Patients' and their family members' experiences of participation in care following an acute exacerbation in chronic obstructive pulmonary disease: A phenomenological-hermeneutic study

被引:15
作者
Andersen, Ingrid Charlotte [1 ,2 ,3 ]
Thomsen, Thora Grothe [4 ,5 ,6 ]
Bruun, Poul [7 ]
Bodtger, Uffe [6 ,9 ]
Hounsgaard, Lise [1 ,2 ,8 ]
机构
[1] Odense Univ Hosp, Odense Patient Data Explorat Network OPEN, Odense, Denmark
[2] Univ Southern Denmark, Dept Clin Res, Odense, Denmark
[3] Slagelse Hosp, Dept Med, Slagelse, Denmark
[4] Zealand Univ Hosp, Roskilde, Denmark
[5] Zealand Univ Hosp, Koege, Denmark
[6] Univ Southern Denmark, Inst Reg Hlth Res, Odense, Denmark
[7] Univ Coll Lillebaelt, Hlth Sci Res Ctr, Res, Vejle, Denmark
[8] Univ Coll Lillebaelt, Hlth Sci Res Ctr, Vejle, Denmark
[9] Naestved Hosp, Dept Resp Med, Naestved, Denmark
关键词
chronic obstructive pulmonary disease; family members' perspective; family-centred care; participant observation; participation in care; patients' perspective; professional-family relations; self-management; semistructured interview; QUALITY-OF-LIFE; UNDERSTAND PATIENTS; SELF-MANAGEMENT; CHRONIC ILLNESS; HOSPITAL-CARE; COPD PATIENTS; CHALLENGES; INTERVIEWS; PARTNER; IMPACTS;
D O I
10.1111/jocn.13963
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Aim and objectivesTo explore the experiences of patients with chronic obstructive pulmonary disease and their family members relating both to participation in care during hospitalisation for an acute exacerbation in chronic obstructive pulmonary disease, and to the subsequent day-to-day care at home. BackgroundWhen recovering from an exacerbation, the challenges associated with an unpredictable health condition dominate everyday life for patients and can involve their family members. Proper patient and family participation in care during discharge and follow-up can help patients to improve self-management. However, knowledge of the significance of patient and family participation for recovery and subsequent everyday life is still limited. DesignThis study adopted a longitudinal design informed by ethnographic fieldwork principles. MethodsParticipant observations and interviews with 15 patients and 12 family members were conducted on a Danish hospital ward and twice at the participants' homes. A phenomenological-hermeneutic approach inspired by Ricoeur's theory of interpretation guided the data analysis. ResultsParticipation in care was perceived as valuable, but could be associated with tensions and increased uncertainty. While patients mostly demonstrated a reactive approach to care, family members strived to be more proactive. In hospital, preparing for discharge included an effort to find a balance between powerlessness and influence during interactions with healthcare professionals. At home, managing further recovery and self-management were characterised by navigating between mutual pressure and consideration within the family. ConclusionFamily members play an important role in ensuring that patients are seen, heard and understood, but want to be acknowledged more by healthcare professionals. Appropriate interactions with healthcare professionals are crucial in order to support discharge and daily self-management. Relevance to clinical practiceKnowledge of the challenges that patients with chronic obstructive pulmonary disease and their family members face in participating in care activities could inform future development of family-centred care approaches tailored to individual needs.
引用
收藏
页码:4877 / 4889
页数:13
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