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A model for identifying potentially inappropriate medication used in older people with dementia: a machine learning study. 识别老年痴呆症患者潜在用药不当的模型:一项机器学习研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-07-09 DOI: 10.1007/s11096-024-01730-0
Qiaozhi Hu, Mengnan Zhao, Fei Teng, Gongchao Lin, Zhaohui Jin, Ting Xu

Background: Older adults with dementia often face the risk of potentially inappropriate medication (PIM) use. The quality of PIM evaluation is hindered by researchers' unfamiliarity with evaluation criteria for inappropriate drug use. While traditional machine learning algorithms can enhance evaluation quality, they struggle with the multilabel nature of prescription data.

Aim: This study aimed to combine six machine learning algorithms and three multilabel classification models to identify correlations in prescription information and develop an optimal model to identify PIMs in older adults with dementia.

Method: This study was conducted from January 1, 2020, to December 31, 2020. We used cluster sampling to obtain prescription data from patients 65 years and older with dementia. We assessed PIMs using the 2019 Beers criteria, the most authoritative and widely recognized standard for PIM detection. Our modeling process used three problem transformation methods (binary relevance, label powerset, and classifier chain) and six classification algorithms.

Results: We identified 18,338 older dementia patients and 36 PIMs types. The classifier chain + categorical boosting (CatBoost) model demonstrated superior performance, with the highest accuracy (97.93%), precision (95.39%), recall (94.07%), F1 score (95.69%), and subset accuracy values (97.41%), along with the lowest Hamming loss value (0.0011) and an acceptable duration of the operation (371s).

Conclusion: This research introduces a pioneering CC + CatBoost warning model for PIMs in older dementia patients, utilizing machine-learning techniques. This model enables a quick and precise identification of PIMs, simplifying the manual evaluation process.

背景:患有痴呆症的老年人经常面临潜在用药不当(PIM)的风险。由于研究人员不熟悉不适当用药的评估标准,因此影响了不适当用药评估的质量。本研究旨在结合六种机器学习算法和三种多标签分类模型来识别处方信息中的相关性,并开发一种最佳模型来识别老年痴呆症患者的 PIM:本研究于 2020 年 1 月 1 日至 2020 年 12 月 31 日进行。我们采用集群抽样的方式获取 65 岁及以上痴呆症患者的处方数据。我们使用 2019 Beers 标准对 PIM 进行了评估,该标准是最权威、最广为人知的 PIM 检测标准。我们的建模过程使用了三种问题转换方法(二元相关性、标签幂集和分类器链)和六种分类算法:我们确定了 18338 名老年痴呆症患者和 36 种 PIMs 类型。分类器链+分类提升(CatBoost)模型表现优异,准确率(97.93%)、精确率(95.39%)、召回率(94.07%)、F1得分(95.69%)和子集准确率值(97.41%)最高,汉明损失值(0.0011)最低,操作时间(371s)可接受:本研究利用机器学习技术,针对老年痴呆症患者的 PIMs 引入了一种开创性的 CC + CatBoost 预警模型。该模型可快速、准确地识别 PIM,简化人工评估过程。
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引用次数: 0
Optimisation of medication reconciliation using queueing theory: a computer experiment. 利用排队理论优化药物调节:计算机实验。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-05-10 DOI: 10.1007/s11096-024-01722-0
W J Kruik-Kollöffel, G A W Moltman, M D Wu, A Braaksma, F Karapinar, R J Boucherie

Background: Medication reconciliation (MedRec) in hospitals is an important tool to enhance the continuity of care, but completing MedRec is challenging.

Aim: The aim of this study was to investigate whether queueing theory could be used to compare various interventions to optimise the MedRec process to ultimately reduce the number of patients discharged prior to MedRec being completed. Queueing theory, the mathematical study of waiting lines or queues, has not been previously applied in hospital pharmacies but enables comparisons without interfering with the baseline workflow.

Method: Possible interventions to enhance the MedRec process (replacing in-person conversations with telephone conversations, reallocating pharmacy technicians (PTs) or adjusting their working schedule) were compared in a computer experiment. The primary outcome was the percentage of patients with an incomplete discharge MedRec. Due to the COVID-19 pandemic, it was possible to add a real-life post hoc intervention (PTs starting their shift later) to the theoretical interventions. Descriptive analysis was performed.

