Billing Deprescribing Interventions: Portrait of an Initiative in Québec, Canada

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Alexandre Campeau Calfat, Maude Gosselin, Caroline Sirois
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Abstract

Background

Deprescribing is a patient-centred process in which a healthcare professional reduces or stops medications to improve health outcomes. Since late 2022, community pharmacists in Québec, Canada, have been able to bill for deprescribing interventions, enabling more robust deprescribing research in large cohort studies.

Objective

This study aimed to assess the prevalence of deprescribing claims in Québec community pharmacies from January 1, 2023, to November 30, 2024, and to identify the most commonly deprescribed medication classes.

Methods

We analysed the total number of deprescribing claims submitted by pharmacists during this period and categorized deprescribed medications using the American Hospital Formulary Service classification.

Findings

Over 90 000 claims were submitted for deprescribing interventions, with most involving central nervous system medications. Although the number of claims increased over time, the overall volume remained modest.

Conclusion

While limitations remain, such as the gradual adoption of billing interventions, Québec's reimbursement model for deprescribing interventions provides an important framework for research, offering a mechanism to study deprescribing in real-world settings.

Abstract Image

开单、减少处方干预:加拿大quacimbec的一项倡议
开处方是一个以患者为中心的过程,在这个过程中,医疗保健专业人员减少或停止使用药物以改善健康结果。自2022年底以来,加拿大quacimbec的社区药剂师已经能够为处方减少干预措施收费,从而能够在大型队列研究中进行更有力的处方减少研究。目的评估2023年1月1日至2024年11月30日曲海社区药店的处方主张患病率,并确定最常开处方的药物类别。方法分析药师在此期间提交的减处方索赔总数,并使用美国医院处方服务分类对减处方药物进行分类。调查结果:超过9万份要求减少处方干预的索赔,其中大多数涉及中枢神经系统药物。尽管索赔的数量随着时间的推移而增加,但总体数量仍然不大。尽管存在局限性,如计费干预措施的逐步采用,但quamesim的处方解除干预补偿模型为研究提供了一个重要的框架,为研究现实环境中的处方解除提供了一种机制。
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来源期刊
CiteScore
5.60
自引率
6.50%
发文量
126
审稿时长
1 months
期刊介绍: Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.
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