Literature DB >> 30722800

Well-being in dementia: a cross-sectional dyadic study of the impact of multiple dimensions of strain on persons living with dementia and their family care partners.

Lyndsey M Miller1, Jeffrey A Kaye1, Karen S Lyons2, Christopher S Lee2, Carol J Whitlatch3, Michael S Caserta4.   

Abstract

ABSTRACTBackground and Purpose:The impact of dementia-related stressors and strains have been examined for their potential to threaten the well-being of either the person with dementia or the family care partner, but rarely have studies considered the dyadic nature of well-being in dementia. The purpose of this study was to examine the dyadic effects of multiple dimensions of strain on the well-being of dementia care dyads.
METHODS: Using multilevel modeling to account for the inter-relatedness of individual well-being within dementia care dyads, we examined cross-sectional responses collected from 42 dyads comprised of a hospitalized patient diagnosed with a primary progressive dementia (PWD) and their family care partner (CP). Both PWDs and CPs self-reported on their own well-being using measures of quality of life (QOL-Alzheimer's Disease scale) and depressive symptoms (Center for Epidemiological Studies Depression Scale).
RESULTS: In adjusted models, the PWD's well-being (higher QOL and lower depressive symptoms) was associated with significantly less strain in the dyad's relationship. The CP's well-being was associated with significantly less care-related strain and (for QOL scale) less relationship strain.
CONCLUSIONS: Understanding the impact of dementia on the well-being of PWDs or CPs may require an assessment of both members of the dementia care dyad in order to gain a complete picture of how dementia-related stressors and strains impact individual well-being. These results underscore the need to assess and manage dementia-related strain as a multi-dimensional construct that may include strain related to the progression of the disease, strain from providing care, and strain on the dyad's relationship quality.

Entities:  

Keywords:  Stress Process Model; dementia; depression; dyadic analysis; family caregiving; quality-of-life

Mesh:

Year:  2019        PMID: 30722800      PMCID: PMC6579645          DOI: 10.1017/S104161021800203X

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


  30 in total

Review 1.  Touchscreen interventions and the well-being of people with dementia and caregivers: a systematic review.

Authors:  Charlie Tyack; Paul M Camic
Journal:  Int Psychogeriatr       Date:  2017-04-27       Impact factor: 3.878

2.  Caregiver rating bias in mild cognitive impairment and mild Alzheimer's disease: impact of caregiver burden and depression on dyadic rating discrepancy across domains.

Authors:  Livia Pfeifer; Reinhard Drobetz; Sonja Fankhauser; Moyra E Mortby; Andreas Maercker; Simon Forstmeier
Journal:  Int Psychogeriatr       Date:  2013-05-07       Impact factor: 3.878

3.  Religiosity and quality of life: a dyadic perspective of individuals with dementia and their caregivers.

Authors:  Neha Nagpal; Allison R Heid; Steven H Zarit; Carol J Whitlatch
Journal:  Aging Ment Health       Date:  2014-09-04       Impact factor: 3.658

4.  The Theory of Dyadic Illness Management.

Authors:  Karen S Lyons; Christopher S Lee
Journal:  J Fam Nurs       Date:  2018-01-20       Impact factor: 3.818

5.  Caregivers' relationship closeness with the person with dementia predicts both positive and negative outcomes for caregivers' physical health and psychological well-being.

Authors:  Elizabeth Fauth; Kyle Hess; Kathy Piercy; Maria Norton; Chris Corcoran; Peter Rabins; Constantine Lyketsos; JoAnn Tschanz
Journal:  Aging Ment Health       Date:  2012       Impact factor: 3.658

6.  Factors related to perceived quality of life in patients with Alzheimer's disease: the patient's perception compared with that of caregivers.

Authors:  Josep Lluís Conde-Sala; Josep Garre-Olmo; Oriol Turró-Garriga; Secundino López-Pousa; Joan Vilalta-Franch
Journal:  Int J Geriatr Psychiatry       Date:  2009-06       Impact factor: 3.485

7.  Dyadic relationship scale: a measure of the impact of the provision and receipt of family care.

Authors:  Margaret D Sebern; Carol J Whitlatch
Journal:  Gerontologist       Date:  2007-12

8.  Quality of Life for Dementia Caregiving Dyads: Effects of Incongruent Perceptions of Everyday Care and Values.

Authors:  Heehyul Moon; Aloen L Townsend; Carol J Whitlatch; Peggye Dilworth-Anderson
Journal:  Gerontologist       Date:  2017-08-01

9.  Self and carer perspectives of quality of life in dementia using the QoL-AD.

Authors:  Vasiliki Orgeta; Martin Orrell; Barry Hounsome; Bob Woods
Journal:  Int J Geriatr Psychiatry       Date:  2014-05-02       Impact factor: 3.485

10.  Understanding and Measuring the Wellbeing of Carers of People With Dementia.

Authors:  Nicola A Cunningham; Tom R Cunningham; Jane M Roberston
Journal:  Gerontologist       Date:  2019-09-17
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  1 in total

1.  Experiences of Family Caregivers of People with Dementia during the COVID-19 Pandemic.

Authors:  Melissa L Harris; Marita G Titler
Journal:  West J Nurs Res       Date:  2021-10-29       Impact factor: 1.774

  1 in total

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