IMPLEMENTING MANAGED ENTRY AGREEMENTS IN PRACTICE- THE DUTCH REALITY CHECK
Author(s)
Makady A1, van Veelen A2, de Boer A2, Hillege JL3, Klungel O2, Goettsch W1
1The National Healthcare Institute (ZIN), Diemen, The Netherlands, 2Utrecht University, Utrecht, The Netherlands, 3University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
OBJECTIVES: In 2006, the National Healthcare Institute (ZIN) initiated conditional financing (CF) of expensive hospital drugs as an example of conditional reimbursement schemes (CRS). CF is a 4-year procedure encompassing initial HTA assessment (T=0) followed by additional data collection via outcomes research (separately assessing appropriate use & cost effectiveness in routine practice) and re-assessment (T=4). This study aims to retrospectively evaluate the CF framework, focusing on Health Technology Assessment (HTA) procedures. METHODS: All dossiers for drugs that underwent the full CF procedure were reviewed. Using a standardised data extraction form, 2 researchers independently extracted information on procedural, methodological and decision-making aspects from HTA reports of drugs selected for CF. RESULTS: CONCLUSIONS: Theoretically, CF provides a valuable option for enabling quick but conditional access to medicines in the Netherlands. However, procedural, methodological and decision-making considerations related to scheme design and implementation may affect its value in decision-making practice. Shortcomings and learnings identified should inform recommendations for the development of future managed entry agreements worldwide.
Conference/Value in Health Info
2017-11, ISPOR Europe 2017, Glasgow, Scotland
Value in Health, Vol. 20, No. 9 (October 2017)
Code
PHP289
Topic
Health Policy & Regulatory, Health Technology Assessment
Topic Subcategory
Coverage with Evidence Development & Adaptive Pathways, Decision & Deliberative Processes, Reimbursement & Access Policy, Risk-sharing Approaches
Disease
Multiple Diseases