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Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
Rolf, Bradley A; Schneider, Jennifer L; Amendola, Laura M; Davis, James V; Mittendorf, Kathleen F; Schmidt, Mark A; Jarvik, Gail P; Wilfond, Benjamin S; Goddard, Katrina A B; Ezzell Hunter, Jessica.
Afiliação
  • Rolf BA; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Schneider JL; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Amendola LM; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Davis JV; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Mittendorf KF; Department of Translational and Applied Genomics, Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Schmidt MA; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Jarvik GP; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Wilfond BS; Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital and Research Institute, Seattle, WA, USA.
  • Goddard KAB; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, USA.
  • Ezzell Hunter J; Department of Translational and Applied Genomics, Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
J Genet Couns ; 31(1): 230-241, 2022 02.
Article em En | MEDLINE | ID: mdl-34302314
ABSTRACT
Openness about identity as lesbian, gay, bisexual, transgender, queer, and other sexual orientations and gender identities (LGBTQ+) may cause strain on relationships between family members, which could lead to limited knowledge of cancer family history and reduced communication with family members. As a result, members of the LGBTQ+ community may have more difficulty accessing genetic counseling services for inherited cancer risk. We applied a mixed-methods approach to explore potential barriers to knowledge of cancer family history and family communication among participants of the Cancer Health Assessments Reaching Many (CHARM) study who self-identified as LGBTQ+. We assessed perceptions of family functioning and communication of genetic test results to family members using survey tools and supplemented these data with 20 in-depth interviews to further assess participant perspectives and experiences. LGBTQ+ participants were more likely to report unhealthy family functioning on the survey tool, and some interviewees endorsed that openness about their LGBTQ+ identity led to strained family relationships and reduced communication about their family history of cancer. Overall, this study identified barriers that may be faced by members of the LGBTQ+ community which could limit their ability to access genetic counseling services for inherited cancer risk.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article