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Projecting financial sustainability for clinical pharmacy services: An implementation science brief report 预测临床药学服务的财务可持续性:一份实施科学简报。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-06 DOI: 10.1016/j.japh.2025.102988
Ashley W. Ellis, Cori C. Grant, Christopher K. Finch, Reginald F. Frye, Todd D. Sorensen

Background

The United States faces a projected shortage of 86,000 physicians by 2036, disproportionately affecting rural areas. Meanwhile, 90% of Americans live within 5 miles of a pharmacy, positioning pharmacists to help address care gaps. Despite demonstrated clinical value, pharmacist integration into primary care is hindered by unclear compensation pathways.

Objectives

This study developed and piloted the Pharmacist Revenue and Integration Modeling Engine (PRIME), a novel tool to support financial decision-making for pharmacist integration. Objectives included (1) developing PRIME, (2) exploring implementation strategies, and (3) modeling financial viability.

Methods

The University of Tennessee Health Science Center partnered with an academic family medicine clinic in Memphis, TN, to re-establish clinical pharmacy services. PRIME used the 2025 Medicare Physician Fee Schedule, adjusted for Medicaid, private insurance, and self-pay, to model revenue across 4 service delivery scenarios. A full-time pharmacist (40 h/wk, 46 wk/y) was assumed, and projected revenue was compared to personnel costs.

Results

Financial viability varied by service type and volume. Preventive care and collaborative physician-pharmacist visits (e.g., annual wellness visits and 99,214 E/M codes) were key revenue drivers. The most successful model (approach 1.5) blended preventive and collaborative services, generating $286,700 in annual revenue and a net surplus of $105,500 (ROI 1.58:1). This led to a clinic-academic partnership placing 2 pharmacists (1 full-time equivalent) in the clinic.

Conclusion

Strategic use of billing codes can make clinical pharmacy services financially self-sustaining in primary care. PRIME offers a customizable roadmap for clinics to evaluate and implement pharmacist integration. This model supports workforce expansion, training opportunities, and improved access to care.
背景:到2036年,美国预计将面临8.6万名医生的短缺,这对农村地区的影响尤为严重。与此同时,90%的美国人居住在距离药店5英里的范围内,这使得药剂师可以帮助解决医疗缺口。尽管证明了临床价值,药剂师融入初级保健是阻碍不明确的补偿途径。目的:本研究开发并试点了药师收入与整合建模引擎(PRIME),这是一个支持药师整合财务决策的新工具。目标包括:(1)开发PRIME;(2)探索实施策略;(3)建模财务可行性。方法:田纳西大学健康科学中心与田纳西州孟菲斯的一个学术家庭医学诊所合作,重建临床药学服务。PRIME使用2025年医疗保险医师收费表(根据医疗补助、私人保险和自费进行调整)来模拟四种服务提供方案的收入。假设一名全职药剂师(每周40小时,每年46周),并将预计收入与人员成本进行比较。结果:财务可行性因服务类型和数量而异。预防保健和医师-药剂师协作访问(例如,年度健康访问和99214 E/M代码)是主要的收入驱动因素。最成功的模式(方法1.5)混合了预防和协作服务,每年产生286,700美元的收入和105,500美元的净盈余(ROI 1.58:1)。这导致了一个临床-学术合作伙伴关系放置两个药剂师(1 FTE)在诊所。结论:有策略地使用计费码可使初级保健的临床药学服务在财务上自给自足。PRIME为诊所评估和实施药剂师整合提供了可定制的路线图。这种模式支持劳动力扩张、培训机会和改善获得医疗服务的机会。
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引用次数: 0
Bridging the gap between expanded pharmacy services and payment models: A jurisdictional scan 弥合扩大药房服务和支付模式之间的差距:司法管辖区扫描。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-05 DOI: 10.1016/j.japh.2025.102989
Amarildo Ceka, Bhuvi Juneja, Olivia Tseng, Wei Zhang, I Fan Kuo, Nick Bansback, Michael R. Law, Larry D. Lynd, Peter J. Zed, Craig Mitton

Background

Over the past few decades, pharmacists' roles have expanded beyond dispensing to include medication reviews, minor ailment prescribing, and vaccinations. In British Columbia, Canada, the fee-for-service model has been recognized as a barrier to service uptake. To design future payment models that support uptake, it is important to examine the impacts of models used in other jurisdictions.

