Beyond "safe and effective": the role of the federal government in supporting and disseminating comparative-effectiveness research.

Annals of health law Pub Date : 2012-01-01
Maggie H Francis
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Abstract

Over the past century, medical advancements have resulted in tremendous health gains for Americans. Although the federal government has played a prominent role in ensuring that new treatments are safe and effective, questions about which medical treatments work best under which circumstances have largely remained unanswered. Thus, the federal government's recent major investments in comparative-effectiveness research have potential to play a significant role in helping both patients and health care providers navigate the vast array of available treatment options, as well as in improving the quality, efficiency, and delivery of health care system-wide. Yet, the controversial nature of the government's foray into comparative-effectiveness research also suggests that the path toward realizing these goals may be treacherous. This Article describes the rationales for federal support of comparative-effectiveness research and potential models for that involvement, analyzes the federal government's recent investments in the research, and concludes with predictions about the probable outcomes of these investments. While increased federal support for comparative-effectiveness research is unlikely to achieve all of the benefits anticipated by its supporters, it is a crucial step toward ensuring that Americans are able to take full advantage of the benefits of medical innovation

超越“安全有效”:联邦政府在支持和传播比较有效性研究方面的作用。
在过去的一个世纪里,医学的进步为美国人带来了巨大的健康收益。尽管联邦政府在确保新疗法安全有效方面发挥了重要作用,但在何种情况下哪种疗法效果最好的问题在很大程度上仍未得到解答。因此,联邦政府最近在比较有效性研究方面的主要投资有可能在帮助患者和医疗保健提供者在大量可用治疗方案中导航方面发挥重要作用,并在提高医疗保健系统的质量、效率和交付方面发挥重要作用。然而,政府涉足比较有效性研究的争议性也表明,实现这些目标的道路可能是危险的。本文描述了联邦政府支持比较有效性研究的基本原理和参与的潜在模型,分析了联邦政府最近对研究的投资,并对这些投资的可能结果进行了预测。虽然增加联邦政府对比较有效性研究的支持不太可能实现支持者所期望的所有好处,但这是确保美国人能够充分利用医疗创新好处的关键一步
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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