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A multicenter retrospective study of antidepressant use in outpatient clinics in China pre- and post-COVID. 中国门诊抗抑郁药物使用前后的多中心回顾性研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-08-14 DOI: 10.1007/s11096-024-01776-0
Mengqiang Zhao, Luyao Chang, Jing Yu, Jianxin Wang, Yang Song, Shi Su, Chaoli Chen, Yang Lun, Fangfang Cheng, Yuanyuan Zhao, Chunhua Zhou

Background: Analyzing antidepressant prescribing in real-world settings can provide clinicians and health policymakers valuable information.

Aim: This epidemiological study examined the status and trends in antidepressant prescribing among the Chinese population from July 1, 2017, to June 30, 2022.

Method: A retrospective study was conducted in three hospitals. Data were collected 2.5 years before and 2.5 years after the onset of the COVID-19 pandemic. We analyzed the number of patients diagnosed with depression and their corresponding antidepressant prescriptions. Using the chi-square test, stratified analyses were performed to explore the characteristics of these prescriptions in different ages and sexes.

Results: The study included 124,355 patients and 400,840 antidepressant prescriptions. We observed fluctuating upward trends in the number of patients and antidepressant prescriptions. Post-COVID-19, the number of patients increased by 37.1% compared to the pre-pandemic period, and the number of antidepressant prescriptions rose by 88.3%. The three most frequently prescribed antidepressants for adolescents were sertraline, citalopram, and escitalopram. Among adults, citalopram, escitalopram, and sertraline were most common, while in older adults, citalopram, escitalopram, and mirtazapine were predominant. Male patients used mirtazapine, venlafaxine, paroxetine, bupropion, fluvoxamine, vortioxetine, and clomipramine more frequently compared to female patients, who were more likely to be prescribed citalopram, flupentixol/melitracen, agomelatine, and fluoxetine. Antidepressant monotherapy represented 76.6% of prescriptions, with the most common combination being antidepressants and anxiolytics.

Conclusion: Over the past 5 years, both the number of patients and antidepressant prescriptions have shown upward trends, and the COVID-19 pandemic has impacted prescribing. Understanding the changes in antidepressant prescriptions can identify adherence to national guidelines.

背景:目的:本流行病学研究调查了2017年7月1日至2022年6月30日期间中国人群中抗抑郁药物的处方现状和趋势:方法:在三家医院开展了一项回顾性研究。数据收集于 COVID-19 大流行之前 2.5 年和之后 2.5 年。我们分析了被诊断为抑郁症的患者人数及其相应的抗抑郁药处方。我们使用卡方检验法进行了分层分析,以探讨这些处方在不同年龄和性别中的特点:研究包括 124,355 名患者和 400,840 份抗抑郁药处方。我们观察到患者和抗抑郁药物处方数量呈波动上升趋势。与大流行前相比,COVID-19 后的患者人数增加了 37.1%,抗抑郁药处方数量增加了 88.3%。青少年最常处方的三种抗抑郁药是舍曲林、西酞普兰和艾司西酞普兰。在成年人中,西酞普兰、艾司西酞普兰和舍曲林最为常见,而在老年人中,西酞普兰、艾司西酞普兰和米氮平占主导地位。与女性患者相比,男性患者更常使用米氮平、文拉法辛、帕罗西汀、安非他酮、氟伏沙明、伏硫西汀和氯米帕明,而女性患者则更常使用西酞普兰、氟哌噻醇/美利曲辛、阿戈美拉汀和氟西汀。抗抑郁药单药治疗占处方的76.6%,最常见的组合是抗抑郁药和抗焦虑药:结论:在过去 5 年中,患者人数和抗抑郁药处方量均呈上升趋势,COVID-19 大流行也对处方量产生了影响。了解抗抑郁药处方的变化可以确定国家指导方针的遵守情况。
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引用次数: 0
Measuring the impact of pharmaceutical care bundle delivery on patient outcomes: an observational study. 衡量药物护理捆绑服务对患者疗效的影响:一项观察性研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-05-28 DOI: 10.1007/s11096-024-01750-w
Martin Luke Canning, Ross McDougall, Stephanie Yerkovich, Michael Barras, Ian Coombes, Clair Sullivan, Karen Whitfield

Background: Clinical pharmacists perform activities to optimise medicines use and prevent patient harm. Historically, clinical pharmacy quality indicators have measured individual activities not linked to patient outcomes.

Aim: To determine the proportion of patients who receive a pharmaceutical care bundle (PCB) (consisting of a medication history, medication review, discharge medication list and medicines information on the discharge summary) as well as investigate the relationship between delivery of this PCB and patient outcomes.

