Abstract

BackgroundUncertainty in model-based cost-utility analyses is commonly assessed in a probabilistic sensitivity analysis. Model parameters are implemented as distributions and values are sampled from these distributions in a Monte Carlo simulation. Bootstrapping is an alternative method that requires fewer assumptions and incorporates correlations between model parameters.MethodsA Markov model-based cost–utility analysis comparing oromucosal spray containing delta-9-tetrahidrocannabinol + cannabidiol (Sativex®, nabiximols) plus standard care versus standard spasticity care alone in the management of multiple sclerosis spasticity was performed over a 5-year time horizon from the Belgian healthcare payer perspective. The probabilistic sensitivity analysis was implemented using a bootstrap approach to ensure that the correlations present in the source clinical trial data were incorporated in the uncertainty estimates.ResultsAdding Sativex® spray to standard care was found to dominate standard spasticity care alone, with cost savings of €6,068 and a quality-adjusted life year gain of 0.145 per patient over the 5-year analysis. The probability of dominance increased from 29% in the first year to 94% in the fifth year, with the probability of QALY gains in excess of 99% for all years considered.ConclusionsAdding Sativex® spray to spasticity care was found to dominate standard spasticity care alone in the Belgian healthcare setting. This study showed the use of bootstrapping techniques in a Markov model probabilistic sensitivity analysis instead of Monte Carlo simulations. Bootstrapping avoided the need to make distributional assumptions and allowed the incorporation of correlating structures present in the original clinical trial data in the uncertainty assessment.

Highlights

  • Cost-effectiveness analysis (CEA) of new and current health services and technologies has become key in decision-making and health policy [1, 2]

  • Our base case resulted in SoC + Sativex® being the dominant strategy for time horizons of 2 or more years, with ICERs between €22,187 for a 1-year time horizon decreasing to negative €41,942 for a 5-year time horizon (Table 2)

  • The results from the probabilistic sensitivity analysis (PSA) showed that the probability that SoC + Sativex® is dominant compared to SoC alone varied from 28.9% for a time horizon of 1 year to 94.1% for a time horizon of 5 years

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Summary

Introduction

Cost-effectiveness analysis (CEA) of new and current health services and technologies has become key in decision-making and health policy [1, 2]. Rather than sampling values from the distribution of each model parameter separately (as is done in a Monte Carlo simulation), values of the model parameters for the PSA can be calculated jointly for each bootstrap of the clinical trial data on which they are based. This ensures that any correlating structures present in these data sources are preserved and reflected in the estimates of the uncertainty from the PSA. The probabilistic sensitivity analysis was implemented using a bootstrap approach to ensure that the correlations present in the source clinical trial data were incorporated in the uncertainty estimates. Bootstrapping avoided the need to make distributional assumptions and allowed the incorporation of correlating structures present in the original clinical trial data in the uncertainty assessment

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