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Comprehensive Medication Reviews for Adults With Intellectual or Developmental Disabilities 成人智力或发育障碍的综合药物评价
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-20 DOI: 10.1002/jac5.70120
Steven R. Erickson, Ariana Nigoghosian, Brianna Marzolf, Beatrice Palazzolo, Dawn Michael, Muhammad Othman, Michael M. McKee

Introduction

People with intellectual or developmental disabilities face an elevated risk of adverse medication and health outcomes due to polypharmacy, medication interactions, and adherence issues. This study's objective was to assess the feasibility of virtual and in-home comprehensive medication reviews (CMRs) to identify and, when necessary, intervene on medication-related problems (MRPs) among patients with intellectual or developmental disabilities (IDD) residing in community group homes and to assess the caregivers' satisfaction with the CMRs.

Methods

Patients with IDD taking 5 or more medications were detected by using the health system's data warehouse. CMR steps included meeting with the patient and caregiver, assessing for MRP using the American Pharmacist Association/National Association of Chain Drug Stores framework, and providing a summary report for the patient/caregiver/prescriber. The report was reviewed with the caregiver 2 weeks after the initial CMR visit and sent to the prescriber. Outcomes measured included changes in the number of medications in patients' regimens, the number of MRPs identified, and a description of the MRPs.

Results

Twenty-nine patients with IDD received the CMR intervention. A median and interquartile range (IQR) of 4 (3.0, 4.0) MRPs were identified for each patient. The most common MRPs were inaccurate medication list in the medical record (n = 21), duplication of therapy (n = 13), no indication for medication use documented (n = 8), and a potential problem present but not treated (n = 7). There was a statistically significant difference in the median number of medications prior to and after CMR (p = 0.046), which decreased from 16 (12, 19) to 14.5 (10.8, 18.3). Caregivers were highly satisfied with the CMR process.

Conclusion

These results support the feasibility of conducting CMR both virtually and in-home. Implementation of a CMR program on a larger scale and conducting outcomes assessment are the next steps, with the goal to ensure safe and effective use of their medications by patients who have IDD.

由于多种用药、药物相互作用和依从性问题,智力或发育障碍患者面临药物不良反应和健康后果的高风险。本研究的目的是评估虚拟和家庭综合药物评估(cmr)的可行性,以识别并在必要时干预居住在社区团体之家的智力或发育障碍(IDD)患者的药物相关问题(mrp),并评估照顾者对cmr的满意度。方法利用卫生系统数据仓库对服用5种及以上药物的IDD患者进行检测。CMR步骤包括与患者和护理人员会面,使用美国药剂师协会/全国连锁药店协会框架评估MRP,并为患者/护理人员/处方者提供总结报告。在初次CMR访问后2周与护理人员一起审查该报告并发送给处方者。测量的结果包括患者方案中药物数量的变化,确定的mrp数量以及mrp的描述。结果29例IDD患者接受了CMR干预。每个患者的中位和四分位数范围(IQR)为4(3.0,4.0)个mrp。最常见的mrp是医疗记录中不准确的药物清单(n = 21),重复治疗(n = 13),没有药物使用的指征(n = 8),以及存在潜在问题但未治疗(n = 7)。CMR前后用药中位数差异有统计学意义(p = 0.046),由16次(12,19次)减少至14.5次(10.8,18.3次)。护理人员对CMR过程非常满意。结论本研究结果支持在虚拟和家庭中进行CMR的可行性。接下来的步骤是在更大范围内实施CMR计划并进行结果评估,目标是确保IDD患者安全有效地使用他们的药物。
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引用次数: 0
Capabilities of Large Language Models in Detecting and Managing Drug Interactions During Medication Reviews: Potential Implications as A Digital Assistant for Pragmatic Pharmacy Practice in Thailand 大型语言模型在药物审查过程中检测和管理药物相互作用的能力:作为泰国实用药学实践的数字助理的潜在含义
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-18 DOI: 10.1002/jac5.70115
Nuntapong Boonrit, Achiraya Thaweechai, Bussabong Kessarin, Warit Ruanglertboon

Introduction

The emerging capabilities of large language models (LLMs) have drawn increasing attention across various fields, including pharmacy practice in Thailand. Given the extensive number of available medications and the complex, often perplexing prescribing patterns, medication review remains a critical responsibility for pharmacists. This study explored the potential role of LLMs in supporting the medication review process within the Thai health care context, specifically focusing on their ability to detect drug interactions (DIs) and suggest context-sensitive management strategies.

