Literature DB >> 7662327

Family burden in the care of the demented and nondemented elderly--a longitudinal study.

M Grafström1, B Winblad.   

Abstract

This study describes how the situation will change with time when a close relative cares for a demented or nondemented elderly. The changes over a period of time in cognitive and behavioral deterioration, perceived burden, and social support were examined in a population-based, longitudinal study. Spouses and adult children were interviewed at a 2.5-year interval. Although the support from social services had not increased, the relatives reported less burden and decreased behavioral problems in the demented elderly group. They also reported improved physical health. On the contrary, this long-term follow-up indicated a small increase in social limitation and deteriorated physical health in the group of relatives of mentally healthy elderly. One-third of the demented elderly were admitted to an institution during Time 1 and Time 2, and this may be one reason for the decreased burden.

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Year:  1995        PMID: 7662327     DOI: 10.1097/00002093-199509020-00004

Source DB:  PubMed          Journal:  Alzheimer Dis Assoc Disord        ISSN: 0893-0341            Impact factor:   2.703


  8 in total

1.  Caring for elderly people at home: the consequences to caregivers.

Authors:  E Grunfeld; R Glossop; I McDowell; C Danbrook
Journal:  CMAJ       Date:  1997-10-15       Impact factor: 8.262

Review 2.  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

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Authors:  Anders Wimo; Bengt Winblad; Albrecht Stöffler; Yvonne Wirth; Hans-Jörg Möbius
Journal:  Pharmacoeconomics       Date:  2003       Impact factor: 4.981

4.  The psychosocial health status of carers of persons with dementia: a comparison with the chronically ill.

Authors:  D LoGiudice; N Kerse; K Brown; S J Gibson; C Burrows; D Ames; D Young; L Flicker
Journal:  Qual Life Res       Date:  1998-05       Impact factor: 4.147

5.  Defining the role of the caregiver in Alzheimer's disease treatment.

Authors:  Henry Brodaty; Alisa Green
Journal:  Drugs Aging       Date:  2002       Impact factor: 3.923

6.  Balneotherapy, prevention of cognitive decline and care the Alzheimer patient and his family: outcome of a multidisciplinary workgroup.

Authors:  M Secher; M Soto; S Gillette; S Andrieu; H Villars; B Vellas; C Tabone; J-B Chareyras; O Dubois; C-F Roques; B Dubois
Journal:  J Nutr Health Aging       Date:  2009-11       Impact factor: 4.075

7.  Addressing the challenges to successful recruitment and retention in Alzheimer's disease clinical trials.

Authors:  Joshua D Grill; Jason Karlawish
Journal:  Alzheimers Res Ther       Date:  2010-12-21       Impact factor: 6.982

8.  Effects of a caregiver-inclusive assistive technology intervention: a randomized controlled trial.

Authors:  W Ben Mortenson; Louise Demers; Marcus J Fuhrer; Jeffrey W Jutai; Jessica Bilkey; Michelle Plante; Frank DeRuyter
Journal:  BMC Geriatr       Date:  2018-04-18       Impact factor: 3.921

  8 in total

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