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Identifying factors of activities of daily living important for cost and caregiver outcomes in Alzheimer's disease

Published online by Cambridge University Press:  26 August 2015

Catherine Reed*
Affiliation:
Global Health Outcomes, Lilly Research Centre, Eli Lilly and Company Limited, Windlesham, Surrey, UK
Mark Belger
Affiliation:
Global Health Outcomes, Lilly Research Centre, Eli Lilly and Company Limited, Windlesham, Surrey, UK
Bruno Vellas
Affiliation:
Gerontopole, Alzheimer's Disease Research and Clinical Center, INSERM 1027, Toulouse University Hospital, Toulouse, France
Jeffrey Scott Andrews
Affiliation:
Health Outcomes Research, Eli Lilly and Company Limited, Indianapolis, IN, USA
Josep M. Argimon
Affiliation:
Divisió d’avaluació, Servei Català de la Salut, Barcelona, Spain
Giuseppe Bruno
Affiliation:
Clinica della Memoria, Department of Neurological Sciences, University of Rome “Sapienza”, Rome, Italy
Richard Dodel
Affiliation:
Department of Neurology, Philipps-University, Marburg, Germany
Roy W. Jones
Affiliation:
The Research Institute for the Care of Older People (RICE), The RICE Centre, Royal United Hospital, Bath, UK
Anders Wimo
Affiliation:
Division of Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institute, Stockholm, Sweden
Josep Maria Haro
Affiliation:
Parc Santari Sant Joan de Déu, CIBERSAM, Universitat de Barcelona, Sant Boi de Llobregat, Barcelona, Spain
*
Correspondence should be addressed to: Dr Catherine Reed, PhD, Global Health Outcomes, Eli Lilly and Company, Erl Wood Manor, Sunninghill Road, Windlesham, Surrey GU20 6PH, UK. Phone: +44-1276-483243; Fax: +44-1276-483192. Email: reed_catherine@lilly.com.

Abstract

Background:

We aimed to obtain a better understanding of how different aspects of patient functioning affect key cost and caregiver outcomes in Alzheimer's disease (AD).

Methods:

Baseline data from a prospective observational study of community-living AD patients (GERAS) were used. Functioning was assessed using the Alzheimer's Disease Cooperative Study – Activities of Daily Living Scale. Generalized linear models were conducted to analyze the relationship between scores for total activities of daily living (ADL), basic ADL (BADL), instrumental ADL (IADL), ADL subdomains (confirmed through factor analysis) and individual ADL questions, and total societal costs, patient healthcare and social care costs, total and supervision caregiver time, and caregiver burden.

Results:

Four distinct ADL subdomains were confirmed: basic activities, domestic/household activities, communication, and outside activities. Higher total societal costs were associated with impairments in all aspects of ADL, including all subdomains; patient costs were associated with total ADL and BADL, and basic activities subdomain scores. Both total and supervision caregiver hours were associated with total ADL and IADL scores, and domestic/household and outside activities subdomain scores (greater hours associated with greater functional impairments). There was no association between caregiver burden and BADL or basic activities subdomain scores. The relationship between total ADL, IADL, and the outside activities subdomain and outcomes differed between patients with mild and moderate-to-severe AD.

Conclusions:

Identification of ADL subdomains may lead to a better understanding of the association between patient function and costs and caregiver outcomes at different stages of AD, in particular the outside activities subdomain within mild AD.

Type
Research Article
Copyright
Copyright © International Psychogeriatric Association 2015 

