Farghaly Mohamed Naser, Al Dallal Sara Ahmad Mohammad, Fasseeh Ahmad Nader, Monsef Nahed AbdulKhaleq, Suliman Eldaw Abdalla Mohamed Ali, Tahoun Mohamed Attia, Abaza Sherif, Kaló Zoltán
Dubai Health Insurance Corporation, Dubai Health Authority, Dubai, United Arab Emirates.
Doctoral School of Sociology, Eötvös Loránd University, Budapest, Hungary.
Front Pharmacol. 2021 Jun 8;12:680737. doi: 10.3389/fphar.2021.680737. eCollection 2021.
In recent periods the United Arab Emirates (UAE) has strengthened economic measures in its pharmaceutical policy by promoting local manufacturing and facilitating the use of generic medicines. International examples indicate the importance of quality control elements in the implementation of cost containment policies. Multicriteria Decision Analysis (MCDA) is increasingly used in health care to facilitate health care decision based on multiple objectives. Our objective was to develop a pilot MCDA tool for repeated use to support the value-based purchasing of generic medicines in the UAE. An international evidence framework was adapted to UAE in a multistakeholder workshop organized by Dubai Health Authority. After validating the relevance of nine criteria in the local jurisdiction, participants decided the ranking and weight of each criterion by anonymous voting. The top four criteria focused on quality elements starting with real-world clinical or economic outcomes (with 19.8% weight), followed by the quality assurance of manufacturing (17.3%), then evidence on the equivalence with the original product (14.8%), and drug formulation and stability (12.3%). The pharmaceutical acquisition cost criteria ranked fifth with 9.4% weight. The bottom four criteria, including reliability of drug supply, macroeconomic benefit, pharmacovigilance and added value services related to the product had similar weights in the range of 5.5-7.7%. Policy-makers in Dubai put high emphasis of value-based health care by incentivizing manufacturers of off-patent pharmaceuticals to generate additional scientific evidence compared to the mandatory minimum and acknowledging efforts to improve quality standards. The MCDA tool is considered suitable to improve the transparency and consistency of decision making in UAE for off-patent pharmaceuticals, and subsequently for other health technologies.
近年来,阿拉伯联合酋长国(阿联酋)通过促进本地生产和便利使用仿制药,加强了其药品政策中的经济措施。国际案例表明了质量控制要素在实施成本控制政策中的重要性。多标准决策分析(MCDA)在医疗保健领域越来越多地被用于促进基于多目标的医疗保健决策。我们的目标是开发一种可重复使用的MCDA试点工具,以支持阿联酋基于价值的仿制药采购。在迪拜卫生局组织的一次多利益相关方研讨会上,一个国际证据框架被调整以适用于阿联酋。在验证了九个标准在当地司法管辖区的相关性之后,参与者通过匿名投票决定了每个标准的排名和权重。排名前四的标准侧重于质量要素,首先是真实世界的临床或经济结果(权重为19.8%),其次是生产的质量保证(17.3%),然后是与原研产品等效性的证据(14.8%),以及药物剂型和稳定性(12.3%)。药品采购成本标准以9.4%的权重排名第五。排名靠后的四个标准,包括药品供应的可靠性、宏观经济效益、药物警戒以及与产品相关的增值服务,权重相似,在5.5%-7.7%的范围内。迪拜的政策制定者高度重视基于价值的医疗保健,通过激励非专利药品制造商提供比法定最低要求更多的科学证据,并认可其提高质量标准的努力。MCDA工具被认为适合提高阿联酋非专利药品决策的透明度和一致性,进而提高其他医疗技术决策的透明度和一致性。