对加拿大高风险阿片类药物处方的医院阿片类药物管理计划的评估:中断时间序列分析。

IF 3.2 2区 医学 Q1 SUBSTANCE ABUSE
Lianping Ti, Tamara Mihic, Arielle Beauchesne, Cameron Grant, Ingrid Frank, Nooreen Haji, Michael Legal, Stephen Shalansky, Seonaid Nolan
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引用次数: 0

摘要

背景:高风险阿片类药物处方(例如,每日高剂量阿片类药物,同时使用阿片类镇静剂)在医院很普遍,并与不良后果有关。阿片类药物管理计划(OSP)有可能通过审计和反馈建议来减少高风险的阿片类药物处方。方法:我们使用中断时间序列分析评估了2020年1月在加拿大温哥华一家三级保健医院实施的基于审计和反馈的OSP。电子健康记录(EHR)系统与计算机化供应商订单输入(CPOE)同时运行。主要结局是:任何高风险阿片类药物处方(基于10个循证指标),包括高剂量吗啡毫克当量(MME)处方(bbb90 MME),长阿片类药物处方持续时间(>入院后5天),并发阿片类镇静剂处方。结果:在2018年1月至2022年3月期间,纳入了5,477名活跃的阿片类药物患者。虽然osp后总体高危阿片类药物处方没有发生显著变化(p >.05),但每日高剂量MME处方水平显著降低(估计:-0.044;95%置信区间[CI]: -0.082, -0.006)。相反,长阿片类药物持续时间的趋势增加(估计:0.006;95%CI: 0.000, 0.011),可能是由于在实施CPOE的EHR时取消了自动停止日期。osp干预后,我们最初看到并发阿片类镇静剂处方急剧增加(估计:0.013;95%ci: 0.005, 0.020)。2021年5月实施的苯二氮卓类药物订购干预扭转了这一趋势,降低了两者的水平(估计:0.874;95%CI: 0.374, 1.375)和斜率(估计:-0.022,95%CI: -0.034, -0.011)。结论:与OSP一致的新EHR的实施可能影响了我们的研究结果。虽然我们的研究表明,OSP减少了大剂量阿片类药物的处方,但受EHR系统影响的其他指标并没有从OSP中受益。尽管如此,OSP证明能够通过引入干预措施来减少阿片类药物和镇静剂的并发处方,迅速应对意想不到的后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of a hospital-based opioid stewardship program on high-risk opioid prescribing in a Canadian setting: an interrupted time series analysis.

Evaluation of a hospital-based opioid stewardship program on high-risk opioid prescribing in a Canadian setting: an interrupted time series analysis.

Evaluation of a hospital-based opioid stewardship program on high-risk opioid prescribing in a Canadian setting: an interrupted time series analysis.

Evaluation of a hospital-based opioid stewardship program on high-risk opioid prescribing in a Canadian setting: an interrupted time series analysis.

Background: High-risk opioid prescribing (e.g., high daily dose opioids, concurrent opioid-sedatives) is prevalent in hospitals and linked to adverse outcomes. Opioid stewardship programs (OSP) have the potential to reduce high-risk opioid prescribing through audit-and-feedback recommendations.

Methods: We evaluated an audit-and-feedback based OSP implemented in January 2020 at a Vancouver, Canada tertiary care hospital using interrupted time series analysis. An electronic health record (EHR) system with computerized provider order entry (CPOE) was simultaneously operationalized. The main outcome was: any high-risk opioid prescribing (based on 10 evidence-based indicators), including high daily dose of morphine milligram equivalent (MME) prescribing (> 90MME), long opioid prescription duration (> 5 days post-admission), and concurrent opioid-sedative prescribing.

Results: Between January 2018 and March 2022, 5,477 active opioid patient encounters were included. While no significant change occurred in overall high-risk opioid prescribing post-OSP (p > 0.05), a significant reduction was seen in the level of high daily dose of MME prescriptions (estimate: -0.044; 95% confidence interval [CI]: -0.082, -0.006). Conversely, the trend in long opioid duration increased (estimate: 0.006; 95%CI: 0.000, 0.011), likely due to the removal of automatic stop dates with the implementation of the EHR with CPOE. Post-OSP intervention, we initially saw an acute increase in concurrent opioid-sedative prescriptions (estimate: 0.013; 95%CI: 0.005, 0.020). A benzodiazepine ordering intervention implemented in May 2021 reversed this trend, reducing both the level (estimate: 0.874; 95%CI: 0.374, 1.375) and slope (estimate: -0.022, 95%CI: -0.034, -0.011) of concurrent prescriptions.

Conclusion: The implementation of a new EHR concordant with that of the OSP may have impacted our study's results. While our research suggests the OSP reduced high-dose opioid prescribing, other indicators impacted by the EHR system did not benefit as highly from the OSP. Nevertheless, the OSP proved able to rapidly respond to unintended consequences by introducing interventions to reduce concurrent opioid and sedative prescribing.

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来源期刊
Addiction Science & Clinical Practice
Addiction Science & Clinical Practice Psychology-Clinical Psychology
CiteScore
3.90
自引率
10.80%
发文量
64
审稿时长
28 weeks
期刊介绍: Addiction Science & Clinical Practice provides a forum for clinically relevant research and perspectives that contribute to improving the quality of care for people with unhealthy alcohol, tobacco, or other drug use and addictive behaviours across a spectrum of clinical settings. Addiction Science & Clinical Practice accepts articles of clinical relevance related to the prevention and treatment of unhealthy alcohol, tobacco, and other drug use across the spectrum of clinical settings. Topics of interest address issues related to the following: the spectrum of unhealthy use of alcohol, tobacco, and other drugs among the range of affected persons (e.g., not limited by age, race/ethnicity, gender, or sexual orientation); the array of clinical prevention and treatment practices (from health messages, to identification and early intervention, to more extensive interventions including counseling and pharmacotherapy and other management strategies); and identification and management of medical, psychiatric, social, and other health consequences of substance use. Addiction Science & Clinical Practice is particularly interested in articles that address how to improve the quality of care for people with unhealthy substance use and related conditions as described in the (US) Institute of Medicine report, Improving the Quality of Healthcare for Mental Health and Substance Use Conditions (Washington, DC: National Academies Press, 2006). Such articles address the quality of care and of health services. Although the journal also welcomes submissions that address these conditions in addiction speciality-treatment settings, the journal is particularly interested in including articles that address unhealthy use outside these settings, including experience with novel models of care and outcomes, and outcomes of research-practice collaborations. Although Addiction Science & Clinical Practice is generally not an outlet for basic science research, we will accept basic science research manuscripts that have clearly described potential clinical relevance and are accessible to audiences outside a narrow laboratory research field.
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