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Research and Scholarly Methods: Testing the Null Hypothesis 研究与学术方法:检验零假设
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-12 DOI: 10.1002/jac5.70167
John R. Carr, Susan E. Smith

Null hypothesis significance testing (NHST) is the predominant statistical framework in biomedical research and clinical pharmacy, so maintaining a thorough understanding of NHST and its component parts is essential for practitioners. NHST begins with an assumption the null hypothesis is true, allowing researchers to test for differences while guarding against bias. Type I error (false positive) and type II error (false negative) are the possible misclassifications. Interpretation of the p-value depends on the assumption that the null hypothesis is true, rather than indicating the probability that the null hypothesis is correct. Misinterpretation of this value remains one of the most persistent errors in medical literature. Sound application of NHST requires deliberate study design, prospective specification of outcomes, and safeguards against multiplicity. Interpretation demands attention to more than statistical thresholds alone, emphasizing effect size, clinical significance, biological plausibility, and study quality. Responsible interpretation also requires distinguishing statistical inference from broader scientific inference, which incorporates prior knowledge and theoretical rationale. Practical considerations and illustrative cases highlight common pitfalls and strategies for improvement. In addition, emerging approaches, including reinterpretation of confidence intervals as compatibility intervals, use of false positive risk, and Bayesian analysis offer potential refinements, though controversies regarding their application remain. Understanding NHST as one component of scientific inference, rather than a definitive arbiter of truth, promotes more thoughtful application and interpretation of evidence. Careful statistical reasoning enhances the quality of research, the reliability of peer review, and the translation of findings into patient care.

零假设显著性检验(NHST)是生物医学研究和临床药学的主要统计框架,因此保持对NHST及其组成部分的透彻理解对从业者至关重要。NHST首先假设零假设是正确的,允许研究人员在防止偏差的同时检验差异。类型I错误(假阳性)和类型II错误(假阴性)是可能的错误分类。p值的解释取决于假设原假设为真,而不是表明原假设正确的概率。对这一价值的误解仍然是医学文献中最持久的错误之一。NHST的合理应用需要深思熟虑的研究设计,结果的前瞻性规范,以及对多重性的保障。解释需要关注的不仅仅是统计阈值,还需要强调效应大小、临床意义、生物学合理性和研究质量。负责任的解释还需要将统计推断与更广泛的科学推断区分开来,后者包含了先验知识和理论基础。实际考虑和说明性案例突出了常见的缺陷和改进策略。此外,新兴的方法,包括将置信区间重新解释为兼容区间、使用假阳性风险和贝叶斯分析,提供了潜在的改进,尽管关于它们的应用仍然存在争议。将NHST理解为科学推理的一个组成部分,而不是真理的最终仲裁者,可以促进对证据的更深思熟虑的应用和解释。仔细的统计推理提高了研究的质量,同行评议的可靠性,以及将研究结果转化为患者护理。
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引用次数: 0
Preparing Future Pharmacists for an AI-Enhanced Health Care Environment: Educational Strategies and Implementation Challenges 为人工智能增强的卫生保健环境准备未来的药剂师:教育策略和实施挑战
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-12 DOI: 10.1002/jac5.70162
Khoa A. Nguyen, Cary Mobley, Jodi Taylor, Karen Whalen, Casey Rowe, Tracy Leonard, Chris Egan, Elizabeth Aguirre, Michael Outar, Kaitlin M. Alexander

The rapid advancement of artificial intelligence (AI) technologies has fundamentally transformed health care delivery, creating an urgent need to integrate AI education into pharmacy curricula, yet significant implementation challenges persist despite professional organizations establishing frameworks for AI education in health professions. This paper examines the current landscape of AI integration in pharmacy education through a literature review of recent surveys and an analysis of implementation challenges at a single college of pharmacy. Survey data reveal significant knowledge gaps, with approximately half of pharmacy faculty reporting limited AI familiarity and students expressing inadequate preparation for AI use in practice. Key implementation barriers may include a lack of institutional policies, curriculum overload, faculty development needs, varying student AI literacy levels, and challenges keeping pace with rapid technological advancement. Successful AI integration requires establishing a dedicated team with multidisciplinary representation, developing clear AI competencies and student learning outcomes, implementing active learning opportunities with hands-on AI experiences, and maintaining ongoing faculty development and curriculum review processes.

