Perspectives on Care for Late-Stage Parkinson's Disease.

IF 2.1 4区 医学 Q3 CLINICAL NEUROLOGY Parkinson's Disease Pub Date : 2021-01-01 DOI:10.1155/2021/9475026
Kristina Rosqvist, Marianne Kylberg, Charlotte Löfqvist, Anette Schrag, Per Odin, Susanne Iwarsson
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引用次数: 12

Abstract

In the late stage of Parkinson's disease (PD), there is an increasing disease burden not only for the patients but also for their informal caregivers and the health and social services systems. The aim of this study was to explore experiences of late-stage PD patients' and their informal caregivers' satisfaction with care and support, in order to better understand how they perceive the treatment and care they receive. This qualitative substudy was part of the longitudinal European multicentre Care of Late Stage Parkinsonism (CLaSP) project. Individual semistructured interviews were conducted with patients (n = 11) and informal caregivers (n = 9) in Sweden. Data were analysed through the content analysis technique. The final analyses generated one main category: "We are trying to get by both with and without the formal care" and five subcategories: "Availability of health care is important for managing symptoms and everyday life"; "Dependence on others and scheduled days form everyday life"; "There is a wish to get adequate help when it is needed"; "Mixed feelings on future housing and respite care"; and "Family responsibility and loyalty for a functioning everyday life". Having regular contact with PD-specialised health care was perceived as important. Greater access to physiotherapy was wished for. Maintaining autonomy was perceived as important by patients, in both home health care and a future residential care setting. Responsibility and loyalty between spouses and support from children enabled everyday life to carry on at home, indicating a vulnerability for those without an informal caregiver. The results suggest that regular access to PD-specialised health care is important and that a specialised and multidisciplinary approach to the management of PD symptomatology is likely necessary. Non-PD-specialised staff in home health care and residential care facilities should regularly be given opportunities to obtain PD-specific education and information.

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晚期帕金森病的护理展望。
在帕金森病(PD)的晚期,不仅对患者,而且对他们的非正式照顾者以及卫生和社会服务系统都有越来越大的疾病负担。本研究旨在探讨晚期PD患者及其非正式照顾者对护理和支持的满意度体验,以更好地了解他们对所接受的治疗和护理的看法。该定性子研究是欧洲多中心晚期帕金森病护理(CLaSP)纵向研究项目的一部分。在瑞典,对患者(n = 11)和非正式护理人员(n = 9)进行了个人半结构化访谈。通过内容分析技术对数据进行分析。最后的分析产生了一个主要类别:“我们正在努力通过有和没有正式护理”和五个子类别:“获得卫生保健对控制症状和日常生活很重要”;“对他人的依赖和安排好的日子构成了日常生活”;“人们希望在需要的时候得到足够的帮助”;“对未来住房和临时护理的复杂感受”;以及“对正常日常生活的家庭责任和忠诚”。定期接触pd专业保健服务被认为是重要的。人们希望有更多的机会接受物理治疗。在家庭保健和未来的住宿护理环境中,患者认为保持自主权是重要的。配偶之间的责任和忠诚以及孩子的支持使家庭的日常生活得以继续,这表明那些没有非正式照顾者的人很容易受到伤害。结果表明,定期获得PD专业医疗保健是重要的,并且可能需要一种专门和多学科的方法来管理PD症状。家庭保健和寄宿护理机构的非pd专业人员应定期获得pd专业教育和信息的机会。
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来源期刊
Parkinson's Disease
Parkinson's Disease CLINICAL NEUROLOGY-
CiteScore
5.80
自引率
3.10%
发文量
0
审稿时长
18 weeks
期刊介绍: Parkinson’s Disease is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to the epidemiology, etiology, pathogenesis, genetics, cellular, molecular and neurophysiology, as well as the diagnosis and treatment of Parkinson’s disease.
期刊最新文献
Effectiveness and Feasibility of Nonpharmacological Interventions for People With Parkinson's Disease and Cognitive Impairment on Patient-Centred Outcomes: Systematic Review and Meta-Analysis. Validation and Psychometric Properties of the Spanish Version of King's Parkinson's Disease Pain Scale. A Cognitive-Behavioral Model of Apathy in Parkinson's Disease. Possible Implications of Managing Alexithymia on Quality of Life in Parkinson's Disease: A Systematic Review. Implications of Convolutional Neural Network for Brain MRI Image Classification to Identify Alzheimer's Disease.
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