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Unlocking the future of patient Education: ChatGPT vs. LexiComp® as sources of patient education materials 开启患者教育的未来:作为患者教育材料来源的 ChatGPT 与 LexiComp®。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-01-01 DOI: 10.1016/j.japh.2024.102119
Elizabeth W. Covington, Courtney S. Watts Alexander, Jeanna Sewell, Amber M. Hutchison, Julie Kay, Lucy Tocco, Melanie Hyte

Background

ChatGPT is a conversational artificial intelligence technology that has shown application in various facets of healthcare. With the increased use of AI, it is imperative to assess the accuracy and comprehensibility of AI platforms.

Objective

This pilot project aimed to assess the understandability, readability, and accuracy of ChatGPT as a source of medication-related patient education as compared with an evidence-based medicine tertiary reference resource, LexiComp®.

Methods

Patient education materials (PEMs) were obtained from ChatGPT and LexiComp® for 8 common medications (albuterol, apixaban, atorvastatin, hydrocodone/acetaminophen, insulin glargine, levofloxacin, omeprazole, and sacubitril/valsartan). PEMs were extracted, blinded, and assessed by 2 investigators independently. The primary outcome was a comparison of the Patient Education Materials Assessment Tool-printable (PEMAT-P). Secondary outcomes included Flesch reading ease, Flesch Kincaid grade level, percent passive sentences, word count, and accuracy. A 7-item accuracy checklist for each medication was generated by expert consensus among pharmacist investigators, with LexiComp® PEMs serving as the control. PEMAT-P interrater reliability was determined via intraclass correlation coefficient (ICC). Flesch reading ease, Flesch Kincaid grade level, percent passive sentences, and word count were calculated by Microsoft® Word®. Continuous data were assessed using the Student’s t-test via SPSS (version 20.0).

Results

No difference was found in the PEMAT-P understandability score of PEMs produced by ChatGPT versus LexiComp® [77.9% (11.0) vs. 72.5% (2.4), P=0.193]. Reading level was higher with ChatGPT [8.6 (1.2) vs. 5.6 (0.3), P < 0.001). ChatGPT PEMs had a lower percentage of passive sentences and lower word count. The average accuracy score of ChatGPT PEMs was 4.25/7 (61%), with scores ranging from 29% to 86%.

Conclusion

Despite comparable PEMAT-P scores, ChatGPT PEMs did not meet grade level targets. Lower word count and passive text with ChatGPT PEMs could benefit patients, but the variable accuracy scores prevent routine use of ChatGPT to produce medication-related PEMs at this time.
背景介绍ChatGPT 是一种对话式人工智能(AI)技术,已在医疗保健的各个方面得到应用。随着人工智能应用的增加,对人工智能平台的准确性和可理解性进行评估势在必行:本试点项目旨在评估 ChatGPT 作为药物相关患者教育资源与循证医学三级参考资源 LexiComp® 相比的可理解性、可读性和准确性:从 ChatGPT 和 LexiComp® 中获取了八种常见药物(阿布特罗、阿哌沙班、阿托伐他汀、氢可酮/对乙酰氨基酚、格列酮胰岛素、左氧氟沙星、奥美拉唑和沙库比曲利/缬沙坦)的患者教育资料(PEMs)。由两名研究人员独立提取、盲测和评估 PEM。主要结果是患者教育资料评估工具-可打印版(PEMAT-P)的比较。次要结果包括弗莱什阅读难易度、弗莱什-金凯德等级、被动句百分比、字数和准确性。每种药物的 7 项准确性核对表由药剂师研究人员通过专家共识生成,LexiComp® PEMs 作为对照。通过类内相关系数 (ICC) 测定 PEMAT-P 交互可靠性。Flesch 阅读难易度、Flesch Kincaid 等级、被动句百分比和字数由 Microsoft® Word® 计算。连续数据通过 SPSS(20.0 版)的学生 t 检验进行评估:结果:ChatGPT 与 LexiComp® 制作的 PEM 的 PEMAT-P 可理解性得分没有差异[77.9% (11.0) vs. 72.5% (2.4),P=0.193]。ChatGPT 的阅读水平更高[8.6 (1.2) vs. 5.6 (0.3),P=0.193]:尽管 PEMAT-P 分数相当,但 ChatGPT PEM 未达到年级目标。ChatGPT PEM 的字数较少,文字被动,这可能会使患者受益,但由于准确性分数不一,目前还不能常规使用 ChatGPT 制作药物相关的 PEM。
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引用次数: 0
Implementation of a specialty pharmacy in an ambulatory care setting in Saudi Arabia: Patient experience and operational outcomes 在沙特阿拉伯的门诊护理设置专业药房的实施:患者的经验和操作结果。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-01-01 DOI: 10.1016/j.japh.2024.102302
Abdulrazaq S. Al-Jazairi, Roa'a Al-Gain, Nasser I. Alrubayan, Alhanouf F. Almousa, Lina M. Aldawood, Reem A. Alshammari, Ghayda H. Alzaidi, Qasem A. Bahri, Sakra S. Balhareth, Norah Almalhooq, Yousef Binamer, Hisham Alomran

Background

Specialty pharmacy practice requires unique patient-centric care, emphasizing high-cost medications, complex treatment regimens, and medications requiring special handling.

Objective

We conducted this study to assess the effect of specialty pharmacy practice on patient and healthcare provider (HCP) satisfaction and pharmacy practice–related outcomes.

