Challenges to Ethically Managing Parkinson Disease

This study investigated the current ethical issues in relation to recognizing and managing Parkinson disease (PD) from the patient’s perspective. Methods: Twelve patients living with PD who were from the medical school’s Patients as Educators program were recruited. Semistructured interviews were co...

Full description

Bibliographic Details
Main Authors: Shelagh T Shaw BSc (Hons), MSc, Pirashanthie Vivekananda-Schmidt DPhil, C.Psychol, MEd, SFHEA
Format: Article
Language:English
Published: SAGE Publishing 2017-12-01
Series:Journal of Patient Experience
Online Access:https://doi.org/10.1177/2374373517706836
id doaj-1550c8ba00734c8aab40523601b69ec3
record_format Article
spelling doaj-1550c8ba00734c8aab40523601b69ec32020-11-25T03:55:07ZengSAGE PublishingJournal of Patient Experience2374-37432374-37352017-12-01410.1177/2374373517706836Challenges to Ethically Managing Parkinson DiseaseShelagh T Shaw BSc (Hons), MSc0Pirashanthie Vivekananda-Schmidt DPhil, C.Psychol, MEd, SFHEA1 Wensleydale Podiatry and Chiropody Leyburn, North Yorkshire, UK Sheffield Medical School, Sheffield, UKThis study investigated the current ethical issues in relation to recognizing and managing Parkinson disease (PD) from the patient’s perspective. Methods: Twelve patients living with PD who were from the medical school’s Patients as Educators program were recruited. Semistructured interviews were conducted to record patient experiences in order to identify potential ethical issues in relation to recognizing and managing PD. Thematic analysis was applied to the interview transcripts. Results: Four key themes emerged from the interviews. These were information giving, coping, identity, and future medical treatment. These data indicate variable experiences in relation to communication between patient and health-care professional, better support for both planning end-of-life decisions and in coping with the disease’s impacts on their identity. Patients with PD also struggle with access to support services and support for main carer. Implications: To ensure ethical practice in supporting patients with PD, these emerging themes need further investigation; and management guidelines relevant to PD must be informed by research in this area to ensure ethical care of patients with PD, their carers, and families.https://doi.org/10.1177/2374373517706836
collection DOAJ
language English
format Article
sources DOAJ
author Shelagh T Shaw BSc (Hons), MSc
Pirashanthie Vivekananda-Schmidt DPhil, C.Psychol, MEd, SFHEA
spellingShingle Shelagh T Shaw BSc (Hons), MSc
Pirashanthie Vivekananda-Schmidt DPhil, C.Psychol, MEd, SFHEA
Challenges to Ethically Managing Parkinson Disease
Journal of Patient Experience
author_facet Shelagh T Shaw BSc (Hons), MSc
Pirashanthie Vivekananda-Schmidt DPhil, C.Psychol, MEd, SFHEA
author_sort Shelagh T Shaw BSc (Hons), MSc
title Challenges to Ethically Managing Parkinson Disease
title_short Challenges to Ethically Managing Parkinson Disease
title_full Challenges to Ethically Managing Parkinson Disease
title_fullStr Challenges to Ethically Managing Parkinson Disease
title_full_unstemmed Challenges to Ethically Managing Parkinson Disease
title_sort challenges to ethically managing parkinson disease
publisher SAGE Publishing
series Journal of Patient Experience
issn 2374-3743
2374-3735
publishDate 2017-12-01
description This study investigated the current ethical issues in relation to recognizing and managing Parkinson disease (PD) from the patient’s perspective. Methods: Twelve patients living with PD who were from the medical school’s Patients as Educators program were recruited. Semistructured interviews were conducted to record patient experiences in order to identify potential ethical issues in relation to recognizing and managing PD. Thematic analysis was applied to the interview transcripts. Results: Four key themes emerged from the interviews. These were information giving, coping, identity, and future medical treatment. These data indicate variable experiences in relation to communication between patient and health-care professional, better support for both planning end-of-life decisions and in coping with the disease’s impacts on their identity. Patients with PD also struggle with access to support services and support for main carer. Implications: To ensure ethical practice in supporting patients with PD, these emerging themes need further investigation; and management guidelines relevant to PD must be informed by research in this area to ensure ethical care of patients with PD, their carers, and families.
url https://doi.org/10.1177/2374373517706836
work_keys_str_mv AT shelaghtshawbschonsmsc challengestoethicallymanagingparkinsondisease
AT pirashanthievivekanandaschmidtdphilcpsycholmedsfhea challengestoethicallymanagingparkinsondisease
_version_ 1724470706947751936