Literature DB >> 9646153

Determinants of carer stress in Alzheimer's disease.

C Donaldson1, N Tarrier, A Burns.   

Abstract

OBJECTIVES: To explore the impact of subgroups and individual symptoms of non-cognitive disturbance on the carers of Alzheimer's disease patients.
DESIGN: Cross-sectional study using clinically valid scales to assess patient symptomatology and self-report questionnaires to measure carer variables.
SETTING: Old age psychiatry outreach services in South and Central Manchester.
SUBJECTS: 100 patients with Alzheimer's disease living at home and their carers. MAIN OUTCOME MEASURES: Subjective burden and distress in carers.
RESULTS: Separate statistical analyses were performed for subgroups and individual symptoms of non-cognitive disturbance. For subgroups, multivariate analyses identified depression and behavioural disturbances in patients as significant predictors of subjective burden in carers. Carer distress was predicted by depression, psychosis and cognitive impairments in patients and carer gender. For individual symptoms of non-cognitive disturbance, three features of depression in patients (mood-related signs, physical signs and behaviour changes), walking disruptions and the patient-carer relationship predicted of subjective burden in carers. Variance in the level of carer distress was accounted for by sleep disruptions, hallucinations and mood-related depressive features in patients and carer gender.
CONCLUSION: The findings confirm that the non-cognitive features of Alzheimer's disease are stressful for carers and indicate specific relationships between mood-related and behavioural signs of depression, walking and sleep disruptions and hallucinations in patients and adverse carer outcomes. Patient depression and the mood-related signs of depression in particular were the most consistent and powerful predictors of psychological morbidity in carers. Intervention strategies need to identify and target troublesome behaviours in patients and aim to either change these behaviours or alter the way carers respond to them. Thus, interventions need to be symptoms-rather than service-led and are likely to require multidisciplinary and multi-agency approaches.

Entities:  

Mesh:

Year:  1998        PMID: 9646153     DOI: 10.1002/(sici)1099-1166(199804)13:4<248::aid-gps770>3.0.co;2-0

Source DB:  PubMed          Journal:  Int J Geriatr Psychiatry        ISSN: 0885-6230            Impact factor:   3.485


  48 in total

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

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Review 8.  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.

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Review 9.  Sleep disturbances in patients with Alzheimer's disease: epidemiology, pathophysiology and treatment.

Authors:  M V Vitiello; S Borson
Journal:  CNS Drugs       Date:  2001       Impact factor: 5.749

10.  Marital quality in the context of mild cognitive impairment.

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