Method: Pharmaceutical care bundle activities were defined within state-wide (Queensland, Australia) clinical information systems and datasets were linked. An observational study using routinely recorded data was performed at ten participating sites for adult patients who had a non-same day hospital stay. The association between extent of PCB delivery and three patient outcomes were investigated: length of stay (LOS), unplanned readmission, and mortality.

Results: In total 283,813 patient hospital stays were evaluated. The delivery of the PCB occurred in 26.9% of patients at the ten participating hospital sites, ranging from 0.6 to 61.2% across sites. Patients with a longer LOS were more likely to receive delivery of the complete PCB (P < 0.001). There was no correlation between PCB and hospital standardised mortality ratio (r = 0.03, p = 0.93). Higher rates of delivery of the PCB were associated with lower rates of unplanned readmission within 30 days (r = - 0.993, p < 0.001).

Conclusion: A complete PCB was delivered to 26.9% of patients and was associated with a significantly lower rate of unplanned readmission within 30 days.

背景:临床药剂师的工作旨在优化药物使用和预防对患者的伤害。目的:确定接受药物护理包(PCB)(包括用药史、用药回顾、出院用药清单和出院摘要中的药品信息)的患者比例,并调查该PCB的提供与患者预后之间的关系:方法:在全州(澳大利亚昆士兰州)的临床信息系统中定义药物护理捆绑活动,并将数据集连接起来。在十个参与研究的地点,针对非同日住院的成年患者,使用常规记录数据开展了一项观察性研究。研究调查了多氯联苯交付程度与三种患者结果之间的关系:住院时间(LOS)、非计划再入院和死亡率:结果:共对 283 813 名患者的住院时间进行了评估。在 10 家参与医院中,有 26.9% 的患者接受了多氯联苯治疗,各医院的比例从 0.6% 到 61.2% 不等。住院时间较长的患者更有可能获得完整的多氯联苯(P):有 26.9% 的患者接受了完整的多氯联苯治疗,这与 30 天内非计划再入院率显著降低有关。
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引用次数: 0
Perceived importance of emotional intelligence for clinical pharmacy practice and suggested improvements: a focus group study of postgraduate pharmacists. 情商对临床药学实践的重要性认知及改进建议:研究生药剂师焦点小组研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-06-11 DOI: 10.1007/s11096-024-01748-4
Dejan Senćanski, Ivana Tadić, Dragana Jocić, Valentina Marinković

Background: Emotional intelligence (EI) is a critical set of skills that impacts clinical pharmacists' well-being and positively influences high-level patient-centred care. Describing pharmacists' perceptions may support the integration of EI development approaches into their professional development continuum.

Aim: The aim of this study was to analyse pharmacists' perceptions of the characteristics of emotionally intelligent clinical pharmacists, the importance of EI in clinical practice, and educational models and approaches to enhancing EI.

Method: A qualitative study with a focus group methodology was conducted with pharmacy practitioners using a semi-structured guide grounded in the EI competency framework and existing qualitative research methodology practices. Purposive sampling was conducted until information and meaning saturation occurred. The focus group recordings were transcribed and independently coded by two researchers. The conventional content analysis of qualitative data was applied with the inductive thematic approach at its core.

Results: According to the 17 focus group participants, emotionally intelligent clinical pharmacists are perceived as self-confident communicators who control and manage emotions, work well under pressure, and handle every situation effectively. Emotional self-control, self-awareness, awareness of others, tolerance, understanding, and empathy have emerged as key EI competencies required for challenges in clinical practice. EI lectures with reflections from clinical applications, behaviour modelling, and behaviour-changing methods were perceived to be of particular importance for pharmacist education and development programmes.

Conclusion: Postgraduate pharmacy practitioners perceived EI competencies as necessary for their professional success and high-quality patient-centred care. They suggested that EI competencies be a focal point in pharmacy professional development programmes.