人工智能(AI)技术的快速发展从根本上改变了医疗保健服务,迫切需要将人工智能教育整合到药学课程中,然而,尽管专业组织为卫生专业的人工智能教育建立了框架,但重大的实施挑战仍然存在。本文通过对最近调查的文献综述和对一所药学院实施挑战的分析,研究了人工智能在药学教育中的整合现状。调查数据显示了重大的知识差距,大约一半的药学教师表示对人工智能的熟悉程度有限,学生表示对人工智能在实践中的应用准备不足。关键的实施障碍可能包括缺乏制度政策、课程超载、教师发展需求、学生人工智能素养水平不一,以及与快速技术进步保持同步的挑战。成功的人工智能整合需要建立一个具有多学科代表性的专门团队,开发明确的人工智能能力和学生学习成果,通过人工智能实践经验实现主动学习机会,并保持持续的教师发展和课程审查流程。
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引用次数: 0
Enhancing Pharmacy Students' Competencies in Continuous Glucose Monitoring Counseling: An Objective Structured Clinical Examination-Based Training Evaluation 提高药学学生持续血糖监测咨询能力:客观结构化临床考试培训评估
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-12 DOI: 10.1002/jac5.70163
Florian Kinny, Sabina Schlottau, Stephanie Laeer, Emina Obarcanin

Background

As accessible health care professionals, pharmacists are increasingly expected to engage with wearable technology, such as with continuous glucose monitors (CGM) and their associated data that are driven by the ongoing digital transformation. However, formal education on CGM data and its interpretation as well as related digital tools is not yet routinely integrated into pharmacy curricula, leaving a gap in students' preparation. The aim of this study was to enhance pharmacy students' competencies and confidence in CGM counseling through targeted training and to evaluate the effectiveness of this intervention.

Methods

A 4-h seminar was delivered focusing on CGM data and counseling procedures, including practical examples. Students' performance in CGM-counseling and self-assessment of their CGM competencies were assessed in a pre–post manner using Objective Structured Clinical Examination (OSCE) checklists. Additionally, training satisfaction and perceptions of the future integration of wearables and their role in pharmacy practice were captured.

Results

Following the training intervention, pharmacy students demonstrated a significant improvement in their consultation skills, with OSCE increasing from a mean of 19.12 (±7.66) to 63.47 (±12.34) percentage points (p < 0.001). Additionally, participants reported a significantly higher self-assessed performance and expressed notable satisfaction with the module.

Conclusion

Targeted training in CGM counseling significantly improves pharmacy students' competencies specific to CGM data and enhances their confidence in this area. This training prepares students for interpreting CGM data as one example of digital health solutions and wearables. Whether similar training effects extend to other digital health technologies remains to be determined by future research.

作为可访问的医疗保健专业人员,药剂师越来越多地希望参与可穿戴技术,例如持续血糖监测仪(CGM)及其相关数据,这些数据是由正在进行的数字化转型驱动的。然而,关于CGM数据及其解释以及相关数字工具的正规教育尚未常规地纳入药学课程,这在学生的准备方面留下了空白。本研究旨在透过有针对性的训练,提高药学院学生进行心理咨询的能力和信心,并评估干预的效果。方法进行为期4小时的研讨会,重点介绍CGM数据和咨询程序,包括实例。使用客观结构化临床检查(OSCE)检查表,以前后方式评估学生在CGM咨询和CGM能力自我评估方面的表现。此外,还捕获了培训满意度和对可穿戴设备未来整合及其在药房实践中的作用的看法。结果在培训干预后,药学专业学生的咨询技能有了显著提高,OSCE从平均19.12(±7.66)个百分点增加到63.47(±12.34)个百分点(p < 0.001)。此外,参与者报告了显着更高的自我评估绩效,并对该模块表达了显着的满意度。结论针对性的CGM咨询培训能显著提高药学专业学生的CGM数据能力,增强他们在该领域的信心。该培训使学生能够将CGM数据解释为数字健康解决方案和可穿戴设备的一个例子。类似的培训效果是否延伸到其他数字医疗技术,还有待未来的研究确定。
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引用次数: 0
Cost-Utility of Pharmacist-Led Deprescribing Interventions for Community-Dwelling Older Adults: A Systematic Review 药师主导的社区老年人处方干预的成本-效用:一项系统综述
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-12 DOI: 10.1002/jac5.70166
Chiranjeev Sanyal, Ronald Watema-Lord, Feng Xie

Background

Inappropriate medications continue to be dispensed to older adults. Deprescribing is an intervention carried out under the supervision of a health care professional, where medications that may cause harm or are no longer beneficial are reduced or withdrawn. Pharmacists play a crucial role in deprescribing potentially inappropriate medications. This systematic review aimed to summarize available evidence regarding the costs and cost-utility of pharmacist-led (or involved) deprescribing interventions for community-dwelling older adults.

