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应对因 COVID-19 公共卫生紧急事件而导致的监管变化,丁丙诺啡的处方和治疗可及性。

Buprenorphine prescribing and treatment accessibility in response to regulation changes due to the COVID-19 public health emergency.

机构信息

Substance Use Epidemiology Program, Center for Health Data Analysis, Rhode Island Department of Health, Providence, RI, USA.

Department of Emergency Medicine, Alpert Medical School of Brown University, Providence, RI, USA.

出版信息

J Subst Use Addict Treat. 2024 Jul;162:209382. doi: 10.1016/j.josat.2024.209382. Epub 2024 Apr 25.

Abstract

BACKGROUND

In 2021, over 80,000 fatal overdoses occurred in the United States. Since 2020, the federal government has enacted multiple regulatory changes around buprenorphine prescribing for opioid use disorder (OUD) to increase access to buprenorphine. This study aims to explore trends in buprenorphine treatment initiation pre- and post-public health emergency to evaluate changes in the context of X-waiver relaxations and telehealth allowances.

METHODS

In a cross-sectional study, all RI residents who filled a buprenorphine prescription at a pharmacy in Rhode Island (RI), Massachusetts, and Connecticut between January 2017 and December 2023 were obtained from the RI Prescription Drug Monitoring Program (PDMP). The study excluded buprenorphine products not approved for OUD treatment from the analysis. Identified individuals had initiated buprenorphine for OUD during the study period if they did not have a prior prescription or if they had >30 days without buprenorphine exposure between their prescriptions. Spearman's rank correlation tests were used to identify significant associations between outcomes and regulation changes.

RESULTS

The average number of patients dispensed buprenorphine did not significantly change over the study period, however the average number of initiates significantly decreased (ρ = -0.38255, p = .0003). The average number of providers prescribing CII-CV substances in RI has increased 3.4 % over the study period. The average percentage of prescribers in the PDMP prescribing buprenorphine for OUD doubled (ρ = 0.96075, p < .0001).

CONCLUSION

Though efforts have been made to increase buprenorphine initiation, buprenorphine initiates remain well below pre-PHE levels. Efforts must continue to eliminate existing barriers to treatment and improve access to individuals seeking treatment.

摘要

背景

2021 年,美国有超过 8 万人死于过量用药。自 2020 年以来,联邦政府围绕阿片类药物使用障碍(OUD)的丁丙诺啡处方制定了多项监管规定变更,以增加丁丙诺啡的可及性。本研究旨在探讨公共卫生紧急事件前后丁丙诺啡治疗启动的趋势,以评估 X 豁免放宽和远程医疗许可的背景下的变化。

方法

在一项横断面研究中,从罗德岛州处方药物监测计划(PDMP)中获取了 2017 年 1 月至 2023 年 12 月期间在罗德岛州、马萨诸塞州和康涅狄格州的一家药房领取丁丙诺啡处方的所有罗德岛居民。本研究将未经批准用于 OUD 治疗的丁丙诺啡产品排除在分析之外。如果患者在研究期间没有之前的处方,或者他们在处方之间有超过 30 天没有丁丙诺啡暴露,那么他们被认为是开始丁丙诺啡治疗 OUD。使用 Spearman 等级相关检验来确定结果与监管变化之间的显著关联。

结果

研究期间,配发丁丙诺啡的患者数量平均没有显著变化,但启动人数明显减少(ρ=-0.38255,p=0.0003)。在研究期间,罗德岛州开具 CII-CV 物质的医生数量增加了 3.4%。PDMP 中开具丁丙诺啡治疗 OUD 的医生比例增加了一倍(ρ=0.96075,p<0.0001)。

结论

尽管已经做出努力来增加丁丙诺啡的启动,但丁丙诺啡的启动人数仍远低于公共卫生紧急事件前的水平。必须继续努力消除治疗障碍,并改善寻求治疗的个人的治疗途径。

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