Results: The queueing model showed that the number of patients with an incomplete discharge MedRec decreased from 37.2% in the original scenario to approximately 16% when the PTs started their shift 2 h earlier and 1 PT was reassigned to prepare the discharge MedRec. The number increased with the real-life post hoc intervention (PTs starting later), which matches a decrease in the computer experiment when started earlier.

Conclusion: Using queueing theory in a computer experiment could identify the most promising theoretical intervention to decrease the percentage of patients discharged prior to MedRec being completed.

背景:目的:本研究旨在探讨是否可以使用排队理论来比较各种干预措施,以优化用药核对流程,最终减少在用药核对完成前出院的患者人数。排队理论是对等待线或队列的数学研究,以前从未在医院药房中应用过,但可以在不干扰基线工作流程的情况下进行比较:方法:在计算机实验中比较了加强医疗记录流程的可能干预措施(用电话交谈取代面对面交谈、重新分配药房技术人员(PTs)或调整他们的工作时间表)。主要结果是出院医疗记录不完整的患者比例。由于 COVID-19 大流行,在理论干预的基础上增加了一项现实生活中的事后干预(药剂师推迟上班时间)。对结果进行了描述性分析:排队模型显示,当护理人员提前 2 小时开始轮班,并重新指派 1 名护理人员准备出院医疗记录时,出院医疗记录不完整的患者人数从最初方案的 37.2% 降至约 16%。现实生活中的事后干预(PT 开始得晚一些)使这一数字上升,这与计算机实验中提前开始时的下降相吻合:结论:在计算机实验中使用排队理论,可以找出最有希望的理论干预措施,以降低在医疗记录完成前出院病人的比例。
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引用次数: 0
Critical care pharmacy service provision and workforce in adult extracorporeal membrane oxygenation centres: a multicentre cross-sectional survey. 成人体外膜肺氧合中心的重症监护药学服务供应和劳动力:一项多中心横断面调查。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-03-29 DOI: 10.1007/s11096-024-01719-9
Christopher Remmington, Lynda Cameron, Fraser Hanks, Ya-Hui Liang, Linda Barrow, Ruth Coxhead, Reena Mehta, Nisha Bhudia, Haifa Lyster, Sarah Cooke, James Gilmartin, Phillisa Lee, Rhona Sloss, Cathrine McKenzie

Background: There is good evidence describing pharmacy workforce and service provision in general critical care units. However, no data exist from adult extracorporeal membrane oxygenation (ECMO) centres.

Aim: To describe workforce characteristics, pharmacy service provision, and pharmaceutical care activities in critical care units (CCUs) providing an adult ECMO service in the United Kingdom (UK) and compare to national staffing standards for CCUs.

Method: We conducted a multicentre, cross-sectional electronic survey inviting one pharmacy professional response per UK ECMO centre. We collated information on workforce, service provision, and pharmaceutical care activities provided by pharmacy teams in adult CCUs with an ECMO service.

Results: The survey response rate was 90.9%: representatives of 10/11 tertiary hospitals providing ECMO services responded. Median critical care pharmacist to critical care bed was 1:12.1 (IQR: 1:9.4-1:14.9). Most centres (90.0%) did not meet national standards for pharmacy professionals to critical care bed staffing ratios for weekday services. Total critical care beds covered by the critical care pharmacy team varied across the UK: median (IQR) - 45 (37-80) beds. Two centres funded pharmacist time for ECMO activity, and one centre funded a pharmacy technician post. Median peak ECMO activity was 4 ECMO patients in a single day (IQR: 3-5). Most respondents reported reduced pharmacy service at weekends compared to weekday, with limited on-site support.

Conclusion: Most responding ECMO centres in the UK reported pharmacy staffing ratios below nationally agreed critical care standards. There was high variability in clinical pharmacy services to ECMO patients over 7 days.

