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高剂量阿片类药物处方用于急性疼痛患者:评估美国州阿片类药物政策的影响。

High-Dose Opioid Prescribing in Individuals with Acute Pain: Assessing the Effects of US State Opioid Policies.

机构信息

School of Public Policy, Georgia Institute of Technology, Atlanta, GA, USA.

School of Public Health, Department of Health Management and Policy, University of Michigan, Ann Arbor, MI, USA.

出版信息

J Gen Intern Med. 2024 Nov;39(14):2689-2697. doi: 10.1007/s11606-024-08947-9. Epub 2024 Jul 19.

Abstract

BACKGROUND

How state opioid policy environments with multiple concurrent policies affect opioid prescribing to individuals with acute pain is unknown.

OBJECTIVE

To examine how prescription drug monitoring programs (PDMPs), pain management clinic regulations, initial prescription duration limits, and mandatory continued medical education affected total and high-dose prescribing.

DESIGN

A county-level multiple-policy difference-in-difference event study framework.

SUBJECTS

A total of 2,425,643 individuals in a large national commercial insurance deidentified claims database (aged 12-64 years) with acute pain diagnoses and opioid prescriptions from 2007 to 2019.

MAIN MEASURES

The total number of acute pain opioid treatment episodes and number of episodes containing high-dose (> 90 morphine equivalent daily dosage (MEDD)) prescriptions.

KEY RESULTS

Approximately 7.5% of acute pain episodes were categorized as high-dose episodes. Prescription duration limits were associated with increases in the number of total episodes; no other policy was found to have a significant impact. Beginning five quarters after implementation, counties in states with pain management clinic regulations experienced a sustained 50% relative decline in the number of episodes containing > 90 MEDD prescriptions (95 CIs: (Q5: - 0.506, - 0.144; Q12: - 1.000, - 0.290)). Mandated continuing medical education regarding the treatment of pain was associated with a 50-75% relative increase in number of high-dose episodes following the first year-and-a-half of enactment (95 CIs: (Q7: 0.351, 0.869; Q12: 0.413, 1.107)). Initial prescription duration limits were associated with an initial relative reduction of 25% in high-dose prescribing, with the effect increasing over time (95 CI: (Q12: - 0.967, - 0.335). There was no evidence that PDMPs affected high-dose opioids dispensed to individuals with acute pain. Other high-risk prescribing indicators were explored as well; no consistent policy impacts were found.

CONCLUSIONS

State opioid policies may have differential effects on high-dose opioid dispensing in individuals with acute pain. Policymakers should consider effectiveness of individual policies in the presence of other opioid policies to address the ongoing opioid crisis.

摘要

背景

目前尚不清楚同时存在多项政策的州级阿片类药物政策环境会如何影响急性疼痛患者的阿片类药物处方。

目的

研究药品监测计划(PDMP)、疼痛管理诊所法规、初始处方持续时间限制和强制性继续教育如何影响总剂量和高剂量处方。

设计

县一级多政策差异差异事件研究框架。

研究对象

来自大型全国商业保险匿名索赔数据库的 2425643 名患有急性疼痛诊断和阿片类药物处方的个体(年龄在 12-64 岁之间),时间范围为 2007 年至 2019 年。

主要措施

急性疼痛阿片类药物治疗发作的总次数和包含高剂量(>90 吗啡当量日剂量(MEDD))处方的发作次数。

主要结果

约 7.5%的急性疼痛发作被归类为高剂量发作。处方持续时间限制与总发作次数的增加有关;没有发现其他政策有显著影响。从实施后的第五个季度开始,实施疼痛管理诊所法规的州的县经历了含有>90 MEDD 处方的发作次数持续减少 50%(95%CI:(Q5:-0.506,-0.144;Q12:-1.000,-0.290))。强制性继续教育治疗疼痛与实施后的第一年半后高剂量发作次数增加 50-75%相关(95%CI:(Q7:0.351,0.869;Q12:0.413,1.107))。初始处方持续时间限制与高剂量处方的初始相对减少 25%相关,随着时间的推移,这种影响逐渐增加(95%CI:(Q12:-0.967,-0.335))。没有证据表明 PDMP 会影响急性疼痛患者的高剂量阿片类药物的发放。还探讨了其他高危处方指标,但没有发现一致的政策影响。

结论

州级阿片类药物政策可能对急性疼痛患者的高剂量阿片类药物处方产生不同的影响。政策制定者在解决持续存在的阿片类药物危机时,应考虑在存在其他阿片类药物政策的情况下个别政策的有效性。

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本文引用的文献

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The state of the science in opioid policy research.阿片类药物政策研究的科学现状。
Drug Alcohol Depend. 2020 Sep 1;214:108137. doi: 10.1016/j.drugalcdep.2020.108137. Epub 2020 Jun 27.

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