Literature DB >> 21207771

Quality of life in spite of an unpredictable future: the next of kin of patients with multiple sclerosis.

Elisabeth Liedström1, Ann-Kristin Isaksson, Gerd Ahlström.   

Abstract

The aim of the study was to describe the quality of life of the next of kin of patients diagnosed as having multiple sclerosis (MS). Forty-four next of kin were interviewed and thereafter answered the Subjective Quality of Life questionnaire. The next of kin's quality of life emerged as good in terms of both external conditions and interpersonal relationships in both the interviews and the Subjective Quality of Life. In the interviews, most of the next of kin indicated a trusting and secure relationship with the cohabiting partner, but others described a strained situation with an unsatisfactory married/cohabiting life. There was worry about a worsening of the relationship in the future. In addition, the next of kin spoke of a decrease in freedom, self-actualization, and security, also of a more negative general mood and negative emotional experiences. The results of the questionnaire showed that a sense of engagement in life, having energy, self-actualization, self-assuredness, self-acceptance, security, and general mood were significantly correlated with quality of life as a whole. The study confirms that MS is a disease affecting the whole family, and the next of kin were living in uncertainty, facing an unpredictable future. The nurses could start family support groups and help the next of kin to look after their own health, giving advice on health-promoting behavior to make it possible for the person with MS to live at home even if the illness becomes worse.

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Year:  2010        PMID: 21207771     DOI: 10.1097/jnn.0b013e3181f8a5b2

Source DB:  PubMed          Journal:  J Neurosci Nurs        ISSN: 0888-0395            Impact factor:   1.230


  5 in total

1.  Ready or not: planning for health declines in couples with advanced multiple sclerosis.

Authors:  Hannah Chen; Barbara Habermann
Journal:  J Neurosci Nurs       Date:  2013-02       Impact factor: 1.230

Review 2.  Liminality as a conceptual frame for understanding the family caregiving rite of passage: an integrative review.

Authors:  Susanne W Gibbons; Alyson Ross; Margaret Bevans
Journal:  Res Nurs Health       Date:  2014-08-30       Impact factor: 2.228

3.  Intolerance of Uncertainty: Shaping an Agenda for Research on Coping with Multiple Sclerosis.

Authors:  Kevin N Alschuler; Meghan L Beier
Journal:  Int J MS Care       Date:  2015 Jul-Aug

4.  Health-related quality of life in partners of persons with MS: a longitudinal 10-year perspective.

Authors:  Kristina Gottberg; C Chruzander; U Einarsson; S Fredrikson; S Johansson; L Widén Holmqvist
Journal:  BMJ Open       Date:  2014-12-16       Impact factor: 2.692

Review 5.  Intertwined like a double helix: A meta-synthesis of the qualitative literature examining the experiences of living with someone with multiple sclerosis.

Authors:  Anne Parkinson; Crystal Brunoro; Jack Leayr; Vanessa Fanning; Katrina Chisholm; Janet Drew; Jane Desborough; Christine Phillips
Journal:  Health Expect       Date:  2022-02-04       Impact factor: 3.318

  5 in total

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