Method

A systematic literature search was conducted from inception to June 6, 2025, using MEDLINE, EMBASE, CINAHL, and Cochrane Central. The titles and abstracts were screened, followed by eligibility assessment of full texts. The quality of studies was appraised using the Quality of Health Economic Studies (QHES) and Consolidated Health Economic Evaluation Reporting Standards (CHEERS) checklists. The cost-utility results were synthesized narratively.

Results

The search strategies identified a total of 3948 records, of which 9 articles were ultimately included in the systematic review based on inclusion and exclusion criteria. All economic evaluations were performed with a time horizon ranging from 6 to 12 months, and in most studies, the outcomes were derived from a single clinical trial. The cost-utility analyses varied, with some strategies being dominant to an incremental cost-utility ratio of €86 360.00 per quality-adjusted life-year.

Conclusions

The cost-utility analyses indicated that pharmacist-led deprescribing interventions are generally a cost-effective option compared with usual care. While these interventions appear promising from an economic standpoint, more long-term, population-based studies are needed to validate these findings

背景不适当的药物继续被分配给老年人。开处方是在卫生保健专业人员的监督下进行的一种干预措施,即减少或停用可能造成伤害或不再有益的药物。药剂师在处方可能不适当的药物方面起着至关重要的作用。本系统综述旨在总结有关药师主导(或参与)的社区老年人处方干预的成本和成本效用的现有证据。方法采用MEDLINE、EMBASE、CINAHL、Cochrane Central等软件,系统检索自建刊至2025年6月6日的文献。对标题和摘要进行筛选,然后对全文进行合格性评估。采用卫生经济研究质量(QHES)和综合卫生经济评价报告标准(CHEERS)检查表对研究质量进行评价。对成本-效用结果进行了叙述性综合。结果共检索到3948篇文献,其中9篇文献根据纳入和排除标准最终被纳入系统评价。所有的经济评估都是在6到12个月的时间范围内进行的,在大多数研究中,结果来自单一的临床试验。成本效用分析各不相同,一些策略占主导地位,每个质量调整生命年的增量成本效用比为86 360.00欧元。结论成本效用分析表明,与常规护理相比,药剂师主导的处方干预通常是一种具有成本效益的选择。虽然从经济角度来看,这些干预措施似乎很有希望,但需要更长期的、基于人群的研究来验证这些发现
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引用次数: 0
A Pre-Post Assessment of Blood Glucose Control Following Pharmacist-Led Professional Continuous Glucose Monitoring in Rhode Island Primary Care Practices 在罗德岛初级保健实践中,药剂师领导的专业连续血糖监测对血糖控制的前后评估
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-12 DOI: 10.1002/jac5.70171
Kelley Doherty Sanzen, Natalya S. Salganik, Susanne M. Campbell, Carolyn A. Karner, Pano M. Yeracaris, Stephen J. Kogut

Background

Professional continuous glucose monitoring (proCGM) can improve glycemic control and support medication and lifestyle adjustments in people with diabetes. In 2022, the Care Transformation Collaborative of Rhode Island launched a quality improvement initiative to implement pharmacist-led proCGM services in primary care practices. This project aimed to determine the effects of a pharmacist-led proCGM service on glycemic control, overall and by practice site, compared to baseline hemoglobin A1C (A1C) level. A secondary aim was to assess care team members' views of the program impact on patients and the practice environment.

Methods

A pre-post design was employed to assess reduction in A1C level 6 months following the implementation of pharmacist-led proCGM at six primary care sites. Pharmacists placed sensors, interpreted CGM data, and initiated diabetes medication changes. Eligible adult patients had either suboptimal glycemic control, discordant A1C and self-monitoring data, high hypoglycemia risk, or were referred by a provider. Changes in A1C were assessed 3–6 months after proCGM use. Care team surveys captured perceptions of the program's impact and sustainability.

Results

Among 396 patients, mean A1C decreased from 9.36% to 8.25% (p < 0.0001). A ≥ 1% point A1C reduction was achieved in 45.2% of patients. In multivariable analysis, baseline A1C was the strongest predictor of A1C improvement. Patients not using insulin and those who adopted personal CGM after the intervention were also more likely to improve. The majority of 51 care team members who completed the survey strongly agreed the service had positive impacts on patients and staff, and a majority believed the service could be sustainable.

