4.1 Article

Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples

Journal

JOURNAL OF GENETIC COUNSELING
Volume 31, Issue 1, Pages 59-70

Publisher

WILEY
DOI: 10.1002/jgc4.1451

Keywords

exome and genomic sequencing; undiagnosed disorders; healthcare empowerment; genetic counseling; parental perspectives; rare disorders

Funding

  1. NIH Common Fund, through the Office of Strategic Coordination/Office of the NIH Director [U01HG007672, UO1HG007703]
  2. Duke University Health System through Genome Sequencing Clinic

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The Genome Empowerment Scale (GEmS) is a research tool to assess parents' perspectives on empowerment during exome or genome sequencing for children with undiagnosed disorders, with emotion-focused and action-oriented scales. The purpose of the study is to provide a strategy for interpreting GEmS results and present illustrative cases to guide genetic counseling for parents of children with undiagnosed conditions.
The Genome Empowerment Scale (GEmS), developed as a research tool, assesses perspectives of parents of children with undiagnosed disorders about to undergo exome or genome sequencing related to the process of empowerment. We defined genomic healthcare empowerment as follows: perceived ability to understand and seek new information related to the genomic sequencing, manage emotions related to the diagnostic process and outcomes, and utilize genomic sequencing information to the betterment of the individual/child and family. The GEmS consists of four scales, two are primarily emotion-focused (Meaning of a Diagnosis, and Emotional Management of the Process) and two are action-oriented (Seeking Information and Support, and Implications and Planning). The purpose of this research was to provide a strategy for interpreting results from the GEmS and present illustrative cases. These illustrations should serve to facilitate use of the GEmS in the clinical and research arena, particularly with respect to guiding genetic counseling processes for parents of children with undiagnosed conditions.

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