San Francisco Veterans Affairs Health Care System, San Francisco, CA.
University of California, San Francisco, School of Pharmacy, San Francisco, CA.
Am J Health Syst Pharm. 2021 Feb 8;78(4):336-344. doi: 10.1093/ajhp/zxaa406.
Guidelines recommend evaluating the risk of opioid-related adverse events prior to initiating opioid therapy. The orthopedic service at San Francisco Veterans Affairs Health Care System (SFVHCS) has not routinely used risk assessment tools such as the Stratification Tool for Opioid Risk Mitigation, prescription drug monitoring program data, and urine drug screening prior to opioid prescribing. A quality improvement project was conducted to evaluate the number of pharmacist-provided opioid risk mitigation recommendations implemented by orthopedic providers for patients who underwent total hip or knee arthroplasty at SFVHCS.
A pharmacist-led workflow for completing risk mitigation reviews was developed in collaboration with orthopedic providers, and urine drug screening was added to the preoperative laboratory testing protocol. The following recommendations were communicated via electronic medical record: limit postoperative opioids to a 7- or 14-day supply based on risk of suicide and/or overdose, offer naloxone and a medication disposal bag, and order a urine drug screen if not already completed. Risk reviews were completed for 75 patients. Among 64 patients with 2-month postdischarge data available, 88% (7 of 8) of 7-day and 79% (44 of 56) of 14-day opioid supply recommendations were implemented; 41% (26 of 59) of recommendations to issue a medication disposal bag, 17% (2 of 12) recommendations to order a missing urine drug screen, and 9% (5 of 55) of recommendations to offer naloxone were implemented.
Pharmacist-performed risk mitigation reviews paired with individualized recommendations led to high rates of orthopedic provider acceptance of limiting postdischarge opioid day supplies for patients who had total hip or knee arthroplasty. Alternative strategies may increase access to naloxone. Future research should examine the impact of risk mitigation tools in reducing prescribing of long-term opioid therapy and adverse events among orthopedic surgical patients.
指南建议在开始阿片类药物治疗之前,评估与阿片类药物相关的不良事件风险。旧金山退伍军人事务医疗保健系统(SFVHCS)的骨科服务并未常规使用风险评估工具,如阿片类药物风险缓解分层工具、处方药物监测计划数据和尿液药物筛查,以进行阿片类药物处方之前。进行了一项质量改进项目,以评估在 SFVHCS 接受全髋关节或膝关节置换术的患者中,药师提供的阿片类药物风险缓解建议被骨科医生实施的数量。
药师主导的风险缓解审查工作流程是与骨科医生合作开发的,并在术前实验室检测方案中增加了尿液药物筛查。通过电子病历传达了以下建议:根据自杀和/或过量用药风险,将术后阿片类药物的供应限制在 7 天或 14 天;提供纳洛酮和药物处理袋;如果尚未完成,订购尿液药物筛查。共完成了 75 例患者的风险审查。在可获得 2 个月出院后数据的 64 例患者中,7 天供应建议中有 88%(7/8)和 14 天供应建议中有 79%(44/56)得到了实施;41%(26/59)的建议开出药物处理袋,17%(2/12)的建议开出缺少的尿液药物筛查,9%(5/55)的建议开出纳洛酮。
药师进行的风险缓解审查与个性化建议相结合,导致骨科医生接受为接受全髋关节或膝关节置换术的患者限制出院后阿片类药物日供应量的比例很高。替代策略可能会增加纳洛酮的可及性。未来的研究应研究风险缓解工具在减少骨科手术患者长期阿片类药物治疗和不良事件方面的作用。