Objectives

To examine pharmacy remuneration models minor ailments provided by pharmacists across Organization for Economic Co-operation and Development (OECD) countries. The objectives of this study were to (1) identify the structure, funding mechanisms, and provider-level incentives for these models and (2) to assess the reported impacts of these models on service uptake, cost-effectiveness, health care access, and associated barriers and facilitators within community pharmacy settings.

Methods

We conducted a literature review to investigate the payment structures for pharmacists providing expanded services for minor ailments. Guided by Preferred Reporting Items for Systematic Reviews and Meta-Analyses, we searched MEDLINE and EMBASE databases from January 1, 2003, to September 20, 2023, focusing on pharmacy services, remuneration, and minor ailments in OECD countries such as the United Kingdom, Australia, New Zealand, the United States, etc.

Results

The search yielded 1662 records, of which 11 primary studies and 5 systematic reviews met the inclusion criteria, which examined 3 payment models for pharmacies providing minor ailment services: fee-for-service, performance-based payment models (PBPM) and capitation models. Fee-for-service models were found to encourage dispensing based on volume but provided little incentive for quality care. PBPM models were effective in promoting quality care but were noted to lack flexibility. Evidence on capitation models was minimal.

Conclusion

This overview of remuneration models explored alternative payment models to encourage expanded pharmacist services. The review highlights that various payment models come with their own unique benefits, such as cost savings and improved patient care. When designing a payment model, it is essential to prioritize stakeholder engagement and address equity concerns.
背景:在过去的几十年里,药剂师的角色已经从配药扩展到包括药物审查、小病处方和疫苗接种。在加拿大卑诗省,按服务收费的模式被认为是服务普及的障碍。为了设计未来的支付模式,以支持吸收,重要的是要检查在其他司法管辖区使用的模式的影响。目的:研究经合组织国家药剂师提供的小病药房薪酬模型。本研究的目的是:(1)确定这些模式的结构、资助机制和提供者层面的激励机制;(2)评估这些模式对社区药房环境中服务吸收、成本效益、医疗保健获取以及相关障碍和促进因素的影响。方法:对药师提供小病扩展服务的支付结构进行文献回顾。在PRISMA的指导下,我们检索了2003年1月1日至2023年9月20日的MEDLINE和EMBASE数据库,重点研究了OECD国家(如英国、澳大利亚、新西兰、美国等)的药学服务、薪酬和小病。结果:共检索到1662条记录,其中11项初步研究和5项系统评价符合纳入标准,对提供小病服务的药房的3种支付模式进行了考察:按服务收费、基于绩效的支付模式(PBPM)和收费模式。研究发现,按服务收费的模式鼓励按数量分配,但对提高护理质量几乎没有激励作用。PBPM模式在提高护理质量方面是有效的,但缺乏灵活性。关于人头模型的证据很少。结论:本文对薪酬模式进行了概述,探索了鼓励扩大药剂师服务的替代支付模式。该报告强调,各种支付模式都有其独特的好处,比如节省成本和改善病人护理。在设计支付模式时,必须优先考虑利益相关者的参与并解决公平问题。
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引用次数: 0
Development of a community-focused emergency response tool for medication-related preparedness 开发以社区为重点的应急工具,用于与药物有关的准备工作。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-05 DOI: 10.1016/j.japh.2025.102987
Sarah Schneider, Sharon Connor, Kiran Barik, Lauren J. Jonkman, Hoai-An Truong, Joni C. Carroll

Background

Pharmacists are among the first health care providers to respond after a disaster. They serve a vital role through mass medication dispensing or vaccination and triaging the medication needs of the community. Their role during the COVID-19 pandemic and other disasters have highlighted a need to engage pharmacists in local emergency preparation and community planning efforts.

