首页> 外文期刊>Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research >Good research practices for measuring drug costs in cost-effectiveness analyses: an international perspective: the ISPOR Drug Cost Task Force report--Part VI.
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Good research practices for measuring drug costs in cost-effectiveness analyses: an international perspective: the ISPOR Drug Cost Task Force report--Part VI.

机译:在成本效益分析中衡量药物成本的良好研究实践:国际视角:ISPOR药物成本工作组报告第六部分。

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OBJECTIVE: The pharmacoeconomic guidelines available in the literature or promulgated in many countries are either vague or silent about how drug costs should be established or measured so an international comparison of cost-effectiveness analysis (CEA) results can be made. The objective of this report is to provide guidance and recommendations on how drug costs should be measured for CEAs done from an internationally comparative perspective. METHODS: Members of the International Society for Pharmacoeconomics and Outcomes Research (ISPOR) Task Force on Good Research Practices-Use of Drug Costs for Cost Effectiveness Analysis (Drug Cost Task Force [DCTF]) subgroup from several countries were experienced developers or users of CEA models, and worked in academia, industry, and as advisors to governments. They solicited comments on drafts from a core group of 174 external reviewers and more broadly, from the members of the ISPOR at the ISPOR 12th Annual International meeting and via the ISPOR Web site. RESULTS: Drug units should be standardized in terms of volume of active ingredient, regardless of packaging and dosing strength variations across countries. Drug costs should be measured in local currency per unit of active ingredient and should be converted to other currencies using sensitivity analyses of purchasing power parities (PPP) and exchange rates, whichever is more appropriate. When using drug prices from different years, the consumer price index for the local currency should be applied before the PPP and/or exchange rate conversion. CONCLUSION: CEA researchers conducting international pharmacoeconomic analysis should tailor the appropriate measure of drug costs to the international perspective, to maintain clarity and transparency on drug cost measurement in the context of international drug comparison and report the sensitivity of CEA results to reasonable cost conversions.
机译:目的:文献中或许多国家颁布的药物经济学指导方针对于应如何确定或衡量药物成本是模棱两可或无言以对,因此可以对成本效益分析(CEA)结果进行国际比较。本报告的目的是就如何从国际比较的角度对CEA的药物成本进行计量提供指导和建议。方法:国际药物经济学和结果研究学会(ISPOR)良好研究实践工作组的成员-几个国家使用药物成本进行成本效益分析(药物成本工作队[DCTF])小组的成员是经验丰富的CEA开发人员或用户模型,并在学术界,工业界和政府顾问中工作。他们在ISPOR第12届国际年会上通过ISPOR网站征求了由174个核心审阅者组成的核心小组以及更广泛的ISPOR成员对草案的评论。结果:药物单位应按照有效成分的数量进行标准化,而不论各国的包装和剂量强度如何变化。药品成本应以每单位活性成分的当地货币计量,并应使用购买力平价(PPP)和汇率的敏感性分析将其转换为其他货币,以较合适的为准。当使用不同年份的药品价格时,应在购买力平价和/或汇率转换之前应用当地货币的消费者价格指数。结论:进行国际药物经济学分析的CEA研究人员应从国际角度对药物成本进行适当的量度,以在国际药物比较的背景下保持药物成本计量的清晰度和透明度,并报告CEA结果对合理成本转换的敏感性。

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