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用于评估孤儿药的多标准决策分析(MCDA)的国际经验:一项范围综述。

International experiences in multicriteria decision analysis (MCDA) for evaluating orphan drugs: a scoping review.

作者信息

Lasalvia P, Prieto-Pinto L, Moreno M, Castrillón J, Romano G, Garzón-Orjuela N, Rosselli D

机构信息

a NeuroEconomix , Pontificia Universidad Javeriana , Bogota , Colombia.

b NeuroEconomix , MSc Clinical Epidemiology , Bogota , Colombia.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2019 Aug;19(4):409-420. doi: 10.1080/14737167.2019.1633918. Epub 2019 Jul 1.

DOI:10.1080/14737167.2019.1633918
PMID:31210065
Abstract

: Orphan diseases are low-prevalence conditions with chronically debilitating or life-threatening consequences. Their treatments are generally called orphan drugs (OD). Health-technology assessment processes have traditionally considered cost-effectiveness analysis (CEA), when making reimbursement and pricing decisions for health-care plans. Valuing OD with standard CEA raises important issues due to uncertain evidence, inability to meet cost-effectiveness thresholds for reimbursement and high budget impact, among others. Multi-criteria decision analysis (MCDA) allows to overcome these issues and improve the technical and ethical quality of decisions regarding prioritization, coverage, and reimbursement of OD. : A scoping review was conducted in order to characterize MCDA frameworks for assessing OD and implementation experiences. We reviewed electronic databases (Medline, Embase, Cochrane Library, EBSCO, CINAHL, EconLit, Web of Science, LILACS, Google Scholar) key journals (Orphanet Journal of Rare Diseases and Value in Health) and organization repositories. : The theoretical framework for MCDA considers areas related to characteristics of orphan diseases and their technologies' clinical and economic impact. Participation processes are critical in incorporating societal values in weighting different dimensions and constructing decision rules. Local implementation pilots considering different stakeholders are necessary in order to pinpoint specific barriers and opportunities.

摘要

罕见病是发病率低但会导致慢性衰弱或危及生命的疾病。其治疗药物通常被称为孤儿药(OD)。传统上,卫生技术评估流程在为医疗保健计划做出报销和定价决策时会考虑成本效益分析(CEA)。由于证据不确定、无法达到报销的成本效益阈值以及预算影响大等原因,用标准CEA评估孤儿药会引发重要问题。多标准决策分析(MCDA)能够克服这些问题,并提高关于孤儿药的优先级、覆盖范围和报销决策的技术和伦理质量。

为了描述用于评估孤儿药的MCDA框架和实施经验,进行了一项范围综述。我们检索了电子数据库(Medline、Embase、Cochrane图书馆、EBSCO、CINAHL、EconLit、科学网、LILACS、谷歌学术)、关键期刊(《罕见病杂志》和《卫生保健价值》)以及组织知识库。

MCDA的理论框架考虑与罕见病特征及其技术的临床和经济影响相关的领域。参与过程对于将社会价值观纳入不同维度的加权以及构建决策规则至关重要。为了确定具体的障碍和机遇,需要开展考虑不同利益相关者的本地实施试点。

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