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综合管理准入协议审查:机遇与限制。

Integrative Review of Managed Entry Agreements: Chances and Limitations.

机构信息

Graduate Program in Medicines and Pharmaceutical Services, Faculty of Pharmacy, Federal University of Minas Gerais (UFMG), Av. Pres. Antônio Carlos, 6627. Pampulha, Belo Horizonte, 31270-901, Minas Gerais, Brazil.

SUS Collaborating Centre for Technology Assessment and Excellence in Health (CCATES), Belo Horizonte, Minas Gerais, Brazil.

出版信息

Pharmacoeconomics. 2020 Nov;38(11):1165-1185. doi: 10.1007/s40273-020-00943-1.

Abstract

BACKGROUND AND OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景和目的

管理准入协议(MEA)由一系列工具组成,旨在降低新的高价药品的不确定性和预算影响;然而,人们对此仍存在一些担忧。需要对MEA 进行批判性评估,以了解其在巴西的计划引入情况。因此,本文的目的是确定并评估支付方及其顾问对 MEA 的关键属性和关注点,为巴西和其他高收入和中等收入国家提供关键考虑因素。

方法

采用综合审查方法。这涉及到对各国 MEA 的审查。审查问题是“全球范围内应用了哪些卫生技术 MEA?”本综述还补充了高级合著者已知但未在搜索中检索到的研究,包括主要的南美市场。它还涉及高级决策者和顾问,他们就 MEA 的潜在优势、劣势以及前进方向提供指导。

结果

共纳入 25 项研究。大多数 MEA 包括药品(96.8%),侧重于财务安排(43%),并主要包括抗肿瘤药物。大多数国家对关键信息保密,包括折扣或尚未公布此类数据。在南美的文献中很少发现有关细节。我们的研究结果和意见既包括优势,如报销,也包括劣势,如基于结果的方案的数据收集问题。

结论

随着新的高价药品的不断推出,以及对资源的需求不断增加,MEA 的数量可能会增加。虽然基于结果的 MEA 可能是改善新创新药物获得的重要工具,但仍存在一些关键问题需要解决。比较各国的知识、经验和做法对于指导高收入和中等收入国家设计未来的 MEA 至关重要。

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