Methods

This prospective, concurrent, and historically controlled cohort study was performed in an ambulatory care setting for over 6 months and included 6 specialties: neurology, pediatrics, dermatology, gastroenterology, pediatric liver transplantation, and medical genetics. The workflow of the pharmacy was redesigned to serve the objective of specialized counseling and dispensing windows. Patients who visited selected clinics during the study period were included. The primary endpoint was the weighted scores for patient and HCP satisfaction obtained via a validated satisfaction survey. The secondary endpoints included pharmacy operation-related outcomes, such as patient's waiting time, pharmacist intervention, and patient adherence to specialty medications.

Results

Of the 3827 patients approached for study participation, 3620 were recruited (94.5%). Of the 175 HCPs approached, 161 were recruited. Patient satisfaction scores improved from 4.27 to 4.69 after intervention (P < 0.05). Although there was no significant change in pharmacists’ satisfaction, a significant improvement in other HCP satisfaction was observed (3.7–4; P = 0.008). The average wait time was reduced from 25 to 12 min (P < 0.05). The number of documented pharmacist interventions was 3 per 100 patients. Patient adherence improved from 73.6% to 85.6% based on the number of days covered (P = 0.03).

Conclusion

Implementing specialty pharmacies improved the overall satisfaction of patients and health care providers and enhanced work efficiency, as demonstrated by reduced pharmacy waiting time and patient adherence to specialty medications.
背景:专业药房需要独特的以患者为中心的护理,强调高成本药物、复杂的治疗方案和需要特殊处理的药物。目的:我们进行了这项研究,以评估专业药房对患者和医疗保健提供者(HCP)满意度和药学实践相关结果的影响。方法:这项前瞻性、同步、历史对照的队列研究在门诊环境中进行了6个多月,包括6个专业:神经病学、儿科、皮肤病学、胃肠病学、儿童肝移植和医学遗传学。药房的工作流程被重新设计,以服务于专业咨询和配药窗口的目标。在研究期间访问选定诊所的患者被纳入研究范围。主要终点是通过有效的满意度调查获得的患者和HCP满意度的加权分数。次要终点包括药房操作相关的结果,如等待时间、药剂师干预和患者对专业药物的依从性。结果:在3827名参与研究的患者中,有3620名(94.5%)被招募。在接触的175名医护人员中,161人被招募。干预后患者满意度由4.27分提高到4.69分(P < 0.05)。虽然药剂师的满意度没有显著变化,但其他医疗保健提供者的满意度有显著提高(3.7-4;P = 0.008)。平均等待时间由25 min缩短至12 min (P < 0.05)。记录在案的药剂师干预数量为每100名患者3名。根据覆盖天数,患者依从性从73.6%提高到85.6% (P = 0.03)。结论:专科药房的实施提高了患者和医疗服务提供者的整体满意度,提高了工作效率,减少了药房等待时间和患者对专科药物的依从性。
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引用次数: 0
Exploring the pharmacist role in insomnia management and care provision: A scoping review 探讨药师在失眠管理和护理中的作用:范围综述。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-01-01 DOI: 10.1016/j.japh.2024.102312
Mariam M. Basheti, Christopher Gordon, Ronald Grunstein, Bandana Saini

Background

Insomnia is a highly burdensome sleep disorder, with a global prevalence of approximately 30% in adults. Insomnia has negative effects on daily functioning and can play a pivotal role in the development and progression of comorbid mental and physical disease. Therefore, appropriate and timely management is essential. Pharmacists are at the forefront of the primary care workforce and given their expanding roles in care provision, would be able to alleviate the burden of insomnia in the community by delivering evidence-based management.

Objective

To describe the current practice and potential roles of pharmacists in insomnia management.

Methods

The Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews guidelines were followed in this scoping exercise. An extensive search of 5 databases (MEDLINE, Embase, Scopus, IPA, and CINAHL) was conducted, generating 1057 initial results. Titles, abstracts, and full-text articles were screened in a two-step process to identify relevant studies for review inclusion. Studies reporting on insomnia management by pharmacists in primary care settings were included in the review. Articles were reviewed and data extracted, analyzed, and grouped categorically based on study design.

Results

Twenty-eight studies met inclusion criteria with 5 qualitative, 8 observational and 15 interventional studies. Over a third of the studies were conducted in Australia (n = 11). Insomnia management across these studies ranged from 1) screening/assessment services (n = 5), 2) pharmacological and nonpharmacological care provision (n = 16), and 3) sedative-hypnotic deprescribing services (n = 7). It was evident that pharmacological approaches remain the most common treatment modality adopted despite guidelines recommending cognitive behavioral therapy as first-line. The results show that with adequate training and education, pharmacists have the potential to provide insomnia screening, behavioral therapy, and pharmacological deprescribing services, improving overall insomnia management in primary care.

