A Review of Social and Relational Aspects of Deep Brain Stimulation in Parkinson's Disease Informed by Healthcare Provider Experiences

Author:

Bell Emily1,Maxwell Bruce1,McAndrews Mary Pat2,Sadikot Abbas F.3,Racine Eric145

Affiliation:

1. Neuroethics Research Unit, Institut de recherches cliniques de Montréal (IRCM), Montréal, QC, Canada H2W lR7

2. Division of Brain, Imaging & Behaviour-Systems Neuroscience, Toronto Western Research Institute, Toronto, ON, Canada M5G 2M9

3. Montreal Neurological Institute and Hospital, McGill University, Montréal, QC, Canada H3A 2B4

4. Department of Medicine and Department of Social and Preventive Medicine, Université de Montréal, Montréal, QC, Canada H3C 3J7

5. Departments of Medicine and Neurology and Neurosurgery and Biomedical Ethics Unit, McGill University, Montréal, QC, Canada H3A 2T5

Abstract

Background. Although the clinical effectiveness of deep brain stimulation (DBS) in Parkinson's disease is established, there has been less examination of its social aspects.Methods and Results. Building on qualitative comments provided by healthcare providers, we present four different social and relational issues (need for social support, changes in relationships (with self and partner) and challenges with regards to occupation and the social system). We review the literature from multiple disciplines on each issue. We comment on their ethical implications and conclude by establishing the future prospects for research with the possible expansion of DBS for psychiatric indications.Conclusions. Our review demonstrates that there are varied social issues involved in DBS. These issues may have significant impacts on the perceived outcome of DBS by patients. Moreover, the fact that the social impact of DBS is still not well understood in emerging psychiatric indications presents an important area for future examination.

Publisher

Hindawi Limited

Subject

Psychiatry and Mental health,Neurology (clinical),Neuroscience (miscellaneous)

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