
METHOD: Before disclosure of BRCA1/2 test results for hereditary breast/ovarian cancer (T1), questionnaires were filled in by 467 cancer-patients. Another questionnaire (T2) was filled in after disclosure of pathogenic mutation results (n = 30), uninformative results (n = 202) or unclassified-variants (n = 16).
RESULTS: Before and after DNA test result disclosure, overall 58-94% of all counselees experienced unfulfilled NfC regarding the DNA test result, heredity and cancer. Compared with T1, the communication of pathogenic mutations (T2) caused more fulfillment of the NfC about the DNA test result, but less about cancer and heredity (p < .01). Compared with T1, unclassified variants (T2) did not significantly change the extent of fulfillment of all counselees' needs for certainty (NfC > PC). Compared with T1, uninformative results (T2) caused more fulfillments of all needs than before disclosure (p < 0.01). Counselees differentiated NfC and PC between the domains of DNA-test result, heredity and cancer (p < 0.01). The unfulfilled needs for certainty (NfC-PC) were uncorrelated with cognitive understanding of the DNA test result.
CONCLUSION: The counselees' NfC needs more attention in research and practice, for example, when the potential uncertainties of testing are discussed. The counselees' NfC may be assessed and used in tailored, mutual communication of DNA test results.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 22777929     DOI: 10.1002/pon.3125

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


  9 in total

1.  Perceived ambiguity as a barrier to intentions to learn genome sequencing results.

Authors:  Jennifer M Taber; William M P Klein; Rebecca A Ferrer; Paul K J Han; Katie L Lewis; Leslie G Biesecker; Barbara B Biesecker
Journal:  J Behav Med       Date:  2015-05-24

2.  Factors affecting breast cancer patients' need for genetic risk information: From information insufficiency to information need.

Authors:  Soo Jung Hong; Barbara Biesecker; Jennifer Ivanovich; Melody Goodman; Kimberly A Kaphingst
Journal:  J Genet Couns       Date:  2019-01-24       Impact factor: 2.537

3.  Illustrating Cancer Risk: Patient Risk Communication Preferences and Interest regarding a Novel BRCA1/2 Genetic Risk Modifier Test.

Authors:  Jada G Hamilton; Margaux Genoff Garzon; Ibrahim H Shah; Kechna Cadet; Elyse Shuk; Joy S Westerman; Jennifer L Hay; Kenneth Offit; Mark E Robson
Journal:  Public Health Genomics       Date:  2020-03-19       Impact factor: 2.000

Review 4.  Psychological Distress, Anxiety, and Depression of Cancer-Affected BRCA1/2 Mutation Carriers: a Systematic Review.

Authors:  Johanna Ringwald; Christina Wochnowski; Kristin Bosse; Katrin Elisabeth Giel; Norbert Schäffeler; Stephan Zipfel; Martin Teufel
Journal:  J Genet Couns       Date:  2016-04-14       Impact factor: 2.537

5.  Known unknowns: building an ethics of uncertainty into genomic medicine.

Authors:  Ainsley J Newson; Samantha J Leonard; Alison Hall; Clara L Gaff
Journal:  BMC Med Genomics       Date:  2016-09-01       Impact factor: 3.063

6.  Patient-Centered Care in Breast Cancer Genetic Clinics.

Authors:  Anne Brédart; Amélie Anota; Julia Dick; Violetta Kuboth; Olivier Lareyre; Antoine De Pauw; Alejandra Cano; Dominique Stoppa-Lyonnet; Rita Schmutzler; Sylvie Dolbeault; Jean-Luc Kop
Journal:  Int J Environ Res Public Health       Date:  2018-02-12       Impact factor: 3.390

7.  'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations.

Authors:  Niki M Medendorp; Marij A Hillen; Pomme E A van Maarschalkerweerd; Cora M Aalfs; Margreet G E M Ausems; Senno Verhoef; Lizet E van der Kolk; Lieke P V Berger; Marijke R Wevers; Anja Wagner; Barbara A H Caanen; Anne M Stiggelbout; Ellen M A Smets
Journal:  Fam Cancer       Date:  2019-11-26       Impact factor: 2.375

8.  Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?

Authors:  S L van der Steen; E M Bunnik; M G Polak; K E M Diderich; J Verhagen-Visser; L C P Govaerts; M Joosten; M F C M Knapen; A T J I Go; D Van Opstal; M I Srebniak; R J H Galjaard; A Tibben; S R Riedijk
Journal:  J Genet Couns       Date:  2017-07-04       Impact factor: 2.537

9.  "You Always Have It in the Back of Your Mind"-Feelings, Coping, and Support Needs of Women with Pathogenic Variants in Moderate-Risk Genes for Hereditary Breast Cancer Attending Genetic Counseling in Germany: A Qualitative Interview Study.

Authors:  Claudia Stracke; Clarissa Lemmen; Kerstin Rhiem; Rita Schmutzler; Sibylle Kautz-Freimuth; Stephanie Stock
Journal:  Int J Environ Res Public Health       Date:  2022-03-16       Impact factor: 3.390

  9 in total

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