Objective

The objective of this project was to develop an expert-informed medication-related emergency response readiness tool for community-based pharmacists.

Methods

Pharmacists with expertise in the different phases of disaster management informed revisions of an existing emergency response readiness checklist for short-term humanitarian response. The checklist was chosen to adapt because it focuses on pharmacist medication expertise while guiding users through all phases of the disaster management cycle. A variation of nominal group technique was used to gather expert feedback on the checklist and gain consensus on the adapted tool.

Results

The expert panel included 9 pharmacists with collective experience in over 50 emergencies in more than 20 countries. The panel recommended adapting the checklist to a comprehensive tool format to represent the continuousness of disaster management cycle. The panel recommended keeping the tool line items focused on medication access and prompting pharmacists to think about how they can use their medication expertise to ensure equitable access to care during and after an emergency. Most revisions were in the prevention and preparedness phases of the tool and build up capacity for a local response effort through community partnerships.

Conclusion

To our knowledge, this emergency response readiness tool is the first to guide community-based pharmacists through the critical steps required for disaster and emergency medication-related preparation. Medication-related disaster management requires a multiple-step process that is ongoing as the needs of communities change over time.
背景:药剂师是灾难发生后第一批做出反应的卫生保健提供者之一。他们通过大规模药物分配或疫苗接种以及对社区的药物需求进行分类发挥着至关重要的作用。他们在2019冠状病毒病大流行和其他灾害期间的作用凸显了让药剂师参与当地应急准备和社区规划工作的必要性。目标:该项目的目标是为社区药剂师开发一个专家知情的药物相关应急准备工具。方法:在灾害管理不同阶段具有专门知识的药剂师通报了对现有短期人道主义应急准备清单的修订情况。选择清单进行调整,因为它侧重于药剂师的药物专业知识,同时指导用户完成灾害管理周期的所有阶段。标称组技术的一种变化被用来收集专家对清单的反馈,并获得对适应工具的共识。结果:专家组包括9名具有20多个国家50多起突发事件集体经验的药师。小组建议将清单调整为一种全面的工具格式,以表示灾害管理周期的连续性。专家组建议将工具行项目的重点放在药物获取上,并促使药剂师考虑如何利用他们的药物专业知识,确保在紧急情况期间和之后公平获得护理。大多数修订是在工具的预防和准备阶段进行的,并通过社区伙伴关系建立了地方应对工作的能力。结论:据我们所知,这个应急准备工具是第一个指导社区药剂师完成灾害和紧急药物相关准备所需的关键步骤的工具。与药物有关的灾害管理需要一个多步骤的过程,随着社区需求的变化而不断进行。
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引用次数: 0
Misinformation is eroding the foundation of public health 错误信息正在侵蚀公共卫生的基础。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 DOI: 10.1016/j.japh.2025.102492
Benjamin P. Lewis
Robert M. Califf, MD, Commissioner of the Food and Drug Administration (FDA), noted at the end of his term that misinformation was a priority during his tenure; however, COVID-19 vaccines have dissuaded people from getting the vaccine and contributed to preventable deaths. The Incoming Secretary of the Department of Health and Human Services, Robert F. Kennedy, Jr (RFK Jr), which includes the FDA, has now stated that there are not sufficient vaccine safety studies, falsely asserted the government doesn't have good vaccine safety monitoring, and that we don't have good science on almost everything, including vaccines. Additionally, he refused to acknowledge the scientific consensus that childhood vaccines (e.g., measles, mumps, and rubella vaccine) do not cause autism.
Pharmaceutical sponsors study vaccines in clinical trials under an Investigational New Drug Application, which extensively tests vaccines, analyzing thousands of subjects' data for safety and efficacy. Many vaccines have been available for years without reported safety concerns. Conducting comprehensive clinical trials, monitoring, and reporting vaccine safety data are considered good science.
Effective communication about vaccines is crucial as we become increasingly interconnected through world travel, social media, and the internet. Providing accurate information and fostering trust that supports good clinical and scientific knowledge prevents confusion from unsupported statements, such as social media, that can create misinformation. The FDA approves the official prescribing information and fact sheet for vaccines, ensuring they are accurate and well-documented to prevent misinformation. Responsible health science communication must be correct, transparent, and inclusive to the public. Vaccination is a fundamental principle of public health, and clear communication is the basis of mitigating vaccine hesitancy, misinformation, and disinformation. Without this, misinformation will erode the foundation of public health.
美国食品和药物管理局(FDA)局长Robert M.Califf医学博士在任期结束时指出,错误信息是他任期内的首要任务;然而,COVID-19疫苗阻止了人们接种疫苗,并导致了可预防的死亡。即将上任的卫生与公众服务部部长小罗伯特·f·肯尼迪(RFK Jr.),包括食品和药物管理局,现在已经声明没有足够的疫苗安全性研究,错误地断言政府没有良好的疫苗安全监测,我们几乎所有事情都没有良好的科学,包括疫苗。此外,他拒绝承认儿童疫苗(如MMR)不会导致自闭症的科学共识。制药赞助商根据新药研究申请(IND)在临床试验中研究疫苗,该申请对疫苗进行广泛测试,分析数千名受试者的安全性和有效性数据。许多疫苗多年来一直没有安全问题的报道。开展全面的临床试验、监测和报告疫苗安全性数据被认为是良好的科学。随着我们通过世界旅行、社交媒体和互联网日益相互联系,关于疫苗的有效沟通至关重要。提供准确的信息并培养信任,以支持良好的临床和科学知识,防止因未经支持的陈述(如社交媒体)而产生混淆,从而产生错误信息。FDA批准了疫苗的官方处方信息和说明书,确保它们是准确的和有充分记录的,以防止错误信息。负责任的卫生科学传播必须是正确的、透明的和对公众包容的。疫苗接种是公共卫生的一项基本原则,明确的沟通是减轻疫苗犹豫、错误信息和虚假信息的基础。否则,错误信息将侵蚀公共卫生的基础。
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引用次数: 0
Cover 封面
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 DOI: 10.1016/S1544-3191(25)00670-3
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引用次数: 0
The use profile of antimicrobial drugs in neonatal intensive care units: a scoping review protocol 新生儿重症监护病房抗菌药物的使用概况:范围审查。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 DOI: 10.1016/j.japh.2025.102910
Francisco Clébison Chaves Lope , Tayssa Figueiredo Moura , Lucas Amaral-Machado , Gentil Gomes da Fonseca Filho , Klayton Galante Sousa

