Ethical challenges for Health Technology Assessment (HTA) in the evolving evidence landscape.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Pietro Refolo, Katherine Duthie, Björn Hofmann, Michal Stanak, Neil Bertelsen, Bart Bloemen, Rosella Di Bidino, Wija Oortwijn, Costanza Raimondi, Dario Sacchini, Gert Jan van der Wilt, Kenneth Bond
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Abstract

Since its inception, Health Technology Assessment (HTA) has typically determined the value of a technology by collecting information derived from randomized clinical trials (RCTs), in line with the principles of evidence-based medicine (EBM). However, data from RCTs did not constitute the sole source of information, as other types of evidence (such as primary qualitative research) have often been utilized. Recent advances in both generating and collecting other types of evidence are broadening the landscape of evidence, adding complexity to the discussion of "robustness of evidence." What are the consequences of these recent developments for the methodology and conduct of HTA, the HTA community, and its ethical commitments? The aim of this article is to explore some ethical challenges that are emerging in the current evolving evidence landscape, particularly changes in evidence generation and collection (e.g., diversification of data sources), and shifting standards of evidence in the field of HTA (e.g., increasing acceptability of evidence that is thought of as lower quality). Our conclusion is that deciding how to best maintain trustworthiness is common to all these issues.

在不断变化的证据环境中,卫生技术评估(HTA)面临的伦理挑战。
卫生技术评估(HTA)自诞生以来,通常根据循证医学(EBM)的原则,通过收集随机临床试验(RCT)的信息来确定一项技术的价值。然而,来自随机临床试验的数据并不是唯一的信息来源,其他类型的证据(如初级定性研究)也经常被利用。最近,在生成和收集其他类型证据方面取得的进展正在扩大证据的范围,增加了讨论 "证据稳健性 "的复杂性。这些最新进展对 HTA 的方法和行为、HTA 团体及其伦理承诺有什么影响?本文旨在探讨当前不断变化的证据环境中出现的一些伦理挑战,特别是证据生成和收集方面的变化(如数据来源的多样化),以及 HTA 领域证据标准的变化(如被认为质量较低的证据的可接受性不断提高)。我们的结论是,决定如何最好地维护可信度是所有这些问题的共同点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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