Integrative Review of Managed Entry Agreements: Chances and Limitations

SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), Sefako Makgatho Health Sciences University, SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), Souza Cazarim Maurílio,Pantuzza Laís Lessa Neiva, Ribeiro-Junior Nelio Gomes,Pereira André Luiz, SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES),Iunes Roberto, Pippo Tomas,Hauegen Renata Curi,Vassalo Carlos,Laba Tracey-Lea,Simoens Steven, Márquez Sergio,Gomez Carolina,Voncina Luka,Selke Gisbert W.,Garattini Livio, Seoul National University,Gulbinovic Jolanta,Lipinska Aneta,Pomorski Maciej,McClure Lindsay,Fürst Jurij,Gambogi Rosana, Ortiz Carla Hernandez,Canuto Santos Vânia Cristina,Araújo Denizar Vianna, Pontifical Catholic University of Minas Gerais, SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES)

PharmacoEconomics(2020)

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摘要
Managed entry agreements (MEAs) consist of a set of instruments to reduce the uncertainty and the budget impact of new high-priced medicines; however, there are concerns. There is a need to critically appraise MEAs with their planned introduction in Brazil. Accordingly, the objective of this article is to identify and appraise key attributes and concerns with MEAs among payers and their advisers, with the findings providing critical considerations for Brazil and other high- and middle-income countries. An integrative review approach was adopted. This involved a review of MEAs across countries. The review question was ‘What are the health technology MEAs that have been applied around the world?’ This review was supplemented with studies not retrieved in the search known to the senior-level co-authors including key South American markets. It also involved senior-level decision makers and advisers providing guidance on the potential advantages and disadvantages of MEAs and ways forward. Twenty-five studies were included in the review. Most MEAs included medicines (96.8%), focused on financial arrangements (43%) and included mostly antineoplastic medicines. Most countries kept key information confidential including discounts or had not published such data. Few details were found in the literature regarding South America. Our findings and inputs resulted in both advantages including reimbursement and disadvantages including concerns with data collection for outcome-based schemes. We are likely to see a growth in MEAs with the continual launch of new high-priced and often complex treatments, coupled with increasing demands on resources. Whilst outcome-based MEAs could be an important tool to improve access to new innovative medicines, there are critical issues to address. Comparing knowledge, experiences, and practices across countries is crucial to guide high- and middle-income countries when designing their future MEAs.
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