Methods

Ten clinical vignettes were constructed, each depicting a patient with a specific drug regimen seeking assistance from a pharmacist. These cases were tailored to reflect the Thai context and represent commonly encountered DIs in Thailand. Each vignette was submitted to a set of LLMs—ChatGPT-4, ChatGPT-4o, ChatGPT-4o mini, Gemini 1.5, Claude 3.5, Microsoft Copilot, and Alisa 3.0—in both English and Thai. Evaluation metrics were developed and validated using the Index of Item-Objective Congruence. Two independent evaluators assessed all responses, and inter-rater reliability was measured using weighted Cohen's κ. LLM performance was scored based on percentage ranges, and cumulative scores were reported across evaluation domains.

Results

The weighted Cohen's κ values across six domains—(A) ability to identify DIs, (B) completeness, (C) clarity, (D) citation reliability, (E) usefulness, and (F) ability to assess harm—exceeded 0.6, indicating substantial inter-rater agreement. All LLMs showed clinically acceptable performance in both languages. Citation reliability was limited in Alisa 3.0 and Gemini 1.5, while ChatGPT-4o demonstrated the most consistent and well-rounded performance.

Conclusion

The selected LLMs demonstrated their potential as capable digital assistants in medication reviews, although some models require further improvement and careful consideration when applied in real-world settings. Nevertheless, human oversight remains essential; when used in parallel, LLMs and health professionals can work synergistically to enhance patient outcomes.

大型语言模型(llm)的新兴能力在各个领域引起了越来越多的关注,包括泰国的药房实践。鉴于可用药物的大量数量和复杂的,往往令人困惑的处方模式,药物审查仍然是药剂师的关键责任。本研究探讨了法学硕士在支持泰国卫生保健背景下的药物审查过程中的潜在作用,特别关注他们检测药物相互作用(DIs)和提出上下文敏感管理策略的能力。方法构建了10个临床小插图,每个小插图描绘了一个具有特定药物方案的患者向药剂师寻求帮助。这些案例是根据泰国的情况量身定制的,代表了泰国常见的DIs。每个小插图都被提交给一组LLMs-ChatGPT-4, chatgpt - 40, chatgpt - 40 mini, Gemini 1.5, Claude 3.5, Microsoft Copilot和Alisa 3.0 -英语和泰语。使用项目-目标一致性指数开发和验证了评估指标。两名独立评估者对所有反应进行评估,评估者间信度采用加权Cohen’s κ来衡量。LLM的性能是基于百分比范围评分的,并且在评估领域中报告累积分数。结果:六个领域(A)识别DIs的能力,(B)完整性,(C)清晰度,(D)引用可靠性,(E)有用性,(F)评估危害的能力)的加权Cohen's κ值超过0.6,表明评分者之间的一致性很大。所有llm在两种语言中均表现出临床可接受的表现。引用可靠性在Alisa 3.0和Gemini 1.5中受到限制,而chatggt - 40表现出最一致和全面的性能。结论所选择的llm显示了它们作为药物审查数字助理的潜力,尽管一些模型在实际应用时需要进一步改进和仔细考虑。然而,人的监督仍然是必不可少的;当并行使用时,法学硕士和卫生专业人员可以协同工作,以提高患者的治疗效果。
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引用次数: 0
Tipping the Scales: Strategies to Improve Anti-Obesity Medication Access and Affordability 倾斜天平:提高抗肥胖药物获取和负担能力的策略
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-18 DOI: 10.1002/jac5.70118
Anne M. Komé, Amanda R. Boykin, Alayah C. Johnson-Jennings, Andrea D. Coviello

Despite soaring demand and prescribing rates, access to anti-obesity medications (AOM) remains unbalanced due to high manufacturer costs, inadequate insurance coverage, intermittent shortages, and lack of provider knowledge in overcoming medication access barriers. Pharmacists are uniquely positioned to bridge care gaps for people with obesity by facilitating medication management, identifying drug interactions, counseling on lifestyle modification and adverse effects, and providing more frequent follow-up. Further, pharmacists can use their expertise to assist with AOM access, affordability, and therapeutic interchange. This article highlights the challenges routinely encountered in chronic weight management while offering practical pearls for pharmacists about insurance coverage, prior authorizations, current affordability initiatives, navigating shortages, and the importance of education and advocacy for people living with obesity.