Background

Newborns are particularly susceptible to infections due to their immature immune systems. This condition is also exacerbated by the following factors (i) invasive procedures, (ii) length of hospital stay, and (iii) low birth weight.

Objective

This study aims to characterize the utilization profile of antimicrobial drugs in neonatal intensive care units (NICUs) through a scoping review.

Methods

The protocol, developed in accordance with the methodology outlined by the Joanna Briggs Institute, has been registered on the Open Science Framework (OSF) platform (DOI 10.17605/OSF.IO/YB4AG). The search will encompass databases including LILACS, EMBASE, MEDLINE/PubMed, Scientific Electronic Library Online (SciELO), as well as Web of Science and Scopus. Gray literature will be accessed through digital repositories. Search terms will be combined using Boolean operators 'OR' and 'AND,' aligned with the PCC framework (Population, Concept, Context). Identified studies will be managed using the Rayyan app, with duplicates removed. Two independent reviewers will handle study selection and data extraction. Studies will be included if they are available in full and contain at least one of the following pieces of information: data on antimicrobial consumption rates, the most prescribed antimicrobials, the most common indications for antimicrobial use, or off-label prescription of antimicrobials. Studies must have been conducted in NICUs with neonates hospitalized in this setting; if the study involves other settings or populations, the data must be stratifiable for neonates hospitalized in NICUs. The extracted data will be presented schematically or in tables, with a narrative description accompanying the results.

