The next of kin of older people undergoing haemodialysis: a discursive perspective on perceptions of participation

被引:24
作者
Aasen, Elin Margrethe [1 ]
Kvangarsnes, Marit [1 ]
Wold, Bente [2 ]
Heggen, Kare [3 ]
机构
[1] Aalesund Univ Coll, Alesund, Norway
[2] Univ Bergen, Dept Hlth Promot & Dev, N-5020 Bergen, Norway
[3] Volda Univ Coll, Volda, Norway
关键词
discourse analysis; haemodialysis; next of kin; older people; participation; STAGE RENAL-DISEASE; QUALITY-OF-LIFE; PATIENT PARTICIPATION; NURSING-CARE; CAREGIVERS; DIALYSIS; HEALTH; INTERVENTIONS; SUPPORT; NEED;
D O I
10.1111/j.1365-2648.2011.05854.x
中图分类号
R47 [护理学];
学科分类号
101102 [成人与老年护理学];
摘要
aasen e.m., kvangarsnes m., wold b. & heggen k. (2011) The next of kin of older people undergoing haemodialysis: a discursive perspective on perceptions of participation. Journal of Advanced Nursing68(6), 17161725. Abstract Aim. This paper is a report of a study conducted to explore how the family members of older people who will undergo haemodialysis treatment for the rest of their lives perceive participation. Background. The rights of families to participate in treatment and health care are supported by international law, and by national law in Norway since 1999. Method. This study, which employed an explorative qualitative approach, was carried out in Norway in 2008. Data were derived from transcribed interviews with seven family members underwent critical discourse analysis. Findings. Three discourse practices about the next of kin perception of participation were found: (1) to care and take control, (2) to struggle for involvement, and (3) to be forgotten and powerless. The next of kin said that they had no dialogue with the healthcare team, and some fought to be included in the decision-making process. Conclusion. The dominant part of the discourse as expressed by the next of kin seems to be a paternalistic ideology. Thus, finding ways to enable the next of kin to participate in the decision-making process seems to be a major challenge for the healthcare team in the dialysis units.
引用
收藏
页码:1716 / 1725
页数:10
相关论文
共 47 条
[1]
QUALITY OF LIFE PERCEIVED BY CHRONIC HAEMODIALYSIS PATIENTS AND FAMILY MEMBERS [J].
Acaray, A. ;
Pinar, R. .
JOURNAL OF RENAL CARE, 2005, 31 (01) :35-38
[2]
Alvarez-Ude F, 2004, J NEPHROL, V17, P841
[3]
[Anonymous], 2005, 25 DEP HLTH CAR SERV
[4]
Beauchamp TL, 1979, Principles of Biomedical Ethics
[5]
Burden and quality of life of caregivers for hemodialysis patients [J].
Belasco, AG ;
Sesso, R .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 39 (04) :805-812
[6]
Bhargava J, 2009, NEPHROL NEWS ISSUES, V23, P38
[7]
Bhargava Jaya, 2009, Nephrol News Issues, V23, P34
[8]
Hemodialysis in elderly patients [J].
Wendy W. Brown .
International Urology and Nephrology, 2000, 32 (1) :127-135
[9]
Byers Dina J, 2009, Nephrol Nurs J, V36, P599
[10]
Patient participation: A concept analysis [J].
Cahill, J .
JOURNAL OF ADVANCED NURSING, 1996, 24 (03) :561-571