Steuart Shelby R
University of Chicago, Chicago, Illinois, USA.
Health Econ. 2025 Feb;34(2):283-296. doi: 10.1002/hec.4911. Epub 2024 Nov 4.
To date, there is considerable evidence of the medical applications of cannabis, however concerns regarding the safety of cannabis are also mounting. To improve the safety of cannabis, nine states have added medical cannabis to their state PDMPs, helping providers to take patient cannabis use into consideration when making prescribing decisions. Across a variety of models using Medicaid State Drug Utilization claims data, I find statistically significant reductions in severely and moderately contraindicated medication fills across two outcomes. In my main specification, adding cannabis to a state PDMP is associated with a 14.4% (p < 0.01) and 7.74% (p < 0.001) decrease in the units per prescription, for severely and moderately contraindicated medications, respectively, as compared to states with legal medical cannabis dispensaries open. An interesting spillover effect of adding cannabis to PDMPs is an apparent decrease in the prescribing of scheduled narcotics, with Schedule II medications seeing a moderately significant decrease and Schedule IV medications seeing a 11.4% decrease (p < 0.01) in the prescribing rate and a 16.2% decrease (p < 0.001) in the units per prescription. The main analysis was conducted using the Borusyak et al. (2023) Imputation Estimator with a robustness check using the Callaway and Sant'Anna (2021) difference-in-difference. This work presents evidence that adding cannabis to a state PDMP impacts provider prescribing decisions involving medications that are contraindicated for use with cannabis as well as controlled substances. This paper demonstrates that adding cannabis to PDMPs influences prescribing and thus has the potential to make medical cannabis use safer. Conversely, this work indicates providers may have bias against patients who use cannabis and deny them life-improving medications (like controlled ADHD medication or opioids) on the basis of medical cannabis use. This paper also contributes to the literature comparing DD outcomes estimated using Borusyak, Jaravel, and Spiess' (2023) Imputation Estimator and Callaway and Sant'Anna's (2021) DD Estimator.
迄今为止,有大量证据表明大麻具有医学应用价值,然而,对大麻安全性的担忧也在不断增加。为提高大麻的安全性,九个州已将医用大麻纳入其州处方药品监测计划(PDMP),帮助医疗服务提供者在做出处方决定时考虑患者使用大麻的情况。在使用医疗补助州药物利用索赔数据的各种模型中,我发现两个结果中严重和中度禁忌药物的配药数量在统计上有显著减少。在我的主要规范中,与有合法医用大麻药房开业的州相比,将大麻纳入州PDMP与严重和中度禁忌药物的每张处方单位数分别减少14.4%(p<0.01)和7.74%(p<0.001)相关。将大麻纳入PDMP的一个有趣的溢出效应是,处方类麻醉药品的处方量明显减少,其中II类药物的处方量有中度显著下降,IV类药物的处方率下降11.4%(p<0.01),每张处方单位数下降16.2%(p<0.001)。主要分析使用了博鲁西亚克等人(2023年)的插补估计器,并使用卡拉韦和圣安娜(2021年)差异中的差异进行了稳健性检验。这项工作提供了证据,表明将大麻纳入州PDMP会影响医疗服务提供者涉及与大麻或管制物质禁忌使用的药物的处方决定。本文表明,将大麻纳入PDMP会影响处方,因此有可能使医用大麻的使用更安全。相反,这项工作表明医疗服务提供者可能对使用大麻的患者存在偏见,并基于患者使用医用大麻而拒绝给他们开改善生活的药物(如治疗多动症的管制药物或阿片类药物)。本文还为比较使用博鲁西亚克、贾拉韦和斯皮斯(2023年)的插补估计器和卡拉韦与圣安娜(2021年)的差异估计器估计的差异中的差异结果的文献做出了贡献。