Almarsdóttir Anna Birna, Traulsen Janine M
Faculty of Pharmacy, University of Iceland, Hofsvallagata 53, IS-107, Reykjavík, Iceland.
Pharm World Sci. 2006 Feb;28(1):6-12. doi: 10.1007/s11096-006-9011-0. Epub 2006 Jun 30.
In this last article in the series the authors focus on the issue of researching and evaluating pharmaceutical policy. The past five articles made an argument for why pharmaceutical policy is important and why it is different from health policy. The evidence base needed for pharmaceutical policymaking is also somewhat specialized in relation to health policy. Taking these differences into consideration the authors provide their definition of pharmaceutical policy. The knowledge base for good pharmaceutical policymaking needs to be broad and include approaches and methodologies ranging from the highly quantitative and experimental to the purely qualitative. Other policy questions such as those concerned with rational use of medicines and economics illustrate that pharmaceutical policy needs more varied approaches than randomized clinical trials alone can provide. The importance of gaining a thorough overview and understanding of the available design and methodological options for policy analysis is emphasized. Research into pharmaceutical policy has many commonalities with evaluation and policy analysis. Some of the main pitfalls that policymakers, researchers and analysts can fall into when formulating and evaluating pharmaceutical policy are discussed and include: using too narrow evaluation questions; choosing inappropriate methods/designs; and the problem of bias and self-censorship. The authors conclude this series by advocating a strong focus on research and an international evaluation culture around pharmaceutical policy. They emphasize the importance of pharmaceutical specialists' (i.e., pharmacists') involvement in pharmaceutical policy analysis and the policy consultative process.
在本系列的最后一篇文章中,作者聚焦于制药政策的研究与评估问题。过去的五篇文章论证了制药政策为何重要以及它为何不同于卫生政策。与卫生政策相比,制药政策制定所需的证据基础也有一定的专业性。考虑到这些差异,作者给出了他们对制药政策的定义。良好的制药政策制定所需的知识基础应当广泛,涵盖从高度量化和实验性的方法到纯定性的方法和手段。其他政策问题,比如那些与合理用药及经济学相关的问题,表明制药政策需要比单纯的随机临床试验所能提供的更多样化的方法。强调了全面了解和掌握政策分析可用设计及方法选项的重要性。制药政策研究与评估及政策分析有许多共通之处。讨论了政策制定者、研究人员和分析人员在制定和评估制药政策时可能陷入的一些主要陷阱,包括:评估问题过于狭窄;选择不恰当的方法/设计;以及偏差和自我审查问题。作者通过倡导高度关注制药政策研究及围绕其形成国际评估文化来结束本系列。他们强调了制药专家(即药剂师)参与制药政策分析及政策咨询过程的重要性。