“Out of the blue”: A qualitative study exploring the experiences of women and next of kin receiving unexpected results from BRA‐STRAP research gene panel testing

Author:

Morrow April12ORCID,Speechly Catherine2,Young Alison Luk3,Tucker Kathy24,Harris Rebecca5,Poplawski Nicola67,Andrews Lesley23,Nguyen Dumont Tu89,Kirk Judy5,Southey Melissa C.8910,Willis Amanda1112

Affiliation:

1. Implementation to Impact (i2i), School of Population Health, Faculty of Medicine University of New South Wales Sydney New South Wales Australia

2. Hereditary Cancer Centre Prince of Wales Hospital Randwick New South Wales Australia

3. School of Medicine and Public Health University of Newcastle Callaghan New South Wales Australia

4. UNSW Prince of Wales Clinical School Randwick New South Wales Australia

5. Westmead Hospital Familial Cancer Service Crown Princess Mary Cancer Centre Westmead New South Wales Australia

6. Adult Genetics Unit Royal Adelaide Hospital Adelaide South Australia Australia

7. Adelaide Medical School University of Adelaide Adelaide South Australia Australia

8. Department of Clinical Pathology, Melbourne Medical School The University of Melbourne Parkville Victoria Australia

9. Precision Medicine, School of Clinical Sciences at Monash Health Monash University Clayton Victoria Australia

10. Cancer Council Victoria Melbourne Victoria Australia

11. Clinical Translation and Engagement Platform Garvan Institute of Medical Research Darlinghurst New South Wales Australia

12. School of Clinical Medicine, UNSW Medicine & Health, St Vincent's Healthcare Clinical Campus, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia

Abstract

AbstractIn the genomic era, the availability of gene panel and whole genome/exome sequencing is rapidly increasing. Opportunities for providing former patients with new genetic information are also increasing over time and recontacting former patients with new information is likely to become more common. Breast cancer Refined Analysis of Sequence Tests—Risk And Penetrance (BRA‐STRAP) is an Australian study of individuals who had previously undertaken BRCA1 and BRCA2 genetic testing, with no pathogenic variants detected. Using a waiver of consent, stored DNA samples were retested using a breast/ovarian cancer gene panel and clinically significant results returned to the patient (or next of kin, if deceased). This qualitative study aimed to explore patient experiences, opinions, and expectations of recontacting in the Australian hereditary cancer setting. Participants were familial cancer clinic patients (or next of kin) who were notified of a new pathogenic variant identified via BRA‐STRAP. In‐depth, semi‐structured interviews were conducted approximately 6 weeks post‐result. Interviews were transcribed verbatim and analyzed using an inductive thematic approach. Thirty participants (all female; average age = 57; range 36–84) were interviewed. Twenty‐five were probands, and five were next of kin. Most women reported initial shock upon being recontacted with unexpected news, after having obtained a sense of closure related to their initial genetic testing experiences and cancer diagnosis. For most, this initial distress was short‐lived, followed by a process of readjustment, meaning‐making and adaptation that was facilitated by perceived clinical and personal utility of the information. Women were overall satisfied with the waiver of consent approach and recontacting process. Results are in line with previous studies suggesting that patients have positive attitudes about recontacting. Women in this study valued new genetic information gained from retesting and were satisfied with the BRA‐STRAP recontact model. Practice implications to facilitate readjustment and promote psychosocial adaptation were identified.

Publisher

Wiley

Subject

Genetics (clinical)

Reference46 articles.

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