背景:有充分证据表明,普通重症监护病房的药剂人员和服务提供情况良好。目的:描述英国(UK)提供成人 ECMO 服务的重症监护病房(CCU)的员工特点、药学服务提供情况和药物护理活动,并与 CCU 的国家人员配备标准进行比较:我们开展了一项多中心、横断面电子调查,邀请每个英国 ECMO 中心的一名药学专业人员回答。我们整理了拥有 ECMO 服务的成人 CCU 中药剂团队的劳动力、服务提供和药物护理活动等方面的信息:调查回复率为 90.9%:10/11 家提供 ECMO 服务的三级医院的代表进行了回复。重症监护药剂师与重症监护病床的比例中位数为 1:12.1(IQR:1:9.4-1:14.9)。大多数中心(90.0%)的药剂专业人员与重症监护病床平日服务人员配备比不符合国家标准。英国各地重症监护药学团队覆盖的重症监护病床总数不尽相同:中位数(IQR)为 45 (37-80) 张病床。两个中心资助药剂师的 ECMO 活动时间,一个中心资助一个药剂技师职位。单日 ECMO 活动高峰期的中位数为 4 名 ECMO 患者(IQR: 3-5)。大多数受访者表示,与工作日相比,周末的药学服务有所减少,现场支持有限:结论:英国大多数受访 ECMO 中心报告的药剂人员配备比率低于国家商定的重症监护标准。7 天内为 ECMO 患者提供的临床药学服务差异很大。
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引用次数: 0
Comment on "The efficacy of zuranolone versus placebo in postpartum depression and major depressive disorder: a systematic review and meta-analysis". 关于 "祖拉诺龙与安慰剂对产后抑郁症和重度抑郁障碍的疗效:系统综述和荟萃分析 "的评论。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-06-19 DOI: 10.1007/s11096-024-01763-5
Kazumasa Kotake
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引用次数: 0
Development and Delphi consensus validation of the Medication-Related Fall screening and scoring tool. 开发与药物相关跌倒筛查和评分工具,并对其进行德尔菲共识验证。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-05-16 DOI: 10.1007/s11096-024-01734-w
Dima Saeed, Gillian Carter, Ruth Miller, Carmel Darcy, Karen Miller, Kevin Madden, Hilary McKee, Jayne Agnew, Paula Crawford, Carole Parsons

Background: Falls are a significant public health problem and constitute a major cause of injuries and mortality. Risk factors for falls are multifactorial and include medication use.

Aim: To develop and investigate the content validity of the Medication-Related fall (MRF) screening and scoring tool.

Method: The MRF tool was developed from clinical practice guidelines addressing medication-related problems, and additional medications identified by specialist pharmacists across a region of the United Kingdom (Northern Ireland). Medication classes were categorised according to their 'potential to cause falls' as: high-risk (three points), moderate-risk (two points) or low-risk (one point). The overall medication-related falls risk for the patient was determined by summing the scores for all medications. The MRF was validated using Delphi consensus methodology, whereby three iterative rounds of surveys were conducted using SurveyMonkey®. Twenty-two experts from 10 countries determined their agreement with the falls risk associated with each medication on a 5-point Likert scale. Only medications with at least 75% of respondents agreeing or strongly agreeing were retained in the next round.

Results: Consensus was reached for 19 medications/medication classes to be included in the final version of the MRF tool; ten were classified as high-risk, eight as moderate-risk and one as low-risk.

Conclusion: The MRF tool is simple and has the potential to be integrated into medicines optimisation to reduce falls risk and negative fall-related outcomes. The score from the MRF tool can be used as a clinical parameter to assess the need for medication review and clinical interventions.

背景:跌倒是一个重大的公共卫生问题,也是造成伤害和死亡的主要原因。跌倒的风险因素是多方面的,其中包括用药。目的:开发与用药相关的跌倒(MRF)筛查和评分工具,并研究其内容的有效性:方法:MRF 工具是根据解决用药相关问题的临床实践指南以及英国一个地区(北爱尔兰)的专科药剂师确定的其他药物开发的。药物类别根据其 "导致跌倒的可能性 "分为:高风险(3 分)、中度风险(2 分)或低风险(1 分)。患者与药物相关的总体跌倒风险由所有药物的得分总和决定。MRF 采用德尔菲共识法进行验证,即使用 SurveyMonkey® 进行三轮反复调查。来自 10 个国家的 22 位专家通过 5 点李克特量表确定了他们对每种药物相关跌倒风险的认同度。只有至少 75% 的受访者表示同意或非常同意的药物才会被纳入下一轮调查:结果:19 种药物/药物类别被纳入 MRF 工具的最终版本;其中 10 种被归类为高风险,8 种被归类为中度风险,1 种被归类为低风险:MRF工具操作简单,有可能被整合到药物优化中,以降低跌倒风险和与跌倒相关的不良后果。MRF工具的评分可作为临床参数,用于评估药物审查和临床干预的必要性。
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引用次数: 0
Impact of intra-patient variability of tacrolimus on allograft function and CD4 + /CD8 + ratio in kidney transplant recipients: a retrospective single-center study. 肾移植受者体内他克莫司的变化对异体移植功能和 CD4 + /CD8 + 比率的影响:一项回顾性单中心研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-05-30 DOI: 10.1007/s11096-024-01726-w
Xuebin Wang, Zhengyue Liu, Jingxia Chen, Yuhui Chai, Xueqing Shao, Wenmin Xie, Kaile Zheng, Jia You, Zhuo Wang, Meiqing Feng

