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Co-design, implementation, and evaluation of plain language genomic test reports.
Brett, Gemma R; Ward, Aisha; Bouffler, Sophie E; Palmer, Elizabeth E; Boggs, Kirsten; Lynch, Fiona; Springer, Amanda; Nisselle, Amy; Stark, Zornitza.
Afiliação
  • Brett GR; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia. gemma.brett@vcgs.org.au.
  • Ward A; The University of Melbourne, Melbourne, VIC, Australia. gemma.brett@vcgs.org.au.
  • Bouffler SE; The University of Melbourne, Melbourne, VIC, Australia.
  • Palmer EE; Australian Genomics, Melbourne, VIC, Australia.
  • Boggs K; Sydney Children's Hospitals Network, Sydney, NSW, Australia.
  • Lynch F; The University of New South Wales, Sydney, NSW, Australia.
  • Springer A; Australian Genomics, Melbourne, VIC, Australia.
  • Nisselle A; Sydney Children's Hospitals Network, Sydney, NSW, Australia.
  • Stark Z; The University of Melbourne, Melbourne, VIC, Australia.
NPJ Genom Med ; 7(1): 61, 2022 Oct 22.
Article em En | MEDLINE | ID: mdl-36272999
Understanding and communicating genomic results can be challenging for families and health professionals without genetic specialty training. Unlike modifying existing laboratory reports, plain language genomic test reports provide an opportunity for patient/family-centered approaches. However, emerging examples generally lack co-design and/or evaluation in real-world settings. Through co-design involving patient groups, plain language experts, educators, and genetic health professionals, plain language genomic test report templates were produced for common test outcomes in rare diseases. Eight plain language genomic test report templates were developed. These reports were piloted and evaluated as part of a national pediatric ultra-rapid genomic testing program. Family and genetic health professional experiences with report layout, content, and use were explored using surveys. Of 154 families and 107 genetic health professionals issued with reports, 51 families and 57 clinicians responded (RR = 33% and 53%, respectively). Most families (82%) found their report helpful in understanding the result. Reports were shared by 63% of families, predominantly with family members (72%), or health professionals (68%). Clinicians (15%) adapted the reports for other settings. Through co-design, plain language genomic test reports implemented in a real-world setting can facilitate patient/family and caregiver understanding and communication of genomic test purpose, outcome, and potential clinical implications.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Austrália