Clinical pharmacist intervention to ensure safe stimulant prescribing practices at a Veterans Affairs facility.

Bailey B Bass, Lacey J Vann
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Abstract

Introduction: The Psychotropic Drug Safety Initiative (PDSI) is a national Veterans Affairs program that recommends obtaining cardiovascular vital signs semiannually and urine toxicology screening annually for veterans prescribed stimulants. The PDSI also recommends a risk review of concurrent central nervous system (CNS) depressants to ensure the benefits of coadministration with stimulants outweigh the risks. This project's purpose was to evaluate the occurrence of coprescriptions for CNS depressants and stimulants and encourage compliance with the PDSI recommendations to increase safe and appropriate management of veterans prescribed the combination. This study aimed to evaluate the occurrence of coprescriptions for CNS depressants and stimulants, evaluate compliance with stimulant monitoring recommendations, and measure the proportion of pharmacist recommendations implemented by the prescriber.

Methods: This quality improvement project identified veterans with an outpatient prescription for a stimulant and any coprescription(s) for benzodiazepines, sedative-hypnotics, and/or opioids. A pharmacy intervention note was generated to request a risk review, provide recommendations for de-escalation, and notify the stimulant prescriber of overdue monitoring parameters. Impact was measured 60 days after intervention. Descriptive statistics and a McNemar test were used to compare preintervention and postintervention data.

Results: From the 61 patients included, there were 67 unique prescriptions for benzodiazepines (49.3%), sedative-hypnotics (34.3%), and opioids (16.4%) in combination with a stimulant. Pharmacist intervention resulted in de-escalation of coprescribing for 9 patients (16.1%) and was associated with statistically significant improvement in compliance to stimulant monitoring recommendations.

Discussion: Clinical pharmacists can assist in ensuring safe and appropriate monitoring and management of veterans prescribed stimulants.

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临床药剂师进行干预,确保退伍军人事务机构安全开具兴奋剂处方。
导言:精神药物安全倡议(PDSI)是一项全国性的退伍军人事务计划,该计划建议每半年为开具兴奋剂处方的退伍军人采集一次心血管生命体征,每年进行一次尿液毒理学筛查。PDSI 还建议对同时服用的中枢神经系统(CNS)抑制剂进行风险审查,以确保与兴奋剂合用的益处大于风险。该项目的目的是评估中枢神经系统抑制剂和兴奋剂并用处方的发生率,并鼓励遵守 PDSI 建议,以加强对开具这种并用处方的退伍军人进行安全、适当的管理。本研究旨在评估中枢神经系统抑制剂和兴奋剂联合处方的发生率,评估兴奋剂监测建议的依从性,并衡量处方者执行药剂师建议的比例:该质量改进项目确定了门诊处方为兴奋剂和苯二氮卓、镇静催眠药和/或阿片类药物的退伍军人。药房会生成一份干预说明,要求进行风险审查,提供降级建议,并通知兴奋剂处方者监测参数已逾期。干预 60 天后对效果进行测量。使用描述性统计和 McNemar 检验比较干预前和干预后的数据:结果:在纳入的 61 名患者中,苯二氮卓类药物(49.3%)、镇静催眠药(34.3%)和阿片类药物(16.4%)与兴奋剂合用的处方共有 67 个。在药剂师的干预下,9 名患者(16.1%)的联合处方有所减少,并且在统计意义上显著提高了对兴奋剂监测建议的依从性:讨论:临床药剂师可协助确保对退伍军人处方兴奋剂进行安全、适当的监测和管理。
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