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Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies
PURPOSE: This meta-synthesis aimed to synthesise qualitative evidence on experiences of people with Multiple Sclerosis (MS) in receiving a diagnosis, to derive a conceptual understanding of adjustment to MS diagnosis. METHODS: Five electronic databases were systematically searched to identify qualit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928430/ https://www.ncbi.nlm.nih.gov/pubmed/35254195 http://dx.doi.org/10.1080/09638288.2022.2046187 |
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author | Topcu, Gogem Mhizha-Murira, Jacqueline R. Griffiths, Holly Bale, Clare Drummond, Avril Fitzsimmons, Deborah Potter, Kristy-Jane Evangelou, Nikos das Nair, Roshan |
author_facet | Topcu, Gogem Mhizha-Murira, Jacqueline R. Griffiths, Holly Bale, Clare Drummond, Avril Fitzsimmons, Deborah Potter, Kristy-Jane Evangelou, Nikos das Nair, Roshan |
author_sort | Topcu, Gogem |
collection | PubMed |
description | PURPOSE: This meta-synthesis aimed to synthesise qualitative evidence on experiences of people with Multiple Sclerosis (MS) in receiving a diagnosis, to derive a conceptual understanding of adjustment to MS diagnosis. METHODS: Five electronic databases were systematically searched to identify qualitative studies that explored views and experiences around MS diagnosis. Papers were quality-appraised using a standardised checklist. Data synthesis was guided by principles of meta-ethnography, a well-established interpretive method for synthesising qualitative evidence. RESULTS: Thirty-seven papers were selected (with 874 people with MS). Synthesis demonstrated that around the point of MS diagnosis people experienced considerable emotional upheaval (e.g., shock, denial, anger, fear) and difficulties (e.g., lengthy diagnosis process) that limited their ability to make sense of their diagnosis, leading to adjustment difficulties. However, support resources (e.g., support from clinicians) and adaptive coping strategies (e.g., acceptance) facilitated the adjustment process. Additionally, several unmet emotional and informational support needs (e.g., need for personalised information and tailored emotional support) were identified that, if addressed, could improve adjustment to diagnosis. CONCLUSIONS: Our synthesis highlights the need for providing person-centred support and advice at the time of diagnosis and presents a conceptual map of adjustment for designing interventions to improve adjustment following MS diagnosis. IMPLICATIONS FOR REHABILITATION: The period surrounding Multiple Sclerosis diagnosis can be stressful and psychologically demanding. Challenges and disruptions at diagnosis can threaten sense of self, resulting in negative emotions. Adaptive coping skills and support resources could contribute to better adjustment following diagnosis. Support interventions should be tailored to the needs of newly diagnosed people. |
format | Online Article Text |
id | pubmed-9928430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-99284302023-02-15 Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies Topcu, Gogem Mhizha-Murira, Jacqueline R. Griffiths, Holly Bale, Clare Drummond, Avril Fitzsimmons, Deborah Potter, Kristy-Jane Evangelou, Nikos das Nair, Roshan Disabil Rehabil Reviews PURPOSE: This meta-synthesis aimed to synthesise qualitative evidence on experiences of people with Multiple Sclerosis (MS) in receiving a diagnosis, to derive a conceptual understanding of adjustment to MS diagnosis. METHODS: Five electronic databases were systematically searched to identify qualitative studies that explored views and experiences around MS diagnosis. Papers were quality-appraised using a standardised checklist. Data synthesis was guided by principles of meta-ethnography, a well-established interpretive method for synthesising qualitative evidence. RESULTS: Thirty-seven papers were selected (with 874 people with MS). Synthesis demonstrated that around the point of MS diagnosis people experienced considerable emotional upheaval (e.g., shock, denial, anger, fear) and difficulties (e.g., lengthy diagnosis process) that limited their ability to make sense of their diagnosis, leading to adjustment difficulties. However, support resources (e.g., support from clinicians) and adaptive coping strategies (e.g., acceptance) facilitated the adjustment process. Additionally, several unmet emotional and informational support needs (e.g., need for personalised information and tailored emotional support) were identified that, if addressed, could improve adjustment to diagnosis. CONCLUSIONS: Our synthesis highlights the need for providing person-centred support and advice at the time of diagnosis and presents a conceptual map of adjustment for designing interventions to improve adjustment following MS diagnosis. IMPLICATIONS FOR REHABILITATION: The period surrounding Multiple Sclerosis diagnosis can be stressful and psychologically demanding. Challenges and disruptions at diagnosis can threaten sense of self, resulting in negative emotions. Adaptive coping skills and support resources could contribute to better adjustment following diagnosis. Support interventions should be tailored to the needs of newly diagnosed people. Taylor & Francis 2022-03-07 /pmc/articles/PMC9928430/ /pubmed/35254195 http://dx.doi.org/10.1080/09638288.2022.2046187 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Reviews Topcu, Gogem Mhizha-Murira, Jacqueline R. Griffiths, Holly Bale, Clare Drummond, Avril Fitzsimmons, Deborah Potter, Kristy-Jane Evangelou, Nikos das Nair, Roshan Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
title | Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
title_full | Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
title_fullStr | Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
title_full_unstemmed | Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
title_short | Experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
title_sort | experiences of receiving a diagnosis of multiple sclerosis: a meta-synthesis of qualitative studies |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928430/ https://www.ncbi.nlm.nih.gov/pubmed/35254195 http://dx.doi.org/10.1080/09638288.2022.2046187 |
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