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SENSITIVITY ANALYSIS IN MULTI-CRITERIA DECISION (MCDA) MODELS

FOR BENEFIT-RISK ASSESSMENT

Maarten IJzerman, Karin Groothuis-Oudshoorn and Marjan Hummel

University of Twente, Health Technology and Services Research, Enschede, Netherlands

OBJECTIVES: Regulators of medical technologies are facing increasing pressure to make their deliberations concerning

the benefits and risk more transparent. Both benefits and risks are often measured via multiple competing outcomes.

Hence, MCDA models like the Analytic Hierarchy/Network Process are valuable tools in quantifying decision trade-offs.

The objective of this paper is to demonstrate the use of MCDA models for benefit-risk assessment and the use of

sensitivity analysis to assess the impact of uncertainty and patient heterogeneity.

CONCLUSION

:

Deterministic sensitivity analysis by manually adjusting criteria weights is a flexible an easy way to

analyze the impact of uncertainty. PSA, however, is more the more rigourous approach incorporating distributions of

both criteria weights and drug performances. This example demonstrates that the impact of drug performance

uncertainty is larger than uncertainty in the criteria weights.

MCDA CASE on ANTI-DEPRESSANTS1

1. Danner et al: Int J Technol Assess Health Care. 2011 Oct. 7:1–7.

Uncertainty in MCDA models: Structural uncertainty

Uncertainty about the assumptions made in the design of an MCDA decision structure and the methods for elicitation of responses E.g. which attributes were taken and which decision objective.

Stochastic uncertainty

•Heterogeneity: uncertainty about the treatment preferences in subgroups of the population.

•Imprecision: parameter uncertainty, i.e. the uncertainty around the estimation of an individual parameter.

•Uncertainty “sensu stricto”: uncertainty about the decision makers’ knowledge and confidence about the subject matter.

Solutions to stochastic uncertainty in preference data:

• Sampling approach and sample size

Include representative sample of respondents for elicitation. Decide on group panel approach (<15 respondents) or survey methods. Analyze preference heterogeneity.

• Probabilistic Sensitivity Analysis (PSA) and resampling

Use of PSA on preference data and clinical performance data, either with or without resampling methods. Small group decision studies require resampling of preference data.

• PSA based on fuzzy data sets

Calibrate experts to generate fuzzy data sets. Calibration can be done by asking for the magnitude of uncertainty people have in providing their scores.

Example of AHP-MCDA scoring grid

Social function

Anxiety

Pain

Cognitive function

Suicide and attempted suicide

Other serious adverse events Response

Remission

No relaps Efficacy

Sexual dysfunction

Other adverse events

Disease specific QoL

Adverse events

Serious adverse events Adverse events

Prioritize endpoints

Which is most important in selecting an anti-depressant:

Response to depression Remission of depression

Performance of three antidepressants (Odds Ratio):

Approach 1: Deterministic sensitivity analysis of the “impact of decision criteria” and “performance” by manually adjusting priorities

Approach 2 and 3: Probabilistic Sensitivity Analysis of (1) criteria weights and (2) criteria weights and performance of antidepressants

Base-case analysis Sensitivity analysis on “treatment

response” Sensitivity analysis on drug performance on HRQoL

OR transformed to priority weights

Probabilistic Sensitivity Analysis for criteria

weights. Criteria weights (n=12 patients) were resampled using bootstrapping. Base case ORs on drug performance were obtained from the

literature. Drug treatment preferences were calculated.

Probabilistic Sensitivity Analysis for criteria

weights and drug performance. Criteria weights (n=12 patients) were resampled using

bootstrapping. Drug performance was sampled from OR distributions for the three separate

drugs.

Probabilistic Sensitivity Analysis for criteria

weights excluding “relapse” and “HRQoL”. These were not given a preference weight because of insufficient data on drug performance. Criteria weights and drug performances were resampled using bootstrapping (see other cases)

November, 8 2011 11-12 AM

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