Conclusion

Pharmacist-led proCGM services were associated with meaningful short-term A1C reductions, especially in patients with high baseline A1C not using insulin. The model was well-received by care teams and may help expand access to effective diabetes management in primary care settings.

背景:专业的连续血糖监测(proCGM)可以改善糖尿病患者的血糖控制,支持药物和生活方式的调整。2022年,罗德岛护理转型合作组织发起了一项质量改进倡议,在初级保健实践中实施药剂师主导的proCGM服务。本项目旨在确定药剂师主导的proCGM服务对血糖控制的影响,总体上和按实践地点,比较基线血红蛋白A1C (A1C)水平。第二个目的是评估护理团队成员对项目对患者和实践环境影响的看法。方法采用前后设计评估在6个初级保健点实施药师主导的proCGM 6个月后A1C水平的降低情况。药剂师放置传感器,解释CGM数据,并开始改变糖尿病药物。符合条件的成年患者要么血糖控制欠佳、糖化血红蛋白和自我监测数据不一致、低血糖风险高,要么是由医生转诊的。使用proCGM后3-6个月评估A1C的变化。护理团队的调查反映了对项目影响和可持续性的看法。结果396例患者中,平均A1C由9.36%降至8.25% (p < 0.0001)。45.2%的患者A1C降低≥1%。在多变量分析中,基线糖化血红蛋白是糖化血红蛋白改善的最强预测因子。不使用胰岛素的患者和干预后采用个人CGM的患者也更有可能改善。在完成调查的51名护理团队成员中,大多数人强烈认为这项服务对病人和工作人员有积极的影响,而且大多数人认为这项服务可以持续下去。结论:药师主导的proCGM服务与有意义的短期糖化血红蛋白降低相关,特别是在不使用胰岛素的高基线糖化血红蛋白患者中。该模型得到了护理团队的好评,并可能有助于在初级保健机构扩大获得有效的糖尿病管理。
{"title":"A Pre-Post Assessment of Blood Glucose Control Following Pharmacist-Led Professional Continuous Glucose Monitoring in Rhode Island Primary Care Practices","authors":"Kelley Doherty Sanzen,&nbsp;Natalya S. Salganik,&nbsp;Susanne M. Campbell,&nbsp;Carolyn A. Karner,&nbsp;Pano M. Yeracaris,&nbsp;Stephen J. Kogut","doi":"10.1002/jac5.70171","DOIUrl":"https://doi.org/10.1002/jac5.70171","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Professional continuous glucose monitoring (proCGM) can improve glycemic control and support medication and lifestyle adjustments in people with diabetes. In 2022, the Care Transformation Collaborative of Rhode Island launched a quality improvement initiative to implement pharmacist-led proCGM services in primary care practices. This project aimed to determine the effects of a pharmacist-led proCGM service on glycemic control, overall and by practice site, compared to baseline hemoglobin A1C (A1C) level. A secondary aim was to assess care team members' views of the program impact on patients and the practice environment.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A pre-post design was employed to assess reduction in A1C level 6 months following the implementation of pharmacist-led proCGM at six primary care sites. Pharmacists placed sensors, interpreted CGM data, and initiated diabetes medication changes. Eligible adult patients had either suboptimal glycemic control, discordant A1C and self-monitoring data, high hypoglycemia risk, or were referred by a provider. Changes in A1C were assessed 3–6 months after proCGM use. Care team surveys captured perceptions of the program's impact and sustainability.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Among 396 patients, mean A1C decreased from 9.36% to 8.25% (<i>p</i> &lt; 0.0001). A ≥ 1% point A1C reduction was achieved in 45.2% of patients. In multivariable analysis, baseline A1C was the strongest predictor of A1C improvement. Patients not using insulin and those who adopted personal CGM after the intervention were also more likely to improve. The majority of 51 care team members who completed the survey strongly agreed the service had positive impacts on patients and staff, and a majority believed the service could be sustainable.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Pharmacist-led proCGM services were associated with meaningful short-term A1C reductions, especially in patients with high baseline A1C not using insulin. The model was well-received by care teams and may help expand access to effective diabetes management in primary care settings.</p>\u0000 </section>\u0000 </div>","PeriodicalId":73966,"journal":{"name":"Journal of the American College of Clinical Pharmacy : JACCP","volume":"9 2","pages":""},"PeriodicalIF":1.5,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://accpjournals.onlinelibrary.wiley.com/doi/epdf/10.1002/jac5.70171","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145983866","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
Expanding Access to Opioid Use Disorder Treatment: Low-Threshold Buprenorphine Dispensing via an Interprofessional Mobile Medical Unit in Chicago 扩大获得阿片类药物使用障碍治疗:低阈值丁丙诺啡通过芝加哥的跨专业移动医疗单位分配
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-12 DOI: 10.1002/jac5.70170
Abigail T. Elmes-Patel, Jennie B. Jarrett, Antonio D. Jimenez, Stockton M. Mayer, Sarah E. Messmer

