QUANTIFYING HEALTH RELATED QUALITY OF LIFE IN A CHRONIC PAIN POPULATION- PRELIMINARY RESULTS
Author(s)
Anderson Chuck, MPH, Doctoral Student1, A Ohinmaa, PhD, Associate Professor1, Philip Jacobs, DPhil, Research Fellow2, W Adamowicz, PhD, Professor1, Saifudin Rashiq, MD, Associate Professor1, B Dick, PhD, Assistant Professor11University of Alberta, Edmonton, AB, Canada; 2 Institute of Health Economics, Edmonton, AB, Canada
OBJECTIVES: To assess the sensitivity of the EQ-5D in differentiating between severities of pain related health status (PRHS). METHODS: Study is being conducted with chronic pain patients attending a specialty pain centre in Edmonton, Alberta, Canada. Self reported PRHS was determined using standardized clinical measures that included the Pain Disability Index and The Facial Pain Scale. These measures were slightly modified to facilitate comprehension based on information generated from pilot testing. Patients were categorized according to their PRHS and the EQ-5D was administered to quantify their health utility. Linear regressions were used to compare health utilities between severity levels of PHS adjusting for gender, marital status, age, month as a patient, smoking status and income. RESULTS: Sixty four patients have been assessed. The mean utility was 0.5524 (n=30) for persons with moderate disability and severe pain (MDSP), 0.3625 (n=9) for persons with severe disability and extreme pain (SDEP), 0.3358 (n=22) for persons with severe disability and severe pain (SDSP), and 0.2965 (n=3) for persons with moderate disability and extreme pain (MDEP). Compared to persons with MDSP, persons with SDSP were associated with a -0.225 utility decrement (p<0.001), and persons with SDEP associated with a -0.240 utility decrement (p=0.002). All other comparisons between PRHS levels were non-significant. CONCLUSION: The EQ-5D may be sensitive in detecting differences between low and high levels of PRHS but not within severe levels of PRHS.
Conference/Value in Health Info
2007-05, ISPOR 2007, Arlington, VA, USA
Value in Health, Vol. 10, No.3 (May/June 2007)
Code
PPN17
Topic
Patient-Centered Research
Topic Subcategory
Health State Utilities, Patient-reported Outcomes & Quality of Life Outcomes
Disease
Systemic Disorders/Conditions