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Development of a measure of genome sequencing knowledge for young people: The kids-KOGS.
Lewis, Celine; Loe, Bao S; Sidey-Gibbons, Chris; Patch, Christine; Chitty, Lyn S; Sanderson, Saskia C.
Afiliación
  • Lewis C; North East Thames Regional Genetics Services, Great Ormond Street Hospital NHS Foundation Trust, London, UK.
  • Loe BS; UCL Great Ormond Street Institute of Child Health, London, UK.
  • Sidey-Gibbons C; The Psychometrics Centre, University of Cambridge, Cambridge, UK.
  • Patch C; Patient Reported Outcomes, Value and Experience (PROVE) Centre, Brigham and Women's Hospital, Boston, Massachusetts.
  • Chitty LS; Genomics England, Queen Mary University of London, London, UK.
  • Sanderson SC; Counselling, Society and Ethics Research, Wellcome Genome Campus, Cambridge, UK.
Clin Genet ; 96(5): 411-417, 2019 11.
Article en En | MEDLINE | ID: mdl-31323115
Genome sequencing (GS) is increasingly being used to diagnose rare diseases in paediatric patients; however, no measures exist to evaluate their knowledge of this technology. We aimed to develop a robust measure of knowledge of GS (the kids-KOGS') suitable for use in the paediatric setting as well as for general public education. The target age was 11 to 15 year olds. An iterative process involving six sequential stages was conducted to develop a set of draft true/false items. These were then administered to 539 target-age school pupils (mean 12.8; SD ± 1.3), from the United Kingdom. Item-response theory was used to confirm the psychometric suitability of the candidate items. None of the Items was identified as misfits. All 10 items performed well under the two-parameter logistic model. The internal consistency of the test was 0.84 (Cronbach alpha value) indicating excellent reliability. The mean kids-KOGS score in the sample overall was 4.24 (SD; 2.49), where 0 = low knowledge and 10 = high knowledge. Age was positively associated with score in a multivariate linear regression. The kids-KOGS is a short and reliable tool that can be used by researchers and healthcare professionals offering GS to paediatric patients. Further validation in a clinical setting is required.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pediatría / Enfermedades Raras / Secuenciación Completa del Genoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Clin Genet Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pediatría / Enfermedades Raras / Secuenciación Completa del Genoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Clin Genet Año: 2019 Tipo del documento: Article