从纸质到数字:评估电子病历及其在欧洲临床试验中对EMA指南的遵从性。

IF 1.4 Q4 PHARMACOLOGY & PHARMACY
Stefano Stabile, Sara Testoni, Veronica Franchina, Marta Betti, Francesca Mannozzi, Alessandra Ferrari, Irene Federici, Ludovic Doungue, Celeste Cagnazzo
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引用次数: 0

摘要

背景:在过去十年中,在数字技术进步的推动下,从纸质医疗记录管理到数字医疗记录管理已经发生了重大转变。这种转变导致了电子医疗记录(emr)的广泛采用,预计纸质文档将很快被完全取代。作为回应,欧洲药品管理局的“临床试验中计算机化系统指南”概述了验证EMR系统的基本标准,以确保数据完整性和安全性,并为临床试验中的电子源文件设定了标准。方法:从2023年12月到2024年3月,意大利数据管理和临床研究协调员小组(GIDMcrc)在意大利、法国和比利时的临床研究站点进行了一项在线调查,以评估病历和源文件的特征。结果:调查由37个中心完成:70.3%来自意大利,16.2%来自法国,13.5%来自比利时。大多数网站使用混合纸张/电子源文件(SD)系统(72.3%),少数中心使用全电子SD系统(13.5%)或全纸张系统(16.2%)。电子病历系统在70.3%的场所使用,但只有23.8%符合电子病历系统的指导方针。还进行了针对具体国家的分析,以进一步探讨意大利和法国/比利时的情况。结论:尽管意大利、法国和比利时广泛使用电子病历(emr),但意大利在数字化方面落后于其他两个国家。尽管有电子病历,许多中心仍然使用纸质和电子源文件的混合系统。也缺乏对EMA和GCP标准的认识,特别是关于培训和系统测试。意大利各中心较高的回复率突出表明需要在法国和比利时扩大抽样,后续调查将有助于评估进展情况和改进纠正行动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Paper to Digital: Evaluating Electronic Medical Records and their Compliance with EMA Guidelines in European Clinical Trials.

Background: Over the past decade, there has been a significant shift from paper-based to digital medical record management, driven largely by advances in digital technology. This transition has led to widespread adoption of Electronic Medical Records (EMRs), with the expectation that paper documentation will soon be fully replaced. In response, the European Medicines Agency's "Guideline on Computerised Systems in Clinical Trials" outlines essential criteria for validated EMR systems to ensure data integrity and security, and sets standards for electronic source documents in clinical trials.

Methods: From December 2023 to March 2024, the Italian Group of Data Managers and Clinical Research Coordinators (GIDMcrc) conducted an online survey across clinical research sites in Italy, France and Belgium to assess the characteristics of medical records and source documents.

Results: The survey was completed by 37 centres: 70.3% from Italy, 16.2% from France and 13.5% from Belgium. Most sites use a mixed paper/electronic Source Document (SD) system (72.3%), with fewer centres having fully electronic SD systems (13.5%) or fully paper-based systems (16.2%). EMR systems are used in 70.3% of sites, but only 23.8% comply with EMA guidelines for computerised systems. A country-specific analysis was also conducted to further explore the situations in Italy and France/Belgium.

Conclusion: Despite the widespread use of electronic medical records (EMRs) in Italy, France and Belgium, Italy lags behind the other two countries in terms of digitization. Despite the presence of an EMR, many centres still use a mixed system of paper and electronic source documents. There is also a lack of awareness regarding EMA and GCP standards, particularly concerning training and system testing. The higher response rate from Italian centres highlights the need for a larger sample in France and Belgium, and a follow-up survey would be beneficial for assessing progress and refining corrective actions.

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来源期刊
Reviews on recent clinical trials
Reviews on recent clinical trials PHARMACOLOGY & PHARMACY-
CiteScore
3.10
自引率
5.30%
发文量
44
期刊介绍: Reviews on Recent Clinical Trials publishes frontier reviews on recent clinical trials of major importance. The journal"s aim is to publish the highest quality review articles in the field. Topics covered include: important Phase I – IV clinical trial studies, clinical investigations at all stages of development and therapeutics. The journal is essential reading for all researchers and clinicians involved in drug therapy and clinical trials.
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