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Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios

OBJECTIVE: To explore the main psychosocial aspects which have influence on the coping with the disease in patients with Parkinson's disease (PD) and their family carers. DESIGN: An exploratory qualitative study which constitutes the second phase of a mixed-methods project. SETTING: Multicenter...

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Autores principales: Navarta-Sánchez, María Victoria, Caparrós, Neus, Ursúa Sesma, María Eugenia, Díaz de Cerio Ayesa, Sara, Riverol, Mario, Portillo, Mari Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876005/
https://www.ncbi.nlm.nih.gov/pubmed/27566906
http://dx.doi.org/10.1016/j.aprim.2016.06.001
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author Navarta-Sánchez, María Victoria
Caparrós, Neus
Ursúa Sesma, María Eugenia
Díaz de Cerio Ayesa, Sara
Riverol, Mario
Portillo, Mari Carmen
author_facet Navarta-Sánchez, María Victoria
Caparrós, Neus
Ursúa Sesma, María Eugenia
Díaz de Cerio Ayesa, Sara
Riverol, Mario
Portillo, Mari Carmen
author_sort Navarta-Sánchez, María Victoria
collection PubMed
description OBJECTIVE: To explore the main psychosocial aspects which have influence on the coping with the disease in patients with Parkinson's disease (PD) and their family carers. DESIGN: An exploratory qualitative study which constitutes the second phase of a mixed-methods project. SETTING: Multicenter study carried out in Navarre in 2014 in collaboration with Primary Care of Navarre Service of Health-Osasunbidea, Clínica Universidad de Navarra and Navarre Association of Parkinson's patients. PARTICIPANTS: A total of 21 participants: 9 people with PD, 7 family carers and 5 healthcare professionals. METHOD: Participants were selected through purposive sampling. Focus groups were conducted until a suitable saturation data was achieved. Transcriptions were analysed by 2 researchers through a content analysis. RESULTS: Three aspects that affected how patients and family carers coped with PD were identified: features of the clinical practice; family environment, and disease's acceptance. Taking account of these findings, some strategies which could foster these aspects from primary healthcare are suggested in order to improve the adjustment to the disease in patients and family carers. CONCLUSIONS: The healthcare in people with PD should have an integral approach that tackle the symptoms control in patients and also deal with psychosocial aspects that influence on the coping with the disease, in patients and family carers.
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spelling pubmed-68760052019-11-26 Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios Navarta-Sánchez, María Victoria Caparrós, Neus Ursúa Sesma, María Eugenia Díaz de Cerio Ayesa, Sara Riverol, Mario Portillo, Mari Carmen Aten Primaria Originales OBJECTIVE: To explore the main psychosocial aspects which have influence on the coping with the disease in patients with Parkinson's disease (PD) and their family carers. DESIGN: An exploratory qualitative study which constitutes the second phase of a mixed-methods project. SETTING: Multicenter study carried out in Navarre in 2014 in collaboration with Primary Care of Navarre Service of Health-Osasunbidea, Clínica Universidad de Navarra and Navarre Association of Parkinson's patients. PARTICIPANTS: A total of 21 participants: 9 people with PD, 7 family carers and 5 healthcare professionals. METHOD: Participants were selected through purposive sampling. Focus groups were conducted until a suitable saturation data was achieved. Transcriptions were analysed by 2 researchers through a content analysis. RESULTS: Three aspects that affected how patients and family carers coped with PD were identified: features of the clinical practice; family environment, and disease's acceptance. Taking account of these findings, some strategies which could foster these aspects from primary healthcare are suggested in order to improve the adjustment to the disease in patients and family carers. CONCLUSIONS: The healthcare in people with PD should have an integral approach that tackle the symptoms control in patients and also deal with psychosocial aspects that influence on the coping with the disease, in patients and family carers. Elsevier 2017-04 2016-08-25 /pmc/articles/PMC6876005/ /pubmed/27566906 http://dx.doi.org/10.1016/j.aprim.2016.06.001 Text en © 2016 Elsevier España, S.L.U. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Originales
Navarta-Sánchez, María Victoria
Caparrós, Neus
Ursúa Sesma, María Eugenia
Díaz de Cerio Ayesa, Sara
Riverol, Mario
Portillo, Mari Carmen
Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
title Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
title_full Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
title_fullStr Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
title_full_unstemmed Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
title_short Estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de Parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
title_sort estrategias psicosociales para fortalecer el afrontamiento de la enfermedad de parkinson: perspectiva de pacientes, familiares y profesionales sociosanitarios
topic Originales
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6876005/
https://www.ncbi.nlm.nih.gov/pubmed/27566906
http://dx.doi.org/10.1016/j.aprim.2016.06.001
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