Background: Tacrolimus is a critical component of immunosuppressive therapy for kidney transplant recipients. Intra-patient variation (IPV) of tacrolimus levels affects the function of transplanted kidney.

Aim: This study aimed to investigate the impact of tacrolimus IPV on kidney function, examine its association with post-transplant duration, and assess its effect on the immune status of transplant recipients.

Method: This retrospective study was conducted from January 2016 to February 2022. IPV was evaluated using the coefficient of variation (CV) of tacrolimus trough levels from 6 to 48 months after transplantation. Patients were divided into low- and high-IPV groups based on the median CV. Significant differences in kidney function, CD4 + /CD8 + ratio, and post-transplant duration between these groups were analyzed.

Results: Among 189 patients, tacrolimus IPV showed a strong correlation with serum creatinine clearance rate (Ccr) and estimated glomerular filtration rate (eGFR) (p < 0.05). Tacrolimus IPV was significantly correlated with post-transplant duration in only two patients (p < 0.05). Using a median CV of 15.4% to categorize patients, the high IPV group, compared to the low IPV group, exhibited significantly higher eGFR at 6-9 months (p < 0.05), lower Ccr at 9-12 months (p < 0.05), and reduced Ccr and eGFR at 15-18 months (p < 0.05). Six months after transplantation, the high IPV group had a significantly lower CD4 + /CD8 + ratio than the low IPV group (p < 0.05).

Conclusion: This study highlights the significant impact of tacrolimus IPV on transplant kidney function and immune status in transplant patients at various post-transplantation intervals.

