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Perceptive Dialogue for Linking Stakeholders and Units During Care Transitions - A Qualitative Study of People with Stroke, Significant Others and Healthcare Professionals in Sweden
Division of Physiotherapy, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Huddinge, SE.ORCID iD: 0000-0003-3781-7615
Division of Physiotherapy, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Huddinge, SE.
School of Education, Health and Social Studies, Dalarna University, Falun, SE.
Division of Family Medicine and Primary Care, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Huddinge, SE.
2020 (English)In: International journal of integrated care, ISSN 1568-4156, Vol. 20, no 1, p. 11-, article id 11Article in journal (Refereed) Published
Abstract [en]

INTRODUCTION: Care transitions are a complex set of actions that risk poor quality outcomes for patients and their significant others. This study explored the transition process between hospital and continued rehabilitation in the home. The process is explored from the perspectives of people with stroke, significant others and healthcare professionals in Stockholm, Sweden.

METHOD: Focus group interviews (n = 10), semi-structured individual interviews (n = 23) and interviews in dyad (n = 4) were conducted with healthcare professionals, people with stroke and significant others, altogether 71 participants. Data was collected and analyzed using Grounded Theory.

RESULTS: One core category "Perceptive dialogue for a coordinated transition", and two categories "Synthesis of parallel processes for common understanding" and "The forced transformation from passive attendant to uninformed agent" emerged from the analysis. The transition consisted of several parallel processes which made it difficult for the stakeholders to get a common understanding of the transition as a whole. Enabling a perceptive dialogue was as a prerequisite for the creation of a common understanding of the care transition.

CONCLUSION: This study elucidates that a perceptive dialogue with patients/significant others as well as within and across organizations is part of a coordinated and person-centred transition. There is an extensive need for increased involvement of patients and significant others regarding dialogue about health conditions, procedures at the hospital and preparation for self-management after discharge.

Place, publisher, year, edition, pages
Ubiquity Press, Ltd. , 2020. Vol. 20, no 1, p. 11-, article id 11
Keywords [en]
care coordination, continuity of care, patient handoff, rehabilitation, transitional care
National Category
Other Health Sciences
Identifiers
URN: urn:nbn:se:mdh:diva-73792DOI: 10.5334/ijic.4689ISI: 000523257600011PubMedID: 32256255Scopus ID: 2-s2.0-85083294810OAI: oai:DiVA.org:mdh-73792DiVA, id: diva2:2008145
Available from: 2025-10-22 Created: 2025-10-22 Last updated: 2025-12-02Bibliographically approved
In thesis
1. Understanding the links : the exploration of care transitions between hospital and continued rehabilitation in the home after stroke
Open this publication in new window or tab >>Understanding the links : the exploration of care transitions between hospital and continued rehabilitation in the home after stroke
2021 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Background: Uncoordinated care transitions are known to be a risk of a substantial burden for patients and significant others with a risk of adverse events, rehospitalisation and dissatisfaction with services. After acute hospital care, people with stroke often need continued rehabilitation which entails a care transition such as from hospital to continued rehabilitation in the home environment.

Aims: The overall aims of this thesis were to generate knowledge about and describe the care transition process from hospital to the home from the perspective of people with stroke, significant others and healthcare professionals. In addition, the aim was to investigate the concept of participation in a co-design of person-centred care transitions.

Methods and participants: Four papers were included. Paper I and II were based on a prospective observational study including 190 people with stroke and 89 significant others. Data were collected from medical records by standardized questionnaires, performance-based tests, and from the Stockholm Region computerized register of healthcare contacts. Paper I was a prospective observational study where data were analysed with descriptive statistics and regression analysis to explore associations between healthcare utilization and independent variables. Paper II was a cross-sectional study where regression analysis was used to explore associations between perceived quality and independent variables. Paper III was a qualitative grounded theory study of the care transition process including 16 people with stroke, 7 significant others and 48 healthcare professionals. Data was collected through focus group interviews, individual interviews, and interviews in dyads. Paper IV included 3 people with stroke, 1 significant other, 10 healthcare professionals and 1 facilitator. Data was collected using observations, field-notes, interviews and questionnaires and was analysed by qualitative content analysis to investigate how participation manifests itself in a co-design process.

Results: A majority had a very mild or mild stroke. There was a large variation in the number of visits with the neurorehabilitation team and other outpatient contacts which seemed to correspond to the level of functioning and stroke severity. The perceived quality of the care transitions indicated that there is room for improvements in the discharge process, especially regarding preparation for discharge and support for self-management post-discharge. Few clinical characteristics were associated with the perceived quality of the care transition. The care transition was described to consist of several parallel processes in need of synthetization and coordination in order to provide care transitions based on the needs of people with stroke and significant others. Patients and significant others described the care transition as a transformation from a passive attendant at the hospital to becoming an uninformed agent at home after discharge. The manifestation of participation in a co-design process was shown to be affected by multifactorial interrelated links such as the composition of groups, the climate and adaptations among the participants, the balancing of roles and power, a shared understanding, leadership and adaptive process. Participation varied between individuals, groups, steps within the process and the topic of conversation.

Conclusion: The care transition from hospital to continued rehabilitation in the home needs to be adapted to the varying needs of people with stroke and significant others. The preparation for discharge and information and support for self-management need to be enhanced. Patients and significant others need to be involved in their care during all steps of the care transition process. A perceptive dialogue between patients/significant others, healthcare professionals and across organizations is needed to facilitate coordinated and person-centred care transitions. Participation in a co-design process needs to be asserted continuous reflection, discussion and adaption in order to facilitate the unique knowledge and experience of the involved stakeholders.

Place, publisher, year, edition, pages
Stockholm: Karolinska Institutet, 2021. p. 81
National Category
Medical and Health Sciences
Identifiers
urn:nbn:se:mdh:diva-74584 (URN)hdl.handle.net/10616/47384 (DOI)978-91-8016-037-7 (ISBN)
Public defence
2021-01-08, Stockholm, 09:00
Available from: 2025-11-27 Created: 2025-11-26 Last updated: 2025-11-27Bibliographically approved

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