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Provision of maternal health services among Ohio community pharmacists practicing in maternity care deserts. 俄亥俄州孕产妇护理荒漠地区社区药剂师提供的孕产妇保健服务。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-13 DOI: 10.1016/j.japh.2024.102292
Maria Duodu, Natalie DiPietro Mager

Background: Over 2.3 million reproductive-age women in the United States live in a maternity care desert, a county without obstetric services or providers; over 3 million more reside in a county with low access to maternity care. The National Alliance of State Pharmacy Associations (NASPA) issued a toolkit outlining maternal health services community pharmacists are positioned to provide within their scope of practice.

Objectives: The primary objective of this study was to determine whether community pharmacists practicing in maternity care deserts/low access areas in Ohio provide NASPA-recommended maternal health services. Secondary objectives were to assess knowledge and attitudes related to maternal health; interest and barriers for developing new services; and screening and referrals for key social determinants of health.

Methods: An anonymous cross-sectional survey was electronically distributed to Ohio community pharmacists working in maternity care deserts/low access areas (n = 216) in fall/winter 2023 to evaluate their awareness, practices, and attitudes.

Results: Thirty-one pharmacists responded (14%). Almost half knew that maternal mortality had increased in recent years. Although 61% reported familiarity with the term "maternity care desert," only 35% recognized they are currently practicing in one. Provision of NASPA-recommended services to reproductive-age women ranged from 90% (immunizations) to 11% (alcohol use screening/counseling). About 96% believed that community pharmacists can help optimize women's health before and during pregnancy. The majority of respondents reported "never" screening for social determinants of health, but 48% were interested in learning more. While 67% of respondents are interested in providing more services for women at their pharmacy, they also reported obstacles like lack of time and staff.

Conclusion: There is a need to raise awareness about maternal mortality and maternity care deserts among Ohio community pharmacists. Given the interest expressed in providing additional services, pharmacists should receive more support to provide needed care for medically-underserved populations.

背景:美国有 230 多万育龄妇女生活在孕产妇保健荒漠中,即没有产科服务或提供者的县;还有 300 多万人生活在孕产妇保健普及率低的县。全美州药学协会联盟(NASPA)发布了一个工具包,概述了社区药剂师在其执业范围内可提供的孕产妇保健服务:本研究的主要目的是确定在俄亥俄州孕产妇护理荒漠/低获取率地区执业的社区药剂师是否提供 NASPA 推荐的孕产妇保健服务。次要目标是评估与孕产妇健康相关的知识和态度;开发新服务的兴趣和障碍;以及健康的主要社会决定因素的筛查和转介:2023 年秋冬季,向俄亥俄州在孕产妇护理荒漠/低获取率地区工作的社区药剂师(n=216)发放了一份匿名横截面电子调查表,以评估他们的认识、实践和态度:结果:31 名药剂师做出了回复(14%)。近一半的药剂师知道近年来孕产妇死亡率有所上升。尽管 61% 的药剂师表示熟悉 "孕产妇护理荒漠 "这一术语,但只有 35% 的药剂师认识到他们目前正在 "孕产妇护理荒漠 "中执业。为育龄妇女提供 NASPA 推荐服务的比例从 90%(免疫接种)到 11%(酒精使用筛查/咨询)不等。约 96% 的受访者认为社区药剂师可以帮助优化孕前和孕期妇女的健康。大多数受访者表示 "从未 "筛查过健康的社会决定因素,但有 48% 的受访者有兴趣了解更多。虽然 67% 的受访者有兴趣在其药房为妇女提供更多服务,但他们也表示存在时间和人员不足等障碍:结论:有必要提高俄亥俄州社区药剂师对孕产妇死亡率和孕产妇护理荒漠的认识。考虑到药剂师对提供更多服务的兴趣,他们应该获得更多支持,以便为医疗服务不足的人群提供所需的护理服务。
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引用次数: 0
Real-world treatment patterns in drug naïve type 2 diabetes population: Initial combination therapy vs. sequential step-therapy. 新药 2 型糖尿病患者的实际治疗模式:初始联合疗法与序贯阶梯疗法。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-12 DOI: 10.1016/j.japh.2024.102295
Zahra Majd, Hua Chen, Michael L Johnson, Kim K Birtcher, Omar Serna, Susan Abughosh

Background: Despite evidence-based guidelines and available therapies, many patients with type 2 diabetes (T2D) have suboptimal glycemic control. The current standard of care suggests initial monotherapy followed by add-on therapy to achieve and maintain target HbA1c. However, clinical trials revealed that intensive glycemic control, especially at the early stages of the disease, could result in earlier and better long-term glycemic control in addition to reducing diabetes-related complications and mortality risk.

