Investigating barriers to genetic counselling and germline mutation testing in women with suspected Hereditary Breast and Ovarian Cancer Syndrome and Lynch syndrome

Josephine Shaw, Caroline Bulsara, Paul Cohen, Madeleine Gryta, Cassandra B Nichols, Lyn Schofield, Sarah O’Sullivan, Nicholas Pachter, Sarah J Hardcastle

Research output: Contribution to journalArticlepeer-review

23 Citations (Scopus)

Abstract

OBJECTIVE: The aim of the current study was to explore barriers to genetic counseling and testing in women with gynecological cancers deemed at significant risk of carrying a germline mutation.
METHODS:
A qualitative study using semi-structured interviews and inductively analysed thematically. Eight patients with ovarian or endometrial cancer participated in individual semi-structured telephone interviews that assessed motivation for genetic counseling and testing, perceived benefits and barriers, timing of the approach, perceptions of the referral process to genetic services and locus of control in relation to cancer and health.
RESULTS:
Analysis of the interview transcripts revealed five themes relating to perceptions of genetic counseling and testing: Lack of importance; Level of information received; Timing of referral processes; Fear and anxiety; Resistance to and perceptions of counseling.
CONCLUSIONS:
Participants had a limited understanding of hereditary cancer syndromes and did not appreciate the benefits of genetic testing. A consistent approach at the time of referral to genetic services is needed to ensure that the level and format of information is appropriate for patients.
PRACTICE IMPLICATIONS:
The rationale for genetic testing needs to be better explained to patients and the timing of referral should be based both on treatment priorities and patient preferences.
Original languageEnglish
Pages (from-to)938-944
Number of pages7
JournalPatient Education and Counseling
Volume101
Issue number5
Early online date12 Dec 2017
DOIs
Publication statusPublished - May 2018

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