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欧盟的卫生经济数据要求与可得性:对10个欧洲国家的调查结果

Health Economic Data Requirements and Availability in the European Union: Results of a Survey Among 10 European Countries.

作者信息

Skoupá Jana, Annemans Lieven, Hájek Petr

机构信息

Medical Data Center, 1st Medical Faculty, Charles University, Prague, Czech Republic.

Department of Public Health, University of Ghent, Ghent, Belgium.

出版信息

Value Health Reg Issues. 2014 Sep;4:53-57. doi: 10.1016/j.vhri.2014.06.003. Epub 2014 Aug 2.

Abstract

OBJECTIVES

To compare data requirements and their availability for health economic (HE) evaluations in five countries in Central/Eastern Europe (CEE) (Poland, the Czech Republic, Slovakia, Hungary, and Romania) and five countries in Western Europe (WE) (the United Kingdom, France, Germany, The Netherlands, and Sweden).

METHODS

A questionnaire was developed and distributed to market access personnel from Pfizer who were asked to complete the questionnaire either from their own knowledge or with support of external experts. The questionnaire focused on the obligation to conduct HE assessment for reimbursement submissions, local HE guidelines, applied discount rates for future costs and effects, willingness-to-pay thresholds, and available data sources.

RESULTS

HE is mandatory in all CEE and three WE participating countries for reimbursement applications of innovative drugs. Usually, cost-effectiveness analysis and budget-impact analyses are required. The preferred outcome of cost-effectiveness analysis is quality-adjusted-life years. In Romania, France, and the Czech Republic, guidelines could not be identified at the time of the survey. The applicant usually prepares HE evaluations; in Sweden, the United Kingdom, The Netherlands, and Poland, unlocked models have to be presented for scrutiny. Discount rates vary from 1.5% to 5%, and, usually, is the same for costs and outcomes (except in The Netherlands and Poland). Only the United Kingdom, Poland, and Slovakia have an explicit willingness-to-pay threshold. In Poland, it is based on the gross domestic product per capita, and in Slovakia, it is based on multiples of average monthly salary. Differences were found on data availability. In WE, data can be acquired easier than in CEE. Health insurance funds do not provide their data unless they were published. Patient registries are either not available in CEE or difficult to access, so applicants mostly rely on retrospective medical chart data, hospital information systems, or expert panels.

CONCLUSIONS

We found similar requirements for HE analyses in CEE and WE but differences in data availability. This results in less accurate inputs across the CEE, influencing analyses' outcomes.

摘要

目的

比较中东欧(CEE)五个国家(波兰、捷克共和国、斯洛伐克、匈牙利和罗马尼亚)和西欧(WE)五个国家(英国、法国、德国、荷兰和瑞典)卫生经济(HE)评估的数据需求及其可得性。

方法

设计了一份问卷并分发给辉瑞公司的市场准入人员,要求他们根据自身知识或在外部专家支持下完成问卷。问卷重点关注为报销申请进行HE评估的义务、当地HE指南、未来成本和效果的应用贴现率、支付意愿阈值以及可用数据来源。

结果

在所有中东欧和三个西欧参与国,创新药物报销申请都必须进行HE评估。通常需要进行成本效益分析和预算影响分析。成本效益分析的首选结果是质量调整生命年。在罗马尼亚、法国和捷克共和国,调查时未找到指南。申请人通常准备HE评估;在瑞典、英国、荷兰和波兰,必须提交未锁定模型以供审查。贴现率从1.5%到5%不等,通常成本和结果的贴现率相同(荷兰和波兰除外)。只有英国、波兰和斯洛伐克有明确的支付意愿阈值。在波兰,它基于人均国内生产总值,在斯洛伐克,它基于月平均工资的倍数。在数据可得性方面存在差异。在西欧,数据比在中东欧更容易获取。除非已公布,医疗保险基金不会提供其数据。中东欧要么没有患者登记处,要么难以获取,因此申请人大多依赖回顾性病历数据、医院信息系统或专家小组。

结论

我们发现中东欧和西欧对HE分析的要求相似,但在数据可得性方面存在差异。这导致中东欧的输入数据不太准确,影响分析结果。

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