背景:他克莫司是肾移植受者免疫抑制疗法的重要组成部分。目的:本研究旨在调查他克莫司 IPV 对肾功能的影响,研究其与移植后持续时间的关系,并评估其对移植受者免疫状态的影响:这项回顾性研究于2016年1月至2022年2月进行。IPV通过移植后6至48个月期间他克莫司谷值的变异系数(CV)进行评估。根据中位变异系数将患者分为低 IPV 组和高 IPV 组。分析了这两组患者在肾功能、CD4 + /CD8 + 比率和移植后持续时间方面的显著差异:结果:在 189 名患者中,他克莫司 IPV 与血清肌酐清除率(Ccr)和估计肾小球滤过率(eGFR)有很强的相关性(p 结论:在 189 名患者中,他克莫司 IPV 与血清肌酐清除率(Ccr)和估计肾小球滤过率(eGFR)有很强的相关性:本研究强调了他克莫司 IPV 对移植后不同时期移植患者的移植肾功能和免疫状态的重要影响。
{"title":"Impact of intra-patient variability of tacrolimus on allograft function and CD4 + /CD8 + ratio in kidney transplant recipients: a retrospective single-center study.","authors":"Xuebin Wang, Zhengyue Liu, Jingxia Chen, Yuhui Chai, Xueqing Shao, Wenmin Xie, Kaile Zheng, Jia You, Zhuo Wang, Meiqing Feng","doi":"10.1007/s11096-024-01726-w","DOIUrl":"10.1007/s11096-024-01726-w","url":null,"abstract":"<p><strong>Background: </strong>Tacrolimus is a critical component of immunosuppressive therapy for kidney transplant recipients. Intra-patient variation (IPV) of tacrolimus levels affects the function of transplanted kidney.</p><p><strong>Aim: </strong>This study aimed to investigate the impact of tacrolimus IPV on kidney function, examine its association with post-transplant duration, and assess its effect on the immune status of transplant recipients.</p><p><strong>Method: </strong>This retrospective study was conducted from January 2016 to February 2022. IPV was evaluated using the coefficient of variation (CV) of tacrolimus trough levels from 6 to 48 months after transplantation. Patients were divided into low- and high-IPV groups based on the median CV. Significant differences in kidney function, CD4 + /CD8 + ratio, and post-transplant duration between these groups were analyzed.</p><p><strong>Results: </strong>Among 189 patients, tacrolimus IPV showed a strong correlation with serum creatinine clearance rate (Ccr) and estimated glomerular filtration rate (eGFR) (p < 0.05). Tacrolimus IPV was significantly correlated with post-transplant duration in only two patients (p < 0.05). Using a median CV of 15.4% to categorize patients, the high IPV group, compared to the low IPV group, exhibited significantly higher eGFR at 6-9 months (p < 0.05), lower Ccr at 9-12 months (p < 0.05), and reduced Ccr and eGFR at 15-18 months (p < 0.05). Six months after transplantation, the high IPV group had a significantly lower CD4 + /CD8 + ratio than the low IPV group (p < 0.05).</p><p><strong>Conclusion: </strong>This study highlights the significant impact of tacrolimus IPV on transplant kidney function and immune status in transplant patients at various post-transplantation intervals.</p>","PeriodicalId":13828,"journal":{"name":"International Journal of Clinical Pharmacy","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141174502","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
Authors' response to comments on "The efficacy of zuranolone versus placebo in postpartum depression and major depressive disorder: a systematic review and meta-analysis". 作者对 "莪术酮与安慰剂对产后抑郁症和重度抑郁障碍的疗效:系统综述和荟萃分析 "评论的回应。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-07-10 DOI: 10.1007/s11096-024-01771-5
Eric C Nemec, Suzanne J Rose
{"title":"Authors' response to comments on \"The efficacy of zuranolone versus placebo in postpartum depression and major depressive disorder: a systematic review and meta-analysis\".","authors":"Eric C Nemec, Suzanne J Rose","doi":"10.1007/s11096-024-01771-5","DOIUrl":"10.1007/s11096-024-01771-5","url":null,"abstract":"","PeriodicalId":13828,"journal":{"name":"International Journal of Clinical Pharmacy","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141563289","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
Community pharmacists' views and experiences of delivering in-pharmacy medication reviews for people living with severe and persistent mental illness: a qualitative study. 社区药剂师在为严重顽固性精神病患者提供药房内用药复查时的观点和经验:一项定性研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-03-29 DOI: 10.1007/s11096-024-01720-2
Ricki Ng, Sarira El-Den, Jack C Collins, Sara S McMillan, Jie Hu, Amanda J Wheeler, Claire L O'Reilly

Background: People living with severe and persistent mental illness (SPMI) often take multiple medications and are at risk of experiencing medication related problems. Medication review services have the potential to reduce inappropriate use of psychotropic medications and improve adherence. However, there is limited research regarding pharmacists' perspectives when providing such services.

Aim: To explore community pharmacists' views and experiences of providing an in-pharmacy medication review (MedsCheck) for people living with SPMI.

Method: Semi-structured interviews were conducted between November 2021 and May 2022 with community pharmacists participating in the comparator group of the PharMIbridge Randomised Controlled Trial (RCT), which aimed to improve medication adherence and manage physical health concerns for people living with SPMI. Interviews were recorded, transcribed, and analysed using inductive thematic analysis.

Results: Fifteen semi-structured interviews were conducted with community pharmacists including pharmacy owners, managers and employee pharmacists. Most pharmacist participants who were interviewed (n = 10) were aged under 39 and more than half (n = 8) had 10 or more years of pharmacy experience. Five key themes were identified: 1) Pharmacists' roles in the management of SPMI in community pharmacy; 2) Mental health education and training; 3) Pharmacy resources; 4) Challenges with interprofessional collaboration and 5) Impact on professional relationships and consumer outcomes.

Conclusion: Pharmacists are motivated to support people living with SPMI. Mental health training, as well as arrangements regarding pharmacy workflow and appropriate remuneration are needed to enable pharmacists to better support people living with SPMI. Referral pathways should be directly accessible by community pharmacists to assist interprofessional collaboration.

