Perceptions of people with Parkinson’s and their caregivers of falling and falls-related healthcare services- a qualitative study
Perceptions of people with Parkinson’s and their caregivers of falling and falls-related healthcare services- a qualitative study
Introduction
Falls are common in Parkinson’s disease, and a recognised research priority. Falls lead to physical and psychological morbidity in people with Parkinson’s disease and their caregivers, however, those with cognitive impairment/ dementia and caregivers have often been excluded from previous studies. This qualitative study explored how people with Parkinson’s disease and their family caregivers understood and experienced falling and healthcare services relating to falls prevention and management.
Methods
A varied and purposive sample of 20 people with Parkinson’s disease (40% confirmed or suspected cognitive impairment/ dementia) and 18 caregivers took part in semi-structured interviews. Eight people with Parkinson’s disease and their caregivers were interviewed as a dyad, 22 participants were interviewed alone. Interviews were analysed through inductive thematic analysis.
Results
Four themes were developed: (i) struggling with thoughts and feelings about falling, (ii) recognising and managing risks surrounding falling, (iii) navigating health and care provision for falling, and (iv) changing as a couple due to falling. Different aspects of falls provoked a range of negative emotions and a variety of coping strategies were adopted. Falls and trying to avoid falls burdened a couple in a number of ways; beyond physical health they also affected functioning, physiological wellbeing, and relationships. Dyads analysed falls to understand their aetiology and described working together to manage them. This often happened in the absence of adequate support and advice with little involvement of healthcare professionals. When cognitive impairment/ dementia was present this brought additional challenges to falls management, with caregivers taking on a greater and more frustrating role.
Conclusion
Dyads required relevant falls-related information and the difficulties associated with cognitive decline should be recognised by researchers and healthcare professionals. Dyads required support in attributing reasons for falls, and increased awareness of healthcare professionals’ different roles to improve patient- professional communication and facilitate patient-centred care.
Owen, Charlotte
4180f299-b1ca-4e3a-839b-faa6867354bc
Gaulton, Christine
2d790033-7f69-423e-b4fd-c13b21db9afc
Roberts, Helen
5ea688b1-ef7a-4173-9da0-26290e18f253
Dennison, Laura
15c399cb-9a81-4948-8906-21944c033c20
26 October 2022
Owen, Charlotte
4180f299-b1ca-4e3a-839b-faa6867354bc
Gaulton, Christine
2d790033-7f69-423e-b4fd-c13b21db9afc
Roberts, Helen
5ea688b1-ef7a-4173-9da0-26290e18f253
Dennison, Laura
15c399cb-9a81-4948-8906-21944c033c20
Owen, Charlotte, Gaulton, Christine, Roberts, Helen and Dennison, Laura
(2022)
Perceptions of people with Parkinson’s and their caregivers of falling and falls-related healthcare services- a qualitative study.
PLoS ONE, 17 (10 October), [e0276588].
(doi:10.1371/journal.pone.0276588).
Abstract
Introduction
Falls are common in Parkinson’s disease, and a recognised research priority. Falls lead to physical and psychological morbidity in people with Parkinson’s disease and their caregivers, however, those with cognitive impairment/ dementia and caregivers have often been excluded from previous studies. This qualitative study explored how people with Parkinson’s disease and their family caregivers understood and experienced falling and healthcare services relating to falls prevention and management.
Methods
A varied and purposive sample of 20 people with Parkinson’s disease (40% confirmed or suspected cognitive impairment/ dementia) and 18 caregivers took part in semi-structured interviews. Eight people with Parkinson’s disease and their caregivers were interviewed as a dyad, 22 participants were interviewed alone. Interviews were analysed through inductive thematic analysis.
Results
Four themes were developed: (i) struggling with thoughts and feelings about falling, (ii) recognising and managing risks surrounding falling, (iii) navigating health and care provision for falling, and (iv) changing as a couple due to falling. Different aspects of falls provoked a range of negative emotions and a variety of coping strategies were adopted. Falls and trying to avoid falls burdened a couple in a number of ways; beyond physical health they also affected functioning, physiological wellbeing, and relationships. Dyads analysed falls to understand their aetiology and described working together to manage them. This often happened in the absence of adequate support and advice with little involvement of healthcare professionals. When cognitive impairment/ dementia was present this brought additional challenges to falls management, with caregivers taking on a greater and more frustrating role.
Conclusion
Dyads required relevant falls-related information and the difficulties associated with cognitive decline should be recognised by researchers and healthcare professionals. Dyads required support in attributing reasons for falls, and increased awareness of healthcare professionals’ different roles to improve patient- professional communication and facilitate patient-centred care.
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Charlotte PD qual study final manuscript
- Accepted Manuscript
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journal.pone.0276588
- Version of Record
Text
journal.pone.0276588
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More information
Accepted/In Press date: 11 October 2022
Published date: 26 October 2022
Additional Information:
Funding Information:
Funding: The National Institute for Health Research (NIHR) funded this research (https://www.arc-wx.nihr.ac.uk). The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care. CO was supported by the University of Southampton NIHR Academic Clinical Fellow (ACF) training programme (https://www.nihr.ac.uk/funding/nihr-academic-clinical-fellowships-inmedicine-2021/25719). CO and HCR were supported by National Institute for Health Research Applied Research Collaboration (NIHR ARC) Wessex (https://www.arc-wx.nihr.ac.uk). HCR was supported by the NIHR Southampton Biomedical Research Centre (https://www.southamptonbrc.nihr.ac.uk). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2022 Owen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Identifiers
Local EPrints ID: 471681
URI: http://eprints.soton.ac.uk/id/eprint/471681
ISSN: 1932-6203
PURE UUID: b8843f93-99e1-4ab2-8bb4-75a15a235618
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Date deposited: 16 Nov 2022 17:40
Last modified: 17 Mar 2024 03:08
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Author:
Charlotte Owen
Author:
Christine Gaulton
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