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Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI)
BACKGROUND: There is limited evidence on caregiver outcomes associated with mild cognitive impairment in patients with Parkinson’s disease (PD-MCI) and the coping strategies used by these caregivers. METHODS: To investigate this relationship, we examined levels of burden, depression, anxiety, coping...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474856/ https://www.ncbi.nlm.nih.gov/pubmed/28638598 http://dx.doi.org/10.1186/s40035-017-0085-5 |
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author | Jones, Ann J. Kuijer, Roeline G. Livingston, Leslie Myall, Daniel Horne, Kyla MacAskill, Michael Pitcher, Toni Barrett, Paul T. Anderson, Tim J. Dalrymple-Alford, John C. |
author_facet | Jones, Ann J. Kuijer, Roeline G. Livingston, Leslie Myall, Daniel Horne, Kyla MacAskill, Michael Pitcher, Toni Barrett, Paul T. Anderson, Tim J. Dalrymple-Alford, John C. |
author_sort | Jones, Ann J. |
collection | PubMed |
description | BACKGROUND: There is limited evidence on caregiver outcomes associated with mild cognitive impairment in patients with Parkinson’s disease (PD-MCI) and the coping strategies used by these caregivers. METHODS: To investigate this relationship, we examined levels of burden, depression, anxiety, coping strategies and positive aspects of caregiving in the informal caregivers of 96 PD patients. The PD patients were classified using MDS-Task Force Level II criteria as showing either normal cognition (PD-N; n = 51), PD-MCI (n = 30) or with dementia (PDD; n = 15). RESULTS: Mean Zarit Burden Interview (ZBI) score increased significantly between carers of PD-N (M = 13.39, SD = 12.22) compared to those of PD-MCI patients (M = 22.00, SD = 10.8), and between carers of PD-MCI and PDD patients (M = 29.33, SD = 9.59). Moreover, the proportion of carers showing clinically significant levels of burden (ZBI score ≥ 21) also increased as the patients’ cognitive status declined (18% for PD-N; 60% for PD-MCI; and 80% for PDD) and was mirrored by an increasing amount of time spent providing care by the caregivers. Caregiver ZBI score was independent of patient neuropsychiatric symptoms, motor function, disease duration and time that caregivers spent caregiving. Caregiver use of different coping strategies increased with worsening cognition. However, we found only equivocal evidence that the use of problem-focused, emotion-focused and dysfunctional coping mediated the association between patient cognitive status and caregiver burden, because the inverse models that used caregiver burden as the mediator were also significant. CONCLUSIONS: The study highlights the impact of Parkinson’s disease on those providing care when the patient’s cognition is poor, including those with MCI. Caregiver well-being has important implications for caregiver support, nursing home placement and disease course. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40035-017-0085-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5474856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54748562017-06-21 Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) Jones, Ann J. Kuijer, Roeline G. Livingston, Leslie Myall, Daniel Horne, Kyla MacAskill, Michael Pitcher, Toni Barrett, Paul T. Anderson, Tim J. Dalrymple-Alford, John C. Transl Neurodegener Research BACKGROUND: There is limited evidence on caregiver outcomes associated with mild cognitive impairment in patients with Parkinson’s disease (PD-MCI) and the coping strategies used by these caregivers. METHODS: To investigate this relationship, we examined levels of burden, depression, anxiety, coping strategies and positive aspects of caregiving in the informal caregivers of 96 PD patients. The PD patients were classified using MDS-Task Force Level II criteria as showing either normal cognition (PD-N; n = 51), PD-MCI (n = 30) or with dementia (PDD; n = 15). RESULTS: Mean Zarit Burden Interview (ZBI) score increased significantly between carers of PD-N (M = 13.39, SD = 12.22) compared to those of PD-MCI patients (M = 22.00, SD = 10.8), and between carers of PD-MCI and PDD patients (M = 29.33, SD = 9.59). Moreover, the proportion of carers showing clinically significant levels of burden (ZBI score ≥ 21) also increased as the patients’ cognitive status declined (18% for PD-N; 60% for PD-MCI; and 80% for PDD) and was mirrored by an increasing amount of time spent providing care by the caregivers. Caregiver ZBI score was independent of patient neuropsychiatric symptoms, motor function, disease duration and time that caregivers spent caregiving. Caregiver use of different coping strategies increased with worsening cognition. However, we found only equivocal evidence that the use of problem-focused, emotion-focused and dysfunctional coping mediated the association between patient cognitive status and caregiver burden, because the inverse models that used caregiver burden as the mediator were also significant. CONCLUSIONS: The study highlights the impact of Parkinson’s disease on those providing care when the patient’s cognition is poor, including those with MCI. Caregiver well-being has important implications for caregiver support, nursing home placement and disease course. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40035-017-0085-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-19 /pmc/articles/PMC5474856/ /pubmed/28638598 http://dx.doi.org/10.1186/s40035-017-0085-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Jones, Ann J. Kuijer, Roeline G. Livingston, Leslie Myall, Daniel Horne, Kyla MacAskill, Michael Pitcher, Toni Barrett, Paul T. Anderson, Tim J. Dalrymple-Alford, John C. Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) |
title | Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) |
title_full | Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) |
title_fullStr | Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) |
title_full_unstemmed | Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) |
title_short | Caregiver burden is increased in Parkinson’s disease with mild cognitive impairment (PD-MCI) |
title_sort | caregiver burden is increased in parkinson’s disease with mild cognitive impairment (pd-mci) |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474856/ https://www.ncbi.nlm.nih.gov/pubmed/28638598 http://dx.doi.org/10.1186/s40035-017-0085-5 |
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