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CTN-0138:基于社区药店的处方药物监测计划阿片类药物风险评估工具的改编、实施和整群随机试验 - 方案论文。

CTN-0138: adaptation, implementation, and cluster randomized trial of a Community Pharmacy-Based Prescription Drug Monitoring Program Opioid Risk Assessment Tool-a protocol paper.

机构信息

Department of Internal Medicine, University of Utah, Salt Lake City, UT, USA.

Department of Psychological Sciences, Purdue University, West Lafayette, IN, USA.

出版信息

Addict Sci Clin Pract. 2024 Nov 18;19(1):82. doi: 10.1186/s13722-024-00514-1.

Abstract

BACKGROUND

As the opioid epidemic continues to have a major negative impact across the US, community pharmacies have come under scrutiny from legal systems attempting to hold them accountable for their role in over dispensing and lack of patient intervention. While the most available tool for monitoring patients' opioid use is Prescription Drug Monitoring Programs (PDMP), these do not provide pharmacists with actionable information and decision support. Our study addresses this gap through three objectives: [1] incorporate validated opioid risk metric thresholds into a PDMP platform to create the Opioid Risk Reduction Clinical Decision Support (ORRCDS) tool; [2] assess ORRCDS' ability to reduce patient opioid risk; [3] assess ORRCDS' sustainability and viability for broader dissemination in community pharmacy.

METHODS

For objective 1, our team is partnering with leadership from the largest US PDMP organization and a top-five pharmacy chain to implement ORRCDS into the pharmacy chain's workflow following the Guideline Implementation with Decision Support (GUIDES) framework. For objective 2, our team will conduct a type-1 implementation mixed methods study using a 2-arm parallel group clustered randomized design. We anticipate enrolling ~ 6,600 patients with moderate and high opioid use risk during the 6-month enrollment phase across 80 pharmacies. This sample size will provide 96.3% power to detect a 5% or greater difference in responder rate between the intervention and control arm. Responders are patients with moderate-risk at baseline who reduce to low-risk or those with high-risk at baseline who reduce to moderate or low-risk at 180 days post last intervention. To accomplish objective 3, we will use the Consolidated Framework for Implementation Research (CFIR) to develop and execute cross-sectional qualitative interviews with pharmacists (n = 15), pharmacy leaders (n = 15), and PDMP leaders (n = 15) regarding long term adoption and sustainability of the ORRCDS tool.

CONCLUSIONS

A PDMP tool that addresses moderate- and high-risk opioid use is not available in community pharmacy. This study will implement ORRCDS in a large retail pharmacy chain that will include additional screening and guidance to pharmacy staff to address risky opioid medication use. Our results will make critical advancements for protecting patient health and addressing the opioid epidemic.

摘要

背景

随着阿片类药物泛滥在美国持续产生重大负面影响,社区药店受到法律系统的审查,试图追究他们在过度配药和缺乏患者干预方面的责任。虽然监测患者阿片类药物使用情况的最有效工具是处方药物监测计划(PDMP),但这些计划并不能为药剂师提供可行的信息和决策支持。我们的研究通过三个目标来解决这一差距:[1] 将经过验证的阿片类药物风险度量阈值纳入 PDMP 平台,创建阿片类药物风险降低临床决策支持(ORRCDS)工具;[2] 评估 ORRCDS 降低患者阿片类药物风险的能力;[3] 评估 ORRCDS 在社区药店更广泛传播的可持续性和可行性。

方法

为实现目标 1,我们的团队正在与美国最大的 PDMP 组织和前五大连锁药店的领导层合作,按照指南实施与决策支持(GUIDES)框架将 ORRCDS 纳入药店的工作流程。为实现目标 2,我们的团队将使用 2 臂平行组聚类随机设计进行 1 型实施混合方法研究。我们预计将在 6 个月的入组阶段,在 80 家药店中招募约 6600 名中高度阿片类药物使用风险的患者。这个样本量将有 96.3%的能力检测到干预组和对照组之间应答率的差异在 5%或更大。应答者是基线中度风险患者,降至低风险或基线高风险患者,在最后一次干预后 180 天降至中或低风险。为了实现目标 3,我们将使用整合实施研究框架(CFIR),对药剂师(n=15)、药店领导(n=15)和 PDMP 领导(n=15)进行跨部门定性访谈,了解 ORRCDS 工具的长期采用和可持续性。

结论

社区药店没有用于中高度阿片类药物使用风险的 PDMP 工具。本研究将在一家大型零售连锁药店实施 ORRCDS,该药店将包括对药店工作人员的额外筛查和指导,以解决危险的阿片类药物使用问题。我们的研究结果将为保护患者健康和解决阿片类药物泛滥问题做出重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2aa/11572521/5620bd4333e2/13722_2024_514_Fig1_HTML.jpg

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