Objective: This population-based study aimed to investigate treatment initiation patterns among newly diagnosed drug-naïve patients with T2D in real-world clinical settings, focusing on two recommended approaches: initial combination therapy and step-therapy.

Methods: A retrospective study was conducted using claims data from the Merative MarketScan Research Databases between 2017 and 2019. The study included drug-naïve patients with T2D with continuous enrollment in medical and pharmacy plans. Patients were categorized into the initial combination therapy or step-therapy cohorts based on their initial treatment regimen. Baseline characteristics of the cohorts were recorded, and logistic regression analysis was performed to identify factors associated with receiving each approach.

Results: The study included a total of 117,419 patients in the Commercial/Medicare population and 18,574 patients in the Medicaid population. About 10% to 12% of patients received initial combination therapy as their initial pharmacotherapy regimen. Several patient demographic and clinical characteristics were significantly associated with the use of initial combination therapy vs. step-therapy. Results also showed a greater usage of loose-dose combination pills over fixed-dose combinations.

Conclusion: Given the lack of real-world studies on combination vs. step-therapy, the study findings provide insights into the current treatment initiation patterns and associated factors among drug-naïve patients with T2D. These findings contribute to understanding the real-world clinical practices in diabetes management and may help guide clinicians in making informed decisions regarding pharmacotherapy approaches.

背景:尽管有循证指南和可用疗法,但许多 2 型糖尿病(T2D)患者的血糖控制仍不理想。目前的治疗标准建议在初始单药治疗后采用附加疗法,以达到并维持目标 HbA1c。然而,临床试验显示,强化血糖控制,尤其是在疾病的早期阶段,除了能降低糖尿病相关并发症和死亡风险外,还能更早和更好地长期控制血糖:这项基于人群的研究旨在调查现实世界临床环境中新确诊的药物治疗无效的 T2D 患者的治疗启动模式,重点关注两种推荐方法:初始联合疗法和阶梯疗法:利用 Merative™ MarketScan® 研究数据库中 2017 年至 2019 年期间的理赔数据进行了一项回顾性研究。研究对象包括连续加入医疗和药房计划的 T2D 患者。根据患者的初始治疗方案,将其分为初始联合治疗队列或阶梯治疗队列。研究记录了组群的基线特征,并进行了逻辑回归分析,以确定与接受每种方法相关的因素:研究共纳入了 117,419 名商业/医疗保险人群患者和 18,574 名医疗补助人群患者。约有 10-12% 的患者接受了初始联合疗法作为其初始药物治疗方案。一些患者的人口统计学特征和临床特征与使用初始联合疗法和阶梯疗法有显著相关性。结果还显示,松散剂量联合用药的使用率高于固定剂量联合用药:鉴于缺乏关于联合疗法与分步疗法的真实世界研究,本研究结果提供了对目前药物治疗无效的 T2D 患者的治疗启动模式及相关因素的深入了解。这些发现有助于了解糖尿病管理的实际临床实践,并有助于指导临床医生就药物治疗方法做出明智的决定。
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引用次数: 0
Implementation of an adult life-course vaccine review service, VaxCheck, in community pharmacy: A qualitative analysis. 在社区药房实施成人生命周期疫苗审查服务 VaxCheck:定性分析。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-12 DOI: 10.1016/j.japh.2024.102294
Elizabeth Vernon-Wilson, Michaela L Comrie, Kyla Barrera, Molly Yang, Lisa Dolovich, Nancy M Waite, Sherilyn K D Houle

Background: Community pharmacists are well placed to identify and vaccinate unimmunized or under-immunized individuals who can put themselves and communities at risk of preventable disease. We designed and tested VaxCheck, a novel life-course vaccine review service that can be used to raise awareness and guide personal vaccination action plans, in community pharmacies in Ontario, Canada.

Objective: To understand the experiences of community pharmacists and staff directly involved with providing the VaxCheck service as part of initial testing.

Methods: Semi-structured interviews were performed with pharmacy staff from 9 pharmacies who participated in the study. Interviews were conducted at baseline and following each of 3 Plan-Do-Study-Act quality improvement cycles. Activities undertaken to perform VaxCheck were assessed. An inductive thematic analysis was performed to identify dominant themes and subthemes. Activities and descriptive codes were then correlated to the Consolidated Framework for Implementation Research (CFIR).