尽管需求和处方率飙升,但抗肥胖药物(AOM)的获取仍然不平衡,原因是生产成本高、保险覆盖面不足、间歇性短缺以及提供者在克服药物获取障碍方面缺乏知识。药剂师具有独特的优势,可以通过促进药物管理、确定药物相互作用、就改变生活方式和不良反应提供咨询以及提供更频繁的随访,来弥合肥胖患者的护理差距。此外,药剂师可以利用他们的专业知识来协助AOM的获取、负担能力和治疗交换。本文强调了慢性体重管理中经常遇到的挑战,同时为药剂师提供了关于保险覆盖范围、事先授权、当前可负担性举措、导航短缺以及对肥胖患者进行教育和宣传的重要性的实用珍珠。
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引用次数: 0
Comment on “Consensus Recommendations for the Integration of Critical Care Pharmacists on Intensive Care Unit Teams: Endorsed by the American Association of Critical-Care Nurses, American College of Clinical Pharmacy, American Society of Health-System Pharmacists, Institute for Safe Medication Practices, and Society of Critical Care Medicine” 对《重症监护护士协会、美国临床药学学院、美国卫生系统药剂师协会、安全用药实践研究所和重症监护医学学会对重症监护小组整合重症监护药剂师的共识建议》的评论
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-15 DOI: 10.1002/jac5.70117
John Carr, Dustin Orvin
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引用次数: 0
Response to Comment on “Consensus Recommendations for the Integration of Critical Care Pharmacists on Intensive Care Unit Teams: Endorsed by the American Association of Critical-Care Nurses, American College of Clinical Pharmacy, American Society of Health-System Pharmacists, Institute for Safe Medication Practices, and Society of Critical Care Medicine” 对“关于重症监护室团队整合重症监护药剂师的共识建议:由美国重症监护护士协会、美国临床药学学院、美国卫生系统药剂师协会、安全用药实践研究所和重症监护医学学会批准”评论的回应
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-15 DOI: 10.1002/jac5.70116
Mojdeh S. Heavner, Jason J. Heavner, Brian Murray, Andrea Sikora
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引用次数: 0
Comprehensive Framework for Oncology Pharmacist-Led Parenteral Anticancer Therapy Patient Education: The Opinion of the American College of Clinical Pharmacy Hematology/Oncology Practice and Research Network 肿瘤药剂师主导的肠外抗癌治疗患者教育的综合框架:美国临床药学血液学/肿瘤学实践与研究网络学院的意见
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-14 DOI: 10.1002/jac5.70114
Erin Hickey Zacholski, Jack Dierckes, David Hartnett-Quach, Cady Noda, Amanda Sharps, Olivia White, Kyle Zacholski, Shawn P. Griffin

Educating patients and caregivers on anticancer therapy is central to oncology pharmacy practice. As anticancer regimens become more complex, oncology pharmacists need a structured framework that ensures vital information is communicated and personalized to each patient. Though existing organizational guidelines, largely written for nurses, and standards for oral oncolytic therapy counseling provide valuable insight, a dedicated guideline for oncology pharmacists regarding the delivery of patient education for parenteral and combination anticancer therapies is largely bereft. This review addresses that gap, presenting a pharmacist-led model that encompasses the pre-visit assessment, preparation, step-by-step delivery of the teaching session, and practical considerations for maximizing patient understanding and safety.

This narrative review summarizes evidence for effective patient education on parenteral anticancer therapies. The authors propose a structured framework for oncology pharmacist-led patient education on parenteral anticancer therapies that combines pharmacotherapy knowledge and the application of patient-centered care.

