Dependence in Alzheimer's disease and service use costs, quality of life, and caregiver burden: The DADE study
Dependence in Alzheimer's disease and service use costs, quality of life, and caregiver burden: The DADE study
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DOI:
10.1016/j.jalz.2014.03.001
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发表时间:
2015-03-01
影响因子:
14
通讯作者:
Lacey, Loretto
中科院分区:
文献类型:
--
作者:
Jones, Roy W.;Romeo, Renee;Lacey, Loretto
Background: Most models determining how patient and caregiver characteristics and costs change with Alzheimer's disease (AD) progression focus on one aspect, for example, cognition. AD is inadequately defined by a single domain; tracking progression by focusing on a single aspect may mean other important aspects are insufficiently addressed. Dependence has been proposed as a better marker for following disease progression.Methods: This was a cross-sectional observational study (18 UK sites). Two hundred forty-nine community or institutionalized patients, with possible/probable AD, Mini-Mental State Examination (3-26), and a knowledgeable informant participated.Results: Significant associations noted between dependence (Dependence Scale [DS]) and clinical measures of severity (cognition, function, and behavior). Bivariate and multivariate models demonstrated significant associations between DS and service use cost, patient quality of life, and caregiver perceived burden.Conclusion: The construct of dependence may help to translate the combined impact of changes in cognition, function, and behavior into a more readily interpretable form. The DS is useful for assessing patients with AD in clinical trials/research. (C) 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.