Literature DB >> 23651733

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

Livia Pfeifer1, Reinhard Drobetz, Sonja Fankhauser, Moyra E Mortby, Andreas Maercker, Simon Forstmeier.   

Abstract

BACKGROUND: Caregivers of individuals with dementia are biased in their rating of mental health measures of the care receiver. This study examines caregiver burden and depression as predictors of this bias for mild cognitive impairment and mild Alzheimer's disease in different domains.
METHODS: The sample consisted of 202 persons: 60 with mild cognitive impairment, 41 with mild Alzheimer's disease, and 101 caregivers. Discrepancy scores were calculated by subtracting the mean caregiver score from the respective mean patient score on the following assessment instruments: the Geriatric Depression Scale, Apathy Evaluation Scale, Bayer-Activities of Daily Living Scale, and Quality of Life-AD scale. Caregiver burden and depression were assessed by the Zarit Burden Interview and the Center for Epidemiologic Studies Depression Scale.
RESULTS: Intraclass correlation coefficients were low for apathy (0.38), daily functioning (0.38), and quality of life (0.30) and moderate for depression (0.49). These domains showed negative rating discrepancies, which indicates caregiver rating bias for all four domains. Regression analyses revealed that caregiver burden significantly contributed to explaining these discrepancies in the domains apathy, daily functioning, and quality of life.
CONCLUSION: Caregiver rating bias can be attributed to caregiver burden. When caregiver burden is present, data based on caregiver ratings should therefore be interpreted with caution.

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Year:  2013        PMID: 23651733     DOI: 10.1017/S1041610213000562

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


  18 in total

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2.  Association of Apathy With Risk of Incident Dementia: A Systematic Review and Meta-analysis.

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3.  Frequency and impact of informant replacement in Alzheimer disease research.

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4.  Frontal Behavior Syndromes in Idiopathic Normal Pressure Hydrocephalus as a Function of Alzheimer's Disease Biomarker Status.

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5.  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.

Authors:  Lyndsey M Miller; Jeffrey A Kaye; Karen S Lyons; Christopher S Lee; Carol J Whitlatch; Michael S Caserta
Journal:  Int Psychogeriatr       Date:  2019-02-06       Impact factor: 3.878

Review 6.  Reconsidering Gold Standards for Surrogate Decision Making for People with Dementia.

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7.  Informant Report of Financial Capacity for Individuals With Chronic Acquired Brain Injury: An Assessment of Informant Accuracy.

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8.  Differences in Assessment of Everyday Preferences Between People With Cognitive Impairment and Their Care Partners: The Role of Neuropsychiatric Symptoms.

Authors:  James M Wilkins; Joseph J Locascio; Jeanette M Gunther; Liang Yap; Bradley T Hyman; Deborah Blacker; Brent P Forester; Olivia I Okereke
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9.  Network structures and temporal stability of self- and informant-rated affective symptoms in Alzheimer's disease.

Authors:  T T Saari; I Hallikainen; T Hintsa; A M Koivisto
Journal:  J Affect Disord       Date:  2020-07-19       Impact factor: 4.839

10.  Autonomic dysfunction in mild cognitive impairment: evidence from power spectral analysis of heart rate variability in a cross-sectional case-control study.

Authors:  Paola Nicolini; Michele M Ciulla; Gabriella Malfatto; Carlo Abbate; Daniela Mari; Paolo D Rossi; Emanuela Pettenuzzo; Fabio Magrini; Dario Consonni; Federico Lombardi
Journal:  PLoS One       Date:  2014-05-06       Impact factor: 3.240

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