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Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS
OBJECTIVE: The literature that has examined healthcare access and needs of the multiple sclerosis (MS) population is limited. Currently, no research has engaged healthcare providers delivering services to this population to examine their perspectives on the provision of MS care in Canada. We aimed t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018146/ https://www.ncbi.nlm.nih.gov/pubmed/36937527 http://dx.doi.org/10.3389/fneur.2023.1101521 |
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author | Petrin, Julie Marrie, Ruth Ann Devonshire, Virginia Jichici, Draga Hrebicek, Olinka Metz, Luanne M. Morrow, Sarah A. Oh, Jiwon Smyth, Penelope Donkers, Sarah J. |
author_facet | Petrin, Julie Marrie, Ruth Ann Devonshire, Virginia Jichici, Draga Hrebicek, Olinka Metz, Luanne M. Morrow, Sarah A. Oh, Jiwon Smyth, Penelope Donkers, Sarah J. |
author_sort | Petrin, Julie |
collection | PubMed |
description | OBJECTIVE: The literature that has examined healthcare access and needs of the multiple sclerosis (MS) population is limited. Currently, no research has engaged healthcare providers delivering services to this population to examine their perspectives on the provision of MS care in Canada. We aimed to summarize what good MS care should look like according to Canadian healthcare providers working with people with MS, and to identify the supports and resources required, within their care setting, to enable this standard of care. METHODS: A qualitative descriptive approach was taken to analyze data from participants who responded to additional open-ended survey questions, within a larger “MS Models of Care Survey” targeting Canadian healthcare providers working with persons with MS. RESULTS: Currently, a gap exists between what healthcare providers working with persons with MS believe MS care should encompass and what they are able to offer. Participants emphasized that their MS clinics are currently understaffed and patient-to-provider ratios are high, leaving very little time to address the array of healthcare concerns their patients present with. The healthcare providers overwhelmingly described that moving toward multidisciplinary team-based MS care that includes appropriate numbers of MS-trained neurologists, nurses, physiotherapists, occupational therapists, and mental health providers working within one location would be their prioritized approach to comprehensively managing MS care. This model of care enables all professionals to effectively coordinate care and use their time efficiently by only focusing on their area of expertise, all while meeting the needs of their patient in one setting, reducing wait-times and improving overall care. CONCLUSION: To meet the care needs of Canadians with MS, the healthcare system must consider standardizing and funding multidisciplinary team-based MS clinics, comparable to Stroke units, which continue to show favorable health outcomes after years of implementation. |
format | Online Article Text |
id | pubmed-10018146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100181462023-03-17 Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS Petrin, Julie Marrie, Ruth Ann Devonshire, Virginia Jichici, Draga Hrebicek, Olinka Metz, Luanne M. Morrow, Sarah A. Oh, Jiwon Smyth, Penelope Donkers, Sarah J. Front Neurol Neurology OBJECTIVE: The literature that has examined healthcare access and needs of the multiple sclerosis (MS) population is limited. Currently, no research has engaged healthcare providers delivering services to this population to examine their perspectives on the provision of MS care in Canada. We aimed to summarize what good MS care should look like according to Canadian healthcare providers working with people with MS, and to identify the supports and resources required, within their care setting, to enable this standard of care. METHODS: A qualitative descriptive approach was taken to analyze data from participants who responded to additional open-ended survey questions, within a larger “MS Models of Care Survey” targeting Canadian healthcare providers working with persons with MS. RESULTS: Currently, a gap exists between what healthcare providers working with persons with MS believe MS care should encompass and what they are able to offer. Participants emphasized that their MS clinics are currently understaffed and patient-to-provider ratios are high, leaving very little time to address the array of healthcare concerns their patients present with. The healthcare providers overwhelmingly described that moving toward multidisciplinary team-based MS care that includes appropriate numbers of MS-trained neurologists, nurses, physiotherapists, occupational therapists, and mental health providers working within one location would be their prioritized approach to comprehensively managing MS care. This model of care enables all professionals to effectively coordinate care and use their time efficiently by only focusing on their area of expertise, all while meeting the needs of their patient in one setting, reducing wait-times and improving overall care. CONCLUSION: To meet the care needs of Canadians with MS, the healthcare system must consider standardizing and funding multidisciplinary team-based MS clinics, comparable to Stroke units, which continue to show favorable health outcomes after years of implementation. Frontiers Media S.A. 2023-03-02 /pmc/articles/PMC10018146/ /pubmed/36937527 http://dx.doi.org/10.3389/fneur.2023.1101521 Text en Copyright © 2023 Petrin, Marrie, Devonshire, Jichici, Hrebicek, Metz, Morrow, Oh, Smyth and Donkers. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Petrin, Julie Marrie, Ruth Ann Devonshire, Virginia Jichici, Draga Hrebicek, Olinka Metz, Luanne M. Morrow, Sarah A. Oh, Jiwon Smyth, Penelope Donkers, Sarah J. Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS |
title | Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS |
title_full | Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS |
title_fullStr | Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS |
title_full_unstemmed | Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS |
title_short | Good multiple sclerosis (MS) care and how to get there in Canada: Perspectives of Canadian healthcare providers working with persons with MS |
title_sort | good multiple sclerosis (ms) care and how to get there in canada: perspectives of canadian healthcare providers working with persons with ms |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018146/ https://www.ncbi.nlm.nih.gov/pubmed/36937527 http://dx.doi.org/10.3389/fneur.2023.1101521 |
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