Literature DB >> 15331808

Survival of persons with Alzheimer's disease: caregiver coping matters.

McKee J McClendon1, Kathleen A Smyth, Marcia M Neundorfer.   

Abstract

PURPOSE: Although persons with Alzheimer's disease (AD) require increasingly more assistance with activities of daily living as their disease progresses, the caregiving environment has received little attention as a source of predictors of their survival time. We report here on a study to determine whether variation in survival time of persons with AD can be better explained by including caregiver variables such as coping style and depressive symptoms as predictors. DESIGN AND METHODS: A sample of 193 persons with AD residing in the community and their family caregivers was used to estimate the parameters of a Cox regression model of survival time that included both caregiver characteristics and care-recipient impairments as covariates.
RESULTS: Caregiver wishfulness-intrapsychic coping was related to shorter care-recipient survival time, but instrumental and acceptance coping and caregiver depressive symptoms were not associated with survival time. Care-recipient impairments (dependency in activities of daily living, low score on the Mini-Mental State Examination, and problematic behaviors) were associated with shorter survival time. IMPLICATIONS: Because this study is the first to report the link between caregiver coping and care-recipient survival, further study to understand the dynamics is required. We discuss several possible mechanisms, including the possibility that caregivers engaging in wishfulness-intrapsychic coping are less psychologically available to the person with dementia. These caregivers may therefore provide less person-centered care that is responsive to the true capacities of the person with dementia, and thus they may inadvertently contribute to excess disability and consequent accelerated decline. Because wishfulness-intrapsychic coping was uncorrelated with instrumental or acceptance coping, our findings suggest that interventions to enhance coping skills among caregivers, which have focused primarily on increasing problem solving and acceptance coping, also may have to include specific attempts to reduce wishfulness-intrapsychic approaches to benefit not only the caregiver but the care recipient as well.

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Year:  2004        PMID: 15331808     DOI: 10.1093/geront/44.4.508

Source DB:  PubMed          Journal:  Gerontologist        ISSN: 0016-9013


  10 in total

1.  Developing a Measurement Strategy for Assessing Family Caregiver Skills: Conceptual Issues.

Authors:  Carol J Farran; Judith J McCann; Louis G Fogg; Caryn D Etkin
Journal:  Alzheimers care today       Date:  2009

2.  Caregiver appraisals of functional dependence in individuals with dementia and associated caregiver upset: psychometric properties of a new scale and response patterns by caregiver and care recipient characteristics.

Authors:  Laura N Gitlin; David L Roth; Louis D Burgio; David A Loewenstein; Laraine Winter; Linda Nichols; Soledad Argüelles; Mary Corcoran; Robert Burns; Jennifer Martindale
Journal:  J Aging Health       Date:  2005-04

3.  Behavioral symptoms of dementia: a dyadic effect of caregivers' stress process?

Authors:  Judy L M Campbell; Meredeth A Rowe; Michael Marsiske
Journal:  Res Gerontol Nurs       Date:  2010-09-30       Impact factor: 1.571

4.  Caregiver coping strategies predict cognitive and functional decline in dementia: the Cache County Dementia Progression Study.

Authors:  JoAnn T Tschanz; Kathleen Piercy; Chris D Corcoran; Elizabeth Fauth; Maria C Norton; Peter V Rabins; Brian T Tschanz; M Scott Deberard; Christine Snyder; Courtney Smith; Lester Lee; Constantine G Lyketsos
Journal:  Am J Geriatr Psychiatry       Date:  2013-01-02       Impact factor: 4.105

5.  The nature and scope of stressful spousal caregiving relationships.

Authors:  Linda Lindsey Davis; Catherine L Gilliss; Tess Deshefy-Longhi; Deborah H Chestnutt; Margory Molloy
Journal:  J Fam Nurs       Date:  2011-05       Impact factor: 3.818

6.  How much striving is too much? John Henryism active coping predicts worse daily cortisol responses for African American but not white female dementia family caregivers.

Authors:  Marcellus M Merritt; T J McCallum; Thomas Fritsch
Journal:  Am J Geriatr Psychiatry       Date:  2011-05       Impact factor: 4.105

7.  Understanding Internet Use Among Dementia Caregivers: Results of Secondary Data Analysis Using the US Caregiver Survey Data.

Authors:  Heejung Kim
Journal:  Interact J Med Res       Date:  2015-02-23

Review 8.  Quality of family relationships and outcomes of dementia: a systematic review.

Authors:  Hannah B Edwards; Sharea Ijaz; Penny F Whiting; Verity Leach; Alison Richards; Sarah J Cullum; Richard Il Cheston; Jelena Savović
Journal:  BMJ Open       Date:  2018-01-21       Impact factor: 2.692

9.  Online training and support program (iSupport) for informal dementia caregivers: protocol for an intervention study in Portugal.

Authors:  Soraia Teles; Ana Ferreira; Katrin Seeher; Stéfanie Fréel; Constança Paúl
Journal:  BMC Geriatr       Date:  2020-01-08       Impact factor: 3.921

10.  Development of guidelines for family and non-professional helpers on assisting an older person who is developing cognitive impairment or has dementia: a Delphi expert consensus study.

Authors:  K S Bond; A F Jorm; B A Kitchener; C M Kelly; K J Chalmers
Journal:  BMC Geriatr       Date:  2016-07-07       Impact factor: 3.921

  10 in total

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