Consideration for Assessing Data/Models/Tools Expiration Supporting Drug Development and Clinical Decision Making.

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Jeffrey S Barrett, Mark A Turner
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引用次数: 0

Abstract

Decision making of any kind is informed by data and often by models, tools or other solutions built from data. Data are evaluated for such purposes within a specific context of use (COU) but implicitly we often believe the data to be relevant, accurate and of high quality. In reality, this is not always the case. The status of data for various COUs must constantly be revisited for relevance and information value over time. Using drug development as an example, we postulate that there are indeed occasions where data value diminishes over time and consideration for data expiration with respect to its relevance for decision making should be entertained and at least identified with respect to a time-dependent change in status. Other situations exist which will also necessitate periodic review and condition reassessment. For example, considerations for patient privacy and consent along with compliance to regulatory standards must factor into future recommendations as well. Actions regarding data expiration are proposed as initial thoughts to be expanded upon but this assessment is primarily an attempt to explore factors which impact opinions about data information value for both drug development and clinical decision making.

评估支持药物开发和临床决策的数据/模型/工具失效的考虑。
任何类型的决策都是由数据提供信息的,通常是由数据构建的模型、工具或其他解决方案。在特定的使用环境(COU)中对数据进行评估,但我们通常认为数据是相关的、准确的和高质量的。在现实中,情况并非总是如此。随着时间的推移,必须不断地重新检查各种cou的数据状态,以确定其相关性和信息价值。以药物开发为例,我们假设确实存在数据价值随着时间的推移而减少的情况,并且应该考虑数据到期与决策的相关性,并且至少应考虑到与时间相关的状态变化。其他情况也需要定期审查和重新评估。例如,考虑患者隐私和同意以及遵守监管标准也必须考虑到未来的建议。关于数据过期的行动被提议作为初步想法进行扩展,但该评估主要是试图探索影响药物开发和临床决策中数据信息价值的因素。
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
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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