Conclusion

The outcomes of this review highlight a current gap in insomnia management practices carried out by pharmacists and provide evidence for expanded roles and improved care provision when pharmacists are upskilled with specialized training/education.
背景:失眠是一种负担沉重的睡眠障碍,在全球成年人中的发病率约为 30%。失眠会对日常功能产生负面影响,并在合并精神和身体疾病的发生和发展中起到关键作用。因此,适当和及时的管理至关重要。药剂师是基层医疗队伍的中坚力量,鉴于其在提供医疗服务方面不断扩大的作用,他们将能够通过提供循证管理来减轻社区失眠的负担:目的:描述药剂师在失眠症管理方面的现有实践和潜在作用:方法:本次范围界定工作遵循 PRISMA-ScR 指南。对五个数据库(MEDLINE、Embase、Scopus、IPA、CINAHL)进行了广泛检索,得出了 1,057 项初步结果。通过两个步骤对标题、摘要和全文进行筛选,以确定纳入综述的相关研究。报道药剂师在基层医疗机构进行失眠管理的研究被纳入综述。对文章进行了审查,并根据研究设计提取、分析和分类数据:有 28 项研究符合纳入标准,其中包括 5 项定性研究、8 项观察性研究和 15 项干预性研究。超过三分之一的研究在澳大利亚进行(n=11)。在这些研究中,失眠管理的范围包括:1)筛查/评估服务(5 项);2)提供药物和非药物护理(16 项);3)镇静催眠药处方服务(7 项)。很明显,尽管指南建议将认知行为疗法作为第一线治疗方法,但药物疗法仍然是最常用的治疗方式。研究结果表明,通过适当的培训和教育,药剂师有潜力提供失眠筛查、行为疗法和药物处方服务,从而改善基层医疗机构的整体失眠管理:本综述的结果凸显了目前药剂师在失眠管理实践中存在的不足,并为药剂师在接受专业培训/教育后扩大角色和改善护理服务提供了证据。
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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 : 2025-01-01 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。
{"title":"Use of glucagon-like peptide 1 receptor agonist to sustain patients off basal-bolus insulin regimens","authors":"Lauren Blumenfeld,&nbsp;Jillian Morgan,&nbsp;Timothy C. Morgan,&nbsp;Ashley M. Thomas","doi":"10.1016/j.japh.2024.102288","DOIUrl":"10.1016/j.japh.2024.102288","url":null,"abstract":"<div><h3>Background</h3><div>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.</div></div><div><h3>Objective</h3><div>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.</div></div><div><h3>Methods</h3><div>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.</div></div><div><h3>Results</h3><div>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.</div></div><div><h3>Conclusion</h3><div>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.</div></div>","PeriodicalId":50015,"journal":{"name":"Journal of the American Pharmacists Association","volume":"65 1","pages":"Article 102288"},"PeriodicalIF":2.5,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142631458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Alabama community pharmacists’ knowledge and perceptions regarding fentanyl test strips: A cross-sectional survey 阿拉巴马州社区药剂师对芬太尼试纸的了解和看法:横断面调查。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-01-01 DOI: 10.1016/j.japh.2024.102148
Shannon Woods, Erin Blythe, Giovanna Valle-Ramos, Jessica Richardson, Karen Pham, Kavon Diggs, Klaudia Harris, Yi Zhao, Lindsey Hohmann

Background

Fentanyl test strips (FTS) are used to detect the presence of fentanyl in other substances, but Alabama pharmacists’ opinions regarding FTS provision are unknown.

Objective

The purpose of this study was to assess the knowledge and perceptions of Alabama pharmacists regarding FTS and factors influencing pharmacists’ FTS provision intentions across community pharmacy locations and types.

Methods

An anonymous cross-sectional survey was distributed via email to Alabama pharmacists employed in community (retail) pharmacies. The survey consisted of multiple-choice questions and 5-point Likert-type scales (1 = strongly disagree, 5 = strongly agree) informed by the Theory of Planned Behavior. Primary outcome measures included: knowledge; general attitudes; perceived benefits; perceived barriers; self-efficacy; subjective norms; perceived behavioral control (PBC); and intention regarding FTS provision. Outcomes were characterized using descriptive statistics and differences in scales scores across pharmacy locations (rural vs. urban) and types (corporately-vs. independently-owned) were assessed using Mann-Whitney U tests. Predictors of FTS provision intentions were evaluated using multiple linear regression (alpha=0.05).

Results

Respondents (N = 131; 3.82% response rate) were mostly female (64%) and Caucasian (92%). No respondents stocked FTS at their pharmacy and knowledge about FTS was low (mean[SD] knowledge score: 58.7% [15.1]). Despite the existence of perceived barriers (mean [SD] scale score: 3.2 [0.6]), pharmacists’ general attitudes (3.4 [0.5]), perceived benefits (3.7 [0.6]), self-efficacy (3.1 [0.8]), and intentions (3.2[0.7]) were positive. While subjective norms were positive (3.5[0.6]), PBC over FTS decision-making was negative (2.7[0.8]). Subjective norms were higher (P = 0.040) and PBC was lower (P < 0.001) amongst corporately-versus independently-owned pharmacies, but no differences existed between rural and urban locations for any measures. Additionally, perceived benefits (β=0.342, P = 0.002), PBC (β = 0.133, P = 0.045), and self-efficacy (β = 0.142, P = 0.034) were positive predictors and perceived barriers (β = −0.211, P = 0.029) was a negative predictor of intention.