背景:情商(EI)是影响临床药剂师福祉的一套关键技能,并对以患者为中心的高级护理产生积极影响。目的:本研究旨在分析药剂师对情商临床药剂师的特点、情商在临床实践中的重要性以及提高情商的教育模式和方法的看法:方法:以情商能力框架和现有定性研究方法实践为基础,采用半结构化指南,对药剂师进行了焦点小组定性研究。在信息和意义达到饱和之前进行了有目的的抽样。焦点小组的录音由两名研究人员进行转录和独立编码。以归纳式主题方法为核心,对定性数据进行了传统的内容分析:根据 17 位焦点小组参与者的观点,情绪智能型临床药师被认为是自信的沟通者,他们能够控制和管理情绪,在压力下出色地工作,并有效地处理各种情况。情绪自我控制、自我意识、他人意识、宽容、理解和同理心成为临床实践挑战所需的关键 EI 能力。在药剂师教育和发展课程中,包含临床应用反思、行为建模和行为改变方法的情商教育讲座尤为重要:结论:研究生药剂师认为 EI 能力是其专业成功和以患者为中心的高质量护理所必需的。他们建议将 EI 能力作为药剂学专业发展课程的重点。
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引用次数: 0
The Medicines Optimisation Innovation Centre: a dedicated centre driving innovation in medicines optimisation-impact and sustainability. 药物优化创新中心:一个专门推动药物优化-影响和可持续性创新的中心。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-07-23 DOI: 10.1007/s11096-024-01775-1
A Hogg, M Scott, G Fleming, C Scullin, R Huey, S Martin, N Goodfellow, C Harrison

Background: Sub-optimal medicines use is a challenge globally, contributing to poorer health outcomes, inefficiencies and waste. The Medicines Optimisation Innovation Centre (MOIC) was established in Northern Ireland by the Department of Health (DH) in 2015 to support implementation of the Medicines Optimisation Quality Framework.

Aim: To demonstrate how MOIC informs policy and provides support to commissioners to improve population health and wellbeing.

Setting: MOIC is a regional centre with multidisciplinary and multi-sector clinical expertise across Health and Social Care and patient representation.

Development: Core funded by DH, MOIC has a robust governance structure and oversight programme board. An annual business plan is agreed with DH. Rigorous processes have been developed for project adoption and working collaboratively with industry.

Implementation: MOIC has established partnerships with academia, industry, healthcare and representative organisations across Europe, participating in research and development projects and testing integrated technology solutions. A hosting programme has been established and evaluation and dissemination strategies have been developed.

Evaluation: MOIC has established numerous agreements, partnered in three large EU projects and strengthened networks globally with extensive publications and conference presentations. Informing pathway redesign, sustainability and COVID response, MOIC has also assisted in the development of clinical pharmacy services and antimicrobial stewardship in Europe and Africa. Northern Ireland has been recognised as a 4-star European Active and Healthy Ageing Reference Site and the Integrated Medicines Management model as an example of best practice in Central and Eastern Europe.

Conclusion: MOIC has demonstrated considerable success and sustainability and is applicable to health systems globally.

背景:非最佳药物使用是全球面临的一项挑战,它导致了较差的健康结果、低效和浪费。北爱尔兰卫生部(DH)于 2015 年成立了 "药品优化创新中心"(MOIC),以支持 "药品优化质量框架 "的实施:MOIC是一个区域中心,拥有卫生和社会保健领域的多学科和多部门临床专业知识以及患者代表:发展:由卫生部提供核心资金,MOIC 拥有健全的治理结构和监督计划委员会。与卫生部商定了年度业务计划。已经制定了严格的项目采用和与行业合作的流程:MOIC 与欧洲的学术界、工业界、医疗保健和代表组织建立了合作伙伴关系,参与研发项目并测试综合技术解决方案。已经制定了一项托管计划,并制定了评估和传播战略:MOIC 签订了许多协议,与欧盟的三个大型项目建立了伙伴关系,并通过广泛的出版物和会议发言加强了全球网络。在为路径重新设计、可持续性和 COVID 应对措施提供信息的同时,MOIC 还协助欧洲和非洲发展临床药学服务和抗菌药物管理。北爱尔兰被评为 "欧洲积极健康老龄化四星级参考点","综合药品管理模式 "被评为中欧和东欧最佳实践范例:结论:MOIC 已取得相当大的成功,具有可持续性,适用于全球卫生系统。
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引用次数: 0
Protocols versus practice: unravelling clinical checking variations in community pharmacies in England-a multi-method study. 协议与实践:揭示英格兰社区药房临床检查的差异--一项多方法研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-06-01 DOI: 10.1007/s11096-024-01743-9
Ali Elgebli, Jason Hall, Denham L Phipps

Background: Standardisation, a widely accepted concept for risk management, entails designing and implementing task-specific operating procedures. In community pharmacies, Standardised Operating Procedures (SOPs) are a mandatory requirement and are recognised as essential for upholding safety and quality.

Aim: This study aimed to investigate community pharmacists' (CPs) compliance with SOPs when checking prescriptions, and the reasons for variations between standardised protocols and practice.

