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为 NICE 何时应仅在适当设计的证据开发计划背景下推荐使用卫生技术制定决策框架提供信息。

Informing a decision framework for when NICE should recommend the use of health technologies only in the context of an appropriately designed programme of evidence development.

机构信息

Centre for Health Economics, University of York, York, UK.

出版信息

Health Technol Assess. 2012;16(46):1-323. doi: 10.3310/hta16460.

Abstract

BACKGROUND

The general issue of balancing the value of evidence about the performance of a technology and the value of access to a technology can be seen as central to a number of policy questions. Establishing the key principles of what assessments are needed, as well as how they should be made, will enable them to be addressed in an explicit and transparent manner.

OBJECTIVES

The aims of this research are to (1) establish the key principles of what assessments are needed to inform an 'only in research' (OIR) or 'approval with research' (AWR) recommendation, (2) evaluate previous National Institute for Health and Clinical Evidence (NICE) guidance in which OIR or AWR recommendations were made or considered and (3) evaluate a range of alternative options to establish criteria, additional information and/or analysis that could be made available to inform the assessments needed.

DATA SOURCES

All NICE draft and final guidance up to January 2010 was considered in the review of NICE technology appraisal guidance. Four case studies were used to evaluate the range of options of what information and analysis could be made available to inform the assessment required. These were based on a reanalysis of existing health technology appraisals for NICE or the Health Technology Assessment programme.

REVIEW METHODS

A critical review of policies, practice and literature was undertaken using traditional systematic searching based on initial search terms informed by key publications. An iterative approach was adopted using 'pearl growing' evaluated through capture-recapture methods. In addition, grey literature, policy documents and other sources, such as special interest groups and the expertise of the Advisory Group for the project, were used to contribute to this process.

RESULTS

A series of recommendations, or options, for NICE to consider were developed with the involvement of key stakeholders. These establish the key principles and associated criteria that might guide OIR and AWR recommendations and identify what, if any, additional information or analysis might be included in the technology appraisal process, including how such recommendations might be more likely to be implemented through publically funded and sponsored research. To meet these aims the research is broadly structured as follows. A critical review of policy, practice and literature in this area informs the development of a coherent conceptual framework to establish the key principles and the sequence of assessment and judgements required. This sequence of assessment and judgement is represented as an algorithm, which can also be summarised as a simple set of explicit criteria or a 7-point checklist of assessments. A review of previous NICE guidance in which OIR or AWR recommendations were either made or considered was undertaken to examine the extent to which the key principles are evident. The application of the checklist of assessment to a series of four case studies informs considerations of whether or not such assessments can be made based on existing information and analysis in current NICE appraisal and in what circumstances could additional information and/or analysis be useful. Finally, some of the implications that this more explicit assessment of OIR and AWR might have for policy (e.g. NICE guidance and drug pricing), the process of appraisal (e.g. greater involvement of research commissioners) and methods of appraisal (e.g. should additional information, evidence and analysis be required) are drawn together. At each stage this research has been informed by a diverse and international Advisory Group and the feedback from participants at two workshops involving a wide range of key stakeholders, which included members of NICE and its Advisory Committees (including lay members and other NICE programmes), patient advocates, manufacturers, and research and NHS commissioners, as well as relevant academics.

LIMITATIONS

Further research is required to establish how these considerations could be integrated within a practical value-based pricing scheme. In addition, irrecoverable opportunity costs are commonly associated with many health technologies that offer future benefits following treatment. The significance of these types of irrecoverable costs is not widely recognised and further research to demonstrate their potential impact more generally is needed.

CONCLUSIONS

The categories of guidance available to NICE have a wider application than is reflected in the review of previous guidance. Importantly, determining which category of guidance will be appropriate depends only partly on an assessment of expected cost-effectiveness. As well as AWR for technologies expected to be cost-effective and OIR for those not expected to be cost-effective, there are other important circumstances when OIR should be considered. In particular, for technologies expected to be cost-effective, OIR rather than approve may be appropriate when research is not possible with approval and OIR or even reject, rather than AWR or approve, may be appropriate even if research is possible with approval when there are significant irrecoverable costs.

