Literature DB >> 8229112

Multiple sclerosis: stressors and coping strategies in spousal caregivers.

M T O'Brien1.   

Abstract

Community health nurses, who have frequent and prolonged contact with patients afflicted with chronic disease, play a central role in the assessment and care of patients and their families who must deal with the many ramifications of long-term disease. The importance of multiple sclerosis in health care is a result of its worldwide prevalence rate of 57.9 per 100,000 population, its tendency to occur in the young adult, and its chronicity. This exploratory study was designed to describe the stressors of caregivers of individuals with multiple sclerosis, to identify coping behaviors used by caregivers, and to explore the relation between caregiver stress and caregiver coping behavior. The study sample included 20 caregiving spouses of individuals with multiple sclerosis. The data were collected through a semistructured interview of caregiving spouses. Caregiver coping behavior was measured with the Ways of Coping Checklist (Folkman & Lazarus, 1980), and caregiver stress was measured with the Caregiver Strain Index (B. C. Robinson, 1983). Descriptive statistics were calculated for each of the demographic and disability variables. Pearson product-moment correlations were employed to assess the relation between caregiver coping behavior and caregiver stress. Findings revealed significant correlations between caregiver stress and caregiver coping behavior. These findings indicate that as stress in the caregiving role increases, there is an increase in the use of various forms of coping behaviors, both problem focused and emotion focused. Types of stressors and coping strategies used by caregivers are described, and nursing implications are discussed.

Entities:  

Mesh:

Year:  1993        PMID: 8229112     DOI: 10.1207/s15327655jchn1003_1

Source DB:  PubMed          Journal:  J Community Health Nurs        ISSN: 0737-0016            Impact factor:   0.974


  7 in total

1.  The impact of the financial costs of multiple sclerosis on quality of life.

Authors:  Margaret A De Judicibus; Marita P McCabe
Journal:  Int J Behav Med       Date:  2007

Review 2.  Multiple sclerosis: it epidemiological, genetic, and health care impact.

Authors:  R Williams; A S Rigby; M Airey; M Robinson; H Ford
Journal:  J Epidemiol Community Health       Date:  1995-12       Impact factor: 3.710

3.  Caregiver burden in multiple sclerosis: the impact of neuropsychiatric symptoms.

Authors:  Nanna Figved; Kjell-Morten Myhr; Jan-Petter Larsen; Dag Aarsland
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-01-19       Impact factor: 10.154

Review 4.  Neuropsychological aspects of multiple sclerosis.

Authors:  J C Brassington; N V Marsh
Journal:  Neuropsychol Rev       Date:  1998-06       Impact factor: 7.444

5.  Mental health problems in children of somatically ill parents, e.g. multiple sclerosis.

Authors:  Barbara Steck; Felix Amsler; Andrea Grether; Alexandra Schwald Dillier; Christiane Baldus; Miriam Haagen; L Diareme; John Tsiantis; Ludwig Kappos; Dieter Bürgin; Georg Romer
Journal:  Eur Child Adolesc Psychiatry       Date:  2006-11-29       Impact factor: 5.349

6.  Who is Taking Care of the Caregiver?

Authors:  Amy Burleson Sullivan; Deborah Miller
Journal:  J Patient Exp       Date:  2015-05-01

7.  Understanding leisure-time physical activity: Voices of people with MS who have moderate-to-severe disability and their family caregivers.

Authors:  Afolasade Fakolade; Julie Lamarre; Amy Latimer-Cheung; Trisha Parsons; Sarah A Morrow; Marcia Finlayson
Journal:  Health Expect       Date:  2017-07-19       Impact factor: 3.377

  7 in total

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