教育患者和护理人员抗癌治疗是肿瘤药学实践的核心。随着抗癌方案变得越来越复杂,肿瘤药剂师需要一个结构化的框架,以确保重要信息的沟通和个性化给每个病人。虽然现有的组织指南(主要是为护士编写的)和口服肿瘤治疗咨询标准提供了有价值的见解,但在很大程度上缺乏针对肿瘤药剂师提供的关于肠外和联合抗癌治疗的患者教育的专门指南。这篇综述解决了这一差距,提出了一个药剂师主导的模式,包括就诊前评估、准备、逐步交付的教学环节,以及最大限度地提高患者理解和安全的实际考虑。这篇叙述性综述总结了有效的患者肠外抗癌治疗教育的证据。作者提出了一个结构化的框架,以肿瘤药剂师为主导的肠外抗癌治疗患者教育,结合药物治疗知识和以患者为中心的护理应用。
{"title":"Comprehensive Framework for Oncology Pharmacist-Led Parenteral Anticancer Therapy Patient Education: The Opinion of the American College of Clinical Pharmacy Hematology/Oncology Practice and Research Network","authors":"Erin Hickey Zacholski,&nbsp;Jack Dierckes,&nbsp;David Hartnett-Quach,&nbsp;Cady Noda,&nbsp;Amanda Sharps,&nbsp;Olivia White,&nbsp;Kyle Zacholski,&nbsp;Shawn P. Griffin","doi":"10.1002/jac5.70114","DOIUrl":"https://doi.org/10.1002/jac5.70114","url":null,"abstract":"<p>Educating patients and caregivers on anticancer therapy is central to oncology pharmacy practice. As anticancer regimens become more complex, oncology pharmacists need a structured framework that ensures vital information is communicated and personalized to each patient. Though existing organizational guidelines, largely written for nurses, and standards for oral oncolytic therapy counseling provide valuable insight, a dedicated guideline for oncology pharmacists regarding the delivery of patient education for parenteral and combination anticancer therapies is largely bereft. This review addresses that gap, presenting a pharmacist-led model that encompasses the pre-visit assessment, preparation, step-by-step delivery of the teaching session, and practical considerations for maximizing patient understanding and safety.</p><p>This narrative review summarizes evidence for effective patient education on parenteral anticancer therapies. The authors propose a structured framework for oncology pharmacist-led patient education on parenteral anticancer therapies that combines pharmacotherapy knowledge and the application of patient-centered care.</p>","PeriodicalId":73966,"journal":{"name":"Journal of the American College of Clinical Pharmacy : JACCP","volume":"8 11","pages":"1202-1214"},"PeriodicalIF":1.5,"publicationDate":"2025-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://accpjournals.onlinelibrary.wiley.com/doi/epdf/10.1002/jac5.70114","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145493725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
PSAP in JACCP Case Series: Hypertension JACCP病例系列中的PSAP:高血压
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-13 DOI: 10.1002/jac5.70102
Andrew Y. Hwang, Christina H. Sherrill
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引用次数: 0
PSAP in JACCP Recorded Webcast: Behavioral Approaches to Optimize Patient Engagement in a Healthy Lifestyle JACCP的PSAP记录网络广播:优化患者参与健康生活方式的行为方法
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-13 DOI: 10.1002/jac5.70101
Lauren M. Hynicka, Richard J. Rovelli
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引用次数: 0
The Pharmacist's Role in the Use of Incretin-Based Therapies for Weight Management: An Opinion of the Endocrine and Metabolism Practice and Research Network of the American College of Clinical Pharmacy 药剂师在使用肠促胰岛素为基础的体重管理疗法中的作用:美国临床药学学院内分泌和代谢实践和研究网络的观点
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-11 DOI: 10.1002/jac5.70111
Sara Lingow, Nicholas Carris, Jennifer Clements, Lindsay Courtney, Abby Lennon, Christina H. Sherrill, Elizabeth Van Dril

The popularity of incretin-based therapies has increased substantially over the past several years due to their clinically significant efficacy for weight loss and positive impact on weight-related comorbid conditions, yet, few clinical practice guidelines for the management of overweight and obesity have been updated to incorporate these agents. The increased demand for incretin-based therapies for weight management has revealed barriers to their implementation related to cost, availability, and emerging safety concerns. This opinion paper aims to briefly review the available literature on the current role of incretin-based therapy for chronic weight management in persons with overweight or obesity and provide recommendations for clinical pharmacists utilizing these agents. The intent of this opinion paper is to discuss the benefits and risks of incretin-based therapy for weight management, review approaches for clinical pharmacists to overcome barriers to their implementation, and address ongoing questions related to their use. Finally, the authors suggest an approach to the management of people with overweight or obesity with incretin-based therapy using the Pharmacists' Patient Care Process along with actions clinical pharmacists can take to ensure best practices with these agents.

