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Data feedback and behavioural change intervention to improve primary care prescribing safety (EFIPPS):multicentre, three arm, cluster randomised controlled trial

机译:数据反馈和行为改变干预以改善初级保健处方安全性(EFIPPS):多中心,三臂,集群随机对照试验

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摘要

: High-risk prescribing in primary care is common and causes significant harm. Data feedback has been shown to be effective in many contexts, but not for prescribing safety. The aim of this study was to evaluate the effectiveness of prescribing safety feedback compared to moderately enhanced usual care.: Three-arm, highly pragmatic cluster-randomised trial. Practices were randomised to one of three arms by an independent statistician. Allocation was masked to the research team throughout. Analysis was intention to treat, included all eligible patients at every time point, and was adjusted for practice baseline rates for each outcome. There were no protocol changes after the trial started.: 262/278 (94.2%) primary care practices in three Scottish Health Boards. : Practices were randomised to: (1) ‘usual care’ consisting of e-mailed educational material with support for searching to identify patients (88 practices at baseline, 86 analysed; (2) usual care plus feedback on practice high-risk prescribing sent quarterly on five occasions (87 practices, 86 analysed), or (3) usual care plus the same feedback incorporating a behaviour change component (87 practices, 86 analysed). : The primary outcome was a patient-level composite of six prescribing measures relating to high-risk use of antipsychotics, non-steroidal anti-inflammatories and antiplatelets. Secondary outcomes were the six individual measures. The primary analysis compared high-risk prescribing in the two feedback arms to usual care at 15 months. Secondary analysis examined immediate change and change in trend of high-risk prescribing associated with intervention implementation within each arm. : In the primary analysis, high-risk prescribing measured by the primary outcome fell from 6.0% to 5.0% in the usual care arm, compared to 6.0% to 4.5% in the feedback-only arm (OR 0.88 compared to usual care, 95%CI 0.80 to 0.96, p=0.007) and 6.2% to 4.5% in the feedback plus behaviour change component (OR 0.86, 95%CI 0.78 to 0.95, p=0.002). In the pre-specified secondary analysis of change in trend within each arm, the usual care educational intervention had no effect on the existing declining trend in high-risk prescribing. Both types of feedback were associated with significantly more rapid decline in high-risk prescribing after the intervention compared to before.: Feedback of prescribing safety data was effective at reducing high-risk prescribing. The intervention would be feasible to implement at scale in contexts where electronic health records are in general use.
机译::初级保健中的高风险处方很普遍,并且会造成重大伤害。数据反馈已在许多情况下被证明是有效的,但并未规定安全性。这项研究的目的是评估与适当加强常规护理相比开具安全反馈的有效性。:三臂,高度实用的整群随机试验。独立统计学家将实践随机分配到三个部门之一。整个研究团队都掩盖了分配情况。分析旨在治疗,包括每个时间点的所有合格患者,并针对每种结局针对实践基线率进行了调整。试验开始后,没有任何方案变化。:三个苏格兰卫生委员会的262/278(94.2%)基层医疗实践。 :将实践随机化为:(1)通过电子邮件发送的教育材料组成的“常规护理”,以支持搜索以识别患者(基线时有88种实践,分析了86种;(2)常规护理以及对实践高风险处方的反馈已发送每季度五次(87种做法,分析了86种),或(3)常规护理加上包含行为改变成分的相同反馈(87种做法,分析了86种):主要结果是在患者水平上综合了六种处方措施使用抗精神病药,非甾体类抗炎药和抗血小板药的高风险;次要结局是六个单独的指标;主要分析将两个反馈组的高风险处方与常规护理在15个月时进行比较;次要分析检查了即刻变化以及与每个部门内的干预措施实施相关的高风险处方趋势的变化::在主要分析中,以主要结局衡量的高风险处方从6.0下降常规治疗组的百分比为5.0%至5.0%,而仅反馈治疗组的百分比为6.0%至4.5%(与常规治疗相比,OR为0.88,95%CI为0.80至0.96,p = 0.007),常规治疗组为6.2%至4.5%反馈加行为改变分量(或为0.86,95%CI为0.78至0.95,p = 0.002)。在预先确定的每个部门内趋势变化的二次分析中,常规护理教育干预措施对高风险处方中现有的下降趋势没有影响。与之前相比,这两种类型的反馈都与干预后的高风险处方明显更快地下降有关。:处方安全数据的反馈在减少高风险处方方面是有效的。在普遍使用电子健康记录的情况下,大规模实施干预措施是可行的。

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