Method: Eight sets of SOPs underwent hierarchical task analysis (HTA) to generate a normative description of clinical checking execution as per protocols. Subsequently, twelve CPs were engaged in a simulated clinical checking exercise, verbalising their thoughts while checking virtual prescriptions. Transcribed data underwent content analysis, aligned with a descriptive model to uncover engagement patterns, and disparities between SOPs and CPs' practices. Finally, a focus group discussion took place to contextualise the observed variations.

Results: HTA aided in constructing a clinical checking model with six primary subtasks and 28 lower subtasks. CPs often omitted subtasks during checks, diverging from prescribed protocols. These deviations, observed in controlled environment, reveal an ingrained aspect within the professional culture of pharmacists, where there may be a tendency not to strictly adhere to protocols, despite variations in work conditions. Contributing factors to this culture include the exercise of professional judgment, reliance on others, and prioritisation of patient preferences.

Conclusion: This study highlights ongoing deviations from SOPs during clinical prescription checks in community pharmacies, suggesting a cultural tendency. Future research should delve into risk management strategies for these deviations and address the delicate balance between flexibility and stringent compliance.

背景:标准化是一个被广泛接受的风险管理概念,它要求设计和实施针对特定任务的操作程序。目的:本研究旨在调查社区药剂师(CPs)在检查处方时对 SOP 的遵守情况,以及标准化方案与实践之间存在差异的原因:方法:对八套 SOP 进行了分层任务分析 (HTA),以生成按规范执行临床核对的规范描述。随后,12 名临床医师参与了模拟临床核对练习,在核对虚拟处方时说出了自己的想法。对转录的数据进行了内容分析,并与描述性模型相结合,以揭示参与模式以及标准操作规程与临床医师实践之间的差异。最后,还进行了焦点小组讨论,对观察到的差异进行了背景分析:HTA 协助构建了一个临床检查模型,其中包括 6 个主要子任务和 28 个次要子任务。医护人员在检查过程中经常遗漏子任务,偏离规定的方案。在受控环境中观察到的这些偏差揭示了药剂师职业文化中根深蒂固的一个方面,即尽管工作条件不同,但可能存在不严格遵守规程的倾向。造成这种文化的因素包括行使专业判断力、依赖他人以及优先考虑病人的喜好:本研究强调了社区药房在临床处方检查过程中不断偏离 SOP 的情况,表明了一种文化倾向。未来的研究应深入探讨这些偏差的风险管理策略,并解决灵活性与严格合规性之间的微妙平衡问题。
{"title":"Protocols versus practice: unravelling clinical checking variations in community pharmacies in England-a multi-method study.","authors":"Ali Elgebli, Jason Hall, Denham L Phipps","doi":"10.1007/s11096-024-01743-9","DOIUrl":"10.1007/s11096-024-01743-9","url":null,"abstract":"<p><strong>Background: </strong>Standardisation, a widely accepted concept for risk management, entails designing and implementing task-specific operating procedures. In community pharmacies, Standardised Operating Procedures (SOPs) are a mandatory requirement and are recognised as essential for upholding safety and quality.</p><p><strong>Aim: </strong>This study aimed to investigate community pharmacists' (CPs) compliance with SOPs when checking prescriptions, and the reasons for variations between standardised protocols and practice.</p><p><strong>Method: </strong>Eight sets of SOPs underwent hierarchical task analysis (HTA) to generate a normative description of clinical checking execution as per protocols. Subsequently, twelve CPs were engaged in a simulated clinical checking exercise, verbalising their thoughts while checking virtual prescriptions. Transcribed data underwent content analysis, aligned with a descriptive model to uncover engagement patterns, and disparities between SOPs and CPs' practices. Finally, a focus group discussion took place to contextualise the observed variations.</p><p><strong>Results: </strong>HTA aided in constructing a clinical checking model with six primary subtasks and 28 lower subtasks. CPs often omitted subtasks during checks, diverging from prescribed protocols. These deviations, observed in controlled environment, reveal an ingrained aspect within the professional culture of pharmacists, where there may be a tendency not to strictly adhere to protocols, despite variations in work conditions. Contributing factors to this culture include the exercise of professional judgment, reliance on others, and prioritisation of patient preferences.</p><p><strong>Conclusion: </strong>This study highlights ongoing deviations from SOPs during clinical prescription checks in community pharmacies, suggesting a cultural tendency. Future research should delve into risk management strategies for these deviations and address the delicate balance between flexibility and stringent compliance.</p>","PeriodicalId":13828,"journal":{"name":"International Journal of Clinical Pharmacy","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11399187/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141186336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Medication Literacy Test for Older Adults: psychometric analysis and standardization of the new instrument. 老年人用药知识测试:新工具的心理测量分析和标准化。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-06-01 DOI: 10.1007/s11096-024-01744-8
Laís Lessa Neiva Pantuzza, Adriano Max Moreira Reis, Stephanie Ferreira Botelho, Ana Luiza Pereira da Rocha, Maria Auxiliadora Parreiras Martins, Mariana Martins Gonzaga do Nascimento, Liliana Batista Vieira, Ronara Camila de Souza Groia Veloso, Elizabeth do Nascimento

