Literature DB >> 20946567

Living with advanced Parkinson's disease: a constant struggle with unpredictability.

Anita Haahr1, Marit Kirkevold, Elisabeth O C Hall, Karen Ostergaard.   

Abstract

AIM: This paper is a report of an exploration of patients' lifeworld and way of managing life with advanced Parkinson's disease prior to Deep Brain Stimulation and what they expect from life following this treatment.
BACKGROUND: Parkinson's disease is a progressive neurodegenerative disease, which is initially well-treated with L-dopa. Living with Parkinson's disease means living with the experience of continuous loss of independence and self-esteem and unpredictable ON/OFF phenomena. Thus, in the advanced stage of the disease, treatment with Deep Brain Stimulation may become relevant.
METHOD: Eleven patients eligible for Deep Brain Stimulation were interviewed prior to treatment. Data were collected in 2007 and analysed according to the hermeneutic phenomenological methodology of van Manen, using the four existentials as analytic tools.
FINDINGS: Living with advanced Parkinson's disease can be described as the experience of living with and managing unpredictability. The disease gradually took over, and participants had to struggle with unpredictability on a daily basis. Themes in relation to this were: The body - setting the agenda, Always a struggle to be on time, Living in dependence and compromise - being a burden, and Living with restrained space and changes in social life.
CONCLUSION: Parkinson's disease leads to profound bodily restrictions. Living with an unpredictable body affects all aspects of life, and nurses need to be aware of the impact the disease has on the entire lifeworld, and how this may affect the way treatment is perceived.
© 2010 Blackwell Publishing Ltd.

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Year:  2010        PMID: 20946567     DOI: 10.1111/j.1365-2648.2010.05459.x

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  43 in total

1.  Health-related quality of life in Parkinson's: impact of 'off' time and stated treatment preferences.

Authors:  Cicely Kerr; Emily J Lloyd; Charlotte E Kosmas; Helen T Smith; James A Cooper; Karissa Johnston; Emma McIntosh; Andrew J Lloyd
Journal:  Qual Life Res       Date:  2015-12-01       Impact factor: 4.147

2.  Self-management program participation and social support in Parkinson's disease: Mixed methods evaluation.

Authors:  Katherine Pappa; Tasha Doty; Steven D Taff; Kathy Kniepmann; Erin R Foster
Journal:  Phys Occup Ther Geriatr       Date:  2017-03-07

3.  Use of the World Health Organization Quality of Life Assessment Short Version in Mild to Moderate Parkinson Disease.

Authors:  Sarah K Hendred; Erin R Foster
Journal:  Arch Phys Med Rehabil       Date:  2016-06-23       Impact factor: 3.966

4.  Perceptions regarding a range of work-related issues and corresponding support needs of individuals with an intractable disease.

Authors:  Kumiko Imahashi; Reiko Fukatsu; Yasoichi Nakajima; Megumi Nakamura; Tateo Ito; Mariko Horigome; Yuichiro Haruna; Tatsuya Noda; Yasuto Itoyama
Journal:  Intractable Rare Dis Res       Date:  2016-08

Review 5.  Understanding, Impact, and Communication of "Off" Periods in Parkinson's Disease: A Scoping Review.

Authors:  Tara Rastgardani; Melissa J Armstrong; Anna R Gagliardi; Connie Marras
Journal:  Mov Disord Clin Pract       Date:  2018-10-09

6.  It's About Time: The Temporal Burden of Lower Urinary Tract Symptoms Among Women.

Authors:  Beverly Rosa Williams; Keith Vargo; Diane K Newman; D Yvette Lacoursiere; Elizabeth R Mueller; John Connett; Lisa Kane Low; Aimee S James; Ariana L Smith; Kathryn H Schmitz; Kathryn L Burgio
Journal:  Urol Nurs       Date:  2020 Nov-Dec

7.  Living with Long term condition Scale: A pilot validation study of a new person centred tool in the UK.

Authors:  Leire Ambrosio; Kelly Hislop-Lennie; Hannah Barker; David Culliford; Mari Carmen Portillo
Journal:  Nurs Open       Date:  2021-03-15

8.  Understanding the creative processes of phenomenological research: The life philosophy of Løgstrup.

Authors:  Annelise Norlyk; Pia Dreyer; Anita Haahr; Bente Martinsen
Journal:  Int J Qual Stud Health Well-being       Date:  2011-11-08

9.  Psychosocial needs of patients and spouses justify a position of psychosocial health professionals in the multidisciplinary care for Parkinson's disease.

Authors:  Annelien Duits; Colin van der Heijden; Masja van Het Hoofd; Gabriel Roodbol; Mark Tiemessen; Marten Munneke; Maxime Steppe
Journal:  Clin Park Relat Disord       Date:  2020-07-03

10.  Using Information and Communication Technology in Home Care for Communication between Patients, Family Members, and Healthcare Professionals: A Systematic Review.

Authors:  Birgitta Lindberg; Carina Nilsson; Daniel Zotterman; Siv Söderberg; Lisa Skär
Journal:  Int J Telemed Appl       Date:  2013-04-10
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