Results: Twenty-six interviews were conducted. Pharmacy staff described VaxCheck activities as spanning 3 stages: (1) Promotion/offering of VaxCheck, (2) Completing the VaxCheck, and (3) Enacting recommendations and follow-up. VaxCheck activities were compatible with workflow related to delivery of other vaccines and medication reviews. Thematic analysis found 3 considerations guided VaxCheck adoption: (1) Aligning VaxCheck with workflow through flexible integration, (2) Enabling patient-oriented vaccination services, and (3) Contributing to community healthcare provision. Data aligned with all CFIR domains with strengths noted in constructs from the "Innovation characteristics" and "Individuals" domains. Barriers to implementation were identified in "Inner setting," "Outer setting," and "Process" domains, such as pharmacy workflow capacity, patient knowledge about vaccination, availability of vaccine records, and interactions with other healthcare providers.

Conclusion: Community pharmacists found VaxCheck to be a valuable, accessible service that was well-received by patients and supported adult vaccination reviews and individualized recommendations. VaxCheck was compatible with pharmacy workflow but needed additional resources for sustainability and promotion with stakeholders.

背景:社区药剂师非常适合识别未接种疫苗或接种疫苗不足的个人并为其接种疫苗,这些人可能会使自己和社区面临可预防疾病的风险。我们在加拿大安大略省的社区药房设计并测试了 VaxCheck,这是一种新颖的终身疫苗审查服务,可用于提高认识和指导个人疫苗接种行动计划:了解直接参与提供 VaxCheck 服务的社区药剂师和工作人员的经验,作为初步测试的一部分:对参与研究的九家药房的药剂师进行了半结构式访谈。访谈分别在基线和三个 "计划-实施-研究-行动 "质量改进周期之后进行。对为执行 VaxCheck 而开展的活动进行了评估。进行了归纳式主题分析,以确定主导主题和次主题。然后将活动和描述性代码与实施研究综合框架(CFIR)相关联。药房工作人员将 VaxCheck 活动描述为三个阶段:(1) 宣传/提供 VaxCheck,(2) 完成 VaxCheck,(3) 执行建议和后续行动。VaxCheck 活动与提供其他疫苗和药物审查的相关工作流程是一致的。专题分析发现,采用 VaxCheck 有三个考虑因素:(1) 通过灵活整合使 VaxCheck 与工作流程相一致,(2) 实现以患者为导向的疫苗接种服务,以及 (3) 为社区医疗保健服务做出贡献。数据符合 CFIR 的所有领域,其中 "创新特征 "和 "个人 "领域的构建具有优势。在 "内部环境"、"外部环境 "和 "过程 "领域发现了实施障碍,如药房工作流程能力、患者对疫苗接种的了解、疫苗记录的可用性以及与其他医疗服务提供者的互动:社区药剂师发现 VaxCheck 是一项有价值、可获得的服务,深受患者欢迎,并支持成人疫苗接种审查和个性化建议。VaxCheck 与药房工作流程兼容,但需要更多资源才能持续开展并向利益相关者推广。
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引用次数: 0
Pharmacy in 2050: To succeed, we must adapt. 2050 年的药学:要想成功,我们必须适应。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-11 DOI: 10.1016/j.japh.2024.102287
Spencer E Harpe
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引用次数: 0
Systematic review and meta-analysis on effectiveness of strategies for enhancing adverse drug reaction reporting. 关于加强药物不良反应报告策略有效性的系统回顾和元分析。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-09 DOI: 10.1016/j.japh.2024.102293
Niphonh Mongkhonmath, Phayom Sookaneknun Olson, Panupong Puttarak, Nathorn Chaiyakunapruk, Ratree Sawangjit

Background: Pharmacovigilance is essential for patient safety, but underreporting adverse drug reactions (ADRs) is a global challenge.

Objectives: This review evaluated the effectiveness of strategies for enhancing ADR reporting by healthcare professionals (HCPs).

Methods: This systematic review was conducted following the Cochrane and the PRISMA guidelines. Five international databases were searched from inception to December 2023 and updated search to September 2024. Randomized clinical controlled trials (RCTs) and non-RCTs on enhancing ADR reporting were included. The primary outcomes were the number of overall ADR and high-quality ADR reports. Study quality was assessed using the Effective Practice and Organization of Care risk of bias (ROB), and ROBIN-I for RCT, and non-RCT. All data were evaluated using a random-effects model, and heterogeneity was assessed using I2 statistic and chi-squared tests.