Background: Low medication literacy is prevalent among older adults and is associated with adverse drug events. The Medication Literacy Test for Older Adults (TELUMI) was developed and content validated in a previously published study.

Aim: To evaluate the psychometric properties and provide norms for TELUMI scores.

Method: This was a cross-sectional methodological study with older adults selected from the community and from two outpatient services. Descriptive item-analysis, exploratory factor analysis (EFA), item response theory (IRT), reliability, and validity analysis with schooling and health literacy were performed to test the psychometric properties of the TELUMI. The classification of the TELUMI scores was performed using percentile norms.

Results: A total of 344 participants, with a mean age of 68.7 years (standard deviation = 6.7), were included; most were female (66.6%), black/brown (61.8%), had low schooling level (60.2%) and low income (55.2%). The EFA pointed to the one-dimensional structure of TELUMI. A three-parameter logistic model was adopted for IRT. All items had an adequate difficulty index. One item had discrimination < 0.65, and three items had an unacceptable guessing index (< 0.35) and were excluded. The 29-item version of TELUMI had excellent internal consistency (KR20 = 0.89). There was a positive and strong association between TELUMI scores and health literacy and education level. The scores were classified as inadequate medication literacy (≤ 10.0 points), medium medication literacy (11-20 points), and adequate medication literacy (≥ 21 points).

Conclusion: The results suggest that the 29-item version of TELUMI is psychometrically adequate for measuring medication literacy in older adults.

背景:老年人普遍存在用药知识不足的问题,这与药物不良反应有关。老年人用药知识测试(TELUMI)是在之前发表的一项研究中开发并经过内容验证的。目的:评估TELUMI的心理测量特性,并提供TELUMI分数的标准:这是一项横断面方法学研究,研究对象是从社区和两个门诊服务机构挑选出来的老年人。通过描述性项目分析、探索性因素分析(EFA)、项目反应理论(IRT)、信度和效度分析,结合学校教育和健康素养,对 TELUMI 的心理测量特性进行了测试。采用百分位数标准对TELUMI得分进行了分类:共纳入 344 名参与者,平均年龄为 68.7 岁(标准差 = 6.7);大多数为女性(66.6%)、黑人/棕色人种(61.8%)、低学历(60.2%)和低收入(55.2%)。EFA 结果表明,TELUMI 具有一维结构。IRT 采用了三参数逻辑模型。所有项目都有适当的难度指数。有一个项目存在辨别结论:结果表明,29 个条目版本的 TELUMI 在心理测量学上足以测量老年人的用药知识。
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引用次数: 0
Cost avoidance of pharmacist-led deprescribing using STOPPFrail for older adults in nursing homes. 使用 STOPPFrail 为疗养院中的老年人提供药剂师指导的处方避免成本。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-07-05 DOI: 10.1007/s11096-024-01749-3
Eoin Hurley, Stephen Byrne, Elaine Walsh, Tony Foley, Noel Woods, Kieran Dalton

Background: The Screening Tool of Older Persons Prescriptions in Frail adults with limited life expectancy (STOPPFrail) criteria aim to reduce inappropriate/unnecessary medications in frail older adults, which should minimise adverse drug events and additional healthcare expenditure. Little is known about the economic outcomes of applying these criteria as an intervention.

Aim: To evaluate cost avoidance of pharmacist-led application of STOPPFrail to frail older nursing home residents with limited life expectancy.

Method: Pharmacist-identified STOPPFrail-defined potentially inappropriate medications that were deprescribed by patients' general practitioners were assigned a rating by a multidisciplinary panel, i.e. the probability of an adverse drug event occurring if the medication was not deprescribed. The intervention's net cost benefit and cost-benefit ratio were then determined by factoring in adverse drug event cost avoidance (calculated from probability of adverse drug event ratings), direct cost savings (deprescribed medication costs/reimbursement fees), and healthcare professionals' salaries.

