Literature DB >> 9677500

Family caregiving in dementia: prediction of caregiver burden 12 months after relocation to group-living care.

S Elmståhl1, B Ingvad, L Annerstedt.   

Abstract

The strain of caregiving associated with the care of demented persons living at home often continues after relocation and group-living care units (GL), designed for a small number of subjects, have been developed. The aim was to prospectively describe caregiver burden in relationship to symptoms of patients with dementia after relocation to GL. Sixty-four caregivers and 64 demented patients were assessed before, 6 months after, and 12 months after relocation. Thirty-six caregivers were children, 7 were spouses, and 21 were others. Validated scales were used for caregiver burden and dementia symptoms. Total burden of caregivers decreased after 12 months, but the degree of isolation was unchanged and feeling of disappointment increased significantly. The burden was not related to changes of activities of daily life or disorientation. Patients' lack of vitality at relocation independently predicted caregiver's burden 1 year later. Hallucinations and changes of symptoms during the first year associated with less caregiver burden, probably due to greater detachment of the relationship. The caregiver burden remains 1 year after relocation and any support to the caregiver should consider patients' symptoms, especially lack of vitality.

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Year:  1998        PMID: 9677500     DOI: 10.1017/s1041610298005249

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  6 in total

Review 1.  The problem with "problem behaviors": a systematic review of the association between individual patient behavioral and psychological symptoms and caregiver depression and burden within the dementia patient-caregiver dyad.

Authors:  Katherine Ornstein; Joseph E Gaugler
Journal:  Int Psychogeriatr       Date:  2012-05-22       Impact factor: 3.878

2.  Spouses, adult children, and children-in-law as caregivers of older adults: a meta-analytic comparison.

Authors:  Martin Pinquart; Silvia Sörensen
Journal:  Psychol Aging       Date:  2011-03

3.  The association between medical diagnosis and caregiver burden: a cross-sectional study of recipients of informal support and caregivers from the general population study 'Good Aging in Skåne', Sweden.

Authors:  Sölve Elmståhl; Beth Dahlrup; Henrik Ekström; Eva Nordell
Journal:  Aging Clin Exp Res       Date:  2017-12-13       Impact factor: 3.636

4.  Neuropsychiatric symptoms as a predictor of caregiver burden in Alzheimer's disease.

Authors:  Ricardo F Allegri; Diego Sarasola; Cecilia M Serrano; Fernando E Taragano; Raúl L Arizaga; Judith Butman; Leandro Loñ
Journal:  Neuropsychiatr Dis Treat       Date:  2006-03       Impact factor: 2.570

Review 5.  Health economics research into supporting carers of people with dementia: a systematic review of outcome measures.

Authors:  Carys Jones; Rhiannon Tudor Edwards; Barry Hounsome
Journal:  Health Qual Life Outcomes       Date:  2012-11-26       Impact factor: 3.186

6.  Emotional Burden and Perceived Social Support in Male Partners of Women with Cancer.

Authors:  Marcin J Jabłoński; Francisco García-Torres; Paulina Zielińska; Alicja Bułat; Piotr Brandys
Journal:  Int J Environ Res Public Health       Date:  2020-06-12       Impact factor: 3.390

  6 in total

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