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dc.contributor.authorMathers, J
dc.contributor.authorRick, C
dc.contributor.authorJenkinson, C
dc.contributor.authorGarside, R
dc.contributor.authorPall, H
dc.contributor.authorMitchell, R
dc.contributor.authorBayliss, S
dc.contributor.authorJones, LL
dc.date.accessioned2017-02-02T09:28:33Z
dc.date.issued2016-06-23
dc.description.abstractOBJECTIVE: To review and synthesise qualitative research studies that have explored patients' experience of deep brain stimulation (DBS) in advanced Parkinson's disease (PD). DESIGN: Systematic review and meta-synthesis of 7 original papers, using metaethnography. SETTING: Studies conducted in Denmark, France and Sweden. PARTICIPANTS: 116 patients who had undergone DBS and 9 spouses of patients. RESULTS: Prior to surgery, the experience of advancing PD is one of considerable loss and a feeling of loss of control. There are significant hopes for what DBS can bring. Following surgery, a sense of euphoria is described by many, although this does not persist and there is a need for significant transitions following this. We suggest that normality as a concept is core to the experience of DBS and that a sense of control may be a key condition for normality. Experience of DBS for patients and spouses, and of the transitions that they must undertake, is influenced by their hopes of what surgery will enable them to achieve, or regain (ie, a new normality). CONCLUSIONS: There is a need for further qualitative research to understand the nature of these transitions to inform how best patients and their spouses can be supported by healthcare professionals before, during and after DBS. In assessing the outcomes of DBS and other treatments in advanced PD, we should consider how to capture holistic concepts such as normality and control. Studies that examine the outcomes of DBS require longer term follow-up.en_GB
dc.description.sponsorshipThis work was part funded by the Medical Research Council Midland Hub for Trials Methodology Research (Grant Number: G0800808). RG is partially supported by the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care (CLAHRC) for the South West Peninsula (PenCLAHRC).en_GB
dc.identifier.citationVol. 6, pp. e011525en_GB
dc.identifier.doi10.1136/bmjopen-2016-011525
dc.identifier.otherbmjopen-2016-011525
dc.identifier.urihttp://hdl.handle.net/10871/25556
dc.language.isoenen_GB
dc.publisherBMJ Publishing Groupen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/27338883en_GB
dc.rightsCopyright © 2016 by the BMJ Publishing Group Ltd. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) 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/4.0/en_GB
dc.subjectDeep Brain Stimulationen_GB
dc.subjectPatient experienceen_GB
dc.subjectQUALITATIVE RESEARCHen_GB
dc.titlePatients' experiences of deep brain stimulation for Parkinson's disease: a qualitative systematic review and synthesis.en_GB
dc.typeArticleen_GB
dc.date.available2017-02-02T09:28:33Z
exeter.place-of-publicationEnglanden_GB
dc.descriptionPublished onlineen_GB
dc.descriptionJournal Articleen_GB
dc.descriptionThis is the final version of the article. Available from BMJ Publishing Group via the DOI in this record.en_GB
dc.identifier.eissn2044-6055
dc.identifier.journalBMJ Openen_GB


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