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同时解决采用和研究设计决策:样本信息分析价值的作用。

Addressing adoption and research design decisions simultaneously: the role of value of sample information analysis.

机构信息

Centre for Health Economics (CM, KC) University of York, York, UK

Department of Economics and Related Studies (KC) University of York, York, UK

出版信息

Med Decis Making. 2011 Nov-Dec;31(6):853-65. doi: 10.1177/0272989X11399921. Epub 2011 Mar 10.

Abstract

METHODS

to estimate the cost-effectiveness of technologies are well developed with increasing experience of their application to inform adoption decisions in a timely way. However, the experience of using similarly explicit methods to inform the associated research decisions is less well developed despite appropriate methods being available with an increasing number of applications in health. The authors demonstrate that evaluation of both adoption and research decisions is feasible within typical time and resource constraints relevant to policy decisions, even in situations in which data are sparse and formal elicitation is required. In addition to demonstrating the application of expected value of sample information (EVSI) in these circumstances, the authors examine and carefully distinguish the impact that the research decision is expected to have on patients while enrolled in the trial, those not enrolled, and once the trial reports. In doing so, the authors are able to account for the range of opportunity cost associated with research and evaluate a number of

RESEARCH DESIGN

s including length of follow-up and sample size. The authors also explore the implications for research design of conducting research while the technology is approved for widespread use and whether approval should be withheld until research reports. In doing so, the authors highlight the impact of irrecoverable opportunity costs when the initial costs of a technology are compensated only by later gains in health outcome.

摘要

方法

随着应用经验的增加,技术的成本效益评估已经得到很好的发展,可以及时为采用决策提供信息。然而,尽管在健康领域有越来越多的应用,类似的明确方法在为相关研究决策提供信息方面的经验却不太成熟。作者证明,即使在数据稀缺且需要正式 elicitation 的情况下,在与政策决策相关的典型时间和资源限制内,评估采用和研究决策是可行的。除了在这些情况下展示预期样本信息价值(EVSI)的应用外,作者还研究并仔细区分了研究决策在试验中招募的患者、未招募的患者以及试验报告发布后的预期影响。通过这样做,作者能够考虑与研究相关的机会成本范围,并评估包括随访时间和样本量在内的一系列研究设计。作者还探讨了在技术广泛使用批准后进行研究以及在研究报告发布之前是否应暂停批准对研究设计的影响。通过这样做,作者强调了当技术的初始成本仅由后期健康结果的收益来补偿时,不可挽回的机会成本的影响。

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