Moving from physician-centered care towards patient-centered care for Parkinson's disease patients

Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but the present health care system–which is organized primarily from the provider's perspective–is not yet prepared for this developme...

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Published inParkinsonism & related disorders Vol. 19; no. 11; pp. 923 - 927
Main Authors van der Eijk, Martijn, Nijhuis, Frouke A.P., Faber, Marjan J., Bloem, Bastiaan R.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.11.2013
Subjects
Online AccessGet full text
ISSN1353-8020
1873-5126
1873-5126
DOI10.1016/j.parkreldis.2013.04.022

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Abstract Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but the present health care system–which is organized primarily from the provider's perspective–is not yet prepared for this development. Here, we argue that an alternative way to organize health care, namely more from the patient's perspective, may help to contain costs, while improving the quality, safety and access to care. This involves a redefinition of the patient–doctor relationship, such that patients are no longer regarded as passive objects, but rather as active subjects who work as partners with health care professionals to optimize health (‘participatory medicine’). The opportunities that come with such a collaborative and patient-centered care model are reviewed within the context of patients with Parkinson's disease. We also discuss societal and Parkinson-specific barriers that could impede implementation of this alternative care model to the management of Parkinson's disease and other chronic conditions.
AbstractList Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but the present health care system-which is organized primarily from the provider's perspective-is not yet prepared for this development. Here, we argue that an alternative way to organize health care, namely more from the patient's perspective, may help to contain costs, while improving the quality, safety and access to care. This involves a redefinition of the patient-doctor relationship, such that patients are no longer regarded as passive objects, but rather as active subjects who work as partners with health care professionals to optimize health ('participatory medicine'). The opportunities that come with such a collaborative and patient-centered care model are reviewed within the context of patients with Parkinson's disease. We also discuss societal and Parkinson-specific barriers that could impede implementation of this alternative care model to the management of Parkinson's disease and other chronic conditions.Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but the present health care system-which is organized primarily from the provider's perspective-is not yet prepared for this development. Here, we argue that an alternative way to organize health care, namely more from the patient's perspective, may help to contain costs, while improving the quality, safety and access to care. This involves a redefinition of the patient-doctor relationship, such that patients are no longer regarded as passive objects, but rather as active subjects who work as partners with health care professionals to optimize health ('participatory medicine'). The opportunities that come with such a collaborative and patient-centered care model are reviewed within the context of patients with Parkinson's disease. We also discuss societal and Parkinson-specific barriers that could impede implementation of this alternative care model to the management of Parkinson's disease and other chronic conditions.
Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but the present health care system-which is organized primarily from the provider's perspective-is not yet prepared for this development. Here, we argue that an alternative way to organize health care, namely more from the patient's perspective, may help to contain costs, while improving the quality, safety and access to care. This involves a redefinition of the patient-doctor relationship, such that patients are no longer regarded as passive objects, but rather as active subjects who work as partners with health care professionals to optimize health ('participatory medicine'). The opportunities that come with such a collaborative and patient-centered care model are reviewed within the context of patients with Parkinson's disease. We also discuss societal and Parkinson-specific barriers that could impede implementation of this alternative care model to the management of Parkinson's disease and other chronic conditions.
Abstract Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but the present health care system–which is organized primarily from the provider's perspective–is not yet prepared for this development. Here, we argue that an alternative way to organize health care, namely more from the patient's perspective, may help to contain costs, while improving the quality, safety and access to care. This involves a redefinition of the patient–doctor relationship, such that patients are no longer regarded as passive objects, but rather as active subjects who work as partners with health care professionals to optimize health (‘participatory medicine’). The opportunities that come with such a collaborative and patient-centered care model are reviewed within the context of patients with Parkinson's disease. We also discuss societal and Parkinson-specific barriers that could impede implementation of this alternative care model to the management of Parkinson's disease and other chronic conditions.
Author Nijhuis, Frouke A.P.
van der Eijk, Martijn
Bloem, Bastiaan R.
Faber, Marjan J.
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  givenname: Martijn
  surname: van der Eijk
  fullname: van der Eijk, Martijn
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  givenname: Frouke A.P.
  surname: Nijhuis
  fullname: Nijhuis, Frouke A.P.
  organization: Department of Neurology, Nijmegen Centre for Evidence Based Practice, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  givenname: Marjan J.
  surname: Faber
  fullname: Faber, Marjan J.
  organization: Scientific Institute for Quality of Healthcare (IQ healthcare), Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
– sequence: 4
  givenname: Bastiaan R.
  surname: Bloem
  fullname: Bloem, Bastiaan R.
  email: b.bloem@neuro.umcn.nl
  organization: Department of Neurology, Donders Institute for Brain Cognition and Behaviour, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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Keywords Participatory medicine
Parkinson's disease
Health 2.0
Chronic disease
Patient-centered care
Collaborative care
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Snippet Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no exception, but...
Abstract Today's society is changing rapidly and individuals increasingly favor an active role in designing their own lives. Contemporary patients are no...
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SubjectTerms Chronic disease
Collaborative care
Disease Management
Health 2.0
Humans
Neurology
Parkinson Disease - diagnosis
Parkinson Disease - therapy
Parkinson's disease
Participatory medicine
Patient Participation - methods
Patient Participation - trends
Patient-centered care
Patient-Centered Care - methods
Patient-Centered Care - trends
Physician-Patient Relations
Title Moving from physician-centered care towards patient-centered care for Parkinson's disease patients
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https://dx.doi.org/10.1016/j.parkreldis.2013.04.022
https://www.ncbi.nlm.nih.gov/pubmed/23742970
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