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在一家大型学术医疗中心利用重新调整的临床研究基础设施来实施临床研究管理系统。

Leveraging retooled clinical research infrastructure for Clinical Research Management System implementation at a large Academic Medical Center.

作者信息

Mullen Catherine G, Houlihan Jessica Y, Stroo Marissa, Deeter Christine E, Freel Stephanie A, Padget Angela M, Snyder Denise C

机构信息

Duke Office of Clinical Research, Duke University School of Medicine, Durham, NC, USA.

Clinical and Translational Science Institute, Duke University, Durham, NC, USA.

出版信息

J Clin Transl Sci. 2023 May 18;7(1):e127. doi: 10.1017/cts.2023.550. eCollection 2023.

Abstract

Quality clinical research is essential for health care progress and is the mission of academic health centers. Yet ensuring quality depends on an institution's ability to measure, control, and respond to metrics of trial performance. Uninformed clinical research provides little benefit to health care, drains institutional resources, and may waste participants' time and commitment. Opportunities for ensuring high-quality research are multifactorial, including training, evaluation, and retention of research workforces; operational efficiencies; and standardizing policies and procedures. Duke University School of Medicine has committed to improving the quality and informativeness of our clinical research enterprise through investments in infrastructure with significant focus on optimizing research management system integration as a foundational element for quality management. To address prior technology limitations, Duke has optimized Advarra's OnCore for this purpose by seamlessly integrating with the IRB system, electronic health record, and general ledger. Our goal was to create a standardized clinical research experience to manage research from inception to closeout. Key drivers of implementation include transparency of research process data and generating metrics aligned with institutional goals. Since implementation, Duke has leveraged OnCore data to measure, track, and report metrics resulting in improvements in clinical research conduct and quality.

摘要

高质量的临床研究对于医疗保健的进步至关重要,也是学术医疗中心的使命。然而,确保质量取决于机构衡量、控制和回应试验绩效指标的能力。缺乏信息的临床研究对医疗保健益处甚微,耗费机构资源,还可能浪费参与者的时间和精力。确保高质量研究的机会是多方面的,包括研究人员的培训、评估和留用;运营效率;以及政策和程序的标准化。杜克大学医学院致力于通过对基础设施的投资来提高我们临床研究事业的质量和信息含量,重点是优化研究管理系统集成,将其作为质量管理的基础要素。为了解决先前技术的局限性,杜克大学为此对Advarra的OnCore进行了优化,使其与机构审查委员会(IRB)系统、电子健康记录和总账无缝集成。我们的目标是创建一个标准化的临床研究体验,以管理从研究启动到结束的整个过程。实施的关键驱动因素包括研究过程数据的透明度以及生成与机构目标一致的指标。自实施以来,杜克大学利用OnCore数据来衡量、跟踪和报告指标,从而改善了临床研究的开展和质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/044d/10260330/8c9136840b38/S2059866123005502_fig1.jpg

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