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美沙酮-药师合作在阿片类药物使用障碍患者管理中的作用:来自国家药物滥用治疗临床试验网络的多地点研究结果。

Buprenorphine physician-pharmacist collaboration in the management of patients with opioid use disorder: results from a multisite study of the National Drug Abuse Treatment Clinical Trials Network.

机构信息

Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.

Department of Medicine, Division of General Internal Medicine, Duke University School of Medicine, Durham, NC, USA.

出版信息

Addiction. 2021 Jul;116(7):1805-1816. doi: 10.1111/add.15353. Epub 2021 Jan 11.

Abstract

BACKGROUND AND AIMS

Physician and pharmacist collaboration may help address the shortage of buprenorphine-waivered physicians and improve care for patients with opioid use disorder (OUD). This study investigated the feasibility and acceptability of a new collaborative care model involving buprenorphine-waivered physicians and community pharmacists.

DESIGN

Nonrandomized, single-arm, open-label feasibility trial.

SETTING

Three office-based buprenorphine treatment (OBBT) clinics and three community pharmacies in the United States.

PARTICIPANTS

Six physicians, six pharmacists, and 71 patients aged ≥18 years with Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) OUD on buprenorphine maintenance.

INTERVENTION

After screening, eligible patients' buprenorphine care was transferred from their OBBT physician to a community pharmacist for 6 months.

MEASUREMENTS

Primary outcomes included recruitment, treatment retention and adherence, and opioid use. Secondary outcomes were intervention fidelity, pharmacists' use of prescription drug monitoring program (PDMP), participant safety, and satisfaction with treatment delivery.

FINDINGS

A high proportion (93.4%, 71/76) of eligible participants enrolled into the study. There were high rates of treatment retention (88.7%) and adherence (95.3%) at the end of the study. The proportion of opioid-positive urine drug screens (UDSs) among complete cases (i.e. those with all six UDSs collected during 6 months) at month 6 was (4.9%, 3/61). Intervention fidelity was excellent. Pharmacists used PDMP at 96.8% of visits. There were no opioid-related safety events. Over 90% of patients endorsed that they were "very satisfied with their experience and the quality of treatment offered," that "treatment transfer from physician's office to the pharmacy was not difficult at all," and that "holding buprenorphine visits at the same place the medication is dispensed was very or extremely useful/convenient." Similarly, positive ratings of satisfaction were found among physicians/pharmacists.

CONCLUSIONS

A collaborative care model for people with opioid use disorder that involves buprenorphine-waivered physicians and community pharmacists appears to be feasible to operate in the United States and have high acceptability to patients.

摘要

背景和目的

医生和药剂师的合作可能有助于解决具有豁免权的丁丙诺啡医生短缺的问题,并改善阿片类药物使用障碍(OUD)患者的护理。本研究调查了涉及具有豁免权的丁丙诺啡医生和社区药剂师的新协作护理模式的可行性和可接受性。

设计

非随机、单臂、开放标签可行性试验。

地点

美国的三个基于办公室的丁丙诺啡治疗(OBBT)诊所和三个社区药房。

参与者

六位医生、六位药剂师和 71 位年龄在 18 岁以上的符合《精神障碍诊断与统计手册》第五版(DSM-5)OUD 的患者,正在接受丁丙诺啡维持治疗。

干预措施

筛选后,合格患者的丁丙诺啡治疗将从他们的 OBBT 医生转移到社区药剂师,为期 6 个月。

测量

主要结果包括招募、治疗保留和依从性以及阿片类药物的使用。次要结果是干预的忠实度、药剂师对处方药物监测计划(PDMP)的使用、参与者的安全性以及对治疗交付的满意度。

结果

符合条件的参与者中有很高的比例(93.4%,71/76)入组了该研究。研究结束时,治疗保留率(88.7%)和依从性(95.3%)很高。在 6 个月期间收集的所有 6 个尿液药物筛查(UDS)中,完全案例(即接受 6 个月期间所有 6 次 UDS 检测的患者)中阿片类药物阳性 UDS 的比例为(4.9%,3/61)。干预的忠实度非常好。药剂师在 96.8%的就诊时使用 PDMP。没有阿片类药物相关的安全事件。超过 90%的患者表示“对他们的体验和所提供的治疗质量非常满意”,“将治疗从医生办公室转移到药房一点也不难”,“在发放药物的同一地点进行丁丙诺啡治疗非常或极其有用/方便”。同样,医生/药剂师也对满意度给予了积极评价。

结论

涉及具有豁免权的丁丙诺啡医生和社区药剂师的阿片类药物使用障碍患者协作护理模式在美国似乎可行,并且患者接受度很高。

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