Background

Less than 25% of individuals with opioid use disorder access medication treatment. Lower income and segregated Black and Hispanic communities often have little to no access to services. In 2021, the Drug Enforcement Administration authorized opioid treatment programs to add mobile units to their licensure, extending treatment to disproportionately affected communities. The objectives of this study were to describe the service outcomes and buprenorphine dispensing of a mobile medical unit that leverages an interprofessional team incorporating clinical pharmacists to provide low-threshold buprenorphine and primary care in Chicago neighborhoods with high opioid overdose rates.

Methods

This retrospective cohort study was conducted via chart review for all patients seen by the mobile medical unit between July 1, 2022 and June 30, 2024. Variables collected were demographics (i.e., age, race/ethnicity, gender, and substance use history), amount of buprenorphine dispensed, and reasons that buprenorphine was not dispensed (if applicable). Descriptive statistics were used for analysis.

Results

During the study period, 737 patients were seen for buprenorphine across 2413 visits. The average patient was a 47-year-old Black male using five bags of opioids daily via insufflation for 20 years. Over 90% (n = 591) of patients reported polysubstance use. Two-thirds of patients (67.0%, n = 494) were dispensed buprenorphine across 1219 (70.5%) visits, including 697 (57.2%) 7-day, 291 (23.9%) 2-day, and 231 (18.9%) 3-day supplies. Reasons for not directly receiving buprenorphine when it was available to dispense included: longer duration indicated (25.9%, n = 132), shorter duration indicated (8.5%, n = 43), patient required different dosing from protocol (10.4%, n = 53), suspected diversion (6.7%, n = 34), patient taking or interested in methadone (2.8%, n = 14), or other (11.0%, n = 56).

Conclusion

Mobile medical services with an interprofessional low-threshold approach and direct buprenorphine dispensing offer a unique opportunity to involve clinical pharmacists in life-saving treatment and recovery support for communities with limited buprenorphine access.

不到25%的阿片类药物使用障碍患者获得药物治疗。低收入和种族隔离的黑人和西班牙裔社区往往很少或根本无法获得服务。2021年,美国缉毒局授权阿片类药物治疗项目在其许可证中增加移动单位,将治疗范围扩大到不成比例的受影响社区。本研究的目的是描述一个流动医疗单位的服务结果和丁丙诺啡配药,该单位利用包括临床药剂师在内的跨专业团队,在阿片类药物过量率高的芝加哥社区提供低门槛丁丙诺啡和初级保健。方法采用回顾性队列研究方法,对2022年7月1日至2024年6月30日在流动医疗单元就诊的所有患者进行回顾性队列研究。收集的变量包括人口统计数据(即年龄、种族/民族、性别和药物使用史)、丁丙诺啡的配药量以及丁丙诺啡未配药的原因(如果适用)。采用描述性统计进行分析。结果在研究期间,2413次就诊中有737例患者接受丁丙诺啡治疗。患者平均为47岁的黑人男性,20年来每天通过注射使用5袋阿片类药物。超过90% (n = 591)的患者报告使用多种药物。三分之二的患者(67.0%,n = 494)在1219次(70.5%)就诊中配发丁丙诺啡,其中7天697次(57.2%),2天291次(23.9%),3天231次(18.9%)。可配发丁丙诺啡时未直接服用丁丙诺啡的原因包括:适应期较长(25.9%,n = 132)、适应期较短(8.5%,n = 43)、患者需要与方案不同的剂量(10.4%,n = 53)、疑似分流(6.7%,n = 34)、患者正在服用或对美沙酮感兴趣(2.8%,n = 14)或其他(11.0%,n = 56)。结论采用跨专业低门槛方法的流动医疗服务和丁丙诺啡直接配药为临床药师参与丁丙诺啡获取有限社区的救生治疗和康复支持提供了独特的机会。
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引用次数: 0
Need for More HIV-Trained Pharmacists due to Unmet Needs and Expanding Opportunities: An Opinion of the HIV Practice and Research Network of the American College of Clinical Pharmacy 由于未满足的需求和不断扩大的机会,需要更多的HIV培训药剂师:美国临床药学学院HIV实践和研究网络的意见
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-08 DOI: 10.1002/jac5.70160
Radhika S. Polisetty, Spencer H. Durham, Roxane Rohani, David B. Cluck, Elizabeth Sherman, Crystal K. Hodge, Emily Huesgen, Eric Sahloff, Salin Nhean, Melissa Badowski, Marisa Brizzi, Kristy M. Shaeer

