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A scoping review of parents' disclosure of BRCA1/2 genetic alteration test results to underage children.

作者信息

Diez de Los Rios de la Serna Celia, Dowling Maura, McNamara Nichola, Ivory John D, Hanhauser Yvonne, Murphy Meghan, Dean Marleah

机构信息

School of Medicine, Dentistry & Nursing, University of Glasgow, UK.

School of Nursing and Midwifery, University of Galway, Ireland.

出版信息

Patient Educ Couns. 2025 Feb;131:108561. doi: 10.1016/j.pec.2024.108561. Epub 2024 Nov 27.

DOI:10.1016/j.pec.2024.108561
PMID:39626451
Abstract

BACKGROUND

Individuals with BRCA1/2 mutations have a notably higher than average lifetime risk of developing cancer as adults. Some parents with BRCA1/2 mutations wish to share this information with their children, yet they struggle to know how, when, and what information to share.

OBJECTIVE

The objective of this review was to identify what communication strategies/interventions exist for parents communicating their BRCA1/2 status to their minor children, and what communication interventions do healthcare professionals use to support parents' disclosure process.

METHODS

Scoping review on six databases search for studies with parents and/or healthcare professionals' interventions on supporting communication from parents to children. The review aligned PRISMA guidelines for scoping reviews and used the PAGER recommendations to guide charting and reporting.

RESULTS

22 articles published from 2001 to 2020 were included. Multiple facilitators/motivators of disclosure, how and where parents disclosed, reactions to disclosure were identified. Also, there were no healthcare professionals' interventions in the disclosure process found.

CONCLUSIONS

The review summarizes research on parents' disclosure of their BRCA1/2 status to their underage children and demonstrates a paucity of communication interventions for guiding parents in this difficult process. Parents experience many obstacles communicating the results to their children.

PRACTICE IMPLICATIONS

These findings equip healthcare professionals in their efforts to develop and test interventions which support the communication of genetic risk information. Furthermore, it is evident there is a need for more research to understand how the disclosure process occurs in the families.

摘要

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