Results: Of the 176 potentially inappropriate medications deprescribed across 69 patients, 65 (36.9%) were rated as having a medium or high probability of an adverse drug event occurring if not deprescribed. With €27,162 for direct cost savings, €61,336 for adverse drug event cost avoidance, and €2,589 for healthcare professionals' salary costs, there was a net cost benefit of €85,909 overall. The cost-benefit ratio was 33.2 and remained positive in all scenarios in sensitivity analyses.

Conclusion: Pharmacist-led application of STOPPFrail to frail older nursing home residents is associated with significant cost avoidance. Wider implementation of pharmacist interventions in frail older nursing home residents should be considered to reduce potentially inappropriate medications and patient harm, alongside substantial cost savings for healthcare systems.

背景:预期寿命有限的体弱老年人处方筛选工具(STOPPFrail)标准旨在减少体弱老年人的不适当/不必要用药,从而最大限度地减少不良药物事件和额外医疗支出。目的:评估在药剂师指导下将 STOPPFrail 应用于预期寿命有限的体弱老年疗养院居民所能避免的成本:方法:药剂师确定的 STOPPFrail 定义的潜在不适当药物由患者的全科医生开具处方,并由多学科小组进行评级,即如果不开具处方,发生药物不良事件的概率。然后,将避免不良药物事件成本(根据不良药物事件概率评级计算)、直接节约成本(处方药成本/报销费用)和医护人员工资等因素考虑在内,确定干预措施的净成本效益和成本效益比:在 69 名患者处方的 176 种潜在不当药物中,有 65 种(36.9%)被评为如果不处方,发生药物不良事件的概率为中等或高等。直接节省成本 27,162 欧元,避免不良药物事件成本 61,336 欧元,医护人员工资成本 2,589 欧元,总体净成本效益为 85,909 欧元。成本效益比为 33.2,在敏感性分析的所有方案中均为正值:结论:药剂师主导的 STOPPFrail疗法可为年老体弱的疗养院住户显著降低成本。应考虑对年老体弱的养老院居民更广泛地实施药剂师干预措施,以减少潜在的用药不当和对患者的伤害,同时为医疗保健系统节省大量成本。
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引用次数: 0
Causal impact of statins on susceptibility to osteoarthritis: insights from a two-sample Mendelian randomization analysis. 他汀类药物对骨关节炎易感性的因果影响:双样本孟德尔随机分析的启示。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-07-11 DOI: 10.1007/s11096-024-01754-6
Kefu Yu, Ziming Li, Weizhong Shi, Zhigang Zhao, Li Yang

Background: Osteoarthritis is a widely prevalent cause of pain and disability among older adults. It is an incurable condition, and most treatments are aimed at alleviating symptoms.

Aim: This study aimed to investigate the impact of statins on osteoarthritis by using a two-sample Mendelian randomization approach, using genetic variants associated with statin use as instrumental variables.

Method: Information on single nucleotide polymorphisms associated with statin medication was obtained from the FinnGen study, and data on osteoarthritis were sourced from the UK Biobank. The inverse variance weighted method was used as the primary analytical approach for the Mendelian randomization analysis. Sensitivity analyses were conducted to evaluate horizontal pleiotropy and heterogeneity. To examine the genetic relationship between statins and osteoarthritis, linkage disequilibrium score regression-based estimates were used.

Results: Mendelian randomization analysis indicated a positive effect of statin use on the treatment of osteoarthritis (odds ratio 0.951, 95% confidence interval 0.914-0.99, p < 0.05). This conclusion was supported by various Mendelian randomization methods. Sensitivity analyses revealed no significant directional pleiotropy or influential single nucleotide polymorphisms that could compromise the overall causal inference. Linkage disequilibrium score regression-based estimates suggested a modest genetic correlation between statin use and osteoarthritis (Rg = 0.098, Se = 0.034, p < 0.05), thus reinforcing the robustness of the Mendelian randomization analysis.

Conclusion: Statins reduce the risk of osteoarthritis, aligning with the results of observational studies. Further research is essential to validate these results and explore the underlying mechanisms in detail.