According to the Centers for Disease Control and Prevention, 1.2 million people are living with human immunodeficiency virus (HIV) in the United States, and an estimated 32 000 new HIV infections are reported each year. While pharmacists and pharmacies play major roles in ending the HIV epidemic, harnessing their full potential will require substantial investment in training qualified pharmacy personnel who can provide HIV prevention and treatment services encompassing comprehensive, culturally sensitive care. The purpose of this white paper is to review critical challenges facing the profession of pharmacy that hinder comprehensive HIV care, including the paucity of residency-trained HIV pharmacists due to a lack of HIV-focused post-graduate training programs, inconsistencies in pharmacy curricula, and insufficient or variable reimbursement for pharmacist services. By proposing targeted solutions across pharmacy education, training, research, and reimbursement, we seek to cultivate a robust, well-trained pharmacy workforce who can effectively provide HIV prevention and treatment services.

根据疾病控制和预防中心的数据,美国有120万人感染了人类免疫缺陷病毒(HIV),估计每年有3.2万例新的HIV感染报告。虽然药剂师和药房在结束艾滋病毒流行方面发挥着重要作用,但要充分发挥其潜力,就需要在培训合格的药学人员方面进行大量投资,使他们能够提供艾滋病毒预防和治疗服务,包括对文化有敏感认识的全面护理。本白皮书的目的是回顾阻碍全面艾滋病毒护理的药学专业面临的关键挑战,包括由于缺乏以艾滋病毒为重点的研究生培训计划而缺乏受过住院培训的艾滋病毒药剂师,药学课程的不一致以及药剂师服务的补偿不足或可变。通过在药学教育、培训、研究和报销方面提出有针对性的解决方案,我们寻求培养一支强大的、训练有素的药学劳动力队伍,他们可以有效地提供艾滋病预防和治疗服务。
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引用次数: 0
Low-Dose Buprenorphine Induction in Pregnant and Postpartum Patients: A Retrospective Analysis of Protocol Implementation 低剂量丁丙诺啡诱导孕妇和产后患者:方案实施的回顾性分析
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-08 DOI: 10.1002/jac5.70173
Kaitlyn Zbylut, Alexandra Herman, Michael Herman, Francheska Sevy Gurule, Jessica Taylor Goldstein, Larry Leeman

Background

Low-dose buprenorphine induction (LDBI) is a method using low doses of buprenorphine titrated to maintenance dosing. Literature on LDBI in pregnant and postpartum patients is limited to case series. The purpose of this study was to evaluate the implementation of an LDBI protocol, describe treatment outcomes of pregnant and postpartum patients with OUD who were treated with the protocol, and identify opportunities to improve this protocol.

Methods

An interdisciplinary team, including a clinical pharmacist, at a level IV maternity academic medical center developed and implemented an LDBI protocol. We performed a retrospective descriptive chart review of hospitalized pregnant and postpartum patients with opioid use disorder (OUD) at our institution. The primary outcome was successful LDBI, defined as reaching and discharging on goal dose buprenorphine without serious adverse effects. Secondary outcomes included adverse effects, protocol deviations, and characteristics that may predict success. Outpatient follow-up was also described.

Results

Of the 78 patients included for analysis, 59 (75.6%) successfully completed LDBI. Of the 19 (24.4%) patients that did not, 8 (10.3%) left before achieving goal dose without documented reason, 6 (7.6%) had intolerable withdrawal symptoms, and 5 (5.1%) were discharged with plans to attempt LDBI at a later time. Of these 19 patients, 10 (52.6%) had successful LDBI at subsequent encounters with an overall success rate on serial inductions of 69 (88.5%). There were no recorded serious adverse medication events from the protocol that caused patient harm. Tobacco use disorder without nicotine replacement therapy was associated with unsuccessful LDBI. Flexible protocol deviations or modifications may increase LDBI success.

