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药品市场参考定价的影响:综述

Effects of reference pricing in pharmaceutical markets: a review.

机构信息

Department of Economics, University of Brescia, Brescia, Italy.

出版信息

Pharmacoeconomics. 2011 Jan;29(1):17-33. doi: 10.2165/11537860-000000000-00000.

Abstract

This work aims to provide a systematic and updated survey of original scientific studies on the effect of the introduction of reference pricing (RP) policies in Organisation for Economic Co-operation and Development (OECD) countries. We searched PubMed, EconLit and Web of Knowledge for articles on RP. We reviewed studies that met the inclusion criteria established in the search strategy. From a total of 468 references, we selected the 35 that met all of the inclusion criteria. Some common themes emerged in the literature. The first was that RP was generally associated with a decrease in the prices of the drugs subject to the policy. In particular, price drops seem to have been experienced in virtually every country that implemented a generic RP (GRP) policy. A GRP policy applies only to products with expired patents and generic competition, and clusters drugs according to chemical equivalence (same form and active compound). More significant price decreases were observed in the sub-markets in which drugs were already facing generic competition prior to RP. Price drops varied widely according to the amount of generic competition and industrial strategies: brand-named drugs originally priced above RP values decreased their prices to a greater extent. A second common theme was that both therapeutic RP (TRP) and GRP have been associated with significant and consistent savings in the first years of application. A third general result is that generic market shares significantly increased whenever the firms producing brand-named drugs did not adopt one of the following strategies: lowering prices to RP values; launching new dosages and/or formulations; or marketing substitute drugs still under patent protection. Finally, concerning TRP, although more evidence is needed, studies based on a large number of patient-level observations showed no association between the RP policy and health outcomes.

摘要

本研究旨在对经合组织(OECD)国家引入参考定价(RP)政策的原始科学研究进行系统和最新的综述。我们在 PubMed、EconLit 和 Web of Knowledge 上搜索了有关 RP 的文章。我们审查了符合搜索策略中建立的纳入标准的研究。在总共 468 篇参考文献中,我们选择了符合所有纳入标准的 35 篇。文献中出现了一些共同的主题。首先,RP 通常与受政策影响的药物价格下降有关。特别是,似乎每个实施仿制药 RP(GRP)政策的国家都经历了价格下降。GRP 政策仅适用于专利过期且具有仿制药竞争的产品,并根据化学等效性(相同形式和活性化合物)对药物进行分类。在实施 RP 之前已经面临仿制药竞争的子市场中,观察到的价格降幅更大。根据仿制药竞争的数量和行业策略,价格降幅差异很大:最初定价高于 RP 值的品牌药物降价幅度更大。第二个共同主题是,无论是治疗性 RP(TRP)还是 GRP,在应用的最初几年都与显著且持续的节省相关。第三个普遍结果是,只要生产品牌药物的公司不采取以下策略之一,仿制药市场份额就会显著增加:将价格降至 RP 值;推出新的剂量和/或配方;或销售仍受专利保护的替代药物。最后,关于 TRP,尽管需要更多的证据,但基于大量患者水平观察的研究表明,RP 政策与健康结果之间没有关联。

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