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References

Balardy, L., Voisin, T., Cantet, C., Vellas, B. and REAL.FR Group. (2005). Predictive factors of emergency hospitalisation in Alzheimer's patients: results of one-year follow-up in the REAL.FR cohort. Journal of Nutrition, Health & Aging, 9, 112116.Google Scholar
Brodaty, H., McGilchrist, C., Harris, L. and Peters, K. E. (1993). Time until institutionalization and death in patients with dementia. Role of caregiver training and risk factors. Archives of Neurology, 50, 643650.Google Scholar
Brown, P. J., Devanand, D. P., Liu, X., Caccappolo, E. and Alzheimer's Disease Neuroimaging Initiative. (2011). Functional impairment in elderly patients with mild cognitive impairment and mild Alzheimer's disease. Archives of General Psychiatry, 68, 617626.CrossRefGoogle Scholar
Campbell, P. et al. (2008). Determinants of burden in those who care for someone with dementia. International Journal of Geriatric Psychiatry, 23, 10781085.CrossRefGoogle ScholarPubMed
Del-Pino-Casado, R., Frías-Osuna, A., Palomino-Moral, P. A. and Pancorbo-Hidalgo, P. L. (2011). Coping and subjective burden in caregivers of older relatives: a quantitative systematic review. Journal of Advanced Nursing, 67, 23112322.CrossRefGoogle ScholarPubMed
Evans, C. and Crawford, B. (1999). Patient self-reports in pharmaco-economic studies. Their use and impact on study validity. Pharmacoeconomics, 15, 241256.Google Scholar
Galasko, D. et al. (1997). An inventory to assess activities of daily living for clinical trials in Alzheimer's disease. The Alzheimer's Disease Cooperative Study. Alzheimer's Disease and Associated Disorders, 11 (Suppl. 2), S33S39.CrossRefGoogle ScholarPubMed
Galasko, D., Schmitt, F., Thomas, R., Jin, S., Bennett, D. and Alzheimer's Disease Cooperative Study. (2005). Detailed assessment of activities of daily living in moderate to severe Alzheimer's disease. Journal of the International Neuropsychological Society, 11, 446453.CrossRefGoogle ScholarPubMed
Germain, S. et al. (2009). Does cognitive impairment influence burden in caregivers of patients with Alzheimer's disease? Journal of Alzheimer's Disease, 17, 105114.Google Scholar
Gustavsson, A. et al. (2011). Predictors of costs of care in Alzheimer's disease: a multinational sample of 1,222 patients. Alzheimers & Dementia, 7, 318327.CrossRefGoogle Scholar
Handels, R. L., Wolfs, C. A., Aalten, P., Verhey, F. R. and Severens, J. L. (2013). Determinants of care costs of patients with dementia or cognitive impairment. Alzheimer's Disease and Associated Disorders, 27, 3036.Google Scholar
Haro, J. M. et al. (2014). Analysis of burden in caregivers of people with Alzheimer's disease using self-report and supervision hours. Journal of Nutrition, Health & Aging, 18, 677684. doi:10.1007/s12603-014-0036-0.Google Scholar
Kahle-Wrobleski, K., Coley, N., Lepage, B., Cantet, C., Vellas, B. and Andrieu, S., f or the PLASA/DSA group. (2014). Understanding the complexities of functional ability in Alzheimer's disease: more than just basic and instrumental factors. Current Alzheimer's Research, 11, 357366.Google Scholar
Kim, H., Chang, M., Rose, K. and Kim, S. (2012). Predictors of caregiver burden in caregivers of individuals with dementia. Journal of Advanced Nursing, 68, 846855.Google Scholar
Leicht, H. et al. (2011). Net costs of dementia by disease stage. Acta Psychiatrica Scandinavica, 124, 384395.Google Scholar
Mangone, C. A. et al. (1993). Influence of feelings of burden on the caregiver's perception of the patient's functional status. Dementia, 4, 287293.Google ScholarPubMed
Marshall, G. A., Amariglio, R. E., Sperling, R. A. and Rentz, D. M. (2012). Activities of daily living: where do they fit in the diagnosis of Alzheimer's disease? Neurodegenerative Disease Management, 2, 483491.Google Scholar
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D. and Stadlan, E. M. (1984). Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's disease. Neurology, 34, 939944.CrossRefGoogle ScholarPubMed
Nourhashemi, F. et al. (2010). Effectiveness of a specific care plan in patients with Alzheimer's disease: cluster randomised trial (PLASA study). BMJ, 340, c2466.Google Scholar
Reed, C. et al. (2014). Caregiver burden in Alzheimer's disease: differential associations in adult-child and spousal caregivers in the GERAS observational study. Dementia and Geriatric Cognitive Disorders Extra, 4, 5164.CrossRefGoogle ScholarPubMed
Sacco, G. et al. (2012). Detection of activities of daily living impairment in Alzheimer's disease and mild cognitive impairment using information and communication technology. Clinical Interventions in Aging, 7, 539549.CrossRefGoogle ScholarPubMed
Serrano-Aguilar, P. G., Lopez-Bastida, J. and Yanes-Lopez, V. (2006). Impact on health-related quality of life and perceived burden of informal caregivers of individuals with Alzheimer's disease. Neuroepidemiology, 27, 136142.CrossRefGoogle ScholarPubMed
Snyder, J. R. (2000). Impact of caregiver–receiver relationship quality on burden and satisfaction. Journal of Women & Aging, 12, 147167.Google Scholar
Wattmo, C., Paulsson, E., Minthon, L. and Londos, E. (2013). A longitudinal study of risk factors for community-based home help services in Alzheimer's disease: the influence of cholinesterase inhibitor therapy. Clinical Interventions in Aging, 8, 329339.Google Scholar
Wimo, A., Wetterholm, A.-L., Mastey, V. and Winblad, B. (1998). Evaluation of resource utilization and caregiver time in anti-dementia drug trials − a quantitative battery. In Wimo, A., Jönsson, B., Karlsson, G. and Winblad, B. (eds.), Health Economics of Dementia (pp. 465499). London: John Wiley.Google Scholar
Wimo, A. et al. (2013). The GERAS study: a prospective observational study of costs and resource use in community dwellers with Alzheimer's disease in three European countries – study design and baseline findings. Journal of Alzheimer's Disease, 36, 385399.Google Scholar
Wolfs, C. A. et al. (2012). Predictive factors for the objective burden of informal care in people with dementia: a systematic review. Alzheimer's Disease and Associated Disorders, 26, 197204.Google Scholar
Zanetti, O., Geroldi, C., Frisoni, G. B., Bianchetti, A. and Trabucchi, M. (1999). Contrasting results between caregiver's report and direct assessment of activities of daily living in patients affected by mild and very mild dementia: the contribution of the caregiver's personal characteristics. Journal of the American Geriatrics Society, 47, 196202.Google Scholar
Zarit, S. H., Reever, K. E. and Bach-Peterson, J. (1980). Relatives of the impaired elderly: correlates of feelings of burden. Gerontologist, 20, 649655.CrossRefGoogle ScholarPubMed
Zhu, C. W. et al. (2006). Clinical features associated with costs in early AD: baseline data from the Predictors Study. Neurology, 66, 10211028.Google Scholar
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