QUALITY-OF-LIFE WEIGHTS FOR THE U.S. POPULATION- SELF-REPORTED HEALTH STATUS AND PRIORITY HEALTH CONDITIONS, BY DEMOGRAPHIC CHARACTERISTICS

Author(s)

John A Nyman, PhD, Professor1, Nathan A Barleen, BA, Research Assistant1, Bryan E Dowd, PhD, Professor1, Daniel W. Russell, PhD, Professor2, Stephen Joel Coons, PhD, Professor3, Patrick W. Sullivan, PhD, Assistant Professor41University of Minnesota, Minneapolis, MN, USA; 2 Iowa State University, Ames, IA, USA; 3 University of Arizona, Tucson, AZ, USA; 4 University of Colorado Health Sciences Center, Denver, CO, USA

OBJECTIVES: Many of the large ongoing national surveys of the US population contain a question that asks for the respondent's self-reported health status: “excellent,” “very good,” “good,” “fair” or “poor.” These surveys could be used to conduct cost-utility analyses of health care policies, treatments or other interventions if quality-of-life (QOL) weights for the self-reported health statuses were also available. The objective of this study was to produce nationally representative QOL weights for self-reported health status and for 10 priority health conditions, by a series of demographic variables. METHODS: The Medical Expenditure Panel Survey contains the questions from the EQ-5D health status measure. A recent study has calculated time-trade-off-derived QOL weights corresponding to the EQ-5D health states for a large US sample. We use these data to construct QOL weights for the five self-reported health status categories and 10 priority health conditions, by a series of demographic variables. RESULTS: Mean and median QOL weights were produced for self-reported health status, the 10 priority health conditions, and the demographic variables. We also report QOL weights for the self-reported health state and priority health conditions, by the demographic variables. Finally, ordinary least squares and CLAD regression equations were used to estimate adjusted QOL weights for these variables. CONCLUSION: By providing nationally representative QOL weights for self-reported health status and priority health conditions, by demographic variable, we have facilitated the use of large national surveys for conducting cost-utility analysis and increased their value to researchers and policy makers.

Conference/Value in Health Info

2007-05, ISPOR 2007, Arlington, VA, USA

Value in Health, Vol. 10, No.3 (May/June 2007)

Code

PIH11

Topic

Patient-Centered Research

Topic Subcategory

Patient-reported Outcomes & Quality of Life Outcomes

Disease

Multiple Diseases, Reproductive and Sexual Health

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