背景:骨关节炎是导致老年人疼痛和残疾的一个普遍原因。目的:本研究旨在采用双样本孟德尔随机化方法,将与他汀类药物使用相关的基因变异作为工具变量,调查他汀类药物对骨关节炎的影响:方法:与他汀类药物相关的单核苷酸多态性信息来自芬兰基因研究,骨关节炎数据来自英国生物库。孟德尔随机分析的主要分析方法是反方差加权法。进行了敏感性分析以评估水平多义性和异质性。为了研究他汀类药物与骨关节炎之间的遗传关系,使用了基于连接不平衡得分回归的估计值:孟德尔随机分析表明,使用他汀类药物对治疗骨关节炎有积极作用(几率比 0.951,95% 置信区间 0.914-0.99,P 结论:他汀类药物可降低骨关节炎的风险:他汀类药物可降低骨关节炎的风险,这与观察性研究的结果一致。进一步的研究对于验证这些结果和详细探索其潜在机制至关重要。
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引用次数: 0
Validation of an algorithm to prioritize patients for comprehensive medication management in primary care settings. 验证基层医疗机构对患者进行综合药物管理的优先顺序算法。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-07-23 DOI: 10.1007/s11096-024-01770-6
Martin A Bishop, Hsien-Yen Chang, Christopher Kitchen, Chintan J Pandya, Dannielle Brown, Jonathan P Weiner, Kenneth M Shermock, Kimberly A Gudzune

Background: Comprehensive medication management (CMM) programs optimize the effectiveness and safety of patients' medication regimens, but CMM may be underutilized. Whether healthcare claims data can identify patients appropriate for CMM is not well-studied.

Aim: Determine the face validity of a claims-based algorithm to prioritize patients who likely need CMM.

Method: We used claims data to construct patient-level markers of "regimen complexity" and "high-risk for adverse effects," which were combined to define four categories of claims-based CMM-need (very likely, likely, unlikely, very unlikely) among 180 patient records. Three clinicians independently reviewed each record to assess CMM need. We assessed concordance between the claims-based and clinician-review CMM need by calculating percent agreement as well as kappa statistic.

Results: Most records identified as 'very likely' (90%) by claims-based markers were identified by clinician-reviewers as needing CMM. Few records within the 'very unlikely' group (5%) were identified by clinician-reviewers as needing CMM. Interrater agreement between CMM-based algorithm and clinician review was moderate in strength (kappa = 0.6, p < 0.001).

Conclusion: Claims-based pharmacy measures may offer a valid approach to prioritize patients into CMM-need groups. Further testing of this algorithm is needed prior to implementation in clinic settings.

背景:综合用药管理(CMM)计划可优化患者用药方案的有效性和安全性,但CMM可能未得到充分利用。目的:确定基于报销单的算法的表面有效性,该算法可优先考虑可能需要 CMM 的患者:我们利用理赔数据构建了患者层面的 "治疗方案复杂性 "和 "不良反应高风险 "指标,并将其结合起来,在 180 份病历中定义了基于理赔的 CMM 需求的四个类别(很可能、可能、不可能、非常不可能)。三名临床医生对每份病历进行独立审核,以评估 CMM 需求。我们通过计算一致性百分比和卡帕统计来评估基于索赔的 CMM 需求与临床医生审查的 CMM 需求之间的一致性:临床医生审查人员认为,大多数基于索赔的标记被确定为 "很有可能"(90%)需要 CMM。在 "极不可能 "组中,只有极少数记录(5%)被临床医生评审员确定为需要 CMM。基于 CMM 的算法与临床医生审查之间的互译一致性强度适中(kappa = 0.6,p 结论:基于报销单的药学测量可提供一种有效的方法,将患者分为需要 CMM 的优先群体。在临床环境中实施该算法之前,需要对其进行进一步测试。
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引用次数: 0
Impact of pharmacist-evaluated clinical decision support system alerts on potentially missing or inappropriately prescribed proton pump inhibitors at hospital discharge: a retrospective cross-sectional study. 药剂师评估的临床决策支持系统警报对出院时可能遗漏或不当处方质子泵抑制剂的影响:一项回顾性横断面研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-01 Epub Date: 2024-06-13 DOI: 10.1007/s11096-024-01746-6
Lee Flückiger, Claudia Zaugg, Rico Fiumefreddo

Background: Proton pump inhibitors (PPIs) are among the most prescribed drugs. A clinical decision support system (CDSS) could improve their rational use.

Aim: The impact of an electronic algorithm (e-algorithm) implemented in a CDSS on potentially missing or inappropriately prescribed PPIs at hospital discharge, its specificity and sensitivity, and the outcome of the alerts issued were analysed.

Method: An e-algorithm continuously monitored patients of a tertiary care hospital for missing or inappropriate PPIs. Following relevance assessment by a pharmacist, the alerts raised were either displayed in the patients' electronic record or dismissed. After a three-month period, all adult patients' records were retrospectively reviewed for missing or inappropriate PPIs at discharge. The results were compared with a corresponding period before CDSS introduction. Sensitivity, specificity and outcome of alerts were quantified.