背景:重度和持续性精神疾病(SPMI)患者通常会服用多种药物,并有可能出现与药物相关的问题。药物审查服务有可能减少精神药物的不当使用,并改善用药依从性。目的:探讨社区药剂师在为 SPMI 患者提供药房内用药检查(MedsCheck)时的观点和经验:在2021年11月至2022年5月期间,对参与PharMIbridge随机对照试验(RCT)比较组的社区药剂师进行了半结构化访谈。对访谈进行了记录、转录,并采用归纳式主题分析法进行了分析:我们对社区药剂师进行了 15 次半结构化访谈,其中包括药店业主、经理和雇员药剂师。大多数参与访谈的药剂师(10 人)年龄在 39 岁以下,超过半数(8 人)拥有 10 年或以上的药店从业经验。我们确定了五个关键主题:1)药剂师在社区药房管理 SPMI 中的角色;2)心理健康教育和培训;3)药房资源;4)跨专业合作面临的挑战;5)对专业关系和消费者结果的影响:结论:药剂师有动力为 SPMI 患者提供支持。为使药剂师能够更好地为 SPMI 患者提供支持,需要对他们进行心理健康培训,并就药房工作流程和适当的薪酬做出安排。社区药剂师应能直接使用转介途径,以协助跨专业合作。
{"title":"Community pharmacists' views and experiences of delivering in-pharmacy medication reviews for people living with severe and persistent mental illness: a qualitative study.","authors":"Ricki Ng, Sarira El-Den, Jack C Collins, Sara S McMillan, Jie Hu, Amanda J Wheeler, Claire L O'Reilly","doi":"10.1007/s11096-024-01720-2","DOIUrl":"10.1007/s11096-024-01720-2","url":null,"abstract":"<p><strong>Background: </strong>People living with severe and persistent mental illness (SPMI) often take multiple medications and are at risk of experiencing medication related problems. Medication review services have the potential to reduce inappropriate use of psychotropic medications and improve adherence. However, there is limited research regarding pharmacists' perspectives when providing such services.</p><p><strong>Aim: </strong>To explore community pharmacists' views and experiences of providing an in-pharmacy medication review (MedsCheck) for people living with SPMI.</p><p><strong>Method: </strong>Semi-structured interviews were conducted between November 2021 and May 2022 with community pharmacists participating in the comparator group of the PharMIbridge Randomised Controlled Trial (RCT), which aimed to improve medication adherence and manage physical health concerns for people living with SPMI. Interviews were recorded, transcribed, and analysed using inductive thematic analysis.</p><p><strong>Results: </strong>Fifteen semi-structured interviews were conducted with community pharmacists including pharmacy owners, managers and employee pharmacists. Most pharmacist participants who were interviewed (n = 10) were aged under 39 and more than half (n = 8) had 10 or more years of pharmacy experience. Five key themes were identified: 1) Pharmacists' roles in the management of SPMI in community pharmacy; 2) Mental health education and training; 3) Pharmacy resources; 4) Challenges with interprofessional collaboration and 5) Impact on professional relationships and consumer outcomes.</p><p><strong>Conclusion: </strong>Pharmacists are motivated to support people living with SPMI. Mental health training, as well as arrangements regarding pharmacy workflow and appropriate remuneration are needed to enable pharmacists to better support people living with SPMI. Referral pathways should be directly accessible by community pharmacists to assist interprofessional collaboration.</p>","PeriodicalId":13828,"journal":{"name":"International Journal of Clinical Pharmacy","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11286626/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140326611","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
Developing a machine learning model for predicting venlafaxine active moiety concentration: a retrospective study using real-world evidence. 开发用于预测文拉法辛活性分子浓度的机器学习模型:一项使用真实世界证据的回顾性研究。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-05-16 DOI: 10.1007/s11096-024-01724-y
Luyao Chang, Xin Hao, Jing Yu, Jinyuan Zhang, Yimeng Liu, Xuxiao Ye, Ze Yu, Fei Gao, Xiaolu Pang, Chunhua Zhou

Background: Venlafaxine is frequently prescribed for patients with depression. To control the concentration of venlafaxine within the therapeutic window for the best treatment effect, a model to predict venlafaxine concentration is necessary.

