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The experience of empowerment in the patient-staff encounter: the patient's perspective
Högskolan i Jönköping, Hälsohögskolan, HHJ, Avd. för omvårdnad. Högskolan i Jönköping, Hälsohögskolan, The Jönköping Academy for Improvement of Health and Welfare.
Högskolan i Jönköping, Hälsohögskolan, HHJ, Avd. för omvårdnad. Högskolan i Jönköping, Hälsohögskolan, HHJ. Kvalitetsförbättring och ledarskap inom hälsa och välfärd. (Kvalitetsförbättringar och ledarskap, Briding the Gap I och II, The SAMMI study group)
Högskolan i Jönköping, Hälsohögskolan.
Swedish Institute for Health Sciences (Vårdalinstitutet), Lund University, Lund, Sweden.
2012 (engelsk)Inngår i: Journal of Clinical Nursing, ISSN 0962-1067, E-ISSN 1365-2702, Vol. 21, nr 5/6, s. 897-904Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Aim and objective.  The aim was to explore empowerment within the patient–staff encounter as experienced by out-patients with chronic kidney disease.

Background.  Empowerment has an important role to play in the patient–staff relationship in the case of patients with a chronic disease. When it comes to patients with chronic kidney disease, there has been little research on empowerment, for which reason interviewing such patients about their experiences of empowerment will provide useful knowledge within the context of out-patient care.

Design.  A qualitative interview study was chosen to gain an understanding of empowerment from the patient perspective.

Method.  The study was carried out at an out-patient clinic in Sweden and involved 20 patients with chronic kidney disease. The interviews were subjected to latent content analysis.

Results.  Five of the seven sub-themes emerging from the analysis represented empowerment: Accessibility according to need, Confirming encounter, Trust in the competence of the healthcare staff, Participation in decision-making, Learning enables better self-management. The other two represented non-empowerment: Meeting with nonchalance, Lack of dialogue and influence. From the seven sub-themes, one comprehensive theme was generated: Creation of trust and learning through encounter.

Conclusion.  The main finding regarding the central role of the creation of trust and learning through the patient–staff encounter underlines the importance of understanding empowerment from the patient’s perspective.

Relevance to clinical practice.  Nursing and other healthcare staff need knowledge and understanding of the meaning of empowerment from the patients’ perspective to meet their needs in out-patient care.

sted, utgiver, år, opplag, sider
2012. Vol. 21, nr 5/6, s. 897-904
Emneord [en]
chronic kidney disease, empowerment, nurses, nursing, out-patient care, patient perspective
HSV kategori
Identifikatorer
URN: urn:nbn:se:hj:diva-17012DOI: 10.1111/j.1365-2702.2011.03901.xISI: 000300504000034PubMedID: 22081948Scopus ID: 2-s2.0-84857031316OAI: oai:DiVA.org:hj-17012DiVA, id: diva2:473166
Prosjekter
Briding the Gap ITilgjengelig fra: 2012-01-05 Laget: 2012-01-05 Sist oppdatert: 2018-10-22bibliografisk kontrollert
Inngår i avhandling
1. A quality improvement project on empowerment in chronic kidney care: an interactive research approach
Åpne denne publikasjonen i ny fane eller vindu >>A quality improvement project on empowerment in chronic kidney care: an interactive research approach
2013 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

One way of improving health care has been conceptualized as personcentred care. In person-centred care the concept of empowerment is crucial. This thesis aims was to explore the meaning of empowerment from the perspective of persons with chronic kidney disease (CKD) and their family members and to evaluate the outcomes of an improvement intervention (QI) for the persons with CKD. Furthermore, to explore the implementation of an QI for empowerment in the context of chronic kidney care from a professional perspective. The research was based on an interactive approach in which the findings relating to the experiences of empowerment by persons with CKD and their family members in chronic kidney care were used in developing the QI. The methods of data collection were both qualitative and quantitative. In all, 20 persons with CKD (Study I) and 12 family members (Study II) participated in the interviews. In the quasi-experimental evaluation of the QI, 25 individuals took part in the intervention group and 21 persons in the comparison group (Study III). Twelve healthcare professionals participated in the case study of the QI (Study IV). Empowerment in chronic kidney care for the persons with CKD was described in terms of creation of trust and learning through encounters. The family members of the persons with CKD described empowerment as having the strength to assume responsibility. The outcomes of the QI after 2 years showed significantly higher scores for individualized care in the intervention group than in the comparison group. The facilitators in the QI were the healthcare professionals' moving spirit and encouragement from involved persons. As a barrier, the healthcare professionals referred to the limitation of the organization. In conclusion, the individual’s perspective of empowerment is important, both for quality of care and as a facilitator for QI in chronic kidney care.

sted, utgiver, år, opplag, sider
Jönköping: School of Health Sciences, 2013. s. 93
Serie
Dissertation Series. School of Health Sciences, ISSN 1654-3602 ; 44
HSV kategori
Identifikatorer
urn:nbn:se:hj:diva-21063 (URN)978-91-85835-43-0 (ISBN)
Disputas
2013-05-31, Forum Humanum Hälsohögskolan, Jönköping, 13:00
Opponent
Veileder
Tilgjengelig fra: 2013-04-30 Laget: 2013-04-30 Sist oppdatert: 2016-01-04bibliografisk kontrollert

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