Conclusion

The outcomes will contribute to understanding global variations in antimicrobial utilization, offering evidence to support health care professionals in making informed decisions regarding antimicrobial usage and promoting safer and more effective clinical practices.
新生儿由于免疫系统不成熟,特别容易受到感染。这种情况还会因以下因素而加剧:(1)侵入性手术,(2)住院时间过长,(3)出生体重过低。本研究旨在通过范围审查表征抗菌药物在新生儿重症监护病房的使用概况。方法:该协议根据乔安娜布里格斯研究所(JBI)概述的方法制定,已在开放科学框架(OSF)平台上注册(DOI 10.17605/OSF. io /YB4AG)。搜索将包括LILACS、EMBASE、MEDLINE/PubMed、科学电子图书馆在线(SciELO)以及Web of Science和Scopus等数据库。灰色文献将通过数字资源库访问。搜索词将使用布尔运算符“OR”和“and”进行组合,并与PCC框架(人口、概念、上下文)保持一致。已确定的研究将使用Rayyan应用程序进行管理,并删除重复的研究。两名独立审稿人将负责研究选择和数据提取。如果有完整的研究报告,并包含以下至少一项信息,则将纳入研究报告:抗微生物药物消费率数据、处方最多的抗微生物药物、最常见的抗微生物药物使用指征,或抗微生物药物说明书外处方。研究必须在新生儿重症监护病房进行,在这种环境下住院的新生儿;如果研究涉及其他环境或人群,则必须对新生儿重症监护病房住院的新生儿进行分层。提取的数据将以图表形式或表格形式呈现,并随附结果的叙述性描述。结论:研究结果将有助于了解抗微生物药物使用的全球变化,为卫生保健专业人员做出有关抗微生物药物使用的知情决策提供证据,并促进更安全、更有效的临床实践。
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引用次数: 0
Utilization of an electronic health record dashboard report to monitor unreconciled controlled substance dispenses 利用电子健康记录仪表板报告来监控不协调的受控物质分配。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-30 DOI: 10.1016/j.japh.2025.102968
Christopher Le, John Mellett, Janinah Barreto, Ben Lopez

Background

A medication is considered unreconciled when there is no documented administration or the dispensed amount does not match the amount administered, wasted, or returned. Unreconciled dispenses pose several issues, including inaccurate accounting of controlled substances, potential financial discrepancies, possible masking of controlled substance diversion, and patient safety concerns. Utilization of an electronic health record (EHR) report of unreconciled dispenses is one of several possible surveillance methods to track unreconciled dispenses and detect potential controlled substance diversion.

Objectives

The objective of this study is to determine the extent to which the utilization of an EHR reporting dashboard by nursing leaders decreases the number of unreconciled controlled substance dispenses.

Methods

An existing report available through the EHR will be used to identify a baseline of unreconciled dispenses. A dashboard was built to include the unreconciled dispenses report that provided real-time data as well as a visualization of historical data. This dashboard was integrated into the nursing leadership workflow on several pilot units covering different levels of care and reviewed regularly for potential intervention. Nurse managers were expected to communicate directly with nurses that had unreconciled controlled substance dispenses and re-educate on appropriate documentation procedures.

Results

During the preintervention period, there were a total of 26,101 controlled substance dispenses with 256 unreconciled dispenses (0.98%). Following implementation of the dashboard report, there was a nonsignificant decrease of 0.13% (P = 0.14) with a total of 24,731 controlled substance dispenses and 211 unreconciled dispenses (0.85%).

