Literature DB >> 23947963

Performance-based risk-sharing arrangements-good practices for design, implementation, and evaluation: report of the ISPOR good practices for performance-based risk-sharing arrangements task force.

Louis P Garrison1, Adrian Towse, Andrew Briggs, Gerard de Pouvourville, Jens Grueger, Penny E Mohr, J L Hans Severens, Paolo Siviero, Miguel Sleeper.   

Abstract

There is a significant and growing interest among both payers and producers of medical products for agreements that involve a "pay-for-performance" or "risk-sharing" element. These payment schemes-called "performance-based risk-sharing arrangements" (PBRSAs)-involve a plan by which the performance of the product is tracked in a defined patient population over a specified period of time and the amount or level of reimbursement is based on the health and cost outcomes achieved. There has always been considerable uncertainty at product launch about the ultimate real-world clinical and economic performance of new products, but this appears to have increased in recent years. PBRSAs represent one mechanism for reducing this uncertainty through greater investment in evidence collection while a technology is used within a health care system. The objective of this Task Force report was to set out the standards that should be applied to "good practices"-both research and operational-in the use of a PBRSA, encompassing questions around the desirability, design, implementation, and evaluation of such an arrangement. This report provides practical recommendations for the development and application of state-of-the-art methods to be used when considering, using, or reviewing PBRSAs. Key findings and recommendations include the following. Additional evidence collection is costly, and there are numerous barriers to establishing viable and cost-effective PBRSAs: negotiation, monitoring, and evaluation costs can be substantial. For good research practice in PBRSAs, it is critical to match the appropriate study and research design to the uncertainties being addressed. Good governance processes are also essential. The information generated as part of PBRSAs has public good aspects, bringing ethical and professional obligations, which need to be considered from a policy perspective. The societal desirability of a particular PBRSA is fundamentally an issue as to whether the cost of additional data collection is justified by the benefits of improved resource allocation decisions afforded by the additional evidence generated and the accompanying reduction in uncertainty. The ex post evaluation of a PBRSA should, however, be a multidimensional exercise that assesses many aspects, including not only the impact on long-term cost-effectiveness and whether appropriate evidence was generated but also process indicators, such as whether and how the evidence was used in coverage or reimbursement decisions, whether budget and time were appropriate, and whether the governance arrangements worked well. There is an important gap in the literature of structured ex post evaluation of PBRSAs. As an innovation in and of themselves, PBRSAs should also be evaluated from a long-run societal perspective in terms of their impact on dynamic efficiency (eliciting the optimal amount of innovation).
Copyright © 2013 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  access with evidence development; conditional licensing; coverage with evidence development; managed entry schemes; outcomes-based; patient access schemes; pay for performance; performance-based risk-sharing arrangements; risk-sharing

Mesh:

Year:  2013        PMID: 23947963     DOI: 10.1016/j.jval.2013.04.011

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  56 in total

Review 1.  Present and future challenges in the treatment of haemophilia: the patient's perspective.

Authors:  Romano Arcieri; Angelo C Molinari; Stefania Farace; Giuseppe Mazza; Alberto Garnero; Gabriele Calizzani; Paola Giordano; Emily Oliovecchio; Lorenzo Mantovani; Lamberto Manzoli; Paul Giangrande
Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

2.  A new model for reimbursing genome-based cancer care.

Authors:  Scott D Ramsey; Sean D Sullivan
Journal:  Oncologist       Date:  2013-12-05

3.  Market-access agreements for anti-cancer drugs.

Authors:  Katelijne van de Vooren; Alessandro Curto; Nick Freemantle; Livio Garattini
Journal:  J R Soc Med       Date:  2014-12-08       Impact factor: 5.344

Review 4.  Disinvestment and Value-Based Purchasing Strategies for Pharmaceuticals: An International Review.

Authors:  Bonny Parkinson; Catherine Sermet; Fiona Clement; Steffan Crausaz; Brian Godman; Sarah Garner; Moni Choudhury; Sallie-Anne Pearson; Rosalie Viney; Ruth Lopert; Adam G Elshaug
Journal:  Pharmacoeconomics       Date:  2015-09       Impact factor: 4.981

5.  When do performance-based risk-sharing arrangements make sense?

Authors:  Michael Drummond
Journal:  Eur J Health Econ       Date:  2015-07

Review 6.  Key enablers and barriers to implementing adaptive pathways in the European setting.

Authors:  Juan Carlos Rejon-Parrilla; Pall Jonsson; Jacoline C Bouvy
Journal:  Br J Clin Pharmacol       Date:  2019-04-29       Impact factor: 4.335

Review 7.  Performance-Based Risk-Sharing Arrangements: An Updated International Review.

Authors:  Josh J Carlson; Shuxian Chen; Louis P Garrison
Journal:  Pharmacoeconomics       Date:  2017-10       Impact factor: 4.981

8.  Cost evolution of biological agents for the treatment of spondyloarthritis in a tertiary hospital: influential factors in price.

Authors:  Mariángeles González-Fernández; Elena Villamañán; Inmaculada Jiménez-Nácher; Francisco Moreno; Chamaida Plasencia; Francisco Gaya; Alicia Herrero; Alejandro Balsa
Journal:  Int J Clin Pharm       Date:  2018-09-08

9.  Italian risk-sharing agreements on drugs: are they worthwhile?

Authors:  Livio Garattini; Alessandro Curto; Katelijne van de Vooren
Journal:  Eur J Health Econ       Date:  2015-01

Review 10.  Sustainable Financing of Innovative Therapies: A Review of Approaches.

Authors:  Aidan Hollis
Journal:  Pharmacoeconomics       Date:  2016-10       Impact factor: 4.981

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.