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欧洲罕见病价值评估与资助流程工作组(ORPH-VAL)的建议。

Recommendations from the European Working Group for Value Assessment and Funding Processes in Rare Diseases (ORPH-VAL).

作者信息

Annemans Lieven, Aymé Ségolène, Le Cam Yann, Facey Karen, Gunther Penilla, Nicod Elena, Reni Michele, Roux Jean-Louis, Schlander Michael, Taylor David, Tomino Carlo, Torrent-Farnell Josep, Upadhyaya Sheela, Hutchings Adam, Le Dez Lugdivine

机构信息

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

ICM, CNRS UMR 7225--Inserm U 1127--UPMC-P6 UMR S 1127, Paris, France.

出版信息

Orphanet J Rare Dis. 2017 Mar 10;12(1):50. doi: 10.1186/s13023-017-0601-9.

Abstract

Rare diseases are an important public health issue with high unmet need. The introduction of the EU Regulation on orphan medicinal products (OMP) has been successful in stimulating investment in the research and development of OMPs. Despite this advancement, patients do not have universal access to these new medicines. There are many factors that affect OMP uptake, but one of the most important is the difficulty of making pricing and reimbursement (P&R) decisions in rare diseases. Until now, there has been little consensus on the most appropriate assessment criteria, perspective or appraisal process. This paper proposes nine principles to help improve the consistency of OMP P&R assessment in Europe and ensure that value assessment, pricing and funding processes reflect the specificities of rare diseases and contribute to both the sustainability of healthcare systems and the sustainability of innovation in this field. These recommendations are the output of the European Working Group for Value Assessment and Funding Processes in Rare Diseases (ORPH-VAL), a collaboration between rare disease experts, patient representatives, academics, health technology assessment (HTA) practitioners, politicians and industry representatives. ORPH-VAL reached its recommendations through careful consideration of existing OMP P&R literature and through a wide consultation with expert stakeholders, including payers, regulators and patients. The principles cover four areas: OMP decision criteria, OMP decision process, OMP sustainable funding systems and European co-ordination. This paper also presents a guide to the core elements of value relevant to OMPs that should be consistently considered in all OMP appraisals. The principles outlined in this paper may be helpful in drawing together an emerging consensus on this topic and identifying areas where consistency in payer approach could be achievable and beneficial. All stakeholders have an obligation to work together to ensure that the promise of OMP's is realised.

摘要

罕见病是一个重要的公共卫生问题,未满足的需求很高。欧盟孤儿药品法规(OMP)的出台成功刺激了对孤儿药品研发的投资。尽管有这一进展,但患者无法普遍获得这些新药。有许多因素影响孤儿药品的采用,但最重要的因素之一是在罕见病中做出定价和报销(P&R)决策的困难。到目前为止,对于最合适的评估标准、视角或评估过程几乎没有达成共识。本文提出了九条原则,以帮助提高欧洲孤儿药品定价和报销评估的一致性,并确保价值评估、定价和资金流程反映罕见病的特殊性,同时有助于医疗保健系统的可持续性以及该领域创新的可持续性。这些建议是欧洲罕见病价值评估和资金流程工作组(ORPH-VAL)的成果,该工作组由罕见病专家、患者代表、学者、卫生技术评估(HTA)从业者、政治家和行业代表合作组成。ORPH-VAL通过仔细考虑现有的孤儿药品定价和报销文献,并与包括支付方、监管机构和患者在内的专家利益相关者进行广泛协商,达成了其建议。这些原则涵盖四个领域:孤儿药品决策标准、孤儿药品决策过程、孤儿药品可持续资金系统和欧洲协调。本文还提供了一份指南,介绍了在所有孤儿药品评估中应始终考虑的与孤儿药品相关的价值核心要素。本文概述的原则可能有助于就这一主题形成新的共识,并确定支付方方法可以实现一致性且有益的领域。所有利益相关者都有义务共同努力,以确保孤儿药品的承诺得以实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66c/5345269/9aa2746fafdc/13023_2017_601_Fig1_HTML.jpg

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