FUNDING

The National Institute for Health Research Health Technology Assessment programme.

摘要

背景

权衡技术性能证据的价值与获取技术的价值,这一普遍问题可以被视为许多政策问题的核心。确立需要进行哪些评估的关键原则,以及如何进行这些评估,将使这些问题能够以明确和透明的方式得到解决。

目的

本研究的目的是:(1) 确定为“仅在研究中”(OIR)或“批准加研究”(AWR)建议提供信息所需的评估的关键原则;(2) 评估之前国家卫生与临床优化研究所(NICE)进行过 OIR 或 AWR 建议或考虑过的指南;(3) 评估一系列替代方案,以确定可提供信息的标准、附加信息和/或分析,以告知所需的评估。

数据来源

对截至 2010 年 1 月的所有 NICE 草案和最终指南进行了审查,以了解 NICE 技术评估指南的情况。使用四种案例研究来评估可提供信息和分析的范围,以告知所需的评估。这些案例研究基于对 NICE 或卫生技术评估计划的现有卫生技术评估的重新分析。

审查方法

使用传统的系统搜索方法,根据关键出版物提供的初始搜索词,对政策、实践和文献进行了批判性审查。采用迭代方法,通过捕获-再捕获方法评估“珍珠增长”。此外,还利用灰色文献、政策文件和其他来源,如特别利益集团和项目咨询小组的专业知识,为这一过程提供了帮助。

结果

在关键利益相关者的参与下,为 NICE 制定了一系列建议或选择方案。这些方案确立了指导 OIR 和 AWR 建议的关键原则和相关标准,并确定了在技术评估过程中可能包括的任何额外信息或分析,包括如何通过公共资助和赞助研究更有可能实施这些建议。为了实现这些目标,研究大致分为以下几个方面。对该领域的政策、实践和文献进行批判性审查,为建立关键原则和所需评估和判断的顺序提供了一个连贯的概念框架。该评估和判断的顺序用算法表示,也可以简化为一套明确的标准或 7 点评估检查表。对 NICE 中已经进行或考虑进行 OIR 或 AWR 建议的指南进行了审查,以审查关键原则的明显程度。对一系列四项案例研究的检查表的应用,使我们考虑了是否可以根据现有信息和分析进行这些评估,以及在何种情况下可以提供额外的信息和/或分析。最后,从更明确地评估 OIR 和 AWR 的角度,对政策(如 NICE 指南和药品定价)、评估过程(如研究委托方的更多参与)和评估方法(如是否需要额外的信息、证据和分析)进行了一些思考。在每个阶段,这项研究都得到了一个多样化的国际咨询小组的支持,并且在两次研讨会中,来自广泛的关键利益相关者的反馈也很有帮助,这些研讨会包括 NICE 及其咨询委员会的成员(包括非专业成员和其他 NICE 计划)、患者权益维护者、制造商、研究和 NHS 委托方,以及相关学者。

局限性

需要进一步研究如何将这些考虑纳入实际的基于价值的定价方案中。此外,许多提供治疗后未来效益的卫生技术通常会产生不可挽回的机会成本。这类不可挽回成本的意义尚未得到广泛认识,需要进一步研究以更广泛地证明其潜在影响。

结论

NICE 可用的指导类别应用范围比之前对指南的审查所反映的要广泛。重要的是,确定将适用哪种指导类别,不仅取决于对预期成本效益的评估。除了对预计具有成本效益的技术进行 AWR 和对预计不具有成本效益的技术进行 OIR 外,还有其他重要情况需要考虑 OIR。特别是,对于预计具有成本效益的技术,如果获得批准的研究是不可能的,那么 OIR 而不是批准可能是合适的;或者即使获得批准的研究是可能的,如果存在重大不可挽回的成本,那么 OIR 甚至拒绝,而不是 AWR 或批准,也可能是合适的。

资金来源

国家卫生研究院卫生技术评估计划。

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