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提交给意大利药品管理局的卫生经济评估质量:现状与未来行动

Quality of health economic evaluations submitted to the Italian Medicines Agency: current state and future actions.

作者信息

Carletto Angelica, Zanuzzi Matteo, Sammarco Annalisa, Russo Pierluigi

机构信息

Italian Medicines Agency (AIFA), Rome, Italy.

出版信息

Int J Technol Assess Health Care. 2020 Dec;36(6):560-568. doi: 10.1017/S0266462320000641. Epub 2020 Sep 10.

Abstract

OBJECTIVES

The purpose of this study was to evaluate the current state of health economic evaluations (HEEs) submitted by pharmaceutical companies to the Italian Medicines Agency (AIFA) as part of their pricing and reimbursement (P&R) dossiers, and to explore potential future actions in order to enhance their quality.

METHODS

All company dossiers submitted from October 2016 to December 2018 were reviewed to select those containing pharmacoeconomic studies. The general characteristics of HEEs were described and their quality assessed based on a checklist adapted from Philips et al. (Review of guidelines for good practice in decision-analytic modelling in health technology assessment. Health Technol Assess. 2004;8: 1-158).

RESULTS

Of the 299 dossiers submitted to AIFA, 105 included one or more pharmacoeconomic studies, of which fifty-three were cost-effectiveness analyses. Overall, the compliance of the HEEs with the quality checklist was highly variable: some studies reached high methodological standards whereas others had serious flaws (mean 59.22 percent, range 19.35-90.32 percent). The main weaknesses were the unjustified exclusion of relevant alternatives, poor description and justification of model data and assumptions, and insufficient exploration of uncertainty and study validity. Non-homogeneity across studies was found in study perspectives, discount rates, methods for costing, estimating quality-adjusted life-years and conducting sensitivity analyses.

CONCLUSIONS

Based on the results of this study, the recommended actions for increasing the quality of HEEs within reimbursement submissions in Italy are twofold: first, to set methodological standards for conducting and reporting HEEs; second, to strengthen the internal assessment process, also through the acquisition of companies' models and re-evaluation of results. These actions will hopefully provide greater contribution to the evidence-based P&R decision making.

摘要

目的

本研究旨在评估制药公司作为定价和报销(P&R)档案的一部分提交给意大利药品管理局(AIFA)的健康经济评估(HEE)的现状,并探索未来可能采取的行动以提高其质量。

方法

对2016年10月至2018年12月提交的所有公司档案进行审查,以筛选出包含药物经济学研究的档案。描述了HEE的一般特征,并根据改编自飞利浦等人(《健康技术评估中决策分析模型的良好实践指南综述》。《健康技术评估》。2004年;8:1-158)的清单对其质量进行评估。

结果

在提交给AIFA的299份档案中,105份包含一项或多项药物经济学研究,其中53份为成本效益分析。总体而言,HEE对质量清单的遵守情况差异很大:一些研究达到了较高的方法学标准,而另一些则存在严重缺陷(平均59.22%,范围19.35-90.32%)。主要弱点包括不合理地排除相关替代方案、对模型数据和假设的描述和论证不足,以及对不确定性和研究有效性的探索不够。在研究视角、贴现率、成本计算方法、质量调整生命年的估计和敏感性分析的进行方面,各研究之间存在非同质性。

结论

基于本研究结果,在意大利报销申请中提高HEE质量的建议行动有两方面:第一,为进行和报告HEE设定方法学标准;第二,加强内部评估过程,也可通过获取公司模型和重新评估结果来实现。这些行动有望为基于证据的P&R决策做出更大贡献。

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