Conclusion

Alabama community pharmacists have positive attitudes regarding FTS, but future research should focus on strategies to increase PBC and overcome perceived barriers.
背景:芬太尼试纸(FTS)用于检测其他物质中是否含有芬太尼,但阿拉巴马州药剂师对提供 FTS 的看法尚不清楚:本研究旨在评估阿拉巴马州药剂师对 FTS 的了解和看法,以及影响不同社区药房地点和类型的药剂师提供 FTS 意愿的因素:通过电子邮件向阿拉巴马州社区(零售)药店的药剂师发放匿名横截面调查问卷。调查包括多项选择题和 5 点李克特量表(1=非常不同意,5=非常同意),并参考了计划行为理论。主要结果测量指标包括:知识、一般态度、感知益处、感知障碍、自我效能、主观规范、感知行为控制(PBC)以及对提供 FTS 的意向。研究结果采用描述性统计方法进行描述,并采用 Mann-Whitney U 检验法评估不同药房地点(农村与城市)和类型(公司所有与独立所有)之间的量表评分差异。使用多元线性回归(alpha=0.05)评估了提供免费医疗服务意向的预测因素:受访者(131 人;回复率 3.82%)大多为女性(64%)和白种人(92%)。没有受访者的药房有 FTS 库存,对 FTS 的了解程度也较低(平均[标度]知识得分:58.7%[15.1])。尽管存在感知障碍(平均[标码]量表得分:3.2[0.6]),但药剂师的总体态度(3.4[0.5])、感知益处(3.7[0.6])、自我效能(3.1[0.8])和意向(3.2[0.7])都是积极的。虽然主观规范是积极的(3.5[0.6]),但 PBC 相对于 FTS 决策是消极的(2.7[0.8])。主观标准较高(p=0.040),而 PBC 较低(p结论:阿拉巴马州的社区药剂师对 FTS 持积极态度,但未来的研究应侧重于提高 PBC 和克服感知障碍的策略。
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引用次数: 0
Implementing a telemedicine-led heart failure medication regimen optimization clinic in medically underserved heart failure populations 在医疗服务不足的心力衰竭人群中实施远程医疗主导的心力衰竭药物治疗方案优化诊所。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-01-01 DOI: 10.1016/j.japh.2024.102309
Kazuhiko Kido, Wei Fang, Kimberly Becher, Brittany Carey, George Sokos

Background

Suboptimal guideline-directed medical therapy (GDMT) management for heart failure (HF) is a critical issue in rural communities. Most patients with HF in rural communities are treated in primary care settings. Multidisciplinary telemedicine-led HF medication optimization clinics were implemented to improve access to specialty care and address health disparities in HF care in rural Appalachian areas.

Objectives

The project aimed to evaluate the effect of a multidisciplinary telemedicine HF medication optimization clinic on the use of GDMT in cardiology and primary care services.

Methods

This pilot study was a multicenter prospective cohort study over a 6-month follow-up period. Patients aged > 18 years with HF with reduced ejection fraction or HF with mildly reduced ejection fraction were included. Telemedicine visits were conducted every 2 to 4 weeks. The primary outcome was the use of all 4 GDMT classes.

Results

The use of all 4 GDMT agents was numerically higher in HF cardiology service (n = 70) than the general cardiology cohort (n = 11) at baseline (46% vs. 9%), 1 month (55% vs. 18%), 3 months (58% vs. 18%), and 6 months (52% vs. 18%). The individual use of angiotensin receptor neprilysin inhibitor (ARNI), mineralocorticoid receptor antagonist (MRA), or sodium-glucose cotransporter 2 inhibitor (SGLT2I) was also numerically higher in HF cardiology service over 6 months. In the primary care service (n = 25), the use of all 4 GDMT agents was not significantly changed over 6 months. ARNI and beta-blocker use was numerically increased from the baseline to follow-up periods. MRA use was numerically decreased from baseline to follow-up periods. SGLT2I use was not significantly changed.

Conclusion

The multidisciplinary telemedicine approach was effective in the HF service group for GDMT optimization. However, further academic detailing for primary care and general cardiology services is needed, focusing on the initiation and persistence of MRA and SGLT2I and dose titration of GDMT agents.
背景:心力衰竭(HF)的指导性医疗疗法(GDMT)管理不理想是农村社区的关键问题。农村社区的大多数心衰患者都在初级医疗机构接受治疗。为了改善阿巴拉契亚农村地区心力衰竭患者获得专科治疗的机会,并解决心力衰竭治疗中的健康差距问题,我们开展了多学科远程医疗主导的心力衰竭药物优化诊所:该项目旨在评估多学科远程医疗高血压药物优化诊所对心脏病学和初级保健服务中使用 GDMT 的影响:这项试点研究是一项为期 6 个月的多中心前瞻性队列研究。研究对象包括年龄大于 18 岁的高频低氧血症(HFrEF)或高频低氧血症(HFmrEF)患者。远程医疗访问每 2 至 4 周进行一次。主要结果是使用了所有四类 GDMT:结果:在基线(46 对 9%)、1 个月(55 对 18%)、3 个月(58 对 18%)和 6 个月(52 对 18%)时,高频心脏病学服务(70 人)与普通心脏病学队列(11 人)相比,使用所有四种 GDMT 的人数更多。在高频心脏病服务中,6 个月内单独使用血管紧张素受体肾利酶抑制剂(ARNI)、矿物质皮质激素受体拮抗剂(MRA)或钠-葡萄糖共转运体-2 抑制剂(SGLT 2 I)的人数也更多。在初级保健服务中(25 人),所有四种 GDMT 药物的使用在 6 个月内没有明显变化。从基线到随访期间,ARNI 和 β-受体阻滞剂的使用在数量上有所增加。从基线到随访期间,MRA 的使用在数量上有所减少。SGLT 2 I 的使用没有明显变化:多学科远程医疗方法对高频服务组的 GDMT 优化很有效。然而,还需要对初级保健和普通心脏病学服务进行进一步的学术细化,重点关注 MRA 和 SGLT2I 的启动和持续使用,以及 GDMT 药物的剂量滴定。
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引用次数: 0
Accuracy and applicability of a tool designed to address pharmacy personnel stress 旨在解决药剂人员压力的工具的准确性和适用性。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-01-01 DOI: 10.1016/j.japh.2024.102296
Jon C. Schommer, Paul D. Tieger, Anthony W. Olson, SuHak Lee, Gavin Wilson

Background

Many pharmacy workplaces are so stressful that pharmacy personnel are unable to meet both clinical and nonclinical duties. Adjustments to training, roles, and responsibilities are not able to be made quickly enough to adapt to change and meet expanding responsibilities.

