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A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder
OBJECTIVES: To elucidate the experiences and perceptions of people living with primary frozen shoulder and their priorities for treatment. DESIGN: Qualitative study design using semistructured interviews. SETTING: General practitioner (GP) and musculoskeletal clinics in primary and secondary care in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787409/ https://www.ncbi.nlm.nih.gov/pubmed/24078753 http://dx.doi.org/10.1136/bmjopen-2013-003452 |
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author | Jones, Susan Hanchard, Nigel Hamilton, Sharon Rangan, Amar |
author_facet | Jones, Susan Hanchard, Nigel Hamilton, Sharon Rangan, Amar |
author_sort | Jones, Susan |
collection | PubMed |
description | OBJECTIVES: To elucidate the experiences and perceptions of people living with primary frozen shoulder and their priorities for treatment. DESIGN: Qualitative study design using semistructured interviews. SETTING: General practitioner (GP) and musculoskeletal clinics in primary and secondary care in one National Health Service Trust in England. PARTICIPANTS: 12 patients diagnosed with primary frozen shoulder were purposively recruited from a GP's surgery, community clinics and hospital clinics. Recruitment targeted the phases of frozen shoulder: pain predominant (n=5), stiffness predominant (n=4) and residual stiffness predominant following hospital treatment (n=2). One participant dropped out. Inclusion criteria: adult, male and female patients of any age, attending the clinics, who had been diagnosed with primary frozen shoulder. RESULTS: The most important experiential themes identified by participants were: pain which was severe as well as inexplicable; inconvenience/disability arising from increasing restriction of movement (due to pain initially, gradually giving way to stiffness); confusion/anxiety associated with delay in diagnosis and uncertainty about the implications for the future; and treatment-related aspects. Participants not directly referred to a specialist (whether physiotherapist, physician or surgeon) wanted a faster, better-defined care pathway. Specialist consultation brought more definitive diagnosis, relief from anxiety and usually self-rated improvement. The main treatment priority was improved function, though there was recognition that this might be facilitated by relief of pain or stiffness. There was a general lack of information from clinicians about the condition with over-reliance on verbal communication and very little written information. CONCLUSIONS: Awareness of frozen shoulder should be increased among non-specialists and the best available information made accessible for patients. Our results also highlight the importance of patient participation in frozen shoulder research. |
format | Online Article Text |
id | pubmed-3787409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37874092013-10-15 A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder Jones, Susan Hanchard, Nigel Hamilton, Sharon Rangan, Amar BMJ Open Qualitative Research OBJECTIVES: To elucidate the experiences and perceptions of people living with primary frozen shoulder and their priorities for treatment. DESIGN: Qualitative study design using semistructured interviews. SETTING: General practitioner (GP) and musculoskeletal clinics in primary and secondary care in one National Health Service Trust in England. PARTICIPANTS: 12 patients diagnosed with primary frozen shoulder were purposively recruited from a GP's surgery, community clinics and hospital clinics. Recruitment targeted the phases of frozen shoulder: pain predominant (n=5), stiffness predominant (n=4) and residual stiffness predominant following hospital treatment (n=2). One participant dropped out. Inclusion criteria: adult, male and female patients of any age, attending the clinics, who had been diagnosed with primary frozen shoulder. RESULTS: The most important experiential themes identified by participants were: pain which was severe as well as inexplicable; inconvenience/disability arising from increasing restriction of movement (due to pain initially, gradually giving way to stiffness); confusion/anxiety associated with delay in diagnosis and uncertainty about the implications for the future; and treatment-related aspects. Participants not directly referred to a specialist (whether physiotherapist, physician or surgeon) wanted a faster, better-defined care pathway. Specialist consultation brought more definitive diagnosis, relief from anxiety and usually self-rated improvement. The main treatment priority was improved function, though there was recognition that this might be facilitated by relief of pain or stiffness. There was a general lack of information from clinicians about the condition with over-reliance on verbal communication and very little written information. CONCLUSIONS: Awareness of frozen shoulder should be increased among non-specialists and the best available information made accessible for patients. Our results also highlight the importance of patient participation in frozen shoulder research. BMJ Publishing Group 2013-09-26 /pmc/articles/PMC3787409/ /pubmed/24078753 http://dx.doi.org/10.1136/bmjopen-2013-003452 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Qualitative Research Jones, Susan Hanchard, Nigel Hamilton, Sharon Rangan, Amar A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
title | A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
title_full | A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
title_fullStr | A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
title_full_unstemmed | A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
title_short | A qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
title_sort | qualitative study of patients’ perceptions and priorities when living with primary frozen shoulder |
topic | Qualitative Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787409/ https://www.ncbi.nlm.nih.gov/pubmed/24078753 http://dx.doi.org/10.1136/bmjopen-2013-003452 |
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