That is the title of a new paper out in Value in Health with co-authors Jaehong Kim, Jacob Fajnor, Kyi-Sin Than, Elizabeth S. Mearns , Stacey L. Kowal, Thomas Majda and Jakub P. Hlávka PhD. The abstract is below.
Objectives
To quantify how incorporating patient risk preferences and severity adjustments affect the value of a hypothetical treatment for mobility impairments caused by neurological conditions.
Methods
A 5-state Markov model was developed to measure the health economic value of a hypothetical treatment delaying the progression of mobility impairments by 30.7% versus standard of care for patients who were 45-year-old, minimally impaired, and had received a diagnosis of a neurological condition. A generalized and risk-adjusted cost-effectiveness (GRACE) model was implemented using relative risk aversion estimates from a US general population survey. Treatment value was measured as risk-aversion and severity-adjusted net monetary benefit (NMB), defined as (1) risk-adjusted health gains (generalized risk-adjusted quality-adjusted life-years [GRA-QALYs]) monetized by (2) risk-aversion and severity-adjusted willingness to pay less (3) incremental costs. Risk-neutral results (traditional cost-effectiveness analysis [TCEA]) were compared.
Results
Incorporating risk preferences and disease severity increased the value of health benefits. Incremental health gains from using the hypothetical treatment (vs standard of care) were valued more when accounting for risk preferences with GRACE (1.358 GRA-QALYs vs 1.199 QALY). Willingness to pay for these health gains was higher when computed under GRACE compared with TCEA ($109 656 per GRA-QALY vs $100 000 per QALY). Overall, NMB increased by 11.6% (risk-aversion and severity-adjusted NMB = $278 324 vs TCEA NMB = $249 311) using GRACE versus TCEA. Results were sensitive to risk-aversion estimates and the functional form of patient utility.
Conclusions
In the first application of GRACE within neurology, GRACE increased the health economic value of a hypothetical neurology treatment, suggesting that TCEA may undervalue treatments for mobility-related neurological impairments.
You can read the full paper here.