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Journal of Aging Research
Volume 2011 (2011), Article ID 682470, 8 pages
http://dx.doi.org/10.4061/2011/682470
Research Article

How Does the Canadian General Public Rate Moderate Alzheimer's Disease?

1Programs for Assessment of Technology in Health (PATH) Research Institute, St. Joseph's Healthcare Hamilton, 25 Main Street West, Suite 2000, Hamilton, ON, Canada L8P 1H1
2Department of Clinical Epidemiology and Biostatistics, McMaster University, 1280 Main Street West, Hamilton, ON, Canada L8S 4L8
3McMaster Evidence-Based Practice Centre, McMaster University, DTC Building, 3rd Floor, 50 Main Street East, Hamilton, ON, Canada L8N 1E9
4Centre for Evaluation of Medicines, St. Joseph's Hospital, Martha Wing H321, 50 Charlton Avenue East, Hamilton, Canada L8N 4A6

Received 12 May 2011; Accepted 11 October 2011

Academic Editor: Barbara Shukitt-Hale

Copyright © 2011 Jean-Eric Tarride et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Objectives. The objectives of this study were to elicit health utility scores for moderate Alzheimer's disease (AD) using members of the general public. Methods. Five-hundred Canadians were chosen randomly to participate in a telephone interview. The EQ-5D was administered to estimate the health utility score for respondents' current health status (i.e., no AD) and for a hypothetical moderate AD health state. Regression analyses were conducted to explain the perceived utility decrement associated with AD. Results. The mean age of the respondents was 51 years, 60% were female, and 42% knew someone with AD. Respondents' mean EQ-5D scores for their current health status and a hypothetical moderate AD were 0.873 (SD: 0.138) and 0.638 (SD: 0.194), respectively ( ). Age, gender, and education were significant factors explaining this decrement in utility. Conclusion. Members of the general public may serve as an alternative to patients and caregivers in the elicitation of health-related quality of life in AD.