Results: From 1672 studies, 13 studies (10 RCTs, and 3 non-RCTs) with 28,116 participants were included. Two of 10 RCTs had low ROB while the remaining were judged as unclear and moderate ROB. Most studies were in high-income countries, and the main strategy was educating HCPs through workshops. Meta-analysis showed significant increases in overall ADR reporting through educating HCPs with a rate ratio (RR) of 5.09 (95% CI: 3.36-7.71, I2 = 84.5%, low certainty), and in high-quality reporting with 1.31 (95% CI: 1.09-1.58, I2 = 0.0%, moderate certainty). Subgroup analysis indicated that educating HCPs through face-to-face workshops combined with the Tawai app (RR:10.5, 95% CI: 8.74-12.61), a face-to-face workshop alone (RR:6.69, 95% CI: 5.43-8.25, I2 = 0.0%), and repeated telephone (RR:2.59, 95% CI: 1.75-3.84, I2 = 8.8%) significantly increased the overall number of ADR reports with moderate certainty. Email or letter communications showed no significant effect.

Conclusion: Educating HCPs via interactive strategies like face-to-face workshops with or without a mobile app and repeated phone calls improved ADR reporting. However, long-term, high-quality studies are needed to confirm these findings before recommending widespread implementation in clinical practice, especially in low-and middle-income countries.

背景:药物警戒对患者安全至关重要,但药物不良反应(ADRs)报告不足是一项全球性挑战:本综述评估了加强医疗保健专业人员(HCPs)报告药物不良反应的策略的有效性:本系统性综述遵循 Cochrane 和 PRISMA 指南。检索了五个国际数据库,检索期从开始至 2023 年 12 月,更新检索期至 2024 年 9 月。纳入了有关加强 ADR 报告的随机临床对照试验 (RCT) 和非 RCT。主要结果是总体 ADR 报告和高质量 ADR 报告的数量。研究质量采用 EPOC 偏倚风险 (ROB) 和 ROBIN-I 对 RCT 和非 RCT 进行评估。所有数据均采用随机效应模型进行评估,异质性采用 I2 统计量和卡方检验进行评估:在 1,672 项研究中,共纳入了 13 项研究(10 项 RCT 和 3 项非 RCT),28,116 名参与者。在 10 项研究性试验中,有两项研究的投资回报率较低,其余研究的投资回报率被判定为不明确和中等。大多数研究都在高收入国家进行,主要策略是通过研讨会对保健医生进行教育。Meta 分析表明,通过对 HCPs 进行教育,ADR 报告率 (RR) 明显增加,达到 5.09(95%CI:3.36-7.71,I2=84.5%,低度确定性),高质量报告率为 1.31(95%CI:1.09-1.58,I2=0.0%,中度确定性)。亚组分析表明,通过结合 Tawai 应用程序的面对面研讨会(RR:10.5,95%CI:8.74-12.61)、单独的面对面研讨会(RR:6.69,95%CI:5.43-8.25,I2=0.0%)和重复电话(RR:2.59,95%CI:1.75-3.84,I2=8.8%)对 HCP 进行教育可显著增加 ADR 报告的总数,确定性为中等。电子邮件或信件沟通没有明显效果:结论:通过互动策略(如使用或不使用移动应用程序的面对面研讨会以及反复拨打电话)对初级保健人员进行教育可提高ADR报告率。然而,在建议在临床实践中(尤其是在低收入国家)广泛实施之前,需要进行长期、高质量的研究来证实这些发现。
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引用次数: 0
The role of pharmacy in promoting public health: Pharmacy and public health in 2050. 药学在促进公共健康中的作用:2050 年的药学与公共卫生。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-09 DOI: 10.1016/j.japh.2024.102272
Mark A Strand

From 2000 to 2025, the profession of pharmacy expanded into vaccinations, point-of-care testing, and chronic disease prevention and management. In the next 25 years, pharmacy will continue to advance in new ways. This paper focuses on expanded roles of community and ambulatory care pharmacy to more directly improve public health. Built around the ten essential services of public health, this paper calls upon the profession of pharmacy to stretch beyond traditional roles to assume roles that would strengthen the public health workforce and make seminal contributions to improved population health. Barriers to be overcome in pursuit of that future are also addressed. The paper will conclude with a public health-focused call to pharmacy.

