Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM)

LM Ballard, R Band, AM Lucassen - European Journal of Human …, 2023 - nature.com
Whilst the finding of heritable susceptibility to disease was once relatively rare,
mainstreaming of genetic testing has resulted in a steady increase. Patients are often …

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

M Dowling, N McNamara, JD Ivory, Y Hanhauser… - Patient Education and …, 2024 - Elsevier
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 …

The communication chain of genetic risk: analyses of narrative data exploring proband–provider and proband–family communication in hereditary breast and ovarian …

C Pedrazzani, M Aceti, R Schweighoffer… - Journal of personalized …, 2022 - mdpi.com
Low uptake of genetic services among members of families with hereditary breast and
ovarian cancer (HBOC) suggests limitations of proband-mediated communication of genetic …

[HTML][HTML] Applying the framework for developing and evaluating complex interventions to increase family communication about hereditary cancer

DL Cragun, PP Hunt, M Dean, A Weidner, AK Shields… - PEC innovation, 2023 - Elsevier
Objective Evaluate an intervention to increase family communication (FC) of positive
hereditary cancer test results using the Framework for Developing and Evaluating Complex …

[HTML][HTML] Your family connects: a theory-based intervention to encourage communication about possible inherited cancer risk among ovarian cancer survivors and …

J Zhao, CM McBride, GP Campbell, RD Pentz… - Public health …, 2023 - karger.com
Introduction: Encouraging family communication about possible genetic risk has become
among the most important avenues for achieving the full potential of genomic discovery for …

[HTML][HTML] Perceptions and care recommendations from previvors: qualitative analysis of female BRCA1/2 mutation carriers' experience with genetic testing and …

KE Dibble, LKM Donorfio, PA Britner… - Gynecologic oncology …, 2022 - Elsevier
Introduction It is estimated that 12.5% of women will be diagnosed with breast cancer and
1.10% with ovarian cancer during their lifetime. Although less common, women with these …

What Do Breast Cancer Previvors Tell Us About Their Stories? To Know or Not to Know?

Y Uslu, ER Seda, DS Sezgin, A Yeşilyurt… - Seminars in Oncology …, 2024 - Elsevier
Objectives This study aimed to explore the (1) experiences of breast cancer previvor women
during genetic testing;(2) perceptions of the impact of genetic testing on their personal …

[HTML][HTML] Modes of responsibility in disclosing cancer genetic test results to relatives: An analysis of Swiss and Korean narrative data

M Aceti, M Caiata-Zufferey, C Pedrazzani… - Patient Education and …, 2024 - Elsevier
Objective We examined how responsibility (the “duty to inform relatives about genetic testing
results”) is understood and enacted among Swiss and Korean women carrying BRCA1 or …

An exploration of knowledge, risk perceptions, and communication in a family with multiple genetic risks for Parkinson's disease

EC Daykin, CN Poffenberger, J Do… - Journal of genetic …, 2023 - Wiley Online Library
Genomic testing increasingly challenges health care providers and patients to understand,
share, and use information. The provision of polygenic risks is anticipated to complicate …

Developing and assessing a kin keeping scale with application to identifying central influencers in African American family networks

CG Allen, CM McBride, C Escoffery, Y Guan… - Journal of Community …, 2023 - Springer
Promoting family communication about inherited disease risk is an arena in which family
systems theory is highly relevant. One family systems' construct that can support promotion …