Conclusion

The use of an EHR dashboard report has the potential to improve the documentation of controlled substances by identifying opportunities to correct unreconciled dispenses. However, workflow barriers can impact the utility of and engagement with the dashboard report.
背景:当没有记录给药或配药量与给药量、浪费量或退回量不匹配时,认为药物不协调。不协调的配药造成了几个问题,包括管制物质的不准确会计,潜在的财务差异,可能掩盖管制物质转移,以及患者安全问题。利用电子健康记录(EHR)报告不协调的配药是跟踪不协调配药和检测潜在的受控物质转移的几种可能的监测方法之一。目的:本研究的目的是确定在何种程度上利用电子病历报告仪表板由护理领导减少数量不协调的受控物质分配。方法:现有的报告可通过电子病历将用于确定不协调分配的基线。构建了一个仪表板,以包含不协调分发报告,该报告提供实时数据以及历史数据的可视化。该仪表板被整合到几个覆盖不同护理水平的试点单位的护理领导工作流程中,并定期审查潜在的干预措施。护士管理人员应直接与有不协调的受控物质分配的护士沟通,并就适当的文件程序进行再教育。结果:干预前共有管制药品处方26101个,不调和药品256个,占0.98%。在仪表板报告实施后,共有24,731个受控物质制剂和211个不调和制剂(0.85%)减少了0.13% (p = 0.14)。结论:EHR仪表板报告的使用有可能通过识别纠正不协调配药的机会来改善受控物质的文件。然而,工作流障碍可能会影响仪表板报告的实用性和参与性。
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引用次数: 0
Consumer data insights on pharmacy utilization: Comparative study of 2015 and 2021 surveys 消费者数据对药房利用的洞察:2015年和2021年调查的比较研究。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-30 DOI: 10.1016/j.japh.2025.102964
Pranitha Presingu, Suhila Sawesi, Michael Irungu, Kyle Kane, Mohamed Rashrash, Jon Schommer, Lawrence Brown

Background

Understanding the evolution of consumer behavior in pharmacy selection is crucial for delivering patient-centered and technology-driven health care.

Objective

To identify factors influencing consumer pharmacy choice using 2021 National Consumer Survey on the Medication Experience and Pharmacists' Roles and to examine how these factors have evolved over time using 2015 data as a baseline.

Methods

All variables were harmonized with the 2015 dataset to ensure comparability. Guided by the Andersen Behavioral Model, descriptive analyses and logistic regression were performed on 2021 survey data (N = 1521) to evaluate factors influencing pharmacy selection, and results were compared with 2015 findings to assess evolving trends.

Results

Younger adults (18–33) increasingly favored prescription-only pharmacies (odds ratios [OR] = 3.523), while older adults (70+) preferred mail-order pharmacies. Use of mail prescriptions rose by 11.7% and remained a strong predictor of mail pharmacy use (OR = 30.29). Vaccination (+20%) and drive-thru utilization (+7.8%) increased substantially and were associated with chain pharmacies (OR = 1.404; OR = 2.500). In contrast, traditional predictors such as education, financial hardship, over-the-counter/herbal use, and medication side effects declined in relevance.

Conclusion

Consumer preferences have shifted toward convenience-based and contactless pharmacy models, a trend that has continued beyond 2021. These changes highlight the need for pharmacists to adapt service delivery approaches and for health informatics professionals to strengthen digital infrastructure supporting patient-centered care.
背景:了解消费者在药物选择中的行为演变对于提供以患者为中心和技术驱动的医疗保健至关重要。目的:利用2021年全国消费者用药经验和药剂师角色调查(ncme - pr)确定影响消费者药房选择的因素,并以2015年的数据为基线,研究这些因素如何随时间演变。方法:将所有变量与2015年数据集统一,以确保可比性。在Andersen行为模型的指导下,对2021年调查数据(N = 1521)进行描述性分析和逻辑回归,以评估影响药房选择的因素,并将结果与2015年的调查结果进行比较,以评估其演变趋势。结果:年轻人(18-33岁)越来越喜欢处方药店(OR=3.523),老年人(70岁以上)更喜欢邮购药店。邮件处方的使用增加了11.7%,仍然是邮件药房使用的有力预测因子(OR=30.29)。疫苗接种(+20%)和驾车通道利用率(+7.8%)大幅增加,并与连锁药店相关(OR = 1.404; OR = 2.500)。相比之下,传统的预测因素,如教育、经济困难、OTC/草药使用和药物副作用的相关性下降。结论:消费者偏好已转向便利性和非接触式药房模式,这一趋势将持续到2021年以后。这些变化突出表明,药剂师需要调整服务提供方法,卫生信息学专业人员需要加强支持以患者为中心的护理的数字基础设施。
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引用次数: 0
Evaluation of digital health technology literacy among community pharmacists in Serbia 塞尔维亚社区药师数字卫生技术素养评价
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-28 DOI: 10.1016/j.japh.2025.102958
Dušan Vukmirović, Dušanka Krajnović, Marina Odalović

Background

Community pharmacists' roles are expanding beyond traditional tasks to include digital health interventions. Despite the growing integration of digital health technologies, gaps remain in understanding pharmacists' digital health technology literacy (DHTL). Adequate DHTL is essential for supporting patients and ensuring the effective implementation of digital tools in pharmacy practice.

