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Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study

BACKGROUND AND AIMS: When youth with diabetes transition from pediatric to adult diabetes care, they are at high risk for loss to follow up and worsening glucose control. We aimed to gain insight on how to improve the transition of youth with type 1 diabetes from pediatric to adult diabetes care fro...

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Autores principales: Butalia, Sonia, McGuire, K. Ashlee, Dyjur, David, Mercer, Julia, Pacaud, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7410016/
https://www.ncbi.nlm.nih.gov/pubmed/32782975
http://dx.doi.org/10.1002/hsr2.181
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author Butalia, Sonia
McGuire, K. Ashlee
Dyjur, David
Mercer, Julia
Pacaud, Daniele
author_facet Butalia, Sonia
McGuire, K. Ashlee
Dyjur, David
Mercer, Julia
Pacaud, Daniele
author_sort Butalia, Sonia
collection PubMed
description BACKGROUND AND AIMS: When youth with diabetes transition from pediatric to adult diabetes care, they are at high risk for loss to follow up and worsening glucose control. We aimed to gain insight on how to improve the transition of youth with type 1 diabetes from pediatric to adult diabetes care from the patients' and parents' perspective. METHODS: We conducted focus groups in youth with type 1 diabetes in transition from pediatric to adult diabetes care and their parents, in Calgary, Alberta, between June and August 2014. Eligibility criteria included: (a) type 1 diabetes; (b) aged 15 to 25 years; (c) have or had received care at the pediatric hospital; and, (d) either pre or post‐transfer; or, (e) parents of recently transferred youth. Purposive sampling was used, and the theoretical framework used was the Integrated Behaviour Model. Participants were asked about positive, negative, or challenging experiences related to diabetes and transition, solutions to challenges, and tools and strategies to improve and better support transition. Thematic analysis was conducted after focus groups were recorded and transcribed. RESULTS: Three focus groups were conducted: pre‐transfer youth with diabetes (4 females and 3 males; median age 17.5 years, IQR 1.3 years); post‐transfer young adults with diabetes (2 females and 2 males; median age 23.5 years, IQR 1.2 years); and parents of recently transferred young adults with diabetes (n = 3). Main themes were: (a) communication technology; (b) the need for more transition and diabetes education and preparation during transition; and, (c) the importance and need for social and peer support. CONCLUSION: This study describes specific areas that may improve diabetes transfer and transition from pediatric to adult diabetes care. This information can help inform clinical care delivery for transition and the development of programs, strategies, and interventions to improve transition care.
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spelling pubmed-74100162020-08-10 Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study Butalia, Sonia McGuire, K. Ashlee Dyjur, David Mercer, Julia Pacaud, Daniele Health Sci Rep Research Articles BACKGROUND AND AIMS: When youth with diabetes transition from pediatric to adult diabetes care, they are at high risk for loss to follow up and worsening glucose control. We aimed to gain insight on how to improve the transition of youth with type 1 diabetes from pediatric to adult diabetes care from the patients' and parents' perspective. METHODS: We conducted focus groups in youth with type 1 diabetes in transition from pediatric to adult diabetes care and their parents, in Calgary, Alberta, between June and August 2014. Eligibility criteria included: (a) type 1 diabetes; (b) aged 15 to 25 years; (c) have or had received care at the pediatric hospital; and, (d) either pre or post‐transfer; or, (e) parents of recently transferred youth. Purposive sampling was used, and the theoretical framework used was the Integrated Behaviour Model. Participants were asked about positive, negative, or challenging experiences related to diabetes and transition, solutions to challenges, and tools and strategies to improve and better support transition. Thematic analysis was conducted after focus groups were recorded and transcribed. RESULTS: Three focus groups were conducted: pre‐transfer youth with diabetes (4 females and 3 males; median age 17.5 years, IQR 1.3 years); post‐transfer young adults with diabetes (2 females and 2 males; median age 23.5 years, IQR 1.2 years); and parents of recently transferred young adults with diabetes (n = 3). Main themes were: (a) communication technology; (b) the need for more transition and diabetes education and preparation during transition; and, (c) the importance and need for social and peer support. CONCLUSION: This study describes specific areas that may improve diabetes transfer and transition from pediatric to adult diabetes care. This information can help inform clinical care delivery for transition and the development of programs, strategies, and interventions to improve transition care. John Wiley and Sons Inc. 2020-08-06 /pmc/articles/PMC7410016/ /pubmed/32782975 http://dx.doi.org/10.1002/hsr2.181 Text en © 2020 The Authors. Health Science Reports published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Butalia, Sonia
McGuire, K. Ashlee
Dyjur, David
Mercer, Julia
Pacaud, Daniele
Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study
title Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study
title_full Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study
title_fullStr Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study
title_full_unstemmed Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study
title_short Youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: A qualitative study
title_sort youth with diabetes and their parents' perspectives on transition care from pediatric to adult diabetes care services: a qualitative study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7410016/
https://www.ncbi.nlm.nih.gov/pubmed/32782975
http://dx.doi.org/10.1002/hsr2.181
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