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美国卫生系统支出年度预估更新:基于全国假设性纳洛酮共同开方强制令。

Updated Estimates of Annual U.S. Health System Spending from a Hypothetical National Naloxone Co-Prescribing Mandate.

机构信息

Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

出版信息

Subst Use Misuse. 2023;58(13):1707-1713. doi: 10.1080/10826084.2023.2244065. Epub 2023 Aug 23.

Abstract

Naloxone-prescription opioid co-prescribing mandates have increasingly been proposed and adopted in the U.S., at both the national and state levels, as a public health intervention for mitigating the impacts of opioid overdoses. In this study, we assess whether a hypothetical national, naloxone co-prescribing mandate has become less costly for the U.S. health system since 2018. We expand and update an existing economic model of naloxone co-prescribing to estimate annual health system spending. We refresh the model inputs through 2021 to reflect changes to the opioid and naloxone landscapes, expand the model to account for more types of market responses, and develop additional scenarios around alternate implementation strategies such as bulk purchasing. We estimate annual spending increases across all retail opioid patients of $1.4-$4.0 billion with naloxone nasal sprays and auto-injectors, and $0.6-$0.9 billion with traditional injectable naloxone formulations. We also find that bulk purchasing could lead to higher spending increases in some patient populations absent volume discounts. Our estimates are substantially lower than prior research. Key drivers include lower prices for naloxone, higher current naloxone distribution, a longer approved shelf life for naloxone, and lower estimated sizes for some patient populations. Additional research is needed to estimate the potential benefits of naloxone co-prescribing for mitigating opioid overdoses, and whether they could outweigh spending increases. Steps that could make this policy more beneficial or less costly include targeting higher risk patient populations and promoting large-scale purchasing agreements with volume discounts to help offset potential price increases.

摘要

纳洛酮处方阿片类药物共同处方的规定在美国越来越多地被提出并被采纳,无论是在国家层面还是州层面,作为减轻阿片类药物过量影响的公共卫生干预措施。在这项研究中,我们评估了自 2018 年以来,美国卫生系统实施全国性纳洛酮共同处方规定的成本是否降低了。我们扩展和更新了现有的纳洛酮共同处方经济模型,以估计年度卫生系统支出。我们通过 2021 年更新模型输入,以反映阿片类药物和纳洛酮领域的变化,扩展模型以考虑更多类型的市场反应,并围绕替代实施策略(如批量采购)开发其他方案。我们估计,所有零售阿片类药物患者的年度支出增加了 14 亿至 40 亿美元,用于纳洛酮鼻喷雾剂和自动注射器,以及 6 亿至 9 亿美元,用于传统的可注射纳洛酮制剂。我们还发现,在没有数量折扣的情况下,批量采购可能会导致某些患者群体的支出增加更高。我们的估计值远低于之前的研究。主要驱动因素包括纳洛酮价格降低、当前纳洛酮分布增加、纳洛酮批准的保质期延长,以及某些患者群体的估计规模降低。需要进一步研究以估计纳洛酮共同处方减轻阿片类药物过量的潜在益处,以及它们是否超过支出增加。可以使这项政策更有利或成本更低的措施包括针对高风险患者群体,以及促进有数量折扣的大规模采购协议,以帮助抵消潜在的价格上涨。

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