Artificial intelligence-enabled safety monitoring in Alzheimer's disease clinical trials.

IF 4.3 Q2 BUSINESS
Gustavo A Jimenez-Maggiora, Michael C Donohue, Michael S Rafii, Rema Raman, Paul S Aisen
{"title":"Artificial intelligence-enabled safety monitoring in Alzheimer's disease clinical trials.","authors":"Gustavo A Jimenez-Maggiora, Michael C Donohue, Michael S Rafii, Rema Raman, Paul S Aisen","doi":"10.1016/j.tjpad.2024.100002","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Investigators conducting clinical trials have an ethical, scientific, and regulatory obligation to protect the safety of trial participants. Traditionally, safety monitoring includes manual review and coding of adverse event data by expert clinicians.</p><p><strong>Objectives: </strong>Our study explores the use of natural language processing (NLP) and artificial intelligence (AI) methods to streamline and standardize clinician coding of adverse event data in Alzheimer's disease (AD) clinical trials.</p><p><strong>Design: </strong>Our quantitative retrospective study aimed to develop a gold standard AD adverse event data set, evaluate the predictive performance of NLP-based models to classify adverse events, and determine whether automated coding is more efficient, accurate, reliable, and consistent than clinician coding.</p><p><strong>Setting: </strong>Our study was conducted at the University of Southern California's Alzheimer's Therapeutic Research Institute (ATRI). ATRI serves as the clinical and data coordinating center for the Alzheimer's Clinical Trial Consortium (ACTC).</p><p><strong>Participants: </strong>We collected demographic and adverse event data from eight completed clinical trials in participants (n=1920) with symptomatic AD conducted between 2005 and 2020.</p><p><strong>Measurements: </strong>Original expert clinician-confirmed codes were used for all model performance comparisons. F1 score was used as the primary model selection metric. Final classifier performance was evaluated using predictive accuracy. Clinician effort was measured in time to code, review, and confirm coded adverse events.</p><p><strong>Results: </strong>In a sample of 1000 adverse events, AI-based AE coding achieved higher accuracy (∼20% increase in accuracy) and was more cost-effective (∼80% cost reduction) than traditional clinician coding.</p><p><strong>Conclusions: </strong>Our study results demonstrate how approaches that effectively combine AI and human expertise can improve the efficiency and quality of adverse event coding and clinical trial safety monitoring.</p>","PeriodicalId":22711,"journal":{"name":"The Journal of Prevention of Alzheimer's Disease","volume":"12 1","pages":"100002"},"PeriodicalIF":4.3000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Prevention of Alzheimer's Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.tjpad.2024.100002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BUSINESS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Investigators conducting clinical trials have an ethical, scientific, and regulatory obligation to protect the safety of trial participants. Traditionally, safety monitoring includes manual review and coding of adverse event data by expert clinicians.

Objectives: Our study explores the use of natural language processing (NLP) and artificial intelligence (AI) methods to streamline and standardize clinician coding of adverse event data in Alzheimer's disease (AD) clinical trials.

Design: Our quantitative retrospective study aimed to develop a gold standard AD adverse event data set, evaluate the predictive performance of NLP-based models to classify adverse events, and determine whether automated coding is more efficient, accurate, reliable, and consistent than clinician coding.

Setting: Our study was conducted at the University of Southern California's Alzheimer's Therapeutic Research Institute (ATRI). ATRI serves as the clinical and data coordinating center for the Alzheimer's Clinical Trial Consortium (ACTC).

Participants: We collected demographic and adverse event data from eight completed clinical trials in participants (n=1920) with symptomatic AD conducted between 2005 and 2020.

Measurements: Original expert clinician-confirmed codes were used for all model performance comparisons. F1 score was used as the primary model selection metric. Final classifier performance was evaluated using predictive accuracy. Clinician effort was measured in time to code, review, and confirm coded adverse events.

Results: In a sample of 1000 adverse events, AI-based AE coding achieved higher accuracy (∼20% increase in accuracy) and was more cost-effective (∼80% cost reduction) than traditional clinician coding.

Conclusions: Our study results demonstrate how approaches that effectively combine AI and human expertise can improve the efficiency and quality of adverse event coding and clinical trial safety monitoring.

阿尔茨海默病临床试验中的人工智能安全监测。
背景:开展临床试验的研究者有保护试验参与者安全的伦理、科学和监管义务。传统上,安全监测包括由临床专家对不良事件数据进行人工审查和编码。目的:我们的研究探讨了使用自然语言处理(NLP)和人工智能(AI)方法来简化和规范临床医生对阿尔茨海默病(AD)临床试验中不良事件数据的编码。设计:我们的定量回顾性研究旨在建立一个金标准的AD不良事件数据集,评估基于nlp的不良事件分类模型的预测性能,并确定自动编码是否比临床医生编码更有效、准确、可靠和一致。背景:我们的研究在南加州大学阿尔茨海默病治疗研究所(ATRI)进行。ATRI是阿尔茨海默病临床试验联盟(ACTC)的临床和数据协调中心。参与者:我们收集了2005年至2020年间进行的8项已完成的临床试验(n=1920)中有症状的AD患者的人口统计学和不良事件数据。测量方法:所有模型性能比较均采用原始专家临床确认代码。F1评分作为主要的模型选择指标。最终分类器性能评估使用预测精度。临床医生的努力被及时测量,以编码、审查和确认编码的不良事件。结果:在1000个不良事件的样本中,基于人工智能的AE编码比传统的临床医生编码具有更高的准确性(准确度提高~ 20%),并且更具成本效益(成本降低~ 80%)。结论:我们的研究结果表明,有效结合人工智能和人类专业知识的方法可以提高不良事件编码和临床试验安全监测的效率和质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
自引率
0.00%
发文量
0
期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信