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利用观察性注册研究来为比较有效性研究提供信息。

Leveraging observational registries to inform comparative effectiveness research.

机构信息

Duke Clinical Research Institute, Durham, NC, USA.

出版信息

Am Heart J. 2010 Jul;160(1):8-15. doi: 10.1016/j.ahj.2010.04.012.

Abstract

Comparative effectiveness research (CER) has gained increased prominence over the past few years, but significant confusion surrounds the scope and definition of what constitutes CER. In some circles, CER is heralded as a tool to improve care quality and patient outcomes while simultaneously reducing health care costs. However, others contend that CER will lead to poorly designed studies whose results will be misinterpreted to limit the development and approval of new therapies. Leading to this confusion is the fact that CER spans a wide spectrum of clinical research domains that includes randomized, controlled trials; observational data analyses; and cost-effectiveness analyses. Recent federal mandates have injected significant funds for observational CER priorities, earmarked incentives for technology investments, and recommended a centralized collection of certain medical information, setting the stage for CER and observational data to gain further prominence as the foundation of many new investigations. In this review article, we define CER and highlight opportunities, and potential pitfalls, of observational registries to expand evidence through CER.

摘要

比较效果研究(CER)在过去几年中越来越受到重视,但对于什么构成 CER 的范围和定义仍存在很大的混淆。在一些圈子里,CER 被吹捧为一种提高护理质量和患者结果的工具,同时降低医疗保健成本。然而,其他人则认为 CER 将导致设计不佳的研究,其结果将被误解,以限制新疗法的开发和批准。造成这种混淆的原因是,CER 涵盖了广泛的临床研究领域,包括随机对照试验、观察性数据分析和成本效益分析。最近的联邦指令为观察性 CER 优先事项注入了大量资金,为技术投资设定了激励措施,并建议集中收集某些医疗信息,为 CER 和观察性数据进一步突出成为许多新调查的基础奠定了基础。在这篇综述文章中,我们定义了 CER,并强调了观察性登记处通过 CER 扩大证据的机会和潜在陷阱。

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