加拿大安大略省公共分配呼吸吸入器的成本和使用趋势:一项重复的横断面研究。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Ria Garg, Tianru Wang, Mina Tadrous, Tony Antoniou, Tara Gomes
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引用次数: 0

摘要

目的:几种新的呼吸吸入器最近进入市场,包括联合治疗产品和通用替代品。因此,我们调查了加拿大安大略省公共分配呼吸吸入器的成本和使用情况,以及新市场进入者对这些趋势的影响。方法:我们对2003年1月1日至2023年3月31日期间发放呼吸吸入器的省级药物计划受益人进行了重复横断面研究。我们估计每个受益人每季度在呼吸吸入器上的支出,定义为呼吸吸入器报销成本(2022加元)除以分配呼吸吸入器的受益人数量。采用连接点回归模型来表征趋势变化。结果:从2003年第一季度到2023年第一季度,公共支付者支出增长了160%(从26 206 322美元增长到68 054 816美元),而发放呼吸吸入器的受益人人数增加了92%(从155 893美元增长到299 418美元)。ICS/LABA吸入器的报销占成本的一半(2023年第一季度为33 844 484美元)。每个受益人支出的趋势有六个连接点,其中有季度费用增加和减少的时期。在2003年至2015年期间,每个受益人的支出增加,在2015年第一季度达到248美元/受益人。2015年第二季度,这一趋势首次下降,并持续下降至2018年第二季度(206美元/受益人)。这一趋势在2018年第三季度之后再次上升,并在2019年第三季度达到平稳水平(216美元/受益人)。结论:2015年第二季度,联合治疗吸入器(即LAMA/LABA)的公开处方清单与人均呼吸吸入器支出的显著下降相吻合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trends in the Cost and Utilization of Publicly Dispensed Respiratory Inhalers in Ontario, Canada: A Repeated Cross-Sectional Study.

Purpose: Several new respiratory inhalers have recently entered the market, including combination therapy products and generic alternatives. Therefore, we examined the cost and utilization of publicly dispensed respiratory inhalers in Ontario, Canada, and the impact of new market entrants on these trends.

Methods: We conducted a repeated cross-sectional study among provincial drug program beneficiaries dispensed a respiratory inhaler between January 1, 2003, and March 31, 2023. We estimated per-beneficiary spending on respiratory inhalers per quarter, defined as the cost (2022 Canadian dollars) of respiratory inhalers reimbursement divided by the number of beneficiaries dispensed a respiratory inhaler. Joinpoint regression models were used to characterize changes in the trend.

Results: Between Q1 of 2003 and Q1 of 2023, public payer spending rose 160% ($26 206 322 to $68 054 816), while the number of beneficiaries dispensed a respiratory inhaler increased 92% (155 893 to 299 418). Reimbursement of ICS/LABA inhalers accounted for half the cost ($33 844 484 in Q1 of 2023). The trend for per-beneficiary spending was marked by six joinpoints, with periods of increasing and decreasing quarterly costs. Between 2003 and 2015, per-beneficiary spending increased, reaching $248/beneficiary in Q1 of 2015. In Q2 of 2015, the trend decreased for the first time and continued to decline until Q2 of 2018 ($206/beneficiary). The trend increased again after Q3 of 2018 and reached a plateau in Q3 of 2019 ($216/beneficiary).

Conclusions: Public formulary listing of combination therapy inhalers, namely LAMA/LABA in Q2 of 2015, coincided with a significant decline in per-beneficiary spending on respiratory inhalers.

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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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