首页> 外文期刊>Trials >AUtomated Risk Assessment for Stroke in Atrial Fibrillation (AURAS-AF) - an automated software system to promote anticoagulation and reduce stroke risk: study protocol for a cluster randomised controlled trial
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AUtomated Risk Assessment for Stroke in Atrial Fibrillation (AURAS-AF) - an automated software system to promote anticoagulation and reduce stroke risk: study protocol for a cluster randomised controlled trial

机译:心房颤动的自动风险评估(AURAS-AF)-促进抗凝和降低中风风险的自动化软件系统:一项集群随机对照试验的研究方案

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Background Patients with atrial fibrillation (AF) are at significantly increased risk of stroke. Oral anticoagulants (OACs) substantially reduce this risk, with gains seen across the spectrum of baseline risk. Despite the benefit to patients, OAC prescribing remains suboptimal in the United Kingdom (UK). We will investigate whether an automated software system, operating within primary care electronic medical records, can improve the management of AF by identifying patients eligible for OAC therapy and increasing uptake of this treatment. Methods/Design We will conduct a cluster randomised controlled trial, involving general practices using the Egton Medical Information Systems (EMIS) Web clinical system. We will randomise practices to use an electronic software tool or to continue with usual care. The tool will a) produce (and continually refresh) a list of patients with AF who are eligible for OAC therapy - practices will invite these patients to discuss therapy at the start of the trial - and b) generate electronic screen reminders in the medical records of those eligible, appearing throughout the trial. The software will run for 6?months in 23 intervention practices. A total of 23 control practices will manage their AF register in line with the usual care offered. The primary outcome is change in proportion of eligible patients with AF who have been prescribed OAC therapy after six months. Secondary outcomes are incidence of stroke, transient ischaemic attack, other major thromboembolism, major haemorrhage and reports of inappropriate OAC prescribing in the data collection sample - those deemed eligible for OACs. We will conduct a process evaluation in parallel with the randomised trial. We will use qualitative methods to examine patient and practitioner views of the intervention and its impact on primary care practice, including its time implications. Discussion AURAS-AF will investigate whether a simple intervention, using electronic primary care records, can improve OAC uptake in a high risk group for stroke. Given previous concerns about safety, especially surrounding inappropriate prescribing, we will also examine whether electronic reminders safely impact care in this clinical area. Trial registration http://ISRCTN 55722437 webcite
机译:背景心房颤动(AF)患者的中风风险显着增加。口服抗凝剂(OAC)可以大大降低这种风险,并且在整个基线风险范围内都能看到收益。尽管对患者有益,但OAC处方在英国(UK)仍然不是最佳选择。我们将调查在初级保健电子病历中运行的自动化软件系统是否可以通过确定有资格接受OAC治疗的患者并增加对该治疗的吸收来改善房颤的管理。方法/设计我们将使用Egton医学信息系统(EMIS)Web临床系统进行一项涉及一般实践的整群随机对照试验。我们将使使用电子软件工具或继续进行常规护理的做法随机化。该工具将a)生成(并不断刷新)符合OAC治疗条件的AF患者名单-实践将邀请这些患者在试验开始时讨论治疗方法-b)在病历中生成电子屏幕提醒在整个试验中出现的那些合格者中。该软件将在23种干预措施中运行6个月。总共23种控制措施将按照提供的日常护理措施管理其AF注册。主要结局是六个月后接受OAC治疗的合格房颤患者比例的变化。次要结果是中风的发生率,短暂性脑缺血发作,其他严重的血栓栓塞,严重的出血以及数据收集样本中OAC处方不当的报道-被认为符合OAC资格的人。我们将与随机试验同时进行过程评估。我们将使用定性方法来检查患者和医生对干预措施及其对初级保健实践的影响(包括时间影响)的观点。讨论AURAS-AF将研究使用电子基层医疗记录进行的简单干预是否可以提高中风高危人群的OAC摄入量。鉴于先前对安全性的担忧,尤其是围绕不适当处方的担忧,我们还将研究电子提醒是否会安全地影响该临床领域的护理。试用注册http:// ISRCTN 55722437网站

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