从 2000 年到 2025 年,药剂学专业扩展到疫苗接种、护理点检测以及慢性病预防和管理。未来 25 年,药学将继续以新的方式向前发展。本文重点关注社区和非住院护理药房在更直接地改善公共卫生方面所发挥的更大作用。本文围绕公共卫生的十项基本服务,呼吁药学专业超越传统角色,承担起加强公共卫生人才队伍的角色,为改善人口健康做出开创性贡献。本文还探讨了实现这一未来需要克服的障碍。最后,本文将向药学界发出以公共卫生为重点的呼吁。
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引用次数: 0
Use of glucagon-like peptide 1 receptor agonist to sustain patients off basal-bolus insulin regimens. 使用胰高血糖素样肽 1 受体激动剂维持患者脱离基础胰岛素疗法。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-09 DOI: 10.1016/j.japh.2024.102288
Lauren Blumenfeld, Jillian Morgan, Timothy C Morgan, Ashley M Thomas

Background: The 2024 Standards of Care in Diabetes recommend initiation of glucagon-like peptide 1 receptor agonists (GLP-1 RAs) prior to starting basal insulin and to reconsider initiating a GLP-1 RA before starting bolus insulin if not already initiated. GLP-1 RA addition leads to improved glycemic benefits as well as risk reduction of cardiovascular and renal outcomes in patients with a history of these events. While there is evidence demonstrating the trends of insulin reduction or discontinuation following GLP-1 RA initiation, data regarding longer-term durability of GLP-1 RA use to sustain patients off bolus insulin are lacking.

Objective: This retrospective study aimed to assess the percentage of patients remaining off bolus insulin after transitioning from a basal-bolus regimen to GLP-1 RA therapy with basal insulin over a period of 3 years.

Methods: We conducted a single centered, retrospective study analyzing patient data from July 2018 through July 2023. Patients were included if they had a diagnosis of type 2 diabetes, were on a basal-bolus insulin regimen, had a GLP-1 RA initiated followed by bolus insulin discontinuation within 90 days, and remained on a GLP-1 RA for at least 6 months. The primary outcome was the percentage of patients who were sustained off bolus insulin after 3 years following GLP-1 RA initiation.

Results: There were 252 patients included. At 3 years, 82.6% of patients were sustained off bolus insulin. The mean change in weight at 3 years was -8.5 kg. The mean A1c initially decreased from 8.6% to 7.8%, but then increased slightly to 8.1% at the end of the study timeframe.

Conclusion: This trial demonstrated the majority of patients on basal-bolus regimens where bolus insulin was replaced with a GLP-1 RA were sustained off bolus insulin for a 3 year period of time. These results highlight the promising durability of converting bolus insulin to GLP-1 RAs.

