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成本效果分析(CER)能否成为新药和新技术研发及评估中推动变革的有效工具?

Can CER be an effective tool for change in the development and assessment of new drugs and technologies?

作者信息

Brixner Diana I, Watkins John B

机构信息

University of Utah, Department of Pharmacotherapy, 30 S. 2000 E., Salt Lake City, UT 84112, USA.

出版信息

J Manag Care Pharm. 2012 Jun;18(5 Supp A):S06-11. doi: 10.18553/jmcp.2012.18.s5-a.S06.

Abstract

BACKGROUND

Comparative effectiveness research (CER) has been proposed in the United States as a way to compare new drugs and technologies with established alternatives and determine not just whether a therapy works, but how well it works compared to other options.

OBJECTIVES

To define the current use of CER in the development of new drugs and technologies and explore what is needed for this research approach to reduce or stabilize health care costs in the United States.

SUMMARY

In 2010, the Patient-Centered Outcomes Research Institute (PCORI) was established by the Patient Protection and Affordable Care Act (PPACA) to coordinate federally funded CER and recommend research priorities. Hochman and McCormick's (2010) evaluation of 328 randomized trials, observational studies, and meta-analyses involving medications published between June 2008 and September 2009 in 6 key journals showed that most published research did not fulfill the criteria of CER (defined as comparison to active treatment) and that most study design is driven by FDA requirements rather than the need to develop evidence to facilitates election of the most effective therapy. Since PPACA provides alternative funding for CER, it could encourage funding more studies to help determine which treatment delivers the best value per unit of investment from clinical, humanistic, and economic perspectives. Manufacturers may avoid CER because it increases product development costs, but a drug proven more effective is more likely to be accepted by formulary committees, increasing the drug's market share, whereas payers may reject or limit use of a new drug that performs less effectively in comparative studies.

CONCLUSIONS

CER may not directly reduce expenditures for drugs and medical technologies. The results may vary widely from case to case; however, despite often significantly higher prices for new drugs, it is important to look beyond product costs to the overall impact on health care costs, including medical cost offsets that may occur through improved health or decreased morbidity. To truly decrease cost and improve quality, cost-effectiveness will have to be integrated into CER with the objective of prioritizing efficient therapies in the real-world health care system. If the methods and output of CER improve, the resulting cost-effectiveness ratios will also be more useful to the payer. CER should ultimately, therefore, be a useful tool to help patients, providers, and decision makers provide the most effective and most cost-effective interventions.

摘要

背景

在美国,比较效果研究(CER)被提议作为一种将新药和技术与现有替代方案进行比较的方法,不仅要确定一种疗法是否有效,还要确定与其他选择相比其效果如何。

目的

界定CER在新药和技术研发中的当前应用情况,并探讨这种研究方法需要什么才能在美国降低或稳定医疗保健成本。

总结

2010年,《患者保护与平价医疗法案》(PPACA)设立了以患者为中心的结局研究机构(PCORI),以协调联邦资助的CER并推荐研究重点。霍克曼和麦考密克(2010年)对2008年6月至2009年9月期间在6种主要期刊上发表的涉及药物的328项随机试验、观察性研究和荟萃分析进行的评估表明,大多数已发表的研究不符合CER的标准(定义为与积极治疗进行比较),并且大多数研究设计是由美国食品药品监督管理局(FDA)的要求驱动的,而不是为了开发有助于选择最有效疗法的证据。由于PPACA为CER提供了替代资金,它可能会鼓励资助更多研究,以帮助从临床、人文和经济角度确定哪种治疗每单位投资能带来最佳价值。制造商可能会回避CER,因为它会增加产品开发成本,但一种被证明更有效的药物更有可能被药品目录委员会接受,从而增加该药物的市场份额,而支付方可能会拒绝或限制在比较研究中表现较差的新药的使用。

结论

CER可能不会直接降低药品和医疗技术的支出。结果可能因情况而异;然而,尽管新药价格往往显著更高,但重要的是要超越产品成本,关注对医疗保健成本的总体影响,包括通过改善健康状况或降低发病率可能产生的医疗成本抵消。为了真正降低成本并提高质量,成本效益将必须纳入CER,目标是在现实世界的医疗保健系统中优先选择高效疗法。如果CER的方法和产出得到改进,由此产生的成本效益比也将对支付方更有用。因此,CER最终应该成为帮助患者、医疗服务提供者和决策者提供最有效和最具成本效益干预措施的有用工具。

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