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Co-designing an Integrated Care Network With People Living With Parkinson’s Disease: From Patients’ Narratives to Trajectory Analysis

  • Datos identificativos

    Identificador: imarina:9230388
    Autores:
    Grosjean, SylvieFarre, Jordi ComaGal, OtaLaffan, AoifeSendra, AnnaStuempel, JohanneMestre, Tiago
    Resumen:
    An integrated care model for people living with Parkinson’s disease (PD) offers the promise of meeting complex care needs in a person-centered way that addresses fragmentation and improves quality of life. The purpose of our research was to co-design a care delivery model that supports both social and medical care from the perspective of patients and care partners. In the first step of our co-design approach, participants from five countries were invited to share their experiences of living with PD during a narrative interview. A qualitative analysis of these narrative interviews based on the Corbin and Strauss model was done to map out patients’ trajectories. Three typical trajectories were identified: (a) the “unpredictable” trajectory, (b) the “situated” trajectory, and (c) the “demanding” trajectory. Based on the analysis of these trajectories, we were able to integrate various patient experiences into the design of an integrated care network.
  • Otros:

    Autor según el artículo: Grosjean, Sylvie; Farre, Jordi Coma; Gal, Ota; Laffan, Aoife; Sendra, Anna; Stuempel, Johanne; Mestre, Tiago
    Departamento: Estudis de Comunicació
    Autor/es de la URV: Farré Coma, Jorge / SENDRA TOSET, ANNA
    Palabras clave: Trajectory Quality of life Patients’ experience Participatory design Parkinson’s disease Parkinson disease Narrative interviews Narration Integrated care Humans Europe Delivery of health care, integrated Co-design Canada trajectory services perspective patients' experience parkinson's disease narrative interviews management interviews health-care europe co-design canada
    Resumen: An integrated care model for people living with Parkinson’s disease (PD) offers the promise of meeting complex care needs in a person-centered way that addresses fragmentation and improves quality of life. The purpose of our research was to co-design a care delivery model that supports both social and medical care from the perspective of patients and care partners. In the first step of our co-design approach, participants from five countries were invited to share their experiences of living with PD during a narrative interview. A qualitative analysis of these narrative interviews based on the Corbin and Strauss model was done to map out patients’ trajectories. Three typical trajectories were identified: (a) the “unpredictable” trajectory, (b) the “situated” trajectory, and (c) the “demanding” trajectory. Based on the analysis of these trajectories, we were able to integrate various patient experiences into the design of an integrated care network.
    Áreas temáticas: Sociologia i política Social sciences, interdisciplinary Social sciences, biomedical Saúde coletiva Public health, environmental and occupational health Psicología Nursing Medicina ii Interdisciplinar Information science & library science Health policy & services General o multidisciplinar Farmacia Ensino Enfermagem Educação física Economia Ciencias sociales
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    Direcció de correo del autor: jordi.farre@urv.cat
    Identificador del autor: 0000-0002-4465-911X
    Fecha de alta del registro: 2024-10-12
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Enlace a la fuente original: https://journals.sagepub.com/doi/10.1177/10497323211042605
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Qualitative Health Research. 31 (14): 2585-2601
    Referencia de l'ítem segons les normes APA: Grosjean, Sylvie; Farre, Jordi Coma; Gal, Ota; Laffan, Aoife; Sendra, Anna; Stuempel, Johanne; Mestre, Tiago (2021). Co-designing an Integrated Care Network With People Living With Parkinson’s Disease: From Patients’ Narratives to Trajectory Analysis. Qualitative Health Research, 31(14), 2585-2601. DOI: 10.1177/10497323211042605
    DOI del artículo: 10.1177/10497323211042605
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2021
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Health Policy & Services,Information Science & Library Science,Nursing,Public Health, Environmental and Occupational Health,Social Sciences, Biomedical,Social Sciences, Interdisciplinary
    Trajectory
    Quality of life
    Patients’ experience
    Participatory design
    Parkinson’s disease
    Parkinson disease
    Narrative interviews
    Narration
    Integrated care
    Humans
    Europe
    Delivery of health care, integrated
    Co-design
    Canada
    trajectory
    services
    perspective
    patients' experience
    parkinson's disease
    narrative interviews
    management
    interviews
    health-care
    europe
    co-design
    canada
    Sociologia i política
    Social sciences, interdisciplinary
    Social sciences, biomedical
    Saúde coletiva
    Public health, environmental and occupational health
    Psicología
    Nursing
    Medicina ii
    Interdisciplinar
    Information science & library science
    Health policy & services
    General o multidisciplinar
    Farmacia
    Ensino
    Enfermagem
    Educação física
    Economia
    Ciencias sociales
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