Objectives

Misalignment between a person’s unique personality type and their work dynamics can be associated with a stress reaction, what that reaction looks like, and what strategies would be most effective for reducing stress. The objectives for this study were to: (1) assess variability in the personality types of pharmacy personnel, (2) explore variation in most satisfying job activities and perceptions of stress by personality type, and (3) receive feedback regarding the accuracy, applicability, and recommendations for improving a tool for addressing stress.

Methods

A self-administered online questionnaire was used for collecting data from 1098 pharmacy personnel licensed in Minnesota. After answering four Preferred Communication Style Questionnaire items, a personalized De-Stress Rx report was generated for each respondent’s feedback by answering questions about the tool’s accuracy, applicability to them for helping reduce or manage stress, and recommendations for improving its usefulness. Data were analyzed using content analysis and descriptive statistics.

Results

The findings showed variability in the personality types of pharmacy personnel and that both the most satisfying job activities and stress perceptions vary by personality type. A tool that was designed to address pharmacy personnel stress was found to be both accurate and applicable. Study participants encouraged the expansion of the tool to include resources for follow-up and implementation. Also, they recommended expansion to teach groups and leaders about how to apply this tool to whole organizations, group dynamics, and evolving practice settings.

Conclusion

We propose that the De-Stress Rx Tool can help reduce the stress that is inherent in current pharmacy work settings.
背景:许多药房工作场所压力过大,以至于药剂师无法同时履行临床和非临床职责。对培训、角色和职责的调整无法迅速适应变化和履行不断扩大的职责:一个人独特的人格类型与其工作动力之间的不协调可能与压力反应有关,这种反应是什么样的,以及什么策略对减轻压力最有效。本研究的目标是(1) 评估药剂师人格类型的差异;(2) 探讨不同人格类型的药剂师在最满意的工作活动和对压力的感知方面的差异;(3) 接收有关准确性、适用性的反馈意见,并提出改进压力应对工具的建议:方法:采用自填式在线问卷的方式收集明尼苏达州 1,098 名持证药剂师的数据。在回答了四个首选沟通方式问卷(PCSQ)项目后,我们为每位受访者生成了一份个性化的 "减压RxTM "报告,受访者可通过回答有关该工具的准确性、对其在帮助减轻或管理压力方面的适用性以及改进其实用性的建议等问题来获得反馈意见。采用内容分析法和描述性统计法对数据进行了分析:结果:研究结果表明,药剂师的人格类型存在差异,不同人格类型的药剂师对最满意的工作活动和压力的感知也不尽相同。研究发现,针对药剂师压力设计的工具既准确又适用。研究参与者鼓励扩大该工具的范围,使其包括后续和实施资源。此外,他们还建议扩大范围,向团体和领导者传授如何将这一工具应用于整个组织、团体动态和不断变化的实践环境:我们建议,"减压 RxTM 工具 "可以帮助减轻当前药房工作环境中固有的压力。
{"title":"Accuracy and applicability of a tool designed to address pharmacy personnel stress","authors":"Jon C. Schommer,&nbsp;Paul D. Tieger,&nbsp;Anthony W. Olson,&nbsp;SuHak Lee,&nbsp;Gavin Wilson","doi":"10.1016/j.japh.2024.102296","DOIUrl":"10.1016/j.japh.2024.102296","url":null,"abstract":"<div><h3>Background</h3><div>Many pharmacy workplaces are so stressful that pharmacy personnel are unable to meet both clinical and nonclinical duties. Adjustments to training, roles, and responsibilities are not able to be made quickly enough to adapt to change and meet expanding responsibilities.</div></div><div><h3>Objectives</h3><div>Misalignment between a person’s unique personality type and their work dynamics can be associated with a stress reaction, what that reaction looks like, and what strategies would be most effective for reducing stress. The objectives for this study were to: (1) assess variability in the personality types of pharmacy personnel, (2) explore variation in most satisfying job activities and perceptions of stress by personality type, and (3) receive feedback regarding the accuracy, applicability, and recommendations for improving a tool for addressing stress.</div></div><div><h3>Methods</h3><div>A self-administered online questionnaire was used for collecting data from 1098 pharmacy personnel licensed in Minnesota. After answering four Preferred Communication Style Questionnaire items, a personalized De-Stress Rx report was generated for each respondent’s feedback by answering questions about the tool’s accuracy, applicability to them for helping reduce or manage stress, and recommendations for improving its usefulness. Data were analyzed using content analysis and descriptive statistics.</div></div><div><h3>Results</h3><div>The findings showed variability in the personality types of pharmacy personnel and that both the most satisfying job activities and stress perceptions vary by personality type. A tool that was designed to address pharmacy personnel stress was found to be both accurate and applicable. Study participants encouraged the expansion of the tool to include resources for follow-up and implementation. Also, they recommended expansion to teach groups and leaders about how to apply this tool to whole organizations, group dynamics, and evolving practice settings.</div></div><div><h3>Conclusion</h3><div>We propose that the De-Stress Rx Tool can help reduce the stress that is inherent in current pharmacy work settings.</div></div>","PeriodicalId":50015,"journal":{"name":"Journal of the American Pharmacists Association","volume":"65 1","pages":"Article 102296"},"PeriodicalIF":2.5,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142640114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Increasing SGLT-2 inhibitor prescribing through an integrated case-finding algorithm guided interdisciplinary intervention. 通过综合病例发现算法引导跨学科干预(INSPIRE)增加SGLT-2抑制剂处方。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-27 DOI: 10.1016/j.japh.2024.102320
Cindy Leslie A Roberson, Abby F Hoffman, Pamela Cohen, Victoria Lee Jackson, Susan E Spratt

Background: Use of sodium-glucose cotransporter 2 inhibitors (SGLT-2 inhibitors) falls short of their cardiorenal protective benefits. Patient and provider-level barriers hinder the adoption of these life-saving medications. Innovative practices to provide primary care providers (PCPs) with added clinical-decision support via a dedicated remote interdisciplinary diabetes rounds (IDRs) team could promote SGLT-2 inhibitor selection.

