Suppr超能文献

MEDUCATE试验:门诊中强化教育干预对信息技术介导的药物管理的有效性——一项整群随机对照试验的研究方案

MEDUCATE trial: effectiveness of an intensive EDUCATional intervention for IT-mediated MEDication management in the outpatient clinic - study protocol for a cluster randomized controlled trial.

作者信息

van Stiphout F, Zwart-van Rijkom J E F, Aarts J E C M, Koffijberg H, Klarenbeek-deJonge E, Krulder M, Roes K C B, Egberts A C G, ter Braak E W M T

机构信息

Department of Internal Medicine and Centre for Research and Development of Education, University Medical Centre Utrecht, the Netherlands, Hijmans van den Berghgebouw kamer 4.21, Huispostnummer HB 4.05, Postbus 85500, 3508, GA, Utrecht, The Netherlands.

Department of Clinical Pharmacy, University Medical Centre Utrecht, Heidelberglaan 100, 3584, CX, Utrecht, The Netherlands.

出版信息

Trials. 2015 May 22;16:223. doi: 10.1186/s13063-015-0744-8.

Abstract

BACKGROUND

Using information technology for medication management is an opportunity to help physicians to improve the quality of their documentation and communication and ultimately to improve patient care and patient safety. Physician education is necessary to take full advantage of information technology systems. In this trial, we seek to determine the effectiveness of an intensive educational intervention compared with the standard approach in improving information technology-mediated medication management and in reducing potential adverse drug events in the outpatient clinic.

METHODS/DESIGN: We are conducting a multicenter, cluster randomized controlled trial. The participants are specialists and residents working in the outpatient clinic of internal medicine, cardiology, pulmonology, geriatrics, gastroenterology and rheumatology. The intensive educational intervention is composed of a small-group session and e-learning. The primary outcome is discrepancies between registered medication (by physicians) and actually used medication (by patients). The key secondary outcomes are potential adverse events caused by missed drug-drug interactions. The primary and key secondary endpoints are being assessed shortly after the educational intervention is completed. Sample size will be calculated to ensure sufficient power. A sample size of 40 physicians per group and 20 patients per physician will ensure a power of >90 %, which means we will need a total of 80 physicians and 1,600 patients.

DISCUSSION

We performed an exploratory trial wherein we tested the recruitment process, e-learning, time schedule, and methods for data collection, data management and data analysis. Accordingly, we refined the processes and content: the recruitment strategy was intensified, extra measures were taken to facilitate smooth conductance of the e-learning and parts were made optional. First versions of the procedures for data collection were determined. Data entry and analysis was further standardized by using the G-standard database in the telephone questionnaire.

TRIAL REGISTRATION

ISRCTN registry: ISRCTN50890124 . Registered 10 June 2013.

摘要

背景

利用信息技术进行药物管理是一个帮助医生提高文档记录和沟通质量、最终改善患者护理和患者安全的契机。医生教育对于充分利用信息技术系统是必要的。在本试验中,我们试图确定与标准方法相比,强化教育干预在改善信息技术介导的药物管理以及减少门诊潜在药物不良事件方面的有效性。

方法/设计:我们正在进行一项多中心、整群随机对照试验。参与者是在内科、心脏病学、肺病学、老年医学、胃肠病学和风湿病学门诊工作的专科医生和住院医师。强化教育干预由小组会议和电子学习组成。主要结局是(医生记录的)注册用药与(患者实际使用的)实际用药之间的差异。关键次要结局是漏用药物相互作用导致的潜在不良事件。主要和关键次要终点在教育干预完成后不久进行评估。将计算样本量以确保有足够的效能。每组40名医生、每位医生20名患者的样本量将确保效能>90%,这意味着我们总共需要80名医生和1600名患者。

讨论

我们进行了一项探索性试验,在此试验中我们测试了招募过程、电子学习、时间表以及数据收集、数据管理和数据分析方法。相应地,我们完善了流程和内容:加强了招募策略,采取了额外措施以促进电子学习的顺利进行,并使部分内容成为可选内容。确定了数据收集程序的初稿。通过在电话问卷中使用G标准数据库进一步规范了数据录入和分析。

试验注册

ISRCTN注册库:ISRCTN50890124。2013年6月10日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2269/4447017/f7a4ab7fc9a3/13063_2015_744_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验