Conclusion

Inpatient LDBI at this level IV maternity care center resulted in high success rates and was well tolerated. Several opportunities for improvement in the implementation of inpatient LDBI were identified. Further research is needed on improving transitions of care to the outpatient setting.

背景:低剂量丁丙诺啡诱导(LDBI)是一种使用低剂量丁丙诺啡滴定至维持剂量的方法。关于孕妇和产后LDBI的文献仅限于病例系列。本研究的目的是评估LDBI方案的实施情况,描述接受该方案治疗的孕妇和产后OUD患者的治疗结果,并确定改进该方案的机会。方法一个跨学科团队,包括一名临床药师,在一家四级产科学术医疗中心制定并实施了LDBI方案。我们对我院住院的阿片类药物使用障碍(OUD)孕妇和产后患者进行回顾性描述性图表回顾。主要终点是成功的LDBI,定义为达到并释放目标剂量的丁丙诺啡,没有严重的不良反应。次要结局包括不良反应、方案偏差和可能预测成功的特征。门诊随访也有描述。结果纳入分析的78例患者中,59例(75.6%)成功完成LDBI。在19例(24.4%)患者中,8例(10.3%)患者在达到目标剂量前无理由离开,6例(7.6%)患者有无法忍受的戒断症状,5例(5.1%)患者出院时计划稍后尝试LDBI。在这19例患者中,10例(52.6%)在随后的接触中成功进行LDBI,串联诱导的总成功率为69例(88.5%)。该方案中没有记录严重的药物不良事件,导致患者伤害。没有尼古丁替代治疗的烟草使用障碍与不成功的LDBI相关。灵活的协议偏差或修改可能会增加LDBI的成功。结论我院住院LDBI患者成功率高,耐受性好。确定了住院患者LDBI实施改进的几个机会。需要进一步的研究,以改善护理过渡到门诊设置。
{"title":"Low-Dose Buprenorphine Induction in Pregnant and Postpartum Patients: A Retrospective Analysis of Protocol Implementation","authors":"Kaitlyn Zbylut,&nbsp;Alexandra Herman,&nbsp;Michael Herman,&nbsp;Francheska Sevy Gurule,&nbsp;Jessica Taylor Goldstein,&nbsp;Larry Leeman","doi":"10.1002/jac5.70173","DOIUrl":"https://doi.org/10.1002/jac5.70173","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Low-dose buprenorphine induction (LDBI) is a method using low doses of buprenorphine titrated to maintenance dosing. Literature on LDBI in pregnant and postpartum patients is limited to case series. The purpose of this study was to evaluate the implementation of an LDBI protocol, describe treatment outcomes of pregnant and postpartum patients with OUD who were treated with the protocol, and identify opportunities to improve this protocol.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>An interdisciplinary team, including a clinical pharmacist, at a level IV maternity academic medical center developed and implemented an LDBI protocol. We performed a retrospective descriptive chart review of hospitalized pregnant and postpartum patients with opioid use disorder (OUD) at our institution. The primary outcome was successful LDBI, defined as reaching and discharging on goal dose buprenorphine without serious adverse effects. Secondary outcomes included adverse effects, protocol deviations, and characteristics that may predict success. Outpatient follow-up was also described.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Of the 78 patients included for analysis, 59 (75.6%) successfully completed LDBI. Of the 19 (24.4%) patients that did not, 8 (10.3%) left before achieving goal dose without documented reason, 6 (7.6%) had intolerable withdrawal symptoms, and 5 (5.1%) were discharged with plans to attempt LDBI at a later time. Of these 19 patients, 10 (52.6%) had successful LDBI at subsequent encounters with an overall success rate on serial inductions of 69 (88.5%). There were no recorded serious adverse medication events from the protocol that caused patient harm. Tobacco use disorder without nicotine replacement therapy was associated with unsuccessful LDBI. Flexible protocol deviations or modifications may increase LDBI success.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Inpatient LDBI at this level IV maternity care center resulted in high success rates and was well tolerated. Several opportunities for improvement in the implementation of inpatient LDBI were identified. Further research is needed on improving transitions of care to the outpatient setting.</p>\u0000 </section>\u0000 </div>","PeriodicalId":73966,"journal":{"name":"Journal of the American College of Clinical Pharmacy : JACCP","volume":"9 1","pages":""},"PeriodicalIF":1.5,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145986884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Targeted Antimicrobial Stewardship in a Pediatric Intensive Care Unit: Using the Methicillin-Resistant Staphylococcus aureus (MRSA) Nasal Polymerase Chain Reaction (PCR) to Reduce Vancomycin Days of Therapy 儿科重症监护病房的靶向抗菌药物管理:使用耐甲氧西林金黄色葡萄球菌(MRSA)鼻聚合酶链反应(PCR)减少万古霉素治疗天数
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-08 DOI: 10.1002/jac5.70169
Bailey Bridges, Sara Jones, Whitney Mays, Mary Joyce B. Wingler

