Patient organizations and primary care development: reflections by patients with chronic diseases

To explore how patients with chronic diseases, as well as members of patient organizations, perceive primary care and how they think about how to participate in primary care development. Focus group interviews with 28 patients in three regions in Sweden were conducted. We identified four themes: Ava...

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Autores principales: Britta Berglund, Irene Westerlund
Formato: article
Lenguaje:EN
Publicado: The Beryl Institute 2016
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Acceso en línea:https://doaj.org/article/13a1b14bdae5431e94c147d294a31ac7
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spelling oai:doaj.org-article:13a1b14bdae5431e94c147d294a31ac72021-11-15T04:21:49ZPatient organizations and primary care development: reflections by patients with chronic diseases2372-0247https://doaj.org/article/13a1b14bdae5431e94c147d294a31ac72016-11-01T00:00:00Zhttps://pxjournal.org/journal/vol3/iss2/6https://doaj.org/toc/2372-0247To explore how patients with chronic diseases, as well as members of patient organizations, perceive primary care and how they think about how to participate in primary care development. Focus group interviews with 28 patients in three regions in Sweden were conducted. We identified four themes: Availability of care, How to be met by professionals, Information needs and Continuity and prevention in care. Important was to meet the same doctor at every visit and to be met with empathy and knowledge about your disease. Suggestions about better use of technical information services, introduction of a coordinator in the waiting room and longer and varied open hours came up. The information needs for newly diagnosed and those with a long disease trajectory differed and care treatment plans were asked for by many participants. Discussions between patient organizations about how to participate in education of health care professionals were recommended. Patients’ with chronic diseases want to take more active part in their own care. By promoting more contacts between patient organizations, influence on the politic agendas may be achieved. To achieve effects, the patient organizations should be proposed to be included and to activate themselves about these results. If so, a stronger patient voice may be heard in the society. A change in the paternalistic philosophy in primary health care is also needed so the patients’ rights and contribution will be acknowledged and joint education with health professionals could be one way.Britta BerglundIrene WesterlundThe Beryl Institutearticlefocus groupschronic diseasespatient organizationsprimary caredevelopmentpatient experienceMedicine (General)R5-920Public aspects of medicineRA1-1270ENPatient Experience Journal (2016)
institution DOAJ
collection DOAJ
language EN
topic focus groups
chronic diseases
patient organizations
primary care
development
patient experience
Medicine (General)
R5-920
Public aspects of medicine
RA1-1270
spellingShingle focus groups
chronic diseases
patient organizations
primary care
development
patient experience
Medicine (General)
R5-920
Public aspects of medicine
RA1-1270
Britta Berglund
Irene Westerlund
Patient organizations and primary care development: reflections by patients with chronic diseases
description To explore how patients with chronic diseases, as well as members of patient organizations, perceive primary care and how they think about how to participate in primary care development. Focus group interviews with 28 patients in three regions in Sweden were conducted. We identified four themes: Availability of care, How to be met by professionals, Information needs and Continuity and prevention in care. Important was to meet the same doctor at every visit and to be met with empathy and knowledge about your disease. Suggestions about better use of technical information services, introduction of a coordinator in the waiting room and longer and varied open hours came up. The information needs for newly diagnosed and those with a long disease trajectory differed and care treatment plans were asked for by many participants. Discussions between patient organizations about how to participate in education of health care professionals were recommended. Patients’ with chronic diseases want to take more active part in their own care. By promoting more contacts between patient organizations, influence on the politic agendas may be achieved. To achieve effects, the patient organizations should be proposed to be included and to activate themselves about these results. If so, a stronger patient voice may be heard in the society. A change in the paternalistic philosophy in primary health care is also needed so the patients’ rights and contribution will be acknowledged and joint education with health professionals could be one way.
format article
author Britta Berglund
Irene Westerlund
author_facet Britta Berglund
Irene Westerlund
author_sort Britta Berglund
title Patient organizations and primary care development: reflections by patients with chronic diseases
title_short Patient organizations and primary care development: reflections by patients with chronic diseases
title_full Patient organizations and primary care development: reflections by patients with chronic diseases
title_fullStr Patient organizations and primary care development: reflections by patients with chronic diseases
title_full_unstemmed Patient organizations and primary care development: reflections by patients with chronic diseases
title_sort patient organizations and primary care development: reflections by patients with chronic diseases
publisher The Beryl Institute
publishDate 2016
url https://doaj.org/article/13a1b14bdae5431e94c147d294a31ac7
work_keys_str_mv AT brittaberglund patientorganizationsandprimarycaredevelopmentreflectionsbypatientswithchronicdiseases
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