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IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy

Growing demand for genetic counselling and testing has created a need for innovative service delivery models to provide quality care in an efficient manner. The goal of this study was to develop and evaluate a patient-facing webinar providing pre-test genetic counselling to individuals with hypertro...

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Detalles Bibliográficos
Autores principales: Christian, Susan, Tagoe, Julia, Delday, Lenore, Bernier, Francois P., Kohut, Ruth, Ferrier, Raechel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582342/
https://www.ncbi.nlm.nih.gov/pubmed/34766249
http://dx.doi.org/10.1007/s12687-021-00564-x
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author Christian, Susan
Tagoe, Julia
Delday, Lenore
Bernier, Francois P.
Kohut, Ruth
Ferrier, Raechel
author_facet Christian, Susan
Tagoe, Julia
Delday, Lenore
Bernier, Francois P.
Kohut, Ruth
Ferrier, Raechel
author_sort Christian, Susan
collection PubMed
description Growing demand for genetic counselling and testing has created a need for innovative service delivery models to provide quality care in an efficient manner. The goal of this study was to develop and evaluate a patient-facing webinar providing pre-test genetic counselling to individuals with hypertrophic cardiomyopathy. A patient-facing webinar was developed and implemented between April 2019 and January 2021. It was evaluated using the Alberta Quality Matrix for Health framework, which considers the patient experience across the domains of effectiveness, appropriateness, acceptability, accessibility, and efficiency. The webinar group showed comparable scores to controls with regard to self-perceived knowledge and decisional conflict. The majority of patients reported that the webinar met their expectations and was an acceptable replacement for a 1:1 genetic counselling appointment. Finally, the webinar reduced genetic counsellor time to an average of 24 min per patient. Providing pre-test genetic counselling to index hypertrophic cardiomyopathy patients via a group webinar has achieved a high quality of care, and optimized use of provider and space resources. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12687-021-00564-x.
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spelling pubmed-85823422021-11-12 IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy Christian, Susan Tagoe, Julia Delday, Lenore Bernier, Francois P. Kohut, Ruth Ferrier, Raechel J Community Genet Original Article Growing demand for genetic counselling and testing has created a need for innovative service delivery models to provide quality care in an efficient manner. The goal of this study was to develop and evaluate a patient-facing webinar providing pre-test genetic counselling to individuals with hypertrophic cardiomyopathy. A patient-facing webinar was developed and implemented between April 2019 and January 2021. It was evaluated using the Alberta Quality Matrix for Health framework, which considers the patient experience across the domains of effectiveness, appropriateness, acceptability, accessibility, and efficiency. The webinar group showed comparable scores to controls with regard to self-perceived knowledge and decisional conflict. The majority of patients reported that the webinar met their expectations and was an acceptable replacement for a 1:1 genetic counselling appointment. Finally, the webinar reduced genetic counsellor time to an average of 24 min per patient. Providing pre-test genetic counselling to index hypertrophic cardiomyopathy patients via a group webinar has achieved a high quality of care, and optimized use of provider and space resources. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12687-021-00564-x. Springer Berlin Heidelberg 2021-11-11 2022-02 /pmc/articles/PMC8582342/ /pubmed/34766249 http://dx.doi.org/10.1007/s12687-021-00564-x Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021
spellingShingle Original Article
Christian, Susan
Tagoe, Julia
Delday, Lenore
Bernier, Francois P.
Kohut, Ruth
Ferrier, Raechel
IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
title IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
title_full IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
title_fullStr IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
title_full_unstemmed IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
title_short IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
title_sort impact webinars: improving patient access to genetic counselling and testing using webinars—the alberta experience with hypertrophic cardiomyopathy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582342/
https://www.ncbi.nlm.nih.gov/pubmed/34766249
http://dx.doi.org/10.1007/s12687-021-00564-x
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