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Developing an evidence-based methodological framework to systematically compare HTA coverage decisions: A mixed methods study

机译:建立基于证据的方法框架,系统地比较HTA覆盖范围决策:混合方法研究

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Health Technology Assessment (HTA) often results in different coverage recommendations across countries for a same medicine despite similar methodological approaches. This paper develops and pilots a methodological framework that systematically identifies the reasons for these differences using an exploratory sequential mixed methods research design. The study countries were England, Scotland, Sweden and France. The methodological framework was built around three stages of the HTA process: (a) evidence, (b) its interpretation, and (c) its influence on the final recommendation; and was applied to two orphan medicinal products. The criteria accounted for at each stage were qualitatively analyzed through thematic analysis. Piloting the framework for two medicines, eight trials, 43 clinical end-points and seven economic models were coded 155 times. Eighteen different uncertainties about this evidence were coded 28 times, 56% of which pertained to evidence commonly appraised and 44% to evidence considered by only some agencies. The poor agreement in interpreting this evidence (kappa = 0.183) was partly explained by stakeholder input (n(s) = 48 times), or by agency-specific risk (n(u) = 28 uncertainties) and value preferences (n(oc) = 62 "other considerations"), derived through correspondence analysis. Accounting for variability at each stage of the process can be achieved by codifying its existence and quantifying its impact through the application of this framework. The transferability of this framework to other disease areas, medicines and countries is ensured by its iterative and flexible nature, and detailed description. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:尽管技术方法相似,但卫生技术评估(HTA)经常会导致各国对同一药物的覆盖建议不同。本文开发并试行了一种方法框架,该框架使用探索性顺序混合方法研究设计来系统地识别这些差异的原因。研究国家是英国,苏格兰,瑞典和法国。方法框架是围绕HTA流程的三个阶段建立的:(a)证据,(b)其解释,(c)它对最终建议的影响;并应用于两种孤药。通过主题分析定性分析了每个阶段所占的标准。为两种药物,八项试验,43种临床终点和七种经济模型建立的框架进行了155次编码。关于该证据的十八种不同不确定性被编码了28次,其中56%与通常评估的证据有关,而44%与仅某些机构考虑的证据有关。利益相关者的投入(n(s)= 48次)或机构特定风险(n(u)= 28个不确定性)和价值偏好(n(oc )= 62个“其他注意事项”),通过对应分析得出。可以通过在该过程的每个阶段对可变性进行编码,并通过应用此框架来量化其存在并量化其影响来实现。该框架具有迭代和灵活的性质以及详细的说明,确保了该框架在其他疾病领域,药物和国家的可移植性。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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