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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...

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Autores principales: Petrin, Julie, Marrie, Ruth Ann, Devonshire, Virginia, Jichici, Draga, Hrebicek, Olinka, Metz, Luanne M., Morrow, Sarah A., Oh, Jiwon, Smyth, Penelope, Donkers, Sarah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
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.
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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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