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评估州级处方药监测计划(PDMP)和“药丸磨坊”对药品供应链中阿片类药物消费的影响。

Evaluating State-Level Prescription Drug Monitoring Program (PDMP) and Pill Mill Effects on Opioid Consumption in Pharmaceutical Supply Chain.

作者信息

Sahebi-Fakhrabad Amirreza, Sadeghi Amir Hossein, Handfield Robert

机构信息

Department of Industrial and Systems Engineering, North Carolina State University, Raleigh, NC 27606, USA.

Department of Business Management, Poole College of Management, North Carolina State University, 2806-A Hillsborough St. Building 217, Raleigh, NC 27695, USA.

出版信息

Healthcare (Basel). 2023 Feb 3;11(3):437. doi: 10.3390/healthcare11030437.

Abstract

The opioid crisis in the United States has had devastating effects on communities across the country, leading many states to pass legislation that limits the prescription of opioid medications in an effort to reduce the number of overdose deaths. This study evaluates the impact of two categories of PDMP and Pill Mill regulations on the supply of opioid prescriptions at the level of dispensers and distributors (excluding manufacturers) using ARCOS data. The study uses a difference-in-difference method with a two-way fixed design to analyze the data. The study finds that both of the regulations are associated with reductions in the volume of opioid distribution. However, the study reveals that these regulations may have unintended consequences, such as shifting the distribution of controlled substances to neighboring states. For example, in Tennessee, the implementation of Operational PDMP regulations reduces the in-state distribution of opioid drugs by 3.36% (95% CI, 2.37 to 4.3), while the out-of-state distribution to Georgia, which did not have effective PDMP regulations in place, increases by 16.93% (95% CI, 16.42 to 17.44). Our studies emphasize that policymakers should consider the potential for unintended distribution shifts of opioid drugs to neighboring states with laxer regulations as well as varying impacts on different dispenser types.

摘要

美国的阿片类药物危机对全国各社区造成了毁灭性影响,导致许多州通过立法限制阿片类药物的处方,以努力减少过量用药死亡人数。本研究利用美国处方药监控计划(PDMP)和药丸磨坊监管数据,评估了两类监管措施对配药者和经销商(不包括制造商)层面阿片类药物处方供应的影响。该研究采用双向固定设计的双重差分法来分析数据。研究发现,这两类监管措施都与阿片类药物分发量的减少有关。然而,研究表明这些监管措施可能会产生意想不到的后果,比如将受管制物质的分发转移到邻近州。例如,在田纳西州,实施操作性PDMP监管措施使该州阿片类药物的分发量减少了3.36%(95%置信区间,2.37至4.3),而向没有有效PDMP监管措施的佐治亚州的州外分发量增加了16.93%(95%置信区间,16.42至17.44)。我们的研究强调,政策制定者应考虑到阿片类药物向监管较宽松的邻近州意外转移分发的可能性,以及对不同配药类型的不同影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/772c/9914561/94a419b89272/healthcare-11-00437-g001.jpg

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