评估在临床试验中使用电子健康记录数据确定结果的准备情况--案例研究。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Denise Esserman , Erich J. Greene , Nancy K. Latham , Michael Kane , Charles Lu , Peter N. Peduzzi , Thomas M. Gill , David A. Ganz
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引用次数: 0

摘要

背景:数据质量参差不齐是使用电子健康记录(EHR)数据确定多点临床试验急性期临床结果的一个挑战。不同临床试验机构的电子病历平台和数据全面性不同,特别是如果患者在临床机构网络之外接受治疗,也会影响结果的有效性。克服这些挑战需要一种结构化的方法:方法:我们提出了一个框架并创建了一个核对表,用于评估临床研究机构是否准备好向临床试验提供电子病历数据,以便进行结果确认:研究机构准备情况检查表包括对基础设施(即研究机构医疗保健系统或临床网络的规模和结构)、数据采购(即数据质量)和获取研究数据的成本进行评估。核对表强调,必须了解研究机构如何在其覆盖范围内获取和整合数据,并制定数据采购协议,以确保每个研究机构都能一致、统一地提取数据:我们建议在启动依赖电子病历数据的多站点试验之前,对每个临床站点的数据质量和基础设施进行严格的前瞻性审查。建议的检查表可作为一种指导工具,帮助研究者确保临床试验数据采集的稳健性和公正性:NCT02475850.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing readiness to use electronic health record data for outcome ascertainment in clinical trials – A case study

Background

Variable data quality poses a challenge to using electronic health record (EHR) data to ascertain acute clinical outcomes in multi-site clinical trials. Differing EHR platforms and data comprehensiveness across clinical trial sites, especially if patients received care outside of the clinical site's network, can also affect validity of results. Overcoming these challenges requires a structured approach.

Methods

We propose a framework and create a checklist to assess the readiness of clinical sites to contribute EHR data to a clinical trial for the purpose of outcome ascertainment, based on our experience with the Strategies to Reduce Injuries and Develop Confidence in Elders (STRIDE) study, which enrolled 5451 participants in 86 primary care practices across 10 healthcare systems (sites).

Results

The site readiness checklist includes assessment of the infrastructure (i.e., size and structure of the site's healthcare system or clinical network), data procurement (i.e., quality of the data), and cost of obtaining study data. The checklist emphasizes the importance of understanding how data are captured and integrated across a site's catchment area and having a protocol in place for data procurement to ensure consistent and uniform extraction across each site.

Conclusions

We suggest rigorous, prospective vetting of the data quality and infrastructure of each clinical site before launching a multi-site trial dependent on EHR data. The proposed checklist serves as a guiding tool to help investigators ensure robust and unbiased data capture for their clinical trials.

Original trial registration number

NCT02475850

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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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