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

Grosjean, Sylvie; Farré Coma, Jordi; Gal, Ota; Laffan, Aoife; Sendra, Anna; Stuempel, Johanne; Mestre, Tiago (2021-12-11)

 
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Co_designing_an_Integrated_Care_Network_With_People_Living_With_Parkinson_s_Disease.pdf (2.850Mt)
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Grosjean, Sylvie
Farré Coma, Jordi
Gal, Ota
Laffan, Aoife
Sendra, Anna
Stuempel, Johanne
Mestre, Tiago
11.12.2021

Qualitative Health Research
doi:10.1177/10497323211042605
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202110127535

Kuvaus

Peer reviewed
Tiivistelmä
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.
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste