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Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach
BACKGROUND: Immunosuppression nonadherence may be the most important factor limiting long-term allograft survival. OBJECTIVE: Following user-centered design, we explored the essential priorities and preferences of kidney transplant recipients and healthcare providers (HCP) to inform development of a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808030/ https://www.ncbi.nlm.nih.gov/pubmed/35127106 http://dx.doi.org/10.1177/20543581211072330 |
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author | Schick-Makaroff, Kara Lagendyk, Laura Foster, Bethany Lam, Ngan N. Braam, Branko Bello, Aminu Shojai, Soroush Wen, Kevin |
author_facet | Schick-Makaroff, Kara Lagendyk, Laura Foster, Bethany Lam, Ngan N. Braam, Branko Bello, Aminu Shojai, Soroush Wen, Kevin |
author_sort | Schick-Makaroff, Kara |
collection | PubMed |
description | BACKGROUND: Immunosuppression nonadherence may be the most important factor limiting long-term allograft survival. OBJECTIVE: Following user-centered design, we explored the essential priorities and preferences of kidney transplant recipients and healthcare providers (HCP) to inform development of a smartphone app to improve immunosuppression adherence and communication. DESIGN: A qualitative descriptive research design was used. SETTING: The University of Alberta Hospital adult kidney transplant program in Edmonton, Canada. PARTICIPANTS: Participants were recruited by convenience sampling and included 32 kidney transplant recipients and 11 HCPs. METHODS: Seven focus groups (5 with recipients and 2 with HCPs) were conducted to inform app development. Sessions were recorded, and transcripts were coded to elucidate themes. RESULTS: App development to improve adherence was not a priority for HCP. Recipients prioritized choice: that all features be optional. Recipients preferred support while traveling; access to laboratory results; and use by younger or newly transplanted recipients. Both recipients and HCP preferred linkage to pharmacy; and self-management and accountability. For the app to improve communication, HCPs believed the priorities to be addressed included: clarity on scope of app; legal, ethical, and professional obligations; and charting. Both recipients and HCP prioritized HCP workload, and broader medication and health concerns. Healthcare providers preferred tech support; both recipients and HCPs preferred app access for nontransplant HCP. LIMITATIONS: Limitations include underrepresentation of physicians, recipients with racial/ethnic diversity, and potential selection bias of transplant recipients who perceived themselves to be adhering to immunosuppression medications. CONCLUSION: Future research is needed for the app to become a comprehensive, secure platform for broader communication between recipients and HCP, pharmacies, and nontransplant clinicians while streamlining HCP workload. |
format | Online Article Text |
id | pubmed-8808030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-88080302022-02-03 Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach Schick-Makaroff, Kara Lagendyk, Laura Foster, Bethany Lam, Ngan N. Braam, Branko Bello, Aminu Shojai, Soroush Wen, Kevin Can J Kidney Health Dis Original Clinical Research Qualitative BACKGROUND: Immunosuppression nonadherence may be the most important factor limiting long-term allograft survival. OBJECTIVE: Following user-centered design, we explored the essential priorities and preferences of kidney transplant recipients and healthcare providers (HCP) to inform development of a smartphone app to improve immunosuppression adherence and communication. DESIGN: A qualitative descriptive research design was used. SETTING: The University of Alberta Hospital adult kidney transplant program in Edmonton, Canada. PARTICIPANTS: Participants were recruited by convenience sampling and included 32 kidney transplant recipients and 11 HCPs. METHODS: Seven focus groups (5 with recipients and 2 with HCPs) were conducted to inform app development. Sessions were recorded, and transcripts were coded to elucidate themes. RESULTS: App development to improve adherence was not a priority for HCP. Recipients prioritized choice: that all features be optional. Recipients preferred support while traveling; access to laboratory results; and use by younger or newly transplanted recipients. Both recipients and HCP preferred linkage to pharmacy; and self-management and accountability. For the app to improve communication, HCPs believed the priorities to be addressed included: clarity on scope of app; legal, ethical, and professional obligations; and charting. Both recipients and HCP prioritized HCP workload, and broader medication and health concerns. Healthcare providers preferred tech support; both recipients and HCPs preferred app access for nontransplant HCP. LIMITATIONS: Limitations include underrepresentation of physicians, recipients with racial/ethnic diversity, and potential selection bias of transplant recipients who perceived themselves to be adhering to immunosuppression medications. CONCLUSION: Future research is needed for the app to become a comprehensive, secure platform for broader communication between recipients and HCP, pharmacies, and nontransplant clinicians while streamlining HCP workload. SAGE Publications 2022-01-31 /pmc/articles/PMC8808030/ /pubmed/35127106 http://dx.doi.org/10.1177/20543581211072330 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Clinical Research Qualitative Schick-Makaroff, Kara Lagendyk, Laura Foster, Bethany Lam, Ngan N. Braam, Branko Bello, Aminu Shojai, Soroush Wen, Kevin Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach |
title | Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach |
title_full | Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach |
title_fullStr | Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach |
title_full_unstemmed | Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach |
title_short | Designing an App for Immunosuppression Adherence and Communication: A Qualitative Approach |
title_sort | designing an app for immunosuppression adherence and communication: a qualitative approach |
topic | Original Clinical Research Qualitative |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8808030/ https://www.ncbi.nlm.nih.gov/pubmed/35127106 http://dx.doi.org/10.1177/20543581211072330 |
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