Evaluation of Interprofessional Quality Improvement Interventions Led by an Ambulatory Care Pharmacist on Adherence to a Controlled Substance Agreement Policy.

Innovations in Pharmacy Pub Date : 2023-10-10 eCollection Date: 2023-01-01 DOI:10.24926/iip.v14i2.5464
Insaf Mohammad, Sarah Alsomairy, Mona Mawari, Mohamad Elabdallah, Ruaa Elteriefi, Julie George
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Abstract

Background: A controlled substance agreement (CSA) is a risk mitigation strategy for patients managed on controlled substance medications such as opioids and benzodiazepines. Limited literature exists to describe the role of the clinic pharmacy team to promote adherence to CSA monitoring parameters. Objective: The objective of this study is to evaluate the impact of interprofessional educational and clinical interventions led by an ambulatory care pharmacist on adherence to monitoring parameters within a CSA policy. Methods: This retrospective observational study included patients on long-term controlled substances who had a clinic visit every 3 months during the study period. The primary outcomes were the proportion of patients with a signed CSA in the electronic medical record (EMR), urine drug screen (UDS) completion, and documentation of review of the statewide prescription drug monitoring program (PDMP) in the EMR 8 months prior to as compared to 8 months after implementation of pharmacist interventions. Results: Among 79 patients (mean age 55.7 years, 65.8% female, 54.4% African American), 8.9% pre- vs 88.6% post-interventions had a signed CSA (p<0.001), 35.4% pre- vs 65.8% post-interventions had a UDS completed (p<0.001), and 32.9% pre- vs 57% post-interventions had documentation of PDMP review (p=0.002). Conclusion: Adherence to monitoring parameters within a CSA policy significantly improved after educational and clinical interventions led by an ambulatory care pharmacist.

由门诊药剂师领导的跨专业质量改进干预措施对受控物质协议政策依从性的评估。
背景:受控物质协议(CSA)是一种风险缓解策略,适用于使用阿片类药物和苯二氮卓类药物等受控物质药物的患者。有限的文献描述了临床药学团队在促进CSA监测参数依从性方面的作用。目的:本研究的目的是评估由门诊护理药剂师领导的跨专业教育和临床干预对依从CSA政策内监测参数的影响。方法:本回顾性观察性研究纳入长期服用控制药物的患者,在研究期间每3个月就诊一次。主要结果是在电子病历(EMR)中签署CSA的患者比例,尿药筛查(UDS)完成情况,以及在实施药师干预前8个月与实施药师干预后8个月的EMR中对全州处方药监测计划(PDMP)的审查文件。结果:79例患者(平均年龄55.7岁,65.8%女性,54.4%非洲裔美国人)中,8.9%干预前和88.6%干预后签署了CSA(结论:在门诊护理药剂师领导的教育和临床干预后,CSA政策内监测参数的依从性显著提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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