Maximum Acceptable Risk Estimation based on a Discrete Choice Experiment and Probabilistic Threshold Technique

Jorien Veldwijk*, Rachael L DiSantostefano, Ellen Janssen, Gwenda Simons, Matthias Englbrecht, Schölin Bywall Karin, Christine Radawski, Karim Raza, Brett Hauber, M Falahee

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Objective: To empirically compare Maximum Acceptable Risk (MAR) results estimated using both a Discrete Choice Experiment (DCE) and the Probabilistic Threshold Technique (PTT).

Methods: Members of the UK general public (n = 982) completed an online survey including a DCE and PTT (in random order) measuring their preferences for preventive treatment for rheumatoid arthritis (RA). For the DCE, a Bayesian D-efficient design consisting of 4 blocks of 15 choice tasks was constructed including 6 attributes with varying levels. The PTT used identical risk and benefit attributes. For the DCE, a panel mixed logit model was conducted, both mean and individual estimates were used to calculate MAR. For the PTT, interval regression was used to calculate MAR. Perceived complexity of the choice tasks and preference heterogeneity were investigated for both methods.

Results: MAR confidence intervals of both methods overlapped for serious infection and serious side effects but not for mild side effects (MAR was 32.7 percent-points lower in the PTT). Although, both DCE and PTT tasks overall were considered easy or very easy to understand and answer, significantly more respondents rated the DCE choice tasks as easier to understand compared to those who rated the PTT as easier (7 percentage-point difference; p < 0.05).

Discussion: MAR estimate confidence intervals based on DCE and PTT overlapped for two out of the three included risk attributes. More respondents rated the DCE as easier to understand. This may suggest that the DCE is better suited in studies estimating MAR for multiple risk attributes of differing severity, while PTT may be better suited when measuring heterogeneity in MAR estimates or when investigating one or more serious adverse events.
Original languageEnglish
JournalPatient
Early online date30 Aug 2023
DOIs
Publication statusE-pub ahead of print - 30 Aug 2023

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