在过去的几年中,基于肠促胰岛素的治疗方法的普及程度大大增加,因为它们对减肥的临床显着疗效和对体重相关合并症的积极影响,然而,很少有超重和肥胖管理的临床实践指南被更新以纳入这些药物。对以肠促胰岛素为基础的体重管理疗法的需求增加,揭示了其实施与成本、可用性和新出现的安全问题相关的障碍。这篇观点文章旨在简要回顾现有的关于肠促胰岛素治疗在超重或肥胖人群慢性体重管理中的作用的文献,并为临床药剂师使用这些药物提供建议。这篇观点论文的目的是讨论以肠促胰岛素为基础的体重管理治疗的益处和风险,回顾临床药剂师克服实施障碍的方法,并解决与使用相关的持续问题。最后,作者提出了一种方法来管理超重或肥胖的人与肠促胰岛素为基础的治疗,使用药剂师的病人护理过程和行动,临床药剂师可以采取确保这些药物的最佳实践。
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引用次数: 0
Impact of Community Pharmacists on Reducing Opioid and Alcohol Co-Use: A Pilot Randomized Control Trial of a Medication Therapy Management Intervention 社区药剂师对减少阿片类药物和酒精共同使用的影响:一项药物治疗管理干预的随机对照试验
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-09-10 DOI: 10.1002/jac5.70113
Kenneth C. Hohmeier, Grace Broussard, Melissa Tyszko, Kelly Barland, Kristi Carlston, Yingjia Wei, Craig Field, Adam J. Gordon, Alina Cernasev, Gerald Cochran

Background

Concurrent use of opioids and alcohol can result in respiratory depression, overdose, and death. Prior research has shown that 20%–30% of patients receiving opioid medications in community pharmacies engage in high-risk drinking. We adapted a medication therapy management-based intervention to address co-use and tested its feasibility, acceptability, and preliminary efficacy.

Design

This pilot study enrolled adult, English-speaking community pharmacy patients dispensed opioids who reported current drinking. Participants were randomized to standard medication counseling (SMC) or alcohol-targeted brief intervention-medication therapy management (ABI-MTM). ABI-MTM included two pharmacist-delivered sessions focused on reviewing medications/interactions, motivating participants to discontinue co-use, and providing a written action plan. We assessed enrollment, retention, intervention delivery, satisfaction, drinks per drinking day (DDD), and daily morphine milligram equivalent (MME) at baseline, 2, and 3 months. Outcomes were analyzed using descriptive statistics and generalized linear mixed modeling.

Results

We enrolled 44 patients (110% of target; 22 per group). No significant differences were found in age (mean = 55.8), sex (female = 65.9%), race (White = 95.5%), education (> high school = 95.5%), or health insurance status (insured = 95.5%). Consent and retention rates exceeded 90%, session delivery was ≥ 95%, and ABI-MTM satisfaction ranged from 79% to 89%. At 3 months, 59.1% of ABI-MTM participants versus 45.5% of SMC achieved ≥ 30% reduction in DDD and/or daily MME. Mixed models showed ABI-MTM recipients had 2.10 (95% confidence interval = 0.34–12.95) higher odds of achieving this reduction.

Conclusion

ABI-MTM demonstrated feasibility, acceptability, and preliminary efficacy. A fully powered trial is warranted to evaluate broader implementation.

阿片类药物和酒精同时使用可导致呼吸抑制、过量和死亡。先前的研究表明,20%-30%在社区药房接受阿片类药物治疗的患者参与高危饮酒。我们采用了一种基于药物治疗管理的干预措施来解决共同使用问题,并测试了其可行性、可接受性和初步疗效。设计本初步研究招募了成人,英语社区药房分配阿片类药物的患者,他们报告目前饮酒。参与者被随机分配到标准药物咨询(SMC)或酒精靶向短期干预药物治疗管理(ABI-MTM)。ABI-MTM包括两次由药剂师主持的会议,重点是回顾药物/相互作用,激励参与者停止共同使用,并提供书面行动计划。我们在基线、2个月和3个月时评估了入组、保留、干预交付、满意度、每饮酒日饮酒量(DDD)和每日吗啡毫克当量(MME)。结果分析采用描述性统计和广义线性混合模型。结果共入组44例(110%),每组22例。年龄(平均值= 55.8)、性别(女性= 65.9%)、种族(白人= 95.5%)、教育程度(高中学历= 95.5%)或健康保险状况(投保= 95.5%)均无显著差异。同意率和保留率超过90%,疗程交付率≥95%,ABI-MTM满意度在79%至89%之间。在3个月时,59.1%的ABI-MTM参与者和45.5%的SMC参与者实现了DDD和/或每日mme减少≥30%。混合模型显示,ABI-MTM接受者实现这一减少的几率高出2.10(95%置信区间= 0.34-12.95)。结论ABI-MTM具有可行性、可接受性和初步疗效。有必要进行全面的试验,以评估更广泛的实施情况。
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引用次数: 0
期刊
Journal of the American College of Clinical Pharmacy : JACCP
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