Background

Vancomycin is commonly used in pediatric intensive care units (PICUs) to treat methicillin-resistant Staphylococcus aureus (MRSA) infections. While previous interventions in children's hospitals have successfully targeted vancomycin use, few have incorporated MRSA nasal polymerase chain reaction (PCR) testing. The MRSA PCR has been shown to reliably rule out MRSA infection and reduce vancomycin therapy duration in adults, but data in children are limited. This study aimed to evaluate the impact of an antimicrobial stewardship intervention on vancomycin use.

Methods

This retrospective study included patients less than 18 years old who received vancomycin in the PICU between January 1, 2019 and June 30, 2024. The primary outcome was vancomycin days of therapy (DOT) before and after the antimicrobial stewardship intervention. Secondary outcomes included acute kidney injury (AKI), hospital length of stay, and MRSA PCR sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV).

Results

A total of 251 patients were included, with 126 in the pre-group and 125 in the post-group. The median age was 2 years, and 60% were mechanically ventilated. The most common indication for vancomycin was sepsis of unknown origin (47%). The median vancomycin DOT was 4 days in both groups (p = 0.033). In patients without confirmed MRSA infection, the median duration was shorter in the post-group (4 vs. 3 days, p = 0.009). More patients in the post-group had vancomycin discontinued at 72 h (38.9% vs. 61.6%, p < 0.001). No significant differences were observed in secondary outcomes. The MRSA PCR sensitivity, specificity, PPV, and NPV were 66.7%, 92.7%, 34.5%, and 98.3%, respectively.

Conclusions

This intervention in PICU patients at an academic medical center led to more rapid vancomycin discontinuation and shorter DOT. The MRSA PCR demonstrated a high NPV, supporting its use as an antimicrobial stewardship tool.

背景万古霉素通常用于儿科重症监护病房(picu)治疗耐甲氧西林金黄色葡萄球菌(MRSA)感染。虽然以前儿童医院的干预措施已经成功地针对万古霉素的使用,但很少有纳入MRSA鼻腔聚合酶链反应(PCR)检测。MRSA PCR已被证明可以可靠地排除MRSA感染并缩短成人万古霉素治疗时间,但儿童的数据有限。本研究旨在评估抗菌药物管理干预对万古霉素使用的影响。方法回顾性研究纳入2019年1月1日至2024年6月30日期间在PICU接受万古霉素治疗的18岁以下患者。主要观察指标为抗菌药物管理干预前后的万古霉素治疗天数(DOT)。次要结局包括急性肾损伤(AKI)、住院时间、MRSA PCR敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)。结果共纳入251例患者,其中术前组126例,术后组125例。中位年龄为2岁,60%采用机械通气。万古霉素最常见的适应症是不明原因的败血症(47%)。两组中位万古霉素DOT均为4天(p = 0.033)。在未确诊MRSA感染的患者中,治疗后组的中位持续时间较短(4天vs. 3天,p = 0.009)。治疗后组更多的患者在72小时停止使用万古霉素(38.9%比61.6%,p < 0.001)。次要结局无显著差异。MRSA PCR敏感性、特异性、PPV和NPV分别为66.7%、92.7%、34.5%和98.3%。结论在学术医疗中心的PICU患者中,这种干预可以使万古霉素停药更快,DOT更短。MRSA PCR显示出高净现值,支持其作为抗菌管理工具的使用。
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引用次数: 0
JACCP in 2026: The Evolution of Scholarly Publishing Continues JACCP在2026年:学术出版的演变继续
IF 1.5 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-08 DOI: 10.1002/jac5.70161
Stuart T. Haines
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引用次数: 0
期刊
Journal of the American College of Clinical Pharmacy : JACCP
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