Aim: Our objective was to develop a prediction model for venlafaxine concentration using real-world evidence based on machine learning and deep learning techniques.

Method: Patients who underwent venlafaxine treatment between November 2019 and August 2022 were included in the study. Important variables affecting venlafaxine concentration were identified using a combination of univariate analysis, sequential forward selection, and machine learning techniques. Predictive performance of nine machine learning and deep learning algorithms were assessed, and the one with the optimal performance was selected for modeling. The final model was interpreted using SHapley Additive exPlanations.

Results: A total of 330 eligible patients were included. Five influential variables that affect venlafaxine concentration were venlafaxine daily dose, sex, age, hyperlipidemia, and adenosine deaminase. The venlafaxine concentration prediction model was developed using the eXtreme Gradient Boosting algorithm (R2 = 0.65, mean absolute error = 77.92, root mean square error = 93.58). In the testing cohort, the accuracy of the predicted concentration within ± 30% of the actual concentration was 73.49%. In the subgroup analysis, the prediction accuracy was 69.39% within the recommended therapeutic range of venlafaxine concentration within ± 30% of the actual value.

Conclusion: The XGBoost model for predicting blood concentration of venlafaxine using real-world evidence was developed, guiding the adjustment of regimen in clinical practice.

背景介绍文拉法辛是抑郁症患者的常用处方药。为了将文拉法辛的浓度控制在治疗窗内以达到最佳治疗效果,有必要建立一个预测文拉法辛浓度的模型。目的:我们的目标是基于机器学习和深度学习技术,利用真实世界的证据建立一个文拉法辛浓度预测模型:研究纳入了2019年11月至2022年8月期间接受文拉法辛治疗的患者。采用单变量分析、顺序前向选择和机器学习技术相结合的方法确定了影响文拉法辛浓度的重要变量。评估了九种机器学习和深度学习算法的预测性能,并选择了性能最优的算法进行建模。最终模型使用SHapley Additive exPlanations进行解释:共纳入了 330 名符合条件的患者。影响文拉法辛浓度的五个影响变量为文拉法辛每日剂量、性别、年龄、高脂血症和腺苷脱氨酶。文拉法辛浓度预测模型是采用极梯度提升算法(R2 = 0.65,平均绝对误差 = 77.92,均方根误差 = 93.58)建立的。在测试组群中,预测浓度在实际浓度± 30% 以内的准确率为 73.49%。在亚组分析中,文拉法辛浓度在实际值±30%以内的推荐治疗范围内的预测准确率为69.39%:利用真实世界的证据建立了预测文拉法辛血药浓度的 XGBoost 模型,为临床实践中调整治疗方案提供了指导。
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引用次数: 0
The influence of patients' beliefs about medicines and the relationship with suboptimal medicine use in community-dwelling older adults: a systematic review of quantitative studies. 患者的用药观念对社区老年人的影响及其与次优用药的关系:定量研究的系统回顾。
IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-01 Epub Date: 2024-05-05 DOI: 10.1007/s11096-024-01727-9
Eman Rafhi, Malath Al-Juhaishi, Ieva Stupans, Julie E Stevens, Joon Soo Park, Kate N Wang

Background: Medication use in older adults is increasing, therefore, reducing the risk of suboptimal medicine use is imperative in achieving optimal therapeutic outcomes. Research suggests that factors such as personal beliefs and beliefs about medicines may be associated with non-adherence and inappropriate medicine use.

Aim: To systematically review and identify quantitative research on the influence of beliefs about medicines and the relationship with suboptimal medicine use in older adults.

Method: Searches were conducted on PubMed, EMBASE, CINAHL, and PsycINFO for quantitative studies (inception to March 2023).

Inclusion criteria: (1) exposure: participants' beliefs (personal, cultural, and medication-related), (2) outcomes: polypharmacy, potentially inappropriate medicines use, or non-adherence, and (3) participants: community-dwelling adults 65 years or above. Study selection, data extraction and quality appraisal (Joanna Briggs Institute critical appraisal checklist) were completed independently by two investigators. Data were combined in a narrative synthesis and presented in a summary of findings table.

