Literature DB >> 10763287

Being a close relative of a dying person. Development of the concepts "involvement in the light and in the dark".

B Andershed1, B M Ternestedt.   

Abstract

The current study is based on an earlier article in which relatives' involvement in care was described as "involvement in the light" or "involvement in the dark." Involvement in the light was characterized as the relative being well informed and experiencing a meaningful involvement. The relatives involved in the dark felt uninformed, that they were "grouping around in the dark" when they tried to support the patient. The present study analyzed further the meaning of "involvement in the light" and "involvement in the dark," and investigated whether two different care cultures, the relationship with the staff, and a rapid course of illness influence the involvement of relatives. Relatives of 52 patients who died, 30 at a surgical department and 22 in a hospice ward, were interviewed after the patients' deaths. All the relatives of the patients in the hospice ward and 13 of those in the surgical department were judged to be involved in the light. Of the relatives judged to be involved in the dark, 12 either had a sick relative with a rapid course of illness or felt that the sick relative had died unexpectedly. A pattern was clearly observed: The relatives involved in the light described being met with respect, openness, sincerity, confirmation, and connection, whereas the opposite was experienced by those involved in the dark.

Entities:  

Mesh:

Year:  2000        PMID: 10763287     DOI: 10.1097/00002820-200004000-00012

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  6 in total

1.  Next of kin's experience of powerlessness and helplessness in palliative home care.

Authors:  Anna Milberg; Peter Strang; Maria Jakobsson
Journal:  Support Care Cancer       Date:  2003-12-18       Impact factor: 3.603

2.  Held to ransom: Parents of self-harming adults describe their lived experience of professional care and caregivers.

Authors:  Britt-Marie Lindgren; Sture Aström; Ulla Hällgren Graneheim
Journal:  Int J Qual Stud Health Well-being       Date:  2010-09-24

3.  Support to informal caregivers of patients with severe chronic obstructive pulmonary disease: a qualitative study of caregivers' and professionals' experiences in Swedish hospitals.

Authors:  Susann Strang; Josefin Fährn; Peter Strang; Agneta Ronstad; Louise Danielsson
Journal:  BMJ Open       Date:  2019-08-10       Impact factor: 2.692

4.  Measuring next of kin's experience of participation in the care of older people in nursing homes.

Authors:  Albert Westergren; Lina Behm; Tove Lindhardt; Magnus Persson; Gerd Ahlström
Journal:  PLoS One       Date:  2020-01-31       Impact factor: 3.240

5.  Caregivers' active role in palliative home care - to encourage or to dissuade? A qualitative descriptive study.

Authors:  Anna Weibull; Frede Olesen; Mette Asbjoern Neergaard
Journal:  BMC Palliat Care       Date:  2008-09-16       Impact factor: 3.234

6.  Next of kin's perceptions of the meaning of participation in the care of older persons in nursing homes: a phenomenographic study.

Authors:  Kajsa Ekström; Sanna Spelmans; Gerd Ahlström; Per Nilsen; Åsa Alftberg; Birgitta Wallerstedt; Lina Behm
Journal:  Scand J Caring Sci       Date:  2019-01-03
  6 in total

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