Objective: To evaluate the impact of the IDR's proactive provider outreach on the prescribing rate of SGLT-2 inhibitors and assess the application of an SGLT-2 inhibitor case-finding algorithm to allow targeted intervention in a population-health-based setting.

Methods: This is a quality improvement prospective cohort observational study from October 2021 to May 2022. Patients who met the prespecified criteria for SGLT-2 eligibility were reviewed via IDR with recommendations sent to the PCP via the electronic health record. The primary analysis employed a multivariate logistic regression to assess the difference in SGLT-2 inhibitor prescription rates between reviewed and not reviewed patients, adjusting for variables affecting SGLT-2 inhibitor prescribing. The secondary analysis measured the algorithm's accuracy in identifying patients with compelling indications.

Results: The IDR team reviewed a total of 206 patients (mean age, 63 years; 53.9% women; 42.7% Black; mean A1c 8.3%) with a successful PCP appointment. Patients reviewed by the IDR team had an increased prescribing rate within 90 days of the visit (adjusted odds ratio 5.1, 95% CI 3.06-8.47). The algorithm identified 1084 SGLT-2 inhibitor-eligible patients with a sensitivity of 90.4% (95% CI, 86.4%, 94.4%) and specificity of 85.1% (95% CI, 79.9%, 90.4%).

Conclusion: IDR team's review of eligible patients with recommendations to PCPs was associated with significantly increased SGLT-2 inhibitor prescription rates. Development of an algorithm with high sensitivity and specificity for targeted intervention may provide a pathway for channeling therapy and decreasing clinical inertia in population health management efforts.

背景:钠-葡萄糖共转运蛋白2抑制剂(SGLT-2抑制剂)的使用缺乏其心肾保护作用。患者和提供者层面的障碍阻碍了这些救命药物的采用。通过专门的远程跨学科糖尿病查轮(IDR)团队为初级保健提供者(PCP)提供额外的临床决策支持的创新实践可以促进SGLT-2抑制剂的选择。目的:评估IDR的主动提供者外展对SGLT-2抑制剂处方率的影响,并评估SGLT-2抑制剂病例查找算法的应用,以便在以人群健康为基础的环境中进行有针对性的干预。方法:这是一项质量改善前瞻性队列观察研究,时间为2021年10月至2022年5月。通过IDR对符合SGLT-2资格预定标准的患者进行审查,并通过电子健康记录(EHR)将建议发送给PCP。初步分析采用多变量logistic回归,对影响SGLT-2抑制剂处方的变量进行调整,评估纳入研究的患者与未纳入研究的患者之间SGLT-2抑制剂处方率的差异。第二次分析测量了该算法在识别具有令人信服的适应症的患者方面的准确性。结果:IDR团队共审查了206例患者(平均年龄63岁;53.9%的女性;42.7%是黑人;平均糖化血红蛋白为8.3%),PCP预约成功。IDR小组审查的患者在就诊后90天内的处方率增加(调整优势比[aOR] 5.1, 95% CI 3.06至8.47)。该算法确定了1084例符合SGLT-2抑制剂条件的患者,敏感性为90.4% (95% CI, 86.4%, 94.4%),特异性为85.1% (95% CI, 79.9%, 90.4%)。结论:IDR团队对推荐pcp的合格患者的审查与SGLT-2抑制剂处方率显着增加相关。开发一种具有高灵敏度和特异性的针对性干预算法,可能为引导治疗和减少人群健康管理工作中的临床惰性提供途径。
{"title":"Increasing SGLT-2 inhibitor prescribing through an integrated case-finding algorithm guided interdisciplinary intervention.","authors":"Cindy Leslie A Roberson, Abby F Hoffman, Pamela Cohen, Victoria Lee Jackson, Susan E Spratt","doi":"10.1016/j.japh.2024.102320","DOIUrl":"10.1016/j.japh.2024.102320","url":null,"abstract":"<p><strong>Background: </strong>Use of sodium-glucose cotransporter 2 inhibitors (SGLT-2 inhibitors) falls short of their cardiorenal protective benefits. Patient and provider-level barriers hinder the adoption of these life-saving medications. Innovative practices to provide primary care providers (PCPs) with added clinical-decision support via a dedicated remote interdisciplinary diabetes rounds (IDRs) team could promote SGLT-2 inhibitor selection.</p><p><strong>Objective: </strong>To evaluate the impact of the IDR's proactive provider outreach on the prescribing rate of SGLT-2 inhibitors and assess the application of an SGLT-2 inhibitor case-finding algorithm to allow targeted intervention in a population-health-based setting.</p><p><strong>Methods: </strong>This is a quality improvement prospective cohort observational study from October 2021 to May 2022. Patients who met the prespecified criteria for SGLT-2 eligibility were reviewed via IDR with recommendations sent to the PCP via the electronic health record. The primary analysis employed a multivariate logistic regression to assess the difference in SGLT-2 inhibitor prescription rates between reviewed and not reviewed patients, adjusting for variables affecting SGLT-2 inhibitor prescribing. The secondary analysis measured the algorithm's accuracy in identifying patients with compelling indications.</p><p><strong>Results: </strong>The IDR team reviewed a total of 206 patients (mean age, 63 years; 53.9% women; 42.7% Black; mean A1c 8.3%) with a successful PCP appointment. Patients reviewed by the IDR team had an increased prescribing rate within 90 days of the visit (adjusted odds ratio 5.1, 95% CI 3.06-8.47). The algorithm identified 1084 SGLT-2 inhibitor-eligible patients with a sensitivity of 90.4% (95% CI, 86.4%, 94.4%) and specificity of 85.1% (95% CI, 79.9%, 90.4%).</p><p><strong>Conclusion: </strong>IDR team's review of eligible patients with recommendations to PCPs was associated with significantly increased SGLT-2 inhibitor prescription rates. Development of an algorithm with high sensitivity and specificity for targeted intervention may provide a pathway for channeling therapy and decreasing clinical inertia in population health management efforts.</p>","PeriodicalId":50015,"journal":{"name":"Journal of the American Pharmacists Association","volume":" ","pages":"102320"},"PeriodicalIF":2.5,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142902869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pharmacist perceptions of motivation and well-being using Self-Determination Theory: A qualitative study. 药师对自我决定理论的动机和幸福感的认知:一项定性研究。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-27 DOI: 10.1016/j.japh.2024.102321
Kayla Walker, Alexcia S Carr, Andrew Wash, Leticia R Moczygemba