Objectives

To assess general digital literacy (gDL) and identify specific levels of DHTL among community pharmacists.

Methods

A version of the DHTL Assessment Questionnaire (DHTL-AQ), specifically validated for use by community pharmacists, was distributed via online and paper-based formats. In addition to the DHTL-AQ, the questionnaire also included supplementary items assessing gDL. The sample size was calculated on the basis of the targeted pharmacist population. The data were analysed via SPSS. Receiver operating characteristic curves were used to determine cut-off scores, whereas chi-square and Kruskal-Wallis tests were used to assess group differences and associations.

Results

A total of 368 valid responses were collected. Among the respondents, 15.2% had low, 68.8% had medium, and 16.0% had high gDL. On the basis of these findings, DHTL cut-off scores were defined as low (35.9%), medium (19.6%), and high (44.5%). Significant differences in DHTL levels were associated with years of working experience. While 41.3% did not use social media professionally, Facebook, YouTube, Instagram, and Viber were the most commonly used platforms among pharmacists.

Conclusion

This study provides the first comprehensive assessment of DHTL among Serbian community pharmacists, revealing high gDL but highlighting the need for targeted DHTL training. Future research should focus on expanding the sample size and addressing specific DHTL gaps. The approach used in this study offers a practical framework for assessing DHTL that can be applied internationally to inform the development of relevant, tailored training programs and support the expansion of pharmacist-led services in an increasingly digital health environment.
背景:社区药剂师的角色正在扩展到传统任务之外,包括数字健康干预。尽管数字卫生技术的整合越来越多,但在了解药剂师的数字卫生技术素养(DHTL)方面仍然存在差距。充分的DHTL对于支持患者和确保药房实践中有效实施数字工具至关重要。目的:评估社区药师的总体数字素养(gDL)并确定具体的数字素养水平。方法:DHTL评估问卷(DHTL- aq),专为社区药剂师使用,通过在线和纸质格式分发。问卷除DHTL-AQ外,还包括评估gDL的补充项目。样本量是根据目标药师人群计算的。数据通过SPSS进行分析。ROC曲线用于确定临界值,而卡方检验和Kruskal-Wallis检验用于评估组间差异和相关性。结果:共收集有效问卷368份。受访者中,低gDL占15.2%,中gDL占68.8%,高gDL占16.0%。基于这些发现,DHTL分值被定义为低(35.9%)、中(19.6%)和高(44.5%)。DHTL水平的显著差异与工作年限有关。41.3%的药剂师不专业使用社交媒体,但Facebook、YouTube、Instagram和Viber是药剂师最常用的平台。结论:本研究首次对塞尔维亚社区药剂师的DHTL进行了全面评估,揭示了较高的数字素养,但强调了有针对性的DHTL培训的必要性。未来的研究应侧重于扩大样本量和解决具体的DHTL差距。本研究中使用的方法为评估DHTL提供了一个实用的框架,可以在国际上应用,为制定相关的、量身定制的培训计划提供信息,并支持在日益数字化的卫生环境中扩大药剂师主导的服务。
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引用次数: 0
The three-fer: How biosimilars reduce cost, expand access, and improve margin 三价:生物仿制药如何降低成本、扩大获取和提高利润率。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-27 DOI: 10.1016/j.japh.2025.102953
Tina M. Seekamp, Michael Hamacher, Jason A. Kemper, Richard W. Toner, Joshua K. Sigrist, Kara Suter, James S. Newman, Chelsee J. Jensen

Background

Traditional Medicare Fee for Service (FFS) covers both reference biologics and biosimilars without requiring prior authorization. Biosimilars offer a safe and effective alternative to reference biologics at a lower cost.

