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How to Value Digital Health Interventions? A Systematic Literature Review

机译:如何看重数字健康干预?系统文献综述

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摘要

In Europe, there were almost twice as many patents granted for medical technology (13,795) compared to pharmaceuticals (7441) in 2018. It is important to ask how to integrate such an amount of innovations into routine clinical practice and how to measure the value it brings to the healthcare system. Given the novelty of digital health interventions (DHI), one can even question whether the quality-adjusted life years (QALY) approach developed for pharmaceuticals can be used or whether we need to develop a new DHI’s value assessment framework. We conducted a systematic literature review of published DHIs’ assessment guidelines. Each publication was analyzed with a 12-items checklist based on a EUnetHTA core model enriched with additional criteria such as usability, interoperability, and data security. In total, 11 value assessment guidelines were identified. The review revealed that safety, clinical effectiveness, usability, economic aspects, and interoperability were most often discussed (seven out of 11). More than half of the guidelines addressed organizational impact, data security, choice of comparator, and technical considerations (six out of 11). The unmet medical needs (three out of 11), along with the ethical (two out of 11) and legal aspects (one out of 11), were given the least attention. No author provided an analytical framework for the calculation of clinical and economic outcomes. We elicited five recommendations for the choice of DHI’s value criteria and a methodological suggestion for the pricing and reimbursement framework. Our conclusions lead to the need for a new DHI’s value assessment framework instead of a QALY approach.
机译:在欧洲,2018年获得的医疗技术专利(1​​3,795)几乎是药品(7441)的两倍。重要的是要问如何将如此大量的创新整合到常规临床实践中以及如何衡量其创新价值带到医疗系统。鉴于数字健康干预(DHI)的新颖性,人们甚至可以质疑是否可以使用针对药品开发的质量调整生命年(QALY)方法,或者我们是否需要开发新的DHI价值评估框架。我们对已发布的DHI评估指南进行了系统的文献综述。基于EUnetHTA核心模型的12个项目清单对每个出版物进行了分析,该模型丰富了可用性,互操作性和数据安全性等其他标准。总共确定了11项价值评估指南。审查显示,最经常讨论安全性,临床有效性,可用性,经济性和互操作性(11个中的7个)。一半以上的指南涉及组织影响,数据安全性,比较器选择和技术考虑因素(11个中的6个)。未满足的医疗需求(11个中的3个)以及道德方面(11个中的2个)和法律方面(11个中的1个)受到的关注最少。没有作者提供用于计算临床和经济结果的分析框架。我们为选择DHI的价值标准提出了五项建议,并为定价和报销框架提供了方法论上的建议。我们的结论导致需要新的DHI价值评估框架,而不是QALY方法。

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