TY - JOUR
T1 - Design and evaluation of a visual genomic explainer
T2 - a mixed-methods study
AU - Butler, Grainne
AU - Andersen, Camilla
AU - Buttery, Jim
AU - Gupta, Asheeta
AU - Martyn, Melissa M.
AU - Stark, Zornitza
AU - Wilkins, Ella
AU - Jayasinghe, Kushani
AU - Quinlan, Catherine
PY - 2025/1/24
Y1 - 2025/1/24
N2 - Objective To design and assess a visual genomic explainer focusing on plain language and engaging imagery. The explainer aimed to support doctors' comprehension of complex genomic concepts and results and act as a resource promoting the integration of genomic testing into mainstream care.Design Prospective genomic resource development and questionnaire.Setting Regional and tertiary hospitals in Australia and Ireland, private and community-based clinicians in Australia.Participants Recruitment of paediatricians and nephrologists in Australia and paediatricians in Ireland was multi-faceted. Emails with survey links were circulated through training bodies, advanced trainee networks, departmental heads, and professional societies.Main outcome measures Comprehension, engagement and perception of the visual explainer.Results Most clinicians surveyed (95% (53) Australian group, 100% (29) Irish group) felt that genomics would be a useful tool in their practice. 77% of Australian paediatric respondents and 73% of Irish paediatric respondents felt that genomics was underutilised. Challenges encountered with genomic testing included poor patient comprehension of the testing process and results along with difficulties perceived by clinicians in explaining complex results. 89% of Australian paediatricians and 100% of Irish paediatricians surveyed would recommend the use of the explainer to other professionals in their field.Conclusion This genomic resource was acceptable to clinicians and could be a useful tool to support paediatricians integrating genomic testing into mainstream care.
AB - Objective To design and assess a visual genomic explainer focusing on plain language and engaging imagery. The explainer aimed to support doctors' comprehension of complex genomic concepts and results and act as a resource promoting the integration of genomic testing into mainstream care.Design Prospective genomic resource development and questionnaire.Setting Regional and tertiary hospitals in Australia and Ireland, private and community-based clinicians in Australia.Participants Recruitment of paediatricians and nephrologists in Australia and paediatricians in Ireland was multi-faceted. Emails with survey links were circulated through training bodies, advanced trainee networks, departmental heads, and professional societies.Main outcome measures Comprehension, engagement and perception of the visual explainer.Results Most clinicians surveyed (95% (53) Australian group, 100% (29) Irish group) felt that genomics would be a useful tool in their practice. 77% of Australian paediatric respondents and 73% of Irish paediatric respondents felt that genomics was underutilised. Challenges encountered with genomic testing included poor patient comprehension of the testing process and results along with difficulties perceived by clinicians in explaining complex results. 89% of Australian paediatricians and 100% of Irish paediatricians surveyed would recommend the use of the explainer to other professionals in their field.Conclusion This genomic resource was acceptable to clinicians and could be a useful tool to support paediatricians integrating genomic testing into mainstream care.
KW - Child Health
KW - Genetics
KW - Paediatrics
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=uwapure5-25&SrcAuth=WosAPI&KeyUT=WOS:001349217200001&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1136/archdischild-2024-327650
DO - 10.1136/archdischild-2024-327650
M3 - Article
C2 - 39442982
SN - 0003-9888
VL - 110
SP - 151
EP - 157
JO - Archives of Disease in Childhood
JF - Archives of Disease in Childhood
IS - 2
M1 - archdischild-2024-327650
ER -