Results: In a 3-month period with 5018 patients, the CDSS created 158 alerts for missing PPIs and 464 alerts for inappropriate PPIs. PPI prescribing was proposed 81 times and PPI termination 122 times, with acceptance rates of 73% and 34%, respectively. A specificity of 99.4% and sensitivity of 92.0% for missing PPIs and a specificity of 97.1% and a sensitivity of 69.7% for inappropriate PPIs were calculated. The algorithm reduced incidents of missing PPIs by 63.4% (p < 0.001) and of inappropriate PPIs by 16.2% (p = 0.022).

Conclusion: The algorithm identified patients without necessary gastroprotection or inappropriate PPIs with high specificity and acceptable sensitivity. It positively impacted the rational use of PPIs by reducing incidents of missing and inappropriate PPIs.

背景:质子泵抑制剂(PPI)是处方量最大的药物之一。目的:分析了临床决策支持系统(CDSS)中采用的电子算法(e-algorithm)对出院时可能遗漏或不当处方 PPIs 的影响、其特异性和灵敏度以及发出警报的结果:方法:电子算法持续监测一家三甲医院的患者是否遗漏或不当使用 PPIs。在药剂师进行相关性评估后,发出的警报要么显示在患者的电子病历中,要么被驳回。三个月后,对所有成人患者的病历进行回顾性检查,以发现出院时缺少或不适当的 PPIs。结果与引入 CDSS 之前的相应时期进行了比较。对警报的灵敏度、特异性和结果进行了量化:在对 5018 名患者进行的为期 3 个月的检查中,CDSS 发出了 158 次 PPI 缺失警报和 464 次 PPI 使用不当警报。建议开具 PPI 81 次,终止 PPI 122 次,接受率分别为 73% 和 34%。计算得出,缺失 PPI 的特异性为 99.4%,灵敏度为 92.0%;不当 PPI 的特异性为 97.1%,灵敏度为 69.7%。该算法减少了 63.4% 的 PPIs 丢失率(p 结论:PPIs 丢失率的下降主要是由于 PPIs 的使用不当造成的:该算法能识别出无必要胃保护或不适当 PPIs 的患者,特异性高,灵敏度可接受。该算法减少了漏用和不当使用 PPIs 的情况,对合理使用 PPIs 产生了积极影响。
{"title":"Impact of pharmacist-evaluated clinical decision support system alerts on potentially missing or inappropriately prescribed proton pump inhibitors at hospital discharge: a retrospective cross-sectional study.","authors":"Lee Flückiger, Claudia Zaugg, Rico Fiumefreddo","doi":"10.1007/s11096-024-01746-6","DOIUrl":"10.1007/s11096-024-01746-6","url":null,"abstract":"<p><strong>Background: </strong>Proton pump inhibitors (PPIs) are among the most prescribed drugs. A clinical decision support system (CDSS) could improve their rational use.</p><p><strong>Aim: </strong>The impact of an electronic algorithm (e-algorithm) implemented in a CDSS on potentially missing or inappropriately prescribed PPIs at hospital discharge, its specificity and sensitivity, and the outcome of the alerts issued were analysed.</p><p><strong>Method: </strong>An e-algorithm continuously monitored patients of a tertiary care hospital for missing or inappropriate PPIs. Following relevance assessment by a pharmacist, the alerts raised were either displayed in the patients' electronic record or dismissed. After a three-month period, all adult patients' records were retrospectively reviewed for missing or inappropriate PPIs at discharge. The results were compared with a corresponding period before CDSS introduction. Sensitivity, specificity and outcome of alerts were quantified.</p><p><strong>Results: </strong>In a 3-month period with 5018 patients, the CDSS created 158 alerts for missing PPIs and 464 alerts for inappropriate PPIs. PPI prescribing was proposed 81 times and PPI termination 122 times, with acceptance rates of 73% and 34%, respectively. A specificity of 99.4% and sensitivity of 92.0% for missing PPIs and a specificity of 97.1% and a sensitivity of 69.7% for inappropriate PPIs were calculated. The algorithm reduced incidents of missing PPIs by 63.4% (p < 0.001) and of inappropriate PPIs by 16.2% (p = 0.022).</p><p><strong>Conclusion: </strong>The algorithm identified patients without necessary gastroprotection or inappropriate PPIs with high specificity and acceptable sensitivity. It positively impacted the rational use of PPIs by reducing incidents of missing and inappropriate PPIs.</p>","PeriodicalId":13828,"journal":{"name":"International Journal of Clinical Pharmacy","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11399224/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141310709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
International Journal of Clinical Pharmacy
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