Behavioral Science: Enhancing Our Approach to the Development of Effective Additional Risk Minimization Strategies

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Safety Pub Date : 2024-04-09 DOI:10.1007/s40264-024-01420-w
Joanne Treacy, Elaine H. Morrato, Robert Horne, Michael S. Wolf, Ameet Bakhai, Marie-Claire Wilson, Mark Lightowler, Sibel Guerler, Jeremy Jokinen
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Abstract

Additional risk minimization strategies may be required to assure a positive benefit–risk balance for some therapeutic products associated with serious adverse drug reactions/risks of use, without which these products may be otherwise unavailable to patients. The goals of risk minimization strategies are often fundamentally to influence the behavior of healthcare professionals (HCPs) and/or patients and can include appropriate patient selection, provision of education and counselling, appropriate medication use, adverse drug reaction monitoring, and adoption of other elements to assure safe use, such as pregnancy prevention. Current approaches to additional risk minimization strategy development rely heavily on information provision, without full consideration of the contextual factors and multi-level influences on patient and HCP behaviors that impact adoption and long-term adherence to these interventions. Application of evidence-based behavioral science methods are urgently needed to improve the quality and effectiveness of these strategies. Evidence from the fields of adherence, health promotion, and drug utilization research underscores the value and necessity for using established behavioral science frameworks and methods if we are to achieve clinical safety goals for patients. The current paper aims to enhance additional risk minimization strategy development and effectiveness by considering how a behavioral science approach can be applied, drawing from evidence in understanding of engagement with pharmaceutical medicines as well as wider public health interventions for patients and HCPs.

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行为科学:加强我们制定有效的额外风险最小化战略的方法
对于某些与严重药物不良反应/使用风险相关的治疗产品,可能需要采取额外的风险最小化策略,以确保效益与风险之间的正平衡,否则患者可能无法获得这些产品。风险最小化策略的目标通常从根本上影响医疗保健专业人员(HCPs)和/或患者的行为,可包括适当选择患者、提供教育和咨询、适当用药、药物不良反应监测,以及采用其他确保安全使用的要素,如预防妊娠。目前制定额外风险最小化策略的方法主要依赖于信息提供,而没有充分考虑影响患者和 HCP 行为的背景因素和多层次影响因素,这些因素会影响这些干预措施的采用和长期坚持。迫切需要应用循证行为科学方法来提高这些策略的质量和有效性。如果我们要为患者实现临床安全目标,那么来自依从性、健康促进和药物使用研究领域的证据强调了使用既定行为科学框架和方法的价值和必要性。本论文旨在通过考虑如何应用行为科学方法,借鉴了解患者和 HCP 参与药物治疗以及更广泛的公共卫生干预的证据,从而加强额外风险最小化策略的制定和有效性。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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