背景:2024 年糖尿病治疗标准》建议,在开始使用基础胰岛素之前,先使用胰高血糖素样肽 1 受体激动剂(GLP-1 RA),如果尚未使用,则在开始使用胰岛素前重新考虑使用 GLP-1 RA。对于有心血管和肾脏疾病史的患者,添加 GLP-1 RA 可改善血糖,降低心血管和肾脏疾病风险。虽然有证据表明,在开始使用 GLP-1 RA 后,胰岛素用量会减少或停用,但有关长期使用 GLP-1 RA 使患者不再使用胰岛素的数据还很缺乏:这项回顾性研究旨在评估从基础胰岛素治疗方案过渡到 GLP-1 RA 基础胰岛素治疗方案后,三年内不再使用胰岛素长效胰岛素的患者比例:我们进行了一项单一中心的回顾性研究,分析了从 2018 年 7 月到 2023 年 7 月的患者数据。如果患者确诊为 2 型糖尿病,正在使用基础胰岛素栓剂疗法,开始使用 GLP-1 RA 后在 90 天内停用栓剂胰岛素,并继续使用 GLP-1 RA 至少 6 个月,则将其纳入研究。主要结果是在开始使用 GLP-1 RA 后三年内不再使用胰岛素注射剂的患者比例:结果:共纳入 252 名患者。三年后,82.6%的患者不再使用胰岛素。三年后体重的平均变化为-8.5 千克。平均 A1c 最初从 8.6% 降至 7.8%,但在研究结束时略有上升,达到 8.1%:这项试验表明,在用 GLP-1 RA 取代胰岛素的基础胰岛素治疗方案中,大多数患者都能在三年内持续停用胰岛素。这些结果凸显了将长效胰岛素转换为 GLP-1 RAs 的持久性。
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引用次数: 0
Pharmacy 2050: A new clinical and patient experience 药房 2050:全新的临床和患者体验。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-08 DOI: 10.1016/j.japh.2024.102290
George Bernard Van Antwerp Jr.
With the changing demographics of the U.S. population and evolving shift in urban design, the physical experience at the community level will change how health care is delivered. This will allow for more personalized and localized care complemented by digital technologies and smart devices over the next 25 years. At the same time, the evolution of clinical research with prevention, vaccinations, 3-dimensional printing, drone delivery, clustered interspaced short palindromic repeats, and implantables, will change the pharmaceutical landscape.
Pharmacists and pharmacies have an opportunity to evolve with these changes making their role an integral part of the care team, but it is important that regulations and reimbursement also change. By 2050, pharmacists may play very different roles from clinical specialists to digital coaches and use data, artificial intelligence, and technology to help drive outcomes whereas robots and technology automate many of their current repetitive tasks.
随着美国人口结构的变化和城市设计的发展,社区层面的实际体验将改变医疗服务的提供方式。这将在未来 25 年内实现更加个性化和本地化的医疗服务,并辅以数字技术和智能设备。同时,临床研究与预防、疫苗接种、3D 打印、无人机投递、CRISPR 和植入式设备的发展将改变制药业的格局。药剂师和药房有机会随着这些变化而发展,使自己的角色成为医疗团队中不可或缺的一部分,但重要的是法规和报销也要发生变化。到 2050 年,药剂师可能会扮演非常不同的角色,从临床专家到数字教练,并利用数据、人工智能和技术来帮助推动治疗效果,同时机器人和技术将他们目前的许多重复性任务自动化。
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引用次数: 0
Evaluating a Generative Artificial Intelligence Accuracy in Providing Medication Instructions from Smartphone Images. 评估生成式人工智能从智能手机图像中提供用药指导的准确性。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-06 DOI: 10.1016/j.japh.2024.102284
Yusef Yassin, Thien Nguyen, Krishna Panchal, Katie Nault, Timothy Aungst
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引用次数: 0
Beyond the fill: Navigating pharmacy's technological future in 2050. 超越填充:引领 2050 年药学技术的未来》(Beyond the Fill: Navigating Pharmacy's Technological Future in 2050)。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-11-05 DOI: 10.1016/j.japh.2024.102285
Timothy Dy Aungst

The pharmacy profession stands at a pivotal juncture as it faces unprecedented technological advancements that will rapidly reshape the healthcare landscape by 2050. This commentary explores the implications of technological advancements for pharmacy practice and how it may impact the workforce in the coming decades. The advent of digital health technologies (DHTs), artificial intelligence (AI), and automation is poised to transform patient engagement and care delivery. The Covid-19 pandemic has accelerated this shift, and traditional pharmacy roles have evolved to meet these expectations. As AI and DHT adoption increase, it will push the profession beyond its historical focus on logistics and medication dispensing. Several potential scenarios may unfold by 2050, ranging from a diminished workforce overshadowed by technology to an evolved profession that leverages novel technologies to enhance clinical services and patient care. To prepare for these changes, the profession must address key challenges, including advancing education and training to incorporate new competencies, establishing sustainable financial models for emerging roles, embracing advocacy and navigating regulatory constraints to expand scopes of practice, and overcoming societal resistance to change. By embracing continuous learning and adaptability, pharmacists can seize the opportunity to redefine their roles, ensuring they remain indispensable in an evolving healthcare environment.

药学行业正处于一个关键时刻,因为它面临着前所未有的技术进步,到 2050 年,这些技术将迅速重塑医疗保健行业的格局。这篇评论探讨了技术进步对药学实践的影响,以及它在未来几十年可能对药学人员队伍产生的影响。数字医疗技术 (DHT)、人工智能 (AI) 和自动化的出现将改变患者参与和医疗服务的提供。Covid-19 大流行加速了这一转变,传统的药房角色将不断演变以满足这些期望。随着人工智能和 DHT 应用的增加,它将推动药学行业超越以往对物流和配药的关注。到 2050 年,可能会出现几种潜在的情况,从被技术所掩盖的劳动力减少,到利用新技术加强临床服务和患者护理的专业进化。为了应对这些变化,该行业必须应对主要挑战,包括推进教育和培训以纳入新的能力,为新兴角色建立可持续的财务模式,接受宣传并驾驭监管限制以扩大业务范围,以及克服社会对变革的抵制。通过不断学习和提高适应能力,药剂师可以抓住机遇,重新定义自己的角色,确保他们在不断变化的医疗环境中继续发挥不可或缺的作用。
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Journal of the American Pharmacists Association
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