UCLA School of Law, Los Angeles, California.
NBER, Cambridge, Massachusetts.
Health Serv Res. 2021 Apr;56(2):268-274. doi: 10.1111/1475-6773.13548. Epub 2020 Sep 2.
To develop a legal research protocol for identifying various measures of prescription drug monitoring program (PDMP) start dates, apply the protocol to create a useable PDMP database, and test whether the different legal databases that are meant to contain the same information produce divergent results when used in an illustrative empirical exercise.
Original research from state statutes, regulations, policy statements, and interviews; alternative PDMP data from the National Alliance for Model State Drug Laws and Prescription Drug Abuse Policy System; claims from a 40 percent random sample of Medicare beneficiaries, 2006-2014.
Collaborative research effort among a group of lawyers to develop protocol. Legal research to produce an original database of dates state PDMP laws: (a) were enacted, (b) became operational, and (c) required query before prescribing controlled substances. Descriptive analyses characterize differences in dates of enactment, operation, and must query requirements. Regression analyses estimating, for each beneficiary annually any opioid prescription received in a calendar year, among other measures. Estimates conducted on under age 65 and full Medicare population.
DATA COLLECTION/EXTRACTION METHODS: PDMP legal databases were linked to annual Medicare claims.
An original database differs from commonly used, publicly available data. Outcomes tested depend on the measure of PDMP date used and differ by data source. Must-query laws show the largest effects among all the laws tested.
Data choices likely have had large consequences for study results and may explain contradictory outcomes in prior research. Researchers must understand and report protocol for dates used in PDMP research to ensure that results are internally consistent and verifiable.
制定一项法律研究方案,以确定各种处方药监测计划(PDMP)启动日期的衡量标准,应用该方案创建一个可用的 PDMP 数据库,并测试旨在包含相同信息的不同法律数据库在一个说明性的实证研究中是否会产生不同的结果。
州法规、规章、政策声明和访谈中的原始研究;国家模型州药物法联盟和处方药物滥用政策系统中的替代 PDMP 数据;2006 年至 2014 年,对 Medicare 受益人的 40%随机样本的索赔。
一群律师之间的合作研究,以制定方案。法律研究产生了一个原始的州 PDMP 法律日期数据库:(a)颁布日期,(b)生效日期,(c)规定在开控药物之前必须查询。描述性分析描述了颁布、生效和必须查询要求日期的差异。回归分析估计了每年每个受益人在日历年收到的任何阿片类药物处方,以及其他措施。在 65 岁以下和完全 Medicare 人群中进行估计。
数据收集/提取方法:PDMP 法律数据库与年度 Medicare 索赔相关联。
原始数据库与常用的公开可用数据不同。测试的结果取决于使用的 PDMP 日期衡量标准,并且因数据源而异。必须查询的法律在所有测试的法律中显示出最大的效果。
数据选择可能对研究结果产生了重大影响,并且可能解释了先前研究中相互矛盾的结果。研究人员必须了解并报告 PDMP 研究中使用的日期方案,以确保结果具有内部一致性和可验证性。