Results: Nineteen articles were included: 15 cross-sectional and four cohort studies. Outcomes of included papers were as follows; adherence (n = 18) and potentially inappropriate medicine use (n = 1). Ten studies found stronger beliefs in the necessity of medicines and/or fewer concerns led to better adherence, with one paper contradicting these findings. Three studies did not find associations between adherence and beliefs. One study confirmed an association between unnecessary drug use and a lack of belief in a "powerful other" (e.g. doctor).

Conclusion: Further investigation is necessary to (1) ascertain the importance of necessity or concern beliefs in fostering adherence and, (2) examine the influence of beliefs on polypharmacy and inappropriate medicine use.

背景:老年人的用药量在不断增加,因此,要达到最佳治疗效果,就必须降低次优用药的风险。研究表明,个人信念和对药物的信念等因素可能与不依从性和不适当用药有关。目的:系统回顾并确定有关药物信念的影响以及与老年人次优用药之间关系的定量研究:方法: 在 PubMed、EMBASE、CINAHL 和 PsycINFO 上检索定量研究(开始至 2023 年 3 月):(1) 暴露:参与者的信念(个人、文化和用药相关);(2) 结果:多重用药、潜在用药不当或不依从;(3) 参与者:65 岁或以上居住在社区的成年人。研究选择、数据提取和质量评估(乔安娜-布里格斯研究所关键评估清单)由两名调查人员独立完成。数据以叙述性综述的形式进行合并,并在研究结果摘要表中列出:结果:共纳入 19 篇文章:结果:共纳入 19 篇文章:15 篇横断面研究和 4 篇队列研究。收录论文的结果如下:依从性(18 篇)和潜在用药不当(1 篇)。十项研究发现,对药物必要性的更强信念和/或更少的担忧会导致更好的依从性,有一篇论文与这些研究结果相矛盾。三项研究未发现依从性与信念之间存在关联。一项研究证实,不必要的药物使用与缺乏对 "强大的他人"(如医生)的信念有关:有必要开展进一步调查,以便(1)确定必要性或关注信念在促进坚持用药方面的重要性,以及(2)研究信念对多药疗法和不当用药的影响。
{"title":"The influence of patients' beliefs about medicines and the relationship with suboptimal medicine use in community-dwelling older adults: a systematic review of quantitative studies.","authors":"Eman Rafhi, Malath Al-Juhaishi, Ieva Stupans, Julie E Stevens, Joon Soo Park, Kate N Wang","doi":"10.1007/s11096-024-01727-9","DOIUrl":"10.1007/s11096-024-01727-9","url":null,"abstract":"<p><strong>Background: </strong>Medication use in older adults is increasing, therefore, reducing the risk of suboptimal medicine use is imperative in achieving optimal therapeutic outcomes. Research suggests that factors such as personal beliefs and beliefs about medicines may be associated with non-adherence and inappropriate medicine use.</p><p><strong>Aim: </strong>To systematically review and identify quantitative research on the influence of beliefs about medicines and the relationship with suboptimal medicine use in older adults.</p><p><strong>Method: </strong>Searches were conducted on PubMed, EMBASE, CINAHL, and PsycINFO for quantitative studies (inception to March 2023).</p><p><strong>Inclusion criteria: </strong>(1) exposure: participants' beliefs (personal, cultural, and medication-related), (2) outcomes: polypharmacy, potentially inappropriate medicines use, or non-adherence, and (3) participants: community-dwelling adults 65 years or above. Study selection, data extraction and quality appraisal (Joanna Briggs Institute critical appraisal checklist) were completed independently by two investigators. Data were combined in a narrative synthesis and presented in a summary of findings table.</p><p><strong>Results: </strong>Nineteen articles were included: 15 cross-sectional and four cohort studies. Outcomes of included papers were as follows; adherence (n = 18) and potentially inappropriate medicine use (n = 1). Ten studies found stronger beliefs in the necessity of medicines and/or fewer concerns led to better adherence, with one paper contradicting these findings. Three studies did not find associations between adherence and beliefs. One study confirmed an association between unnecessary drug use and a lack of belief in a \"powerful other\" (e.g. doctor).</p><p><strong>Conclusion: </strong>Further investigation is necessary to (1) ascertain the importance of necessity or concern beliefs in fostering adherence and, (2) examine the influence of beliefs on polypharmacy and inappropriate medicine use.</p>","PeriodicalId":13828,"journal":{"name":"International Journal of Clinical Pharmacy","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11286706/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140854940","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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