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Effects of mandatory prescription drug monitoring program (PDMP) use laws on prescriber registration and use and on risky prescribing.强制性处方药物监测计划(PDMP)使用法规对开方者登记和使用以及高风险处方的影响。
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Internet-based vs. face-to-face cognitive behavior therapy for psychiatric and somatic disorders: an updated systematic review and meta-analysis.基于互联网的与面对面的认知行为疗法治疗精神和躯体障碍:一项更新的系统评价和荟萃分析。
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远程随机多中心临床试验设计考虑因素,评估接受阿片类药物治疗的慢性疼痛患者的电子健康自我管理计划。

Design considerations for a remote randomized multi-site clinical trial evaluating an e-health self-management program for chronic pain patients receiving opioid therapy.

机构信息

Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, 3131 Harvey Avenue, Cincinnati, OH 45229, USA; Center for Addiction Research, University of Cincinnati College of Medicine, 3230 Eden Avenue, Cincinnati, OH 45267, USA.

College of Nursing, Washington State University, 412 E. Spokane Falls Blvd., Spokane, WA 99202, USA.

出版信息

Contemp Clin Trials. 2021 Feb;101:106245. doi: 10.1016/j.cct.2020.106245. Epub 2020 Dec 10.

DOI:10.1016/j.cct.2020.106245
PMID:33309947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7954981/
Abstract

Based on the adverse consequences and inadequate evidence of effectiveness for long-term opioid therapy (LOT), the CDC developed recommendations to decrease the use of LOT and morphine equivalent dose (MED) for patients receiving LOT. However, the majority of these patients report that opioid medication is significantly beneficial for pain management and are hesitant to reduce/decrease its use. Compounding the problem is poor access to non-pharmacologic therapies for many patients due to insurance reimbursement structures and limited pain-service availability. EMPOWER is an intent-to-treat, two-arm, open-label, randomized controlled trial evaluating a web-based self-management chronic pain program (E-Health) that has been found to reduce self-reported MED, while also decreasing pain, in two randomized controlled trials. Approximately 400 chronic pain patients receiving LOT at a daily average prescribed MED ≥ 20 mg at one of two U.S. healthcare systems, located in North Carolina and Ohio, will be randomized in a 1:1 ratio to treatment as usual (TAU) or TAU plus E-Health (E-Health). TAU consists of LOT from a prescribing clinician. E-Health participants are provided with a 4-month E-Health subscription (active treatment phase). All participants will complete web-based self-report measures at baseline, the end of the active treatment phase, and 6-months post-active treatment. Opioid prescription information will be collected from the participants' electronic health record (EHR) from baseline through 6 months post-active treatment. This paper describes design considerations for this unique trial which is conducted completely remotely, with no in-person visits, and utilizes the EHR for participant identification and primary outcome collection.

摘要

基于长期阿片类药物治疗(LOT)的不良后果和有效性证据不足,CDC 制定了减少接受 LOT 和吗啡当量剂量(MED)的建议。然而,大多数患者报告称阿片类药物对疼痛管理有显著益处,他们不愿减少/减少其使用。由于保险报销结构和有限的疼痛服务可及性,许多患者难以获得非药物治疗,这使得问题更加复杂。EMPOWER 是一项意向治疗、双臂、开放标签、随机对照试验,评估了一种基于网络的自我管理慢性疼痛计划(E-Health),该计划已被发现可减少自我报告的 MED,同时在两项随机对照试验中还可减轻疼痛。大约 400 名在北卡罗来纳州和俄亥俄州的两个美国医疗保健系统中接受 LOT 治疗的慢性疼痛患者,每天平均处方 MED≥20mg,将按照 1:1 的比例随机分为常规治疗(TAU)或 TAU 加 E-Health(E-Health)。TAU 包括来自处方临床医生的 LOT。E-Health 参与者将获得为期 4 个月的 E-Health 订阅(主动治疗阶段)。所有参与者将在基线、主动治疗阶段结束和主动治疗后 6 个月完成基于网络的自我报告测量。从基线到主动治疗后 6 个月,将从参与者的电子健康记录(EHR)中收集阿片类药物处方信息。本文介绍了这项独特试验的设计考虑因素,该试验完全在远程进行,没有面对面访问,并且利用 EHR 进行参与者识别和主要结果收集。