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Do research participants share genomic screening results with family members?
Wynn, Julia; Milo Rasouly, Hila; Vasquez-Loarte, Tania; Saami, Akilan M; Weiss, Robyn; Ziniel, Sonja I; Appelbaum, Paul S; Wright Clayton, Ellen; Christensen, Kurt D; Fasel, David; Green, Robert C; Hain, Heather S; Harr, Margaret; Hoell, Christin; Kullo, Iftikhar J; Leppig, Kathleen A; Myers, Melanie F; Pacyna, Joel E; Perez, Emma F; Prows, Cynthia A; Kulchak Rahm, Alanna; Campbell-Salome, Gemme; Sharp, Richard R; Smith, Maureen E; Wiesner, Georgia L; Williams, Janet L; Blout Zawatsky, Carrie L; Gharavi, Ali G; Chung, Wendy K; Holm, Ingrid A.
Afiliação
  • Wynn J; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Milo Rasouly H; Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
  • Vasquez-Loarte T; Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
  • Saami AM; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Weiss R; Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY, USA.
  • Ziniel SI; Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
  • Appelbaum PS; Department of Pediatrics, School of Medicine, University of Colorado, Aurora, CO, USA.
  • Wright Clayton E; Department of Psychiatry, Center for Research on Ethical, Legal & Social Implications of Psychiatric, Neurologic & Behavior Genetics, Columbia University Irving Medical Center, New York, NY, USA.
  • Christensen KD; Center for Biomedical Ethics and Society and Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Fasel D; Department of Population Medicine, Precision Medicine Translational Research (PROMoTeR) Center, Harvard Pilgrim Health Care Institute, Boston, MA, USA.
  • Green RC; Department of Population Medicine, Harvard Medical School, Boston, MA, USA.
  • Hain HS; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
  • Harr M; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Hoell C; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Kullo IJ; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Leppig KA; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Myers MF; Center for Genetic Medicine, Northwestern University, Chicago, IL, USA.
  • Pacyna JE; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
  • Perez EF; Genetic Services and Kaiser Permanente Washington Health Research Institute, Kaiser Permanente of Washington, Seattle, WA, USA.
  • Prows CA; Divisions of Human Genetics and Patient Services, Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Kulchak Rahm A; Biomedical Ethics Program, Mayo Clinic, Rochester, MN, USA.
  • Campbell-Salome G; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Sharp RR; Divisions of Human Genetics and Patient Services, Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Smith ME; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Wiesner GL; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Williams JL; Biomedical Ethics Program, Mayo Clinic, Rochester, MN, USA.
  • Blout Zawatsky CL; Center for Genetic Medicine, Northwestern University, Chicago, IL, USA.
  • Gharavi AG; Division of Genetic Medicine, Department of Medicine, and Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Chung WK; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Holm IA; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
J Genet Couns ; 31(2): 447-458, 2022 04.
Article em En | MEDLINE | ID: mdl-34665896
ABSTRACT
The public health impact of genomic screening can be enhanced by cascade testing. However, cascade testing depends on communication of results to family members. While the barriers and facilitators of family communication have been researched following clinical genetic testing, the factors impacting the dissemination of genomic screening results are unknown. Using the pragmatic Electronic Medical Records and Genomics Network-3 (eMERGE-3) study, we explored the reported sharing practices of participants who underwent genomic screening across the United States. Six eMERGE-3 sites returned genomic screening results for mostly dominant medically actionable disorders and surveyed adult participants regarding communication of results with first-degree relatives. Across the sites, 279 participants completed a 1-month and/or 6-month post-results survey. By 6 months, only 34% of the 156 respondents shared their results with all first-degree relatives and 4% did not share with any. Over a third (39%) first-degree relatives were not notified of the results. Half (53%) of participants who received their results from a genetics provider shared them with all first-degree relatives compared with 11% of participants who received their results from a non-genetics provider. The most frequent reasons for sharing were a feeling of obligation (72%) and that the information could help family members make medical decisions (72%). The most common reasons indicated for not sharing were that the family members were too young (38%), or they were not in contact (25%) or not close to them (25%). These data indicate that the professional returning the results may impact sharing patterns, suggesting that there is a need to continue to educate healthcare providers regarding approaches to facilitate sharing of genetic results within families. Finally, these data suggest that interventions to increase sharing may be universally effective regardless of the origin of the genetic result.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Família / Genômica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Família / Genômica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: J Genet Couns Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
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