Objective

This study aimed to reduce Medicare FFS patient use of reference biologics in oncology and oncology-supportive care by 50%, lower Mayo Clinic Community Accountable Care Organization (MCC ACO) spending, achieve institutional cost savings, and improve revenue by increasing biosimilar use.

Practice description

Using the quality improvement (QI) framework, we expanded upon Mayo Clinic’s biosimilar-first strategy through the use of targeted electronic health record (EHR) reports to identify Medicare patients using reference biologics when biosimilars were available. We requested pharmacists or physicians to convert these patients to less costly, formulary-preferred biosimilars.

Practice innovation

We developed custom EHR reports to pinpoint Medicare patients still on reference biologics despite biosimilar availability and leveraged cost and margin data to promote change. Providers and pharmacists received targeted outreach and education, and pharmacists facilitated transitions to lower-cost biosimilars.

Evaluation methods

EHR reports tracked Medicare patients treated with reference biologics (trastuzumab, rituximab, bevacizumab, pegfilgrastim prefilled syringe, filgrastim) and their biosimilars during baseline and postintervention periods using the QI framework. MCC ACO spend impacts were analyzed using EHR data for Medicare beneficiaries treated at a MCC ACO location. Medication margin impact was extrapolated from internal data using the average sales price minus the contracted acquisition cost for each medication.

Results

Reference biologic use among Medicare patients dropped 47%. MCC ACO spending decreased by $2.62 million, patient count rose by 4.3%, and per-utilizer-per-month spending fell by 13.9% from fiscal year 2022-2023. Medication margin improved by more than $2.2 million for a modeled patient volume of 1000 per drug category.

Conclusion

QI efforts largely reduced reference biologic use in Medicare patients, lowered spending, increased patient access, and improved margins by shifting to biosimilars.
背景:传统的医疗服务收费(FFS)涵盖参考生物制剂和生物仿制药,无需事先授权(PA)。生物仿制药以较低的成本提供了一种安全有效的替代参考生物制剂的方法。目的:减少医疗保险FFS患者在肿瘤和肿瘤支持治疗中参考生物制剂的使用50%,降低梅奥诊所社区责任医疗组织(MCC ACO)的支出,实现机构成本节约,并通过增加生物仿制药的使用来提高收入。实践描述:使用质量改进(QI)框架,我们通过使用有针对性的电子健康记录(EHR)报告,扩展了梅奥诊所的生物仿制药优先战略,以识别在生物仿制药可用时使用参考生物制剂的医疗保险患者。我们要求药剂师或医生将这些患者转换为成本更低,处方首选的生物仿制药。实践创新:我们开发了定制的电子病历报告,以查明尽管有生物仿制药可用,但仍在使用参考生物制剂的医疗保险患者,并利用成本和利润率数据促进变革。提供者和药剂师接受了有针对性的外展和教育,药剂师促进了向低成本生物仿制药的过渡。评估方法:EHR报告在基线和干预后使用QI框架跟踪使用参考生物制剂(曲妥珠单抗、利妥昔单抗、贝伐单抗、pegfilgrastim预填充注射器、非格拉西汀)及其生物仿制药治疗的医保患者。使用在MCC ACO所在地接受治疗的医疗保险受益人的EHR数据分析MCC ACO支出影响。药物边际影响是从内部数据推断出来的,使用平均销售价格减去每种药物的合同采购成本。结果:参照性生物制剂在医保患者中的使用下降了47%。从2022财年到2023财年,MCC ACO的支出减少了262万美元,患者数量增加了4.3%,每位患者每月的支出下降了13.9%。在每个药物类别的模型患者数量为1,000的情况下,药物利润率提高了220多万美元。结论:质量改进工作显著减少了参照物在医保患者中的使用,降低了支出,增加了患者可及性,并通过转向生物类似药提高了利润。
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引用次数: 0
期刊
Journal of the American Pharmacists Association
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