Background: Many US hospitals and health systems have implemented well-being programs to address the clinician well-being and burnout crisis. Most community pharmacists experience at least one symptom of burnout, yet they have been overlooked for inclusion in well-being initiatives.

Objective: To explore community pharmacists' perceptions of how motivation and burnout impact patient care and how fulfillment of basic psychological needs (autonomy, competence, and relatedness) impacts motivation and well-being.

Methods: Focus groups were conducted with 20 community pharmacists. A semistructured focus group guide was developed using Self-Determination Theory (SDT). Transcriptions from the focus groups were analyzed using deductive qualitative analysis with SDT as a framework and inductive analysis to code subthemes.

Results: Our findings revealed that pharmacists who feel burnout experience depersonalization toward patients which lowers the quality of patient-pharmacist interactions. Pharmacists who did not feel burnout expressed a sense of professional fulfillment, which motivated them to provide patient-centered care. Pharmacists indicated that unrealistic expectations from patients and corporate management, such as pressure from patients to fill prescriptions quickly and management expectations to meet prescription fill quotas, negatively impacted autonomy. Conversely, having access to clinical information, workflow optimization, and realistic job expectations supported autonomy. Poor relationships with patients and coworkers negatively impacted relatedness and contributed to communication barriers, workplace negativity, and emotional detachment from work. Relatedness was facilitated by building relationships and mutual respect with patients and coworkers and cultivating a positive work culture. Expectations for perfection and the need for multitasking when understaffed diminished competency. Adequate staffing and allocation of time to complete job duties served to support competency.

Conclusion: Community pharmacists are faced with situations that undermine autonomy, relatedness, and competency, which according to SDT need to be fulfilled to facilitate well-being.

背景:许多美国医院和卫生系统已经实施了福利计划,以解决临床医生的福利和职业倦怠危机。大多数社区药剂师至少经历过一种倦怠症状,但他们在福利倡议中被忽视了。目的:探讨社区药师的动机和倦怠对患者护理的影响,以及基本心理需求(自主性、能力和相关性)的满足对动机和幸福感的影响。方法:对20名社区药师进行焦点小组调查。运用自我决定理论(Self-Determination Theory, SDT)编制了半结构化焦点小组指南。使用SDT为框架的演绎定性分析和编码子主题的归纳分析对焦点小组的转录进行分析。结果:药师有倦怠感时,会对患者产生人格解体,降低医患互动的质量。没有感到倦怠的药剂师表现出一种职业成就感,这促使他们提供以患者为中心的护理。药师表示,来自患者和企业管理层的不切实际的期望,如患者要求快速配药的压力和管理层要求满足配药配额的期望,对自主经营产生了负面影响。相反,获得临床信息、工作流程优化和实际的工作期望支持了自主性。与病人和同事的不良关系会对人际关系产生负面影响,并导致沟通障碍、工作场所的消极情绪和对工作的情感疏离。通过与病人和同事建立关系和相互尊重以及培养积极的工作文化,可以促进关系。在人手不足的情况下,对完美的期望和一心多用的需求削弱了员工的能力。有足够的人员配备和时间分配来完成工作职责,以支持胜任能力。结论:社区药师面临着自主性、相关性和胜任力被削弱的情况,根据SDT需要满足这些情况以促进幸福感。
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引用次数: 0
Comparative effectiveness of buprenorphine adherence with telemedicine Vs. in-person for rural and urban patients. 丁丙诺啡依从性对农村和城市患者远程医疗与现场医疗的比较效果。
IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-12-27 DOI: 10.1016/j.japh.2024.102318
Thomas J Reese, Nana Addo Padi-Adjirackor, Kevin N Griffith, Bryan Steitz, Stephen W Patrick, Ashley A Leech, Andrew D Wiese, Adam Wright, Mauli V Shah, Jessica S Ancker

Background: Policy changes during the COVID-19 pandemic allowed buprenorphine to be prescribed for opioid use disorder via telemedicine without an in-person visit. A recently proposed change will limit buprenorphine access to 30 days without an in-person visit. Given that people living in rural areas may be disproportionally impacted by this change, we sought to better understand how buprenorphine adherence may be impacted by requiring in-person visits.

Objective: Compare buprenorphine adherence after telemedicine to adherence after in-person visits for patients who live in rural and urban areas.

Methods: In this retrospective cohort study, we used electronic health record data from a large medical center. The cohort included all adult patients prescribed buprenorphine for opioid use disorder during 2017-2022. The primary outcome was adherence, characterized by the Medication Possession Ratio (MPR) and gaps in buprenorphine treatment at 30 and 180 days. We conducted a longitudinal analysis at visit level, stratified by patient urbanicity, and controlled for patient, prescriber, prescription, and setting characteristics.

Results: From 511 patients, we followed 3302 in-person and 519 telemedicine visits. Compared to in-person visits we observed no difference in the adherence following telemedicine visits overall. However, telemedicine was associated with higher MPR for rural patients (30 days: adjusted marginal effects [AME], 3.7%; 95% CI, 2.0-5.5; P < 0.001 and 180 days: AME, 8.5%; 95% CI 5.7-11.3; P < 0.001) and fewer gaps (30 days: AME, -6.7%; 95% CI, -9.9 to -0.1; P < 0.001 and 180 days: AME, -9.4%; -14.0 to -4.5; P < 0.001) compared to in-person visits.

Conclusion: These findings suggest that telemedicine is a viable alternative to in-person visits, especially for patients living in rural areas, which should help guide future policies that preserve or increase access to buprenorphine in a manner that can reduce barriers for patients.

背景:COVID-19大流行期间的政策变化允许通过远程医疗为阿片类药物使用障碍(OUD)开具丁丙诺啡处方,而无需亲自就诊。最近提出的一项改变将把丁丙诺啡的使用限制在不亲自就诊的30天内。鉴于生活在农村地区的人们可能受到这一变化的不成比例的影响,我们试图更好地了解要求亲自就诊如何影响丁丙诺啡的依从性。目的:比较城乡患者远程医疗后丁丙诺啡依从性与上门就诊后丁丙诺啡依从性的差异。方法:在这项回顾性队列研究中,我们使用了一家大型医疗中心的电子健康记录数据。该队列包括2017-2022年期间处方丁丙诺啡治疗阿片类药物使用障碍的所有成年患者。主要终点是依从性,以药物占有比(MPR)和30天和180天丁丙诺啡治疗间隙为特征。我们在就诊水平上进行了纵向分析,按患者城市化程度分层,并控制了患者、处方者、处方和环境特征。结果:我们对511例患者进行了3302次现场随访和519次远程医疗随访。与亲自就诊相比,我们观察到远程医疗就诊后的依从性总体上没有差异。然而,远程医疗与农村患者较高的MPR相关(30天:调整边际效应[AME], 3.7%;95% CI, 2.0 ~ 5.5;P < 0.001, 180天:AME, 8.5%;95% CI 5.7 ~ 11.3;P < 0.001)和更少的间隔(30天:AME, -6.7%;95% CI, -9.9 ~ -0.1;P < 0.001, 180天:AME, -9.4%;-14.0 ~ -4.5;P < 0.001)。结论:这些发现表明,远程医疗是面对面就诊的可行替代方案,特别是对于生活在农村地区的患者,这应该有助于指导未来的政策,以减少患者障碍的方式保留或增加丁丙诺啡的获取。
{"title":"Comparative effectiveness of buprenorphine adherence with telemedicine Vs. in-person for rural and urban patients.","authors":"Thomas J Reese, Nana Addo Padi-Adjirackor, Kevin N Griffith, Bryan Steitz, Stephen W Patrick, Ashley A Leech, Andrew D Wiese, Adam Wright, Mauli V Shah, Jessica S Ancker","doi":"10.1016/j.japh.2024.102318","DOIUrl":"10.1016/j.japh.2024.102318","url":null,"abstract":"<p><strong>Background: </strong>Policy changes during the COVID-19 pandemic allowed buprenorphine to be prescribed for opioid use disorder via telemedicine without an in-person visit. A recently proposed change will limit buprenorphine access to 30 days without an in-person visit. Given that people living in rural areas may be disproportionally impacted by this change, we sought to better understand how buprenorphine adherence may be impacted by requiring in-person visits.</p><p><strong>Objective: </strong>Compare buprenorphine adherence after telemedicine to adherence after in-person visits for patients who live in rural and urban areas.</p><p><strong>Methods: </strong>In this retrospective cohort study, we used electronic health record data from a large medical center. The cohort included all adult patients prescribed buprenorphine for opioid use disorder during 2017-2022. The primary outcome was adherence, characterized by the Medication Possession Ratio (MPR) and gaps in buprenorphine treatment at 30 and 180 days. We conducted a longitudinal analysis at visit level, stratified by patient urbanicity, and controlled for patient, prescriber, prescription, and setting characteristics.</p><p><strong>Results: </strong>From 511 patients, we followed 3302 in-person and 519 telemedicine visits. Compared to in-person visits we observed no difference in the adherence following telemedicine visits overall. However, telemedicine was associated with higher MPR for rural patients (30 days: adjusted marginal effects [AME], 3.7%; 95% CI, 2.0-5.5; P < 0.001 and 180 days: AME, 8.5%; 95% CI 5.7-11.3; P < 0.001) and fewer gaps (30 days: AME, -6.7%; 95% CI, -9.9 to -0.1; P < 0.001 and 180 days: AME, -9.4%; -14.0 to -4.5; P < 0.001) compared to in-person visits.</p><p><strong>Conclusion: </strong>These findings suggest that telemedicine is a viable alternative to in-person visits, especially for patients living in rural areas, which should help guide future policies that preserve or increase access to buprenorphine in a manner that can reduce barriers for patients.</p>","PeriodicalId":50015,"journal":{"name":"Journal of the American Pharmacists Association","volume":" ","pages":"102318"},"PeriodicalIF":2.5,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142904002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Journal of the American Pharmacists Association
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