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我们如何应对多重耐药菌的威胁?对法国、英国和德国卫生技术评估机构2016年至2020年抗生素评估的比较。

How do we respond to the threat of multidrug-resistant bacteria? Comparison of antibiotic appraisals from 2016 to 2020 of the French, English, and German HTA agencies.

作者信息

Dumont Rémy, Lengliné Etienne, Delorme Clara, Bru Jean-Pierre, Ansart Sévérine, Aslangul Elisabeth, Kelley Sophie, Cochat Pierre, Chevret Sylvie, Diatta Thierno

机构信息

Assessment and Access to Innovation Direction, Haute Autorité de Santé, Saint-Denis, France.

Haematology Department, AP-HP Saint Louis Hospital, Paris, France.

出版信息

Int J Technol Assess Health Care. 2024 Dec 9;40(1):e72. doi: 10.1017/S0266462324000552.

Abstract

Antimicrobial resistance (AMR) has become a worldwide growing concern over the past decades. Thus, encouraging manufacturers to develop new antibiotics is needed. We hypothesised that transparency on the regulatory appraisals of antibiotics would provide an incentive to pharmaceutical development. We thus aimed at reporting the French health technology assessment (HTA) opinions and reimbursement decision on antibiotics to those German (G-BA) and English (NICE) HTA bodies.A qualitative analysis of the Transparency Committee of the French National Authority for Health (TC-HAS) opinions regarding antibiotics assessment between 2016 and 2020 was performed. Decisions of reimbursement by TC-HAS were compared to those from G-BA and NICE when available. TC-HAS recognized a clinical benefit (CB) for 15/15 evaluated indications, a clinical added value for 9/15, and a public health interest for 8/15. Among the valued antibiotics by HAS, 5 were recommended for restricted use as a "reserve" to protect against the risk of resistance emergence. A comparison of HTA opinions was possible across HTA for only 8 antibiotics. The G-BA granted a reserve status for 4 drugs and NICE a reserve with restricted use for 5 antibiotics. Three of these antibiotics were positioned similarly by the English, German, and French HTA bodies. This qualitative analysis of HTA opinions between different European HTA bodies shows a consistent reimbursement decision of antibiotics against MDR bacteria and tuberculosis besides the differences in the applied assessment methods. This work also shows how HTA bodies could recognize a clinical added value in a context of the emergence of antibiotic resistance.

摘要

在过去几十年里,抗菌药物耐药性(AMR)已成为全球日益关注的问题。因此,需要鼓励制造商开发新的抗生素。我们假设抗生素监管评估的透明度将为药物研发提供激励。因此,我们旨在向德国卫生技术评估机构(G-BA)和英国国家卫生与临床优化研究所(NICE)报告法国对抗生素的卫生技术评估(HTA)意见和报销决定。对法国国家卫生管理局透明度委员会(TC-HAS)2016年至2020年期间关于抗生素评估的意见进行了定性分析。将TC-HAS的报销决定与G-BA和NICE(如有)的决定进行了比较。TC-HAS认可了15项评估适应症中的15项具有临床益处(CB),9项具有临床附加值,8项具有公共卫生利益。在HAS评估的抗生素中,5种被推荐作为“储备”限制使用,以防范耐药性出现的风险。仅对8种抗生素进行了不同HTA机构间HTA意见的比较。G-BA批准4种药物为储备药物,NICE批准5种抗生素为限制使用的储备药物。其中3种抗生素在英国、德国和法国HTA机构中的定位相似。不同欧洲HTA机构间对HTA意见的定性分析表明,除了应用的评估方法存在差异外,对抗多重耐药菌和结核病的抗生素报销决定是一致的。这项工作还展示了HTA机构在抗生素耐药性出现的背景下如何认识到临床附加值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8720/11703620/5335742ac620/S0266462324000552_fig1.jpg

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