The HTA Risk Analysis Chart: Visualising the Need for and Potential Value of Managed Entry Agreements in Health Technology Assessment

Sabine Elisabeth Grimm*, Mark Strong, Alan Brennan, Allan J. Wailoo

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Recent changes to the regulatory landscape of pharmaceuticals may sometimes require reimbursement authorities to issue guidance on technologies that have a less mature evidence base. Decision makers need to be aware of risks associated with such health technology assessment (HTA) decisions and the potential to manage this risk through managed entry agreements (MEAs).

This work develops methods for quantifying risk associated with specific MEAs and for clearly communicating this to decision makers.

We develop the 'HTA risk analysis chart', in which we present the payer strategy and uncertainty burden (P-SUB) as a measure of overall risk. The P-SUB consists of the payer uncertainty burden (PUB), the risk stemming from decision uncertainty as to which is the truly optimal technology from the relevant set of technologies, and the payer strategy burden (PSB), the additional risk of approving a technology that is not expected to be optimal. We demonstrate the approach using three recent technology appraisals from the UK National Institute for Health and Clinical Excellence (NICE), each of which considered a price-based MEA.

The HTA risk analysis chart was calculated using results from standard probabilistic sensitivity analyses. In all three HTAs, the new interventions were associated with substantial risk as measured by the P-SUB. For one of these technologies, the P-SUB was reduced to zero with the proposed price reduction, making this intervention cost effective with near complete certainty. For the other two, the risk reduced substantially with a much reduced PSB and a slightly increased PUB.

The HTA risk analysis chart shows the risk that the healthcare payer incurs under unresolved decision uncertainty and when considering recommending a technology that is not expected to be optimal given current evidence. This allows the simultaneous consideration of financial and data-collection MEA schemes in an easily understood format. The use of HTA risk analysis charts will help to ensure that MEAs are considered within a standard utility-maximising health economic decision-making framework.

Original languageEnglish
Pages (from-to)1287-1296
Number of pages10
JournalPharmacoeconomics
Volume35
Issue number12
DOIs
Publication statusPublished - Dec 2017

Keywords

  • PARTIAL EXPECTED VALUE
  • SENSITIVITY-ANALYSIS SAMPLE
  • STRUCTURAL UNCERTAINTY
  • PERFECT INFORMATION
  • FRAMEWORK
  • DECISIONS
  • MODELS

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