早期临床阶段视觉安全风险评估工具。

IF 1.9 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Kathrin Wawra-Hehenberger , Vanessa Pencelli , January Anne Pardo , Lothar Tremmel , Quazi Ataher , Max Waschbusch
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引用次数: 0

摘要

随着药物警戒风险管理的发展,在临床开发的所有阶段(包括早期试验阶段)对安全风险进行动态评估已成为常态。对直接适用于早期临床评估的实用工具的需求促使作者试点定制通用风险矩阵,以支持基于多个维度的主动安全风险评估。一旦为他们的研究领域定义,定制的安全风险矩阵被应用于可视化一系列已知的风险概况和示例,以及预计的风险缓解效果。研究发现,在早期临床开发阶段的多学科安全性讨论中,在一个简单图表上的双重可视化(风险定位和这些位置的风险缓解效果)特别相关。可视化工具提供了预计安全风险概况的有用快照,促进了参与早期临床开发决策的多个利益相关者的沟通。在现有的风险管理工具箱和流程中增加了一个简单的可视化工具,为临床团队提供了一个基本的蓝图,可以根据与自己研究领域相关的风险维度进行应用和定制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A visual safety risk evaluation tool in early clinical phases
Dynamic evaluation of safety risks across all stages of clinical development, including early trial phases, has become the norm with the evolution of risk management in pharmacovigilance. The need for practical tools directly applicable to early clinical assessment prompted the authors to pilot the customization of a common risk matrix to support proactive safety risk evaluation based on multiple dimensions. Once defined for their research area, the tailored safety risk matrix was applied to visualize a series of known risk profiles and examples, along with projected risk mitigation effects. This two-fold visualization on one simple graph (risks positioning, and effect of risk mitigation of those positions) was found to be particularly relevant in multi-disciplinary safety discussions during early clinical development stages. The visual tool provides useful snapshots of projected safety risk profiles, facilitating communication with multiple stakeholders involved in decisions throughout early clinical development. With the prospect of a simple visual instrument to add to their existing risk management toolbox and processes, clinical teams are also provided with a basic blueprint to apply and tailor based on risk dimensions related to their own research area.
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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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