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目标保险公司强制处方监测对阿片类药物处方模式的影响。

The effect of targeted insurer-mandated prescription monitoring on opioid prescribing patterns.

出版信息

J Am Pharm Assoc (2003). 2020 Jul-Aug;60(4):559-564. doi: 10.1016/j.japh.2019.12.019. Epub 2020 Feb 6.

DOI:10.1016/j.japh.2019.12.019
PMID:32033899
Abstract

OBJECTIVES

The purpose of this study was to determine the impact of a mandate from 2 large insurers in South Carolina for mandatory review of the state's prescription drug monitoring program (PDMP) for controlled substance (CS) prescriptions for more than 5 days' supply on the proportion of opioid prescriptions for less than or equal to 5 days in a statewide adult population. In addition, changes in the mean morphine milligram equivalents (MME) per day for prescriptions for 5 days or less were described to evaluate prescribing changes.

DESIGN, SETTING AND PARTICIPANTS: All prescriptions for opioids written for and filled by adults (≥ 18 years of age) and reported to the PDMP from January 1, 2010, to December 31, 2017, were included in an interrupted time series analysis.

OUTCOME MEASURES

An interrupted time series analysis was performed to determine if there was a significant change in the proportion of opioid prescriptions for less than or equal to 5 days' supply.

RESULTS

Overall opioid prescriptions decreased over the time period by 11.5%, including a decreasing rate of opioid prescriptions for less than or equal to 5 days' supply. There was no statistical difference in the slope between the pre- and postmandate cohorts (P = 0.077, r = 0.951). There was not an identified corresponding increase in the MME per day of prescriptions.

CONCLUSION

Our analysis found that 2 major insurer mandates that occurred in South Carolina in 2016, which required a review of the state PDMP for CS prescriptions for more than 5 days' supply, did not have a significant impact on the proportion of opioid prescriptions for less than or equal to 5 days' supply in the statewide population. In addition, we did not find any concern that prescribers attempted to circumvent the requirement by inappropriately adjusting dosing instructions.

摘要

目的

本研究旨在确定南卡罗来纳州 2 家大型保险公司发布的一项授权要求对全州范围内成年人中少于或等于 5 天供应量的阿片类药物处方比例的影响。该授权要求对超过 5 天供应量的受控物质(CS)处方进行强制性审查。此外,还描述了少于或等于 5 天处方的平均吗啡毫克当量(MME)每日剂量的变化,以评估处方变化。

设计、设置和参与者:纳入了从 2010 年 1 月 1 日至 2017 年 12 月 31 日向 PDMP 报告的所有由成年人(≥ 18 岁)开具和配药的阿片类药物处方,并进行了中断时间序列分析。

结果

进行了中断时间序列分析,以确定少于或等于 5 天供应量的阿片类药物处方比例是否发生显著变化。

结论

我们的分析发现,2016 年南卡罗来纳州的 2 项主要保险公司授权要求,即要求审查 CS 处方的州 PDMP,以确保超过 5 天供应量,对全州人口中少于或等于 5 天供应量的阿片类药物处方比例没有显著影响。此外,我们没有